Core spliceosomal Sm proteins as constituents of cytoplasmic mRNPs in plants
SUMMARY In recent years, research has increasingly focused on the key role of post‐transcriptional regulation of messenger ribonucleoprotein (mRNP) function and turnover. As a result of the complexity and dynamic nature of mRNPs, the full composition of a single mRNP complex remains unrevealed and m...
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Published in | The Plant journal : for cell and molecular biology Vol. 103; no. 3; pp. 1155 - 1173 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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England
Blackwell Publishing Ltd
01.08.2020
John Wiley and Sons Inc |
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Abstract | SUMMARY
In recent years, research has increasingly focused on the key role of post‐transcriptional regulation of messenger ribonucleoprotein (mRNP) function and turnover. As a result of the complexity and dynamic nature of mRNPs, the full composition of a single mRNP complex remains unrevealed and mRNPs are poorly described in plants. Here we identify canonical Sm proteins as part of the cytoplasmic mRNP complex, indicating their function in the post‐transcriptional regulation of gene expression in plants. Sm proteins comprise an evolutionarily ancient family of small RNA‐binding proteins involved in pre‐mRNA splicing. The latest research indicates that Sm could also impact on mRNA at subsequent stages of its life cycle. In this work we show that in the microsporocyte cytoplasm of Larix decidua, the European larch, Sm proteins accumulate within distinct cytoplasmic bodies, also containing polyadenylated RNA. To date, several types of cytoplasmic bodies involved in the post‐transcriptional regulation of gene expression have been described, mainly in animal cells. Their role and molecular composition in plants remain less well established, however. A total of 222 mRNA transcripts have been identified as cytoplasmic partners for Sm proteins. The specific colocalization of these mRNAs with Sm proteins within cytoplasmic bodies has been confirmed via microscopic analysis. The results from this work support the hypothesis, that evolutionarily conserved Sm proteins have been adapted to perform a whole repertoire of functions related to the post‐transcriptional regulation of gene expression in Eukaryota. This adaptation presumably enabled them to coordinate the interdependent processes of splicing element assembly, mRNA maturation and processing, and mRNA translation regulation, and its degradation.
Significance Statement
The study reports the cyclic occurrence of cytoplasmic mRNP accumulations enriched in canonical Sm proteins but not in other spliceosomal components in Larix decidua microsporocytes. Based on transcriptomic analysis, 222 mRNAs were identified as cytoplasmic partners for Sm proteins, which were linked to many gene ontology terms. The results presented show that S‐bodies constitute newly described cytoplasmic domains involved in the post‐transcriptional regulation of highly expressed transcripts, particularly in cells in which mRNA synthesis occurs in transcriptional bursts. |
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AbstractList | In recent years, research has increasingly focused on the key role of post-transcriptional regulation of messenger ribonucleoprotein (mRNP) function and turnover. As a result of the complexity and dynamic nature of mRNPs, the full composition of a single mRNP complex remains unrevealed and mRNPs are poorly described in plants. Here we identify canonical Sm proteins as part of the cytoplasmic mRNP complex, indicating their function in the post-transcriptional regulation of gene expression in plants. Sm proteins comprise an evolutionarily ancient family of small RNA-binding proteins involved in pre-mRNA splicing. The latest research indicates that Sm could also impact on mRNA at subsequent stages of its life cycle. In this work we show that in the microsporocyte cytoplasm of Larix decidua, the European larch, Sm proteins accumulate within distinct cytoplasmic bodies, also containing polyadenylated RNA. To date, several types of cytoplasmic bodies involved in the post-transcriptional regulation of gene expression have been described, mainly in animal cells. Their role and molecular composition in plants remain less well established, however. A total of 222 mRNA transcripts have been identified as cytoplasmic partners for Sm proteins. The specific colocalization of these mRNAs with Sm proteins within cytoplasmic bodies has been confirmed via microscopic analysis. The results from this work support the hypothesis, that evolutionarily conserved Sm proteins have been adapted to perform a whole repertoire of functions related to the post-transcriptional regulation of gene expression in Eukaryota. This adaptation presumably enabled them to coordinate the interdependent processes of splicing element assembly, mRNA maturation and processing, and mRNA translation regulation, and its degradation. SUMMARYIn recent years, research has increasingly focused on the key role of post‐transcriptional regulation of messenger ribonucleoprotein (mRNP) function and turnover. As a result of the complexity and dynamic nature of mRNPs, the full composition of a single mRNP complex remains unrevealed and mRNPs are poorly described in plants. Here we identify canonical Sm proteins as part of the cytoplasmic mRNP complex, indicating their function in the post‐transcriptional regulation of gene expression in plants. Sm proteins comprise an evolutionarily ancient family of small RNA‐binding proteins involved in pre‐mRNA splicing. The latest research indicates that Sm could also impact on mRNA at subsequent stages of its life cycle. In this work we show that in the microsporocyte cytoplasm of Larix decidua, the European larch, Sm proteins accumulate within distinct cytoplasmic bodies, also containing polyadenylated RNA. To date, several types of cytoplasmic bodies involved in the post‐transcriptional regulation of gene expression have been described, mainly in animal cells. Their role and molecular composition in plants remain less well established, however. A total of 222 mRNA transcripts have been identified as cytoplasmic partners for Sm proteins. The specific colocalization of these mRNAs with Sm proteins within cytoplasmic bodies has been confirmed via microscopic analysis. The results from this work support the hypothesis, that evolutionarily conserved Sm proteins have been adapted to perform a whole repertoire of functions related to the post‐transcriptional regulation of gene expression in Eukaryota. This adaptation presumably enabled them to coordinate the interdependent processes of splicing element assembly, mRNA maturation and processing, and mRNA translation regulation, and its degradation. SUMMARY In recent years, research has increasingly focused on the key role of post‐transcriptional regulation of messenger ribonucleoprotein (mRNP) function and turnover. As a result of the complexity and dynamic nature of mRNPs, the full composition of a single mRNP complex remains unrevealed and mRNPs are poorly described in plants. Here we identify canonical Sm proteins as part of the cytoplasmic mRNP complex, indicating their function in the post‐transcriptional regulation of gene expression in plants. Sm proteins comprise an evolutionarily ancient family of small RNA‐binding proteins involved in pre‐mRNA splicing. The latest research indicates that Sm could also impact on mRNA at subsequent stages of its life cycle. In this work we show that in the microsporocyte cytoplasm of Larix decidua, the European larch, Sm proteins accumulate within distinct cytoplasmic bodies, also containing polyadenylated RNA. To date, several types of cytoplasmic bodies involved in the post‐transcriptional regulation of gene expression have been described, mainly in animal cells. Their role and molecular composition in plants remain less well established, however. A total of 222 mRNA transcripts have been identified as cytoplasmic partners for Sm proteins. The specific colocalization of these mRNAs with Sm proteins within cytoplasmic bodies has been confirmed via microscopic analysis. The results from this work support the hypothesis, that evolutionarily conserved Sm proteins have been adapted to perform a whole repertoire of functions related to the post‐transcriptional regulation of gene expression in Eukaryota. This adaptation presumably enabled them to coordinate the interdependent processes of splicing element assembly, mRNA maturation and processing, and mRNA translation regulation, and its degradation. Significance Statement The study reports the cyclic occurrence of cytoplasmic mRNP accumulations enriched in canonical Sm proteins but not in other spliceosomal components in Larix decidua microsporocytes. Based on transcriptomic analysis, 222 mRNAs were identified as cytoplasmic partners for Sm proteins, which were linked to many gene ontology terms. The results presented show that S‐bodies constitute newly described cytoplasmic domains involved in the post‐transcriptional regulation of highly expressed transcripts, particularly in cells in which mRNA synthesis occurs in transcriptional bursts. In recent years, research has increasingly focused on the key role of post‐transcriptional regulation of messenger ribonucleoprotein (mRNP) function and turnover. As a result of the complexity and dynamic nature of mRNPs, the full composition of a single mRNP complex remains unrevealed and mRNPs are poorly described in plants. Here we identify canonical Sm proteins as part of the cytoplasmic mRNP complex, indicating their function in the post‐transcriptional regulation of gene expression in plants. Sm proteins comprise an evolutionarily ancient family of small RNA‐binding proteins involved in pre‐mRNA splicing. The latest research indicates that Sm could also impact on mRNA at subsequent stages of its life cycle. In this work we show that in the microsporocyte cytoplasm of Larix decidua , the European larch, Sm proteins accumulate within distinct cytoplasmic bodies, also containing polyadenylated RNA. To date, several types of cytoplasmic bodies involved in the post‐transcriptional regulation of gene expression have been described, mainly in animal cells. Their role and molecular composition in plants remain less well established, however. A total of 222 mRNA transcripts have been identified as cytoplasmic partners for Sm proteins. The specific colocalization of these mRNAs with Sm proteins within cytoplasmic bodies has been confirmed via microscopic analysis. The results from this work support the hypothesis, that evolutionarily conserved Sm proteins have been adapted to perform a whole repertoire of functions related to the post‐transcriptional regulation of gene expression in Eukaryota. This adaptation presumably enabled them to coordinate the interdependent processes of splicing element assembly, mRNA maturation and processing, and mRNA translation regulation, and its degradation. The study reports the cyclic occurrence of cytoplasmic mRNP accumulations enriched in canonical Sm proteins but not in other spliceosomal components in Larix decidua microsporocytes. Based on transcriptomic analysis, 222 mRNAs were identified as cytoplasmic partners for Sm proteins, which were linked to many gene ontology terms. The results presented show that S‐bodies constitute newly described cytoplasmic domains involved in the post‐transcriptional regulation of highly expressed transcripts, particularly in cells in which mRNA synthesis occurs in transcriptional bursts. In recent years, research has increasingly focused on the key role of post-transcriptional regulation of messenger ribonucleoprotein (mRNP) function and turnover. As a result of the complexity and dynamic nature of mRNPs, the full composition of a single mRNP complex remains unrevealed and mRNPs are poorly described in plants. Here we identify canonical Sm proteins as part of the cytoplasmic mRNP complex, indicating their function in the post-transcriptional regulation of gene expression in plants. Sm proteins comprise an evolutionarily ancient family of small RNA-binding proteins involved in pre-mRNA splicing. The latest research indicates that Sm could also impact on mRNA at subsequent stages of its life cycle. In this work we show that in the microsporocyte cytoplasm of Larix decidua, the European larch, Sm proteins accumulate within distinct cytoplasmic bodies, also containing polyadenylated RNA. To date, several types of cytoplasmic bodies involved in the post-transcriptional regulation of gene expression have been described, mainly in animal cells. Their role and molecular composition in plants remain less well established, however. A total of 222 mRNA transcripts have been identified as cytoplasmic partners for Sm proteins. The specific colocalization of these mRNAs with Sm proteins within cytoplasmic bodies has been confirmed via microscopic analysis. The results from this work support the hypothesis, that evolutionarily conserved Sm proteins have been adapted to perform a whole repertoire of functions related to the post-transcriptional regulation of gene expression in Eukaryota. This adaptation presumably enabled them to coordinate the interdependent processes of splicing element assembly, mRNA maturation and processing, and mRNA translation regulation, and its degradation.In recent years, research has increasingly focused on the key role of post-transcriptional regulation of messenger ribonucleoprotein (mRNP) function and turnover. As a result of the complexity and dynamic nature of mRNPs, the full composition of a single mRNP complex remains unrevealed and mRNPs are poorly described in plants. Here we identify canonical Sm proteins as part of the cytoplasmic mRNP complex, indicating their function in the post-transcriptional regulation of gene expression in plants. Sm proteins comprise an evolutionarily ancient family of small RNA-binding proteins involved in pre-mRNA splicing. The latest research indicates that Sm could also impact on mRNA at subsequent stages of its life cycle. In this work we show that in the microsporocyte cytoplasm of Larix decidua, the European larch, Sm proteins accumulate within distinct cytoplasmic bodies, also containing polyadenylated RNA. To date, several types of cytoplasmic bodies involved in the post-transcriptional regulation of gene expression have been described, mainly in animal cells. Their role and molecular composition in plants remain less well established, however. A total of 222 mRNA transcripts have been identified as cytoplasmic partners for Sm proteins. The specific colocalization of these mRNAs with Sm proteins within cytoplasmic bodies has been confirmed via microscopic analysis. The results from this work support the hypothesis, that evolutionarily conserved Sm proteins have been adapted to perform a whole repertoire of functions related to the post-transcriptional regulation of gene expression in Eukaryota. This adaptation presumably enabled them to coordinate the interdependent processes of splicing element assembly, mRNA maturation and processing, and mRNA translation regulation, and its degradation. |
Author | Smoliński, Dariusz Jan Kołowerzo‐Lubnau, Agnieszka Gołębiewski, Marcin Hyjek‐Składanowska, Malwina Jarmołowski, Artur Nuc, Przemysław Bajczyk, Mateusz |
AuthorAffiliation | 1 Department of Cellular and Molecular Biology Nicolaus Copernicus Univeristy Lwowska 1 87‐100 Torun Poland 3 Department of Gene Expression Institute of Molecular Biology and Biotechnology Adam Mickiewicz University Umultowska 89 Poznan 61‐614 Poland 5 Present address: Laboratory of Protein Structure International Institute of Molecular and Cell Biology 4 Trojdena St. 02‐109 Warsaw Poland 2 Centre For Modern Interdisciplinary Technologies Nicolaus Copernicus University Wilenska 4 87‐100 Torun Poland 4 Department of Plant Physiology and Biotechnology Nicolaus Copernicus Univeristy Lwowska 1 87‐100 Torun Poland |
AuthorAffiliation_xml | – name: 3 Department of Gene Expression Institute of Molecular Biology and Biotechnology Adam Mickiewicz University Umultowska 89 Poznan 61‐614 Poland – name: 1 Department of Cellular and Molecular Biology Nicolaus Copernicus Univeristy Lwowska 1 87‐100 Torun Poland – name: 4 Department of Plant Physiology and Biotechnology Nicolaus Copernicus Univeristy Lwowska 1 87‐100 Torun Poland – name: 2 Centre For Modern Interdisciplinary Technologies Nicolaus Copernicus University Wilenska 4 87‐100 Torun Poland – name: 5 Present address: Laboratory of Protein Structure International Institute of Molecular and Cell Biology 4 Trojdena St. 02‐109 Warsaw Poland |
Author_xml | – sequence: 1 givenname: Malwina orcidid: 0000-0001-8276-4845 surname: Hyjek‐Składanowska fullname: Hyjek‐Składanowska, Malwina email: mhyjek@iimcb.gov.pl organization: Nicolaus Copernicus University – sequence: 2 givenname: Mateusz orcidid: 0000-0001-7043-2827 surname: Bajczyk fullname: Bajczyk, Mateusz organization: Adam Mickiewicz University – sequence: 3 givenname: Marcin orcidid: 0000-0003-2039-8733 surname: Gołębiewski fullname: Gołębiewski, Marcin organization: Nicolaus Copernicus Univeristy – sequence: 4 givenname: Przemysław orcidid: 0000-0002-8380-1166 surname: Nuc fullname: Nuc, Przemysław organization: Adam Mickiewicz University – sequence: 5 givenname: Agnieszka orcidid: 0000-0002-1337-6715 surname: Kołowerzo‐Lubnau fullname: Kołowerzo‐Lubnau, Agnieszka organization: Nicolaus Copernicus University – sequence: 6 givenname: Artur orcidid: 0000-0002-1073-146X surname: Jarmołowski fullname: Jarmołowski, Artur organization: Adam Mickiewicz University – sequence: 7 givenname: Dariusz Jan orcidid: 0000-0002-8272-0196 surname: Smoliński fullname: Smoliński, Dariusz Jan email: darsmol@umk.pl organization: Nicolaus Copernicus University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32369637$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1016/j.ydbio.2008.07.008 10.1371/journal.pgen.1002527 10.1016/j.ydbio.2005.12.011 10.1105/tpc.112.103697 10.1016/0092-8674(86)90072-3 10.1093/molbev/msn175 10.1128/MCB.17.7.3702 10.1007/s00412-011-0339-4 10.4161/psb.26955 10.1371/journal.pbio.0020079 10.3389/fpls.2014.00201 10.1093/emboj/19.7.1661 10.1016/S1097-2765(02)00559-2 10.1128/MCB.19.6.4311 10.1093/emboj/18.20.5789 10.1016/j.tig.2018.09.006 10.1093/nar/gkn176 10.4161/cc.2.5.491 10.1093/jxb/erv399 10.1016/j.molcel.2010.03.014 10.1007/s00709-007-0270-y 10.1371/journal.ppat.1000767 10.1016/j.molcel.2007.02.011 10.1007/s00299-008-0579-9 10.1038/nature12349 10.4161/psb.5.2.10988 10.1016/j.bbapap.2016.02.015 10.1101/gad.1390306 10.1073/pnas.0509260103 10.1093/emboj/20.1.187 10.1073/pnas.1432104100 10.1099/vir.0.2008/002139-0 10.1105/tpc.15.01045 10.1105/tpc.109.070078 10.1016/j.bbamcr.2008.07.025 10.1046/j.1365-2958.2003.03793.x 10.1083/jcb.200502088 10.1093/emboj/16.18.5752 10.1158/0008-5472.CAN-05-3459 10.1002/wrna.1403 10.1371/journal.pone.0117337 10.1002/pld3.12 10.1007/s00412-006-0056-6 10.1016/j.molcel.2004.10.013 10.1007/s00018-007-7447-6 10.1038/43694 10.1105/tpc.106.047605 10.1186/1471-2229-10-44 10.1038/ncb1265 10.1093/emboj/21.11.2746 10.1186/gb-2006-7-11-r113 10.1093/nar/gkr1215 10.1104/pp.17.01468 10.1091/mbc.E11-06-0511 10.1038/nmeth.2089 10.1007/s00418-011-0861-8 10.1186/1471-2164-6-75 10.1016/j.jmb.2013.01.039 10.1101/gad.1282305 10.1002/mrd.1080260209 10.1242/jcs.107.12.3521 10.1242/jcs.01692 10.1111/mmi.12819 10.1261/rna.2340405 10.1111/j.1365-2818.2006.01706.x 10.1110/ps.0224703 10.1111/j.1601-5223.1976.tb01557.x 10.1101/gad.939502 10.1073/pnas.0704977104 10.1007/s00018-004-4190-0 10.1038/nbt.1883 10.1186/gb-2014-15-1-r7 10.1093/nar/gkx1120 10.1016/j.tcb.2016.05.004 10.1016/j.yexcr.2004.05.016 10.1016/j.ydbio.2009.05.553 10.1371/journal.pbio.0040210 10.1261/rna.035469.112 10.1002/wrna.1369 10.1111/j.1365-313X.2008.03623.x 10.1093/emboj/cdg394 10.1038/nature09479 10.1128/MCB.19.10.6554 10.1038/nsmb.2640 10.1007/BF00414179 10.1016/j.cell.2012.05.029 10.1038/nrg2111 10.1073/pnas.1314851111 10.1016/S1097-2765(01)00233-7 10.1038/nature10924 10.1017/S1355838200991957 10.1126/science.1082320 10.1016/S0960-9822(02)01111-9 10.1242/jcs.152975 10.1101/557900 10.1016/j.molcel.2009.11.020 10.1101/cshperspect.a012286 10.1002/j.1460-2075.1995.tb07199.x 10.1007/s00709-009-0042-y 10.3410/B4-16 10.1371/journal.pone.0022463 10.1093/bioinformatics/btr026 10.1016/S0925-4773(03)00181-3 10.3389/fpls.2017.01235 10.1111/nph.15690 10.1242/dev.095034 10.1073/pnas.0906498106 10.1007/s00441-011-1145-2 10.1105/tpc.110.081059 10.1080/07391102.2011.10508593 10.1093/jxb/erw373 10.1105/tpc.114.134494 10.1186/1742-4690-10-55 10.1093/humrep/der176 10.1126/science.1090095 10.1073/pnas.1900084116 10.1101/gad.286404 10.1007/978-1-4939-2444-8_10 10.1016/j.phytochem.2014.01.015 10.1091/mbc.e04-02-0116 10.1371/journal.pone.0045966 10.1093/emboj/cdf322 10.1016/j.biocel.2009.11.018 10.1016/0022-2836(88)90312-9 10.1186/gb-2012-13-3-r17 10.1080/07352689.2011.645431 10.1016/j.jprot.2013.07.010 10.1016/j.pbi.2010.10.003 10.1042/BST0330433 10.1016/j.tibs.2005.07.006 10.1242/dev.042721 10.1104/pp.105.065649 |
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Keywords | stress granules P-bodies cytoplasmic bodies RIP-seq mRNP cajal bodies |
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PublicationTitle | The Plant journal : for cell and molecular biology |
PublicationTitleAlternate | Plant J |
PublicationYear | 2020 |
Publisher | Blackwell Publishing Ltd John Wiley and Sons Inc |
Publisher_xml | – name: Blackwell Publishing Ltd – name: John Wiley and Sons Inc |
References | 2002; 16 2007; 104 1993; 24 2010; 10 2012; 121 2012; 484 2010; 468 2002; 12 2008; 36 2006; 291 2004; 2 2012; 13 2003; 50 2013; 8 2009; 236 2018; 46 2004; 299 2014; 127 2018; 176 2000; 19 2006; 20 2008; 27 2007; 8 2008; 25 2014; 15 2018; 34 2012; 24 2014; 94 2010; 5 2010; 6 1994; 278 2011; 136 2010; 38 2002; 9 2013; 91 2005; 118 2009; 332 2008; 56 2006; 115 2011; 6 2012; 31 2019; 222 2001; 20 2010; 42 2005; 19 1990; 26 2015; 66 2005; 7 2005; 6 2016; 28 2016; 26 2005; 11 2003; 100 2015; 1284 2016; 8 2006; 224 2006; 103 2003; 22 2012; 40 2009; 106 2017; 8 2017; 1 2004; 61 2000; 6 2013; 20 2017; 45 2005; 139 2011; 14 1999; 401 2003; 12 2013; 19 2014; 5 2013; 10 1999; 19 1999; 18 2006; 66 1986; 46 2003; 2 2019; 116 2005; 30 1997; 17 2011; 22 1997; 16 2008; 65 2011; 23 2011; 26 2011; 28 2011; 27 1994; 107 2011; 29 2005; 33 2007; 25 2003; 120 2009; 21 1995; 14 1976; 82 2013; 425 2015; 10 2006; 7 2008 2006; 18 2016; 1864 2006; 4 2013; 140 2008; 323 2014; 111 2012; 150 2009; 36 2011; 344 2015; 27 2008; 1783 2001; 7 2004; 18 2004; 16 2005; 169 2004; 15 2010; 137 2007; 232 2002; 21 2019 2013; 499 2008; 89 1988; 199 2003; 302 2012; 7 2014; 100 2012; 4 2003; 300 2012; 8 2016; 67 2012; 9 e_1_2_9_75_1 e_1_2_9_98_1 e_1_2_9_52_1 Cordelières F.P. (e_1_2_9_32_1) 2008 e_1_2_9_79_1 e_1_2_9_94_1 e_1_2_9_10_1 e_1_2_9_56_1 e_1_2_9_33_1 e_1_2_9_90_1 e_1_2_9_71_1 e_1_2_9_103_1 e_1_2_9_126_1 e_1_2_9_107_1 e_1_2_9_122_1 e_1_2_9_14_1 e_1_2_9_37_1 e_1_2_9_18_1 e_1_2_9_41_1 e_1_2_9_64_1 e_1_2_9_87_1 e_1_2_9_22_1 e_1_2_9_45_1 e_1_2_9_68_1 e_1_2_9_83_1 e_1_2_9_6_1 e_1_2_9_119_1 e_1_2_9_60_1 e_1_2_9_2_1 Knop K. (e_1_2_9_66_1) 2017; 45 e_1_2_9_111_1 e_1_2_9_134_1 e_1_2_9_115_1 e_1_2_9_26_1 e_1_2_9_49_1 e_1_2_9_130_1 e_1_2_9_30_1 e_1_2_9_53_1 e_1_2_9_99_1 e_1_2_9_72_1 e_1_2_9_34_1 e_1_2_9_57_1 e_1_2_9_95_1 e_1_2_9_76_1 e_1_2_9_91_1 e_1_2_9_102_1 e_1_2_9_129_1 e_1_2_9_106_1 e_1_2_9_125_1 e_1_2_9_15_1 e_1_2_9_38_1 e_1_2_9_121_1 e_1_2_9_19_1 e_1_2_9_42_1 e_1_2_9_88_1 e_1_2_9_61_1 e_1_2_9_46_1 e_1_2_9_84_1 e_1_2_9_23_1 e_1_2_9_65_1 e_1_2_9_80_1 e_1_2_9_5_1 e_1_2_9_114_1 e_1_2_9_118_1 e_1_2_9_133_1 e_1_2_9_9_1 e_1_2_9_27_1 e_1_2_9_69_1 e_1_2_9_110_1 e_1_2_9_31_1 e_1_2_9_50_1 e_1_2_9_73_1 e_1_2_9_35_1 e_1_2_9_77_1 e_1_2_9_96_1 e_1_2_9_12_1 e_1_2_9_54_1 e_1_2_9_92_1 e_1_2_9_109_1 e_1_2_9_101_1 e_1_2_9_128_1 e_1_2_9_105_1 e_1_2_9_124_1 e_1_2_9_39_1 e_1_2_9_120_1 e_1_2_9_16_1 e_1_2_9_58_1 Baserga S.J. (e_1_2_9_11_1) 1993; 24 e_1_2_9_20_1 e_1_2_9_62_1 e_1_2_9_89_1 e_1_2_9_24_1 e_1_2_9_43_1 e_1_2_9_85_1 e_1_2_9_8_1 e_1_2_9_81_1 e_1_2_9_4_1 e_1_2_9_113_1 e_1_2_9_117_1 e_1_2_9_136_1 e_1_2_9_28_1 e_1_2_9_47_1 e_1_2_9_132_1 e_1_2_9_74_1 e_1_2_9_51_1 e_1_2_9_78_1 e_1_2_9_13_1 e_1_2_9_55_1 e_1_2_9_97_1 e_1_2_9_93_1 e_1_2_9_108_1 e_1_2_9_70_1 e_1_2_9_127_1 e_1_2_9_100_1 e_1_2_9_123_1 e_1_2_9_104_1 e_1_2_9_17_1 e_1_2_9_36_1 e_1_2_9_59_1 e_1_2_9_63_1 e_1_2_9_40_1 e_1_2_9_21_1 e_1_2_9_67_1 e_1_2_9_44_1 e_1_2_9_86_1 e_1_2_9_7_1 e_1_2_9_82_1 e_1_2_9_3_1 e_1_2_9_112_1 e_1_2_9_116_1 e_1_2_9_135_1 e_1_2_9_25_1 e_1_2_9_131_1 e_1_2_9_48_1 e_1_2_9_29_1 |
References_xml | – volume: 300 start-page: 805 year: 2003 end-page: 808 article-title: Decapping and decay of messenger RNA occur in cytoplasmic processing bodies publication-title: Science – volume: 89 start-page: 2339 year: 2008 end-page: 2348 article-title: Arabidopsis thaliana class II poly(A)‐binding proteins are required for efficient multiplication of turnip mosaic virus publication-title: J. Gen. Virol. – volume: 127 start-page: 4443 year: 2014 end-page: 4456 article-title: Quantifying mRNA targeting to P bodies in living human cells reveals a dual role in mRNA decay and storage publication-title: J. Cell Sci. – volume: 323 start-page: 76 year: 2008 end-page: 87 article-title: Processing bodies and germ granules are distinct RNA granules that interact in C. elegans embryos publication-title: Dev. Biol. – volume: 28 start-page: 426 year: 2016 end-page: 438 article-title: The nuclear ribonucleoprotein SmD1 interplays with splicing, RNA quality control and post‐transcriptional gene silencing in Arabidopsis publication-title: Plant Cell – volume: 4 start-page: 16 year: 2012 article-title: Spatial regulation of translation through RNA localization publication-title: F1000 Biol. Rep. – volume: 36 start-page: 3420 year: 2008 end-page: 3435 article-title: High‐throughput functional annotation and data mining with the Blast2GO suite publication-title: Nucleic Acids Res. – volume: 22 start-page: 4283 year: 2003 end-page: 4293 article-title: A common sequence motif determines the Cajal body‐specific localization of box H/ACA scaRNAs publication-title: EMBO J. – volume: 7 year: 2012 article-title: mRNA decay proteins are targeted to poly(A)+ RNA and dsRNA‐containing cytoplasmic foci that resemble P‐bodies in Entamoeba histolytica publication-title: PLoS ONE – volume: 232 start-page: 109 year: 2007 end-page: 120 article-title: Additional nucleoli and NOR activity during meiotic prophase I in larch (Larix decidua Mill.) publication-title: Protoplasma – volume: 8 year: 2013 article-title: The crosstalk between plant microRNA biogenesis factors and the spliceosome publication-title: Plant Signal. Behav. – volume: 15 start-page: R7 year: 2014 article-title: RIP‐seq analysis of eukaryotic Sm proteins identifies three major categories of Sm‐containing ribonucleoproteins publication-title: Genome Biol. – volume: 278 start-page: 363 year: 1994 end-page: 378 article-title: The immunolocalization of small nuclear ribonucleoprotein particles in testicular cells during the cycle of the seminiferous epithelium of the adult rat publication-title: Cell. Tissue. Res. – volume: 401 start-page: 177 year: 1999 end-page: 180 article-title: Saccharomyces cerevisiae telomerase is an Sm small nuclear ribonucleoprotein particle publication-title: Nature – volume: 104 start-page: 11655 year: 2007 end-page: 11659 article-title: U bodies are cytoplasmic structures that contain uridine‐rich small nuclear ribonucleoproteins and associate with P bodies publication-title: Proc. Natl. Acad. Sci. USA – volume: 19 start-page: 351 year: 2005 end-page: 361 article-title: Recruitment and activation of mRNA decay enzymes by two ARE‐mediated decay activation domains in the proteins TTP and BRF‐1 publication-title: Genes Dev. – volume: 2 start-page: 412 year: 2003 end-page: 414 article-title: HuR in the mammalian genotoxic response: post‐transcriptional multitasking publication-title: Cell Cycle – volume: 20 start-page: 923 year: 2013 end-page: 928 article-title: Polyadenylation site‐induced decay of upstream transcripts enforces promoter directionality publication-title: Nat. Struct. Mol. Biol. – volume: 499 start-page: 360 year: 2013 end-page: 363 article-title: Promoter directionality is controlled by U1 snRNP and polyadenylation signals publication-title: Nature – volume: 65 start-page: 798 year: 2008 end-page: 813 article-title: Post‐transcriptional gene regulation: From genome‐wide studies to principles publication-title: Cell. Mol. Life Sci. – volume: 7 start-page: 633 year: 2005 end-page: 636 article-title: Argonaute 2/RISC resides in sites of mammalian mRNA decay known as cytoplasmic bodies publication-title: Nat. Cell Biol. – volume: 8 year: 2012 article-title: Sequestration of highly expressed mrRNAs in cytoplasmic granules, P‐bodies, and stress granules enhances cell viability publication-title: PLoS Genet. – volume: 19 start-page: 36 year: 2013 end-page: 50 article-title: The association of a La module with the PABP‐interacting motif PAM2 is a recurrent evolutionary process that led to the neofunctionalization of La‐related proteins publication-title: RNA – volume: 82 start-page: 193 year: 1976 end-page: 204 article-title: A new look on the role of the diffuse stage in problems of plant and animal meiosis publication-title: Hereditas – volume: 16 start-page: 587 year: 2004 end-page: 596 article-title: SMG7 acts as a molecular link between mRNA surveillance and mRNA decay publication-title: Mol. Cell – volume: 46 start-page: 905 year: 1986 end-page: 911 article-title: Cap trimethylation of U snRNA is cytoplasmic and dependent on U snRNP protein binding publication-title: Cell – volume: 11 start-page: 717 year: 2005 end-page: 727 article-title: A role for eIF4E and eIF4E‐transporter in targeting mRNPs to mammalian processing bodies publication-title: RNA – volume: 61 start-page: 2560 year: 2004 end-page: 2570 article-title: The special Sm core structure of the U7 snRNP: far‐reaching significance of a small nuclear ribonucleoprotein publication-title: Cell. Mol. Life Sci. – volume: 6 year: 2010 article-title: Universal features of post‐transcriptional gene regulation are critical for Plasmodium zygote development publication-title: PLoS Pathog. – volume: 19 start-page: 4311 year: 1999 end-page: 4323 article-title: Evidence that tristetraprolin binds to AU‐rich elements and promotes the deadenylation and destabilization of tumor necrosis factor alpha mRNA publication-title: Mol. Cell. Biol. – volume: 291 start-page: 132 year: 2006 end-page: 143 article-title: The Sm proteins regulate germ cell specification during early C. elegans embryogenesis publication-title: Dev. Biol. – volume: 50 start-page: 1605 year: 2003 end-page: 1615 article-title: Ssh10b, a conserved thermophilic archaeal protein, binds RNA in vivo publication-title: Mol. Microbiol. – volume: 15 start-page: 2842 year: 2004 end-page: 2852 article-title: An Lsm2–Lsm7 Complex in Saccharomyces cerevisiae Associates with the Small Nucleolar RNA snR5 publication-title: Mol. Biol. Cell – volume: 2 start-page: 0342 year: 2004 end-page: 0354 article-title: Extensive association of functionally and cytotopically related mRNAs with Puf family RNA‐binding proteins in yeast publication-title: PLoS Biol. – volume: 18 start-page: 5789 year: 1999 end-page: 5802 article-title: A doughnut‐shaped heteromer of human Sm‐like proteins binds to the 3’‐end of U6 snRNA, thereby facilitating U4/U6 duplex formation in vitro publication-title: EMBO J. – volume: 30 start-page: 522 year: 2005 end-page: 528 article-title: LSm proteins form heptameric rings that bind to RNA via repeating motifs publication-title: Trends Biochem. Sci. – volume: 91 start-page: 210 year: 2013 end-page: 225 article-title: Global proteomic analysis in trypanosomes reveals unique proteins and conserved cellular processes impacted by arginine methylation publication-title: J. Proteomics – volume: 14 start-page: 88 year: 2011 end-page: 93 article-title: Processing bodies and plant development publication-title: Curr. Opin. Plant Biol. – volume: 425 start-page: 1287 year: 2013 end-page: 1301 article-title: Toxoplasma gondii Alba proteins are involved in translational control of gene expression publication-title: J. Mol. Biol. – volume: 23 start-page: 534 year: 2011 end-page: 549 article-title: The R2R3 MYB transcription factor DUO1 activates a male germline‐specific regulon essential for sperm cell differentiation in Arabidopsis publication-title: Plant Cell – volume: 302 start-page: 1212 year: 2003 end-page: 1215 article-title: CLIP identifies Nova‐regulated RNA networks in the brain publication-title: Science – volume: 176 start-page: 254 year: 2018 end-page: 269 article-title: Polysomes, stress granules, and processing bodies: a dynamic triumvirate controlling cytoplasmic mRNA fate and function publication-title: Plant Physiol. – volume: 344 start-page: 169 year: 2011 end-page: 181 article-title: Nuage morphogenesis becomes more complex: two translocation pathways and two forms of nuage coexist in Drosophila germline syncytia publication-title: Cell Tissue Res. – volume: 16 start-page: 5752 year: 1997 end-page: 5763 article-title: The HIV‐1 5’ LTR poly (A) site is inactivated by U1 snRNP interaction with the downstream major splice donor site publication-title: EMBO J. – volume: 139 start-page: 138 year: 2005 end-page: 150 article-title: Novel CIPK1‐associated proteins in Arabidopsis contain an evolutionarily conserved C‐terminal region that mediates nuclear localization publication-title: Plant Physiol. – volume: 21 start-page: 3270 year: 2009 end-page: 3279 article-title: Arabidopsis decapping 5 is required for mRNA decapping, P‐body formation, and translational repression during postembryonic development publication-title: Plant Cell – volume: 27 start-page: 1687 year: 2008 end-page: 1696 article-title: Development of male gametophyte of Larix leptolepis Gord. with emphasis on diffuse stage of meiosis publication-title: Plant Cell Rep. – volume: 25 start-page: 635 year: 2007 end-page: 646 article-title: P bodies and the control of mRNA translation and degradation publication-title: Mol. Cell – volume: 20 start-page: 531 year: 2006 end-page: 536 article-title: Human telomerase and Cajal body ribonucleoproteins share a unique specificity of Sm protein association publication-title: Genes Dev. – volume: 10 start-page: 55 year: 2013 article-title: U1snRNP‐mediated suppression of polyadenylation in conjunction with the RNA structure controls poly (A) site selection in foamy viruses publication-title: Retrovirology – volume: 26 start-page: 668 year: 2016 end-page: 679 article-title: Principles and properties of stress granules publication-title: Trends Cell Biol. – volume: 40 start-page: 3066 year: 2012 end-page: 3077 article-title: PfAlbas constitute a new eukaryotic DNA/RNA‐binding protein family in malaria parasites publication-title: Nucleic Acids Res. – volume: 1284 start-page: 209 year: 2015 end-page: 219 article-title: Rapid immunopurification of ribonucleoprotein complexes of plants publication-title: Methods Mol. Biol. – volume: 29 start-page: 644 year: 2011 end-page: 652 article-title: Full‐length transcriptome assembly from RNA‐Seq data without a reference genome publication-title: Nat. Biotechnol. – volume: 56 start-page: 517 year: 2008 end-page: 530 article-title: Plant stress granules and mRNA processing bodies are distinct from heat stress granules publication-title: Plant J. – volume: 45 start-page: 2757 year: 2017 end-page: 2775 article-title: Active 5 splice sites regulate the biogenesis efficiency of Arabidopsis microRNAs derived from intron‐containing genes publication-title: Nucleic Acids Res. – volume: 150 start-page: 53 year: 2012 end-page: 64 article-title: U1 snRNP determines mRNA length and regulates isoform expression publication-title: Cell – volume: 6 year: 2011 article-title: Alba‐domain proteins of trypanosoma brucei are cytoplasmic RNA‐Binding proteins that interact with the translation machinery publication-title: PLoS ONE – volume: 332 start-page: 142 year: 2009 end-page: 155 article-title: The spinal muscular atrophy protein SMN affects Drosophila germline nuclear organization through the U body‐P body pathway publication-title: Dev. Biol. – volume: 121 start-page: 37 year: 2012 end-page: 48 article-title: mRNA accumulation in the Cajal bodies of the diplotene larch microsporocyte publication-title: Chromosoma – volume: 6 start-page: 75 year: 2005 article-title: Control of gene expression during T cell activation: alternate regulation of mRNA transcription and mRNA stability publication-title: BMC Genom. – volume: 34 start-page: 972 year: 2018 end-page: 990 article-title: Post‐transcriptional regulatory functions of mammalian Pumilio proteins publication-title: Trends Genet. – volume: 17 start-page: 3702 year: 1997 end-page: 3713 article-title: The sequence of the 5′ end of the U8 small nucleolar RNA is critical for 5.8S and 28S rRNA maturation publication-title: Mol. Cell. Biol. – volume: 24 start-page: 4930 year: 2012 end-page: 4947 article-title: LSM proteins provide accurate splicing and decay of selected transcripts to ensure normal Arabidopsis development publication-title: Plant Cell – volume: 12 start-page: 832 year: 2003 end-page: 847 article-title: The oligomerization and ligand‐binding properties of Sm‐like archaeal proteins (SmAPs) publication-title: Protein Sci. – volume: 100 start-page: 16 year: 2014 end-page: 25 article-title: OsAlba1, a dehydration‐responsive nuclear protein of rice (Oryza sativa L. ssp. indica), participates in stress adaptation publication-title: Phytochemistry – volume: 5 start-page: 1 year: 2014 end-page: 11 article-title: Composition and function of P bodies in Arabidopsis thaliana publication-title: Front. Plant Sci. – volume: 22 start-page: 4205 year: 2011 end-page: 4219 article-title: ALBA proteins are stage regulated during trypanosome development in the tsetse fly and participate in differentiation publication-title: Mol. Biol. Cell – volume: 118 start-page: 981 year: 2005 end-page: 992 article-title: The translational regulator CPEB1 provides a link between dcp1 bodies and stress granules publication-title: J. Cell Sci. – volume: 8 start-page: 533 year: 2007 end-page: 543 article-title: RNA regulons: coordination of post‐transcriptional events publication-title: Nat. Rev. Genet. – volume: 8 start-page: 1235 year: 2017 article-title: Observation of extensive chromosome axis remodeling during the “diffuse‐phase” of meiosis in large genome cereals publication-title: Front. Plant Sci. Sci. – volume: 137 start-page: 2341 year: 2010 end-page: 2351 article-title: Sm proteins specify germ cell fate by facilitating oskar mRNA localization publication-title: Development – volume: 136 start-page: 527 year: 2011 end-page: 541 article-title: Periodic expression of Sm proteins parallels formation of nuclear cajal bodies and cytoplasmic snRNP‐rich bodies publication-title: Histochem. Cell Biol. – volume: 12 start-page: 1502 year: 2002 end-page: 1506 article-title: A novel function for the Sm proteins in germ granule localization during C. elegans embryogenesis publication-title: Curr. Biol. – volume: 46 start-page: 362 year: 2018 end-page: 386 article-title: Identification of diverse target RNAs that are functionally regulated by human pumilio proteins publication-title: Nucleic Acids Res. – volume: 484 start-page: 260 year: 2012 end-page: 264 article-title: Telomerase RNA biogenesis involves sequential binding by Sm and Lsm complexes publication-title: Nature – volume: 20 start-page: 187 year: 2001 end-page: 196 article-title: Sm protein‐Sm site RNA interactions within the inner ring of the spliceosomal snRNP core structure publication-title: EMBO J. – volume: 42 start-page: 828 year: 2010 end-page: 843 article-title: Cytoplasmic ribonucleoprotein (RNP) bodies and their relationship to GW/P bodies publication-title: Int. J. Biochem. Cell Biol. – volume: 21 start-page: 3546 year: 2002 end-page: 3556 article-title: Structures of the pleiotropic translational regulator Hfq and an Hfq‐RNA complex: A bacterial Sm‐like protein publication-title: EMBO J. – volume: 1783 start-page: 2137 year: 2008 end-page: 2144 article-title: Joining the dots: production, processing and targeting of U snRNP to nuclear bodies publication-title: Biochim. Biophys. Acta – volume: 10 year: 2015 article-title: Transcriptional activity in diplotene larch microsporocytes, with emphasis on the diffuse stage publication-title: PLoS ONE – volume: 18 start-page: 755 year: 2004 end-page: 768 article-title: A novel role for shuttling SR proteins in mRNA translation A novel role for shuttling SR proteins in mRNA translation publication-title: Genes Dev. – volume: 1864 start-page: 570 year: 2016 end-page: 583 article-title: The Alba protein family: structure and function publication-title: BBA Proteins Proteom. – volume: 67 start-page: 6111 year: 2016 end-page: 6123 article-title: FIE, a nuclear PRC2 protein, forms cytoplasmic complexes in publication-title: J. Exp. Bot. – volume: 25 start-page: 2255 year: 2008 end-page: 2267 article-title: Evolutionary diversification of the Sm family of RNA‐associated proteins publication-title: Mol. Biol. Evol. – volume: 5 start-page: 190 year: 2010 end-page: 192 article-title: AtTZF gene family localizes to cytoplasmic foci publication-title: Plant Signal. Behav. – volume: 21 start-page: 2746 year: 2002 end-page: 2756 article-title: Cajal body‐specific small nuclear RNAs: a novels class of 2′‐O‐methylation and pseudouridylation guide RNAs publication-title: Embo J. – volume: 9 start-page: 671 year: 2012 end-page: 675 article-title: NIH Image to ImageJ: 25 years of image analysis publication-title: Nat. Methods – volume: 100 start-page: 8354 year: 2003 end-page: 8359 article-title: RNA‐binding protein HuR enhances p53 translation in response to ultraviolet light irradiation publication-title: Proc. Natl. Acad. Sci. USA – volume: 169 start-page: 871 year: 2005 end-page: 884 article-title: Stress granules and processing bodies are dynamically linked sites of mRNP remodeling publication-title: J. Cell Biol. – volume: 31 start-page: 258 year: 2012 end-page: 270 article-title: Cajal bodies and plant RNA metabolism publication-title: CRC Crit. Rev. Plant Sci. – volume: 4 start-page: 1122 year: 2006 end-page: 1136 article-title: Translation repression in human cells by microRNA‐induced gene silencing requires RCK/p54 publication-title: PLoS Biol. – volume: 14 start-page: 2076 year: 1995 end-page: 2088 article-title: snRNP Sm proteins share two evolutionarily conserved sequence motifs which are involved in Sm protein‐protein interactions publication-title: EMBO J. – volume: 1 start-page: 1 year: 2017 end-page: 10 article-title: Two Arabidopsis late pollen transcripts are detected in cytoplasmic granules publication-title: Plant Direct – volume: 27 start-page: 926 year: 2015 end-page: 943 article-title: Tudor staphylococcal nuclease links formation of stress granules and processing bodies with mRNA catabolism in Arabidopsis publication-title: Plant Cell – volume: 19 start-page: 1661 year: 2000 end-page: 1671 article-title: A Sm‐like protein complex that participates in mRNA degradation publication-title: EMBO J. – start-page: 174 year: 2008 end-page: 181 – volume: 18 start-page: 3386 year: 2006 end-page: 3398 article-title: Arabidopsis DCP2, DCP1, and VARICOSE form a decapping complex required for postembryonic development publication-title: Plant Cell – volume: 199 start-page: 259 year: 1988 end-page: 267 article-title: Newly synthesized small nuclear RNAs appear transiently in the cytoplasm publication-title: J. Mol. Biol. – volume: 26 start-page: 150 year: 1990 end-page: 158 article-title: Immunoelectron microscopical visualization of ribonucleoproteins in the chromatoid body of mouse spermatids publication-title: Mol. Reprod. Dev. – volume: 7 start-page: R113 year: 2006 article-title: Genome‐wide identification of functionally distinct subsets of cellular mRNAs associated with two nucleocytoplasmic‐shuttling mammalian splicing factors publication-title: Genome Biol. – volume: 4 start-page: a012286 year: 2012 article-title: P‐bodies and stress granules: possible roles in the control of translation and mRNA degradation publication-title: Cold Spring Harb. Perspect. Biol. – volume: 6 start-page: 170 year: 2000 end-page: 177 article-title: Stem‐loop 1 of the U1 snRNP plays a critical role in the suppression of HIV‐1 polyadenylation publication-title: RNA – volume: 94 start-page: 1085 year: 2014 end-page: 1102 article-title: Altered expression of an RBP‐associated arginine methyltransferase 7 in Leishmania major affects parasite infection publication-title: Mol. Microbiol. – volume: 140 start-page: 4008 year: 2013 end-page: 4019 article-title: Chromatin reprogramming during the somatic‐to‐reproductive cell fate transition in plants publication-title: Development – volume: 36 start-page: 932 year: 2009 article-title: Eukaryotic stress granules : the ins and out of translation publication-title: Mol. Cell – volume: 111 start-page: 2373 year: 2014 end-page: 2378 article-title: Selective mRNA sequestration by OLIGOURIDYLATE‐BINDING PROTEIN 1 contributes to translational control during hypoxia in Arabidopsis publication-title: Proc. Natl. Acad. Sci. USA – volume: 9 start-page: 1161 year: 2002 end-page: 1167 article-title: Eukaryotic mRNPs may represent posttranscriptional operons publication-title: Mol. Cell – volume: 10 start-page: 44 year: 2010 article-title: The Puf family of RNA‐binding proteins in plants: phylogeny, structural modeling, activity and subcellular localization publication-title: BMC Plant Biol. – volume: 16 start-page: 594 year: 2002 end-page: 607 article-title: Stability of a PKCI‐1 ‐related mRNA is controlled by the splicing factor ASF/SF2: a novel function for SR proteins publication-title: Genes Dev. – year: 2019 article-title: mRNA adenosine methylase (MTA) deposits m6A on pri‐miRNAs to modulate miRNA biogenesis in Arabidopsis thaliana publication-title: bioRxiv – volume: 8 start-page: 1 year: 2017 end-page: 17 article-title: The organization and regulation of mRNA‐protein complexes publication-title: Wiley Interdiscip. Rev. RNA – volume: 27 start-page: 863 year: 2011 end-page: 864 article-title: Quality control and preprocessing of metagenomic datasets publication-title: Bioinformatics – volume: 26 start-page: 2165 year: 2011 end-page: 2177 article-title: The competence of germinal vesicle oocytes is unrelated to nuclear chromatin configuration and strictly depends on cytoplasmic quantity and quality in the cat model publication-title: Hum. Reprod. – volume: 236 start-page: 13 year: 2009 end-page: 19 article-title: Poly(A) RNA a new component of Cajal bodies publication-title: Protoplasma – volume: 222 start-page: 1420 year: 2019 end-page: 1433 article-title: Protein and metabolite composition of Arabidopsis stress granules publication-title: New Phytol. – volume: 468 start-page: 664 year: 2010 end-page: 668 article-title: U1 snRNP protects pre‐mRNAs from premature cleavage and polyadenylation publication-title: Nature – volume: 38 start-page: 551 year: 2010 end-page: 562 article-title: Gemin5 delivers snRNA precursors to the SMN complex for snRNP biogenesis publication-title: Mol. Cell – volume: 103 start-page: 4487 year: 2006 end-page: 4492 article-title: Genome‐wide identification of mRNAs associated with the translational regulator PUMILIO in Drosophila melanogaster publication-title: Proc. Natl. Acad. Sci. USA – volume: 13 start-page: R17 year: 2012 article-title: The RNA‐binding landscapes of two SR proteins reveal unique functions and binding to diverse RNA classes publication-title: Genome Biol. – volume: 19 start-page: 6554 year: 1999 end-page: 6565 article-title: Spliceosomal U snRNP core assembly: Sm proteins assemble onto an Sm site RNA nonanucleotide in a specific and thermodynamically stable manner publication-title: Mol. Cell. Biol. – volume: 107 start-page: 3521 year: 1994 end-page: 3534 article-title: Chromatin and microtubule organization during premeiotic, meiotic and early postmeiotic stages of Drosophila melanogaster spermatogenesis publication-title: J. Cell Sci. – volume: 24 start-page: 359 year: 1993 end-page: 381 article-title: The diverse world of small ribonucleoproteins publication-title: RNA World – volume: 299 start-page: 171 year: 2004 end-page: 178 article-title: Sm proteins, the constituents of the spliceosome, are components of nuage and mitochondrial cement in Xenopus oocytes publication-title: Exp. Cell Res. – volume: 8 year: 2016 article-title: Posttranscriptional coordination of splicing and miRNA biogenesis in plants publication-title: Wiley Interdiscip. Rev. RNA – volume: 115 start-page: 343 year: 2006 end-page: 354 article-title: The Cajal body: a meeting place for spliceosomal snRNPs in the nuclear maze publication-title: Chromosoma – volume: 106 start-page: 20989 year: 2009 end-page: 20994 article-title: Live imaging of rapid chromosome movements in meiotic prophase I in maize publication-title: Proc. Natl. Acad. Sci. USA – volume: 7 start-page: 899 year: 2001 end-page: 905 article-title: Splicing factors SRp20 and 9G8 promote the nucleocytoplasmic export of mRNA publication-title: Mol. Cell – volume: 33 start-page: 433 year: 2005 end-page: 438 article-title: Lsm proteins and RNA processing publication-title: Biochem. Soc. Trans. – volume: 116 start-page: 6451 year: 2019 end-page: 6456 article-title: Processing bodies control the selective translation for optimal development of Arabidopsis young seedlings publication-title: Proc. Natl. Acad. Sci. USA – volume: 66 start-page: 1052 year: 2006 end-page: 1061 article-title: Radiation‐induced changes in gene expression involve recruitment of existing messenger RNAs to and away from polysomes publication-title: Cancer Res. – volume: 224 start-page: 213 year: 2006 end-page: 232 article-title: A guided tour into subcellular colocalisation analysis in light microscopy publication-title: J. Microsc. – volume: 28 start-page: 535 year: 2011 end-page: 544 article-title: Genome‐wide identification and evolutionary analysis of Arabidopsis sm genes family publication-title: J. Biomol. Struct. Dyn. – volume: 120 start-page: 979 year: 2003 end-page: 990 article-title: Mouse Tudor Repeat‐1 (MTR‐1) is a novel component of chromatoid bodies/nuages in male germ cells and forms a complex with snRNPs publication-title: Mech. Dev. – volume: 66 start-page: 7019 year: 2015 end-page: 7030 article-title: Spatial regulation of cytoplasmic snRNP assembly at the cellular level publication-title: J. Exp. Bot. – ident: e_1_2_9_40_1 doi: 10.1016/j.ydbio.2008.07.008 – ident: e_1_2_9_71_1 doi: 10.1371/journal.pgen.1002527 – ident: e_1_2_9_9_1 doi: 10.1016/j.ydbio.2005.12.011 – ident: e_1_2_9_94_1 doi: 10.1105/tpc.112.103697 – ident: e_1_2_9_83_1 doi: 10.1016/0092-8674(86)90072-3 – ident: e_1_2_9_107_1 doi: 10.1093/molbev/msn175 – ident: e_1_2_9_93_1 doi: 10.1128/MCB.17.7.3702 – ident: e_1_2_9_114_1 doi: 10.1007/s00412-011-0339-4 – ident: e_1_2_9_122_1 doi: 10.4161/psb.26955 – ident: e_1_2_9_42_1 doi: 10.1371/journal.pbio.0020079 – ident: e_1_2_9_81_1 doi: 10.3389/fpls.2014.00201 – ident: e_1_2_9_21_1 doi: 10.1093/emboj/19.7.1661 – ident: e_1_2_9_63_1 doi: 10.1016/S1097-2765(02)00559-2 – ident: e_1_2_9_70_1 doi: 10.1128/MCB.19.6.4311 – ident: e_1_2_9_2_1 doi: 10.1093/emboj/18.20.5789 – ident: e_1_2_9_45_1 doi: 10.1016/j.tig.2018.09.006 – ident: e_1_2_9_49_1 doi: 10.1093/nar/gkn176 – ident: e_1_2_9_48_1 doi: 10.4161/cc.2.5.491 – ident: e_1_2_9_57_1 doi: 10.1093/jxb/erv399 – ident: e_1_2_9_134_1 doi: 10.1016/j.molcel.2010.03.014 – ident: e_1_2_9_115_1 doi: 10.1007/s00709-007-0270-y – ident: e_1_2_9_80_1 doi: 10.1371/journal.ppat.1000767 – ident: e_1_2_9_92_1 doi: 10.1016/j.molcel.2007.02.011 – ident: e_1_2_9_135_1 doi: 10.1007/s00299-008-0579-9 – ident: e_1_2_9_4_1 doi: 10.1038/nature12349 – ident: e_1_2_9_95_1 doi: 10.4161/psb.5.2.10988 – ident: e_1_2_9_50_1 doi: 10.1016/j.bbapap.2016.02.015 – ident: e_1_2_9_39_1 doi: 10.1101/gad.1390306 – ident: e_1_2_9_43_1 doi: 10.1073/pnas.0509260103 – ident: e_1_2_9_127_1 doi: 10.1093/emboj/20.1.187 – ident: e_1_2_9_84_1 doi: 10.1073/pnas.1432104100 – ident: e_1_2_9_35_1 doi: 10.1099/vir.0.2008/002139-0 – ident: e_1_2_9_36_1 doi: 10.1105/tpc.15.01045 – ident: e_1_2_9_131_1 doi: 10.1105/tpc.109.070078 – ident: e_1_2_9_110_1 doi: 10.1016/j.bbamcr.2008.07.025 – volume: 24 start-page: 359 year: 1993 ident: e_1_2_9_11_1 article-title: The diverse world of small ribonucleoproteins publication-title: RNA World – ident: e_1_2_9_52_1 doi: 10.1046/j.1365-2958.2003.03793.x – ident: e_1_2_9_61_1 doi: 10.1083/jcb.200502088 – ident: e_1_2_9_8_1 doi: 10.1093/emboj/16.18.5752 – ident: e_1_2_9_77_1 doi: 10.1158/0008-5472.CAN-05-3459 – ident: e_1_2_9_120_1 doi: 10.1002/wrna.1403 – ident: e_1_2_9_67_1 doi: 10.1371/journal.pone.0117337 – ident: e_1_2_9_101_1 doi: 10.1002/pld3.12 – ident: e_1_2_9_119_1 doi: 10.1007/s00412-006-0056-6 – ident: e_1_2_9_126_1 doi: 10.1016/j.molcel.2004.10.013 – ident: e_1_2_9_54_1 doi: 10.1007/s00018-007-7447-6 – ident: e_1_2_9_109_1 doi: 10.1038/43694 – ident: e_1_2_9_133_1 doi: 10.1105/tpc.106.047605 – ident: e_1_2_9_123_1 doi: 10.1186/1471-2229-10-44 – ident: e_1_2_9_108_1 doi: 10.1038/ncb1265 – ident: e_1_2_9_33_1 doi: 10.1093/emboj/21.11.2746 – ident: e_1_2_9_41_1 doi: 10.1186/gb-2006-7-11-r113 – ident: e_1_2_9_27_1 doi: 10.1093/nar/gkr1215 – ident: e_1_2_9_25_1 doi: 10.1104/pp.17.01468 – ident: e_1_2_9_121_1 doi: 10.1091/mbc.E11-06-0511 – ident: e_1_2_9_103_1 doi: 10.1038/nmeth.2089 – ident: e_1_2_9_116_1 doi: 10.1007/s00418-011-0861-8 – ident: e_1_2_9_26_1 doi: 10.1186/1471-2164-6-75 – ident: e_1_2_9_44_1 doi: 10.1016/j.jmb.2013.01.039 – ident: e_1_2_9_79_1 doi: 10.1101/gad.1282305 – ident: e_1_2_9_16_1 doi: 10.1002/mrd.1080260209 – ident: e_1_2_9_24_1 doi: 10.1242/jcs.107.12.3521 – ident: e_1_2_9_130_1 doi: 10.1242/jcs.01692 – ident: e_1_2_9_38_1 doi: 10.1111/mmi.12819 – ident: e_1_2_9_5_1 doi: 10.1261/rna.2340405 – ident: e_1_2_9_19_1 doi: 10.1111/j.1365-2818.2006.01706.x – ident: e_1_2_9_88_1 doi: 10.1110/ps.0224703 – ident: e_1_2_9_65_1 doi: 10.1111/j.1601-5223.1976.tb01557.x – ident: e_1_2_9_73_1 doi: 10.1101/gad.939502 – ident: e_1_2_9_74_1 doi: 10.1073/pnas.0704977104 – ident: e_1_2_9_106_1 doi: 10.1007/s00018-004-4190-0 – ident: e_1_2_9_51_1 doi: 10.1038/nbt.1883 – ident: e_1_2_9_78_1 doi: 10.1186/gb-2014-15-1-r7 – ident: e_1_2_9_18_1 doi: 10.1093/nar/gkx1120 – ident: e_1_2_9_96_1 doi: 10.1016/j.tcb.2016.05.004 – ident: e_1_2_9_17_1 doi: 10.1016/j.yexcr.2004.05.016 – ident: e_1_2_9_72_1 doi: 10.1016/j.ydbio.2009.05.553 – ident: e_1_2_9_28_1 doi: 10.1371/journal.pbio.0040210 – ident: e_1_2_9_85_1 doi: 10.1261/rna.035469.112 – ident: e_1_2_9_99_1 doi: 10.1002/wrna.1369 – ident: e_1_2_9_129_1 doi: 10.1111/j.1365-313X.2008.03623.x – ident: e_1_2_9_98_1 doi: 10.1093/emboj/cdg394 – ident: e_1_2_9_60_1 doi: 10.1038/nature09479 – ident: e_1_2_9_97_1 doi: 10.1128/MCB.19.10.6554 – ident: e_1_2_9_89_1 doi: 10.1038/nsmb.2640 – ident: e_1_2_9_87_1 doi: 10.1007/BF00414179 – ident: e_1_2_9_14_1 doi: 10.1016/j.cell.2012.05.029 – ident: e_1_2_9_62_1 doi: 10.1038/nrg2111 – ident: e_1_2_9_117_1 doi: 10.1073/pnas.1314851111 – ident: e_1_2_9_56_1 doi: 10.1016/S1097-2765(01)00233-7 – ident: e_1_2_9_124_1 doi: 10.1038/nature10924 – ident: e_1_2_9_7_1 doi: 10.1017/S1355838200991957 – ident: e_1_2_9_113_1 doi: 10.1126/science.1082320 – ident: e_1_2_9_10_1 doi: 10.1016/S0960-9822(02)01111-9 – ident: e_1_2_9_3_1 doi: 10.1242/jcs.152975 – ident: e_1_2_9_15_1 doi: 10.1101/557900 – ident: e_1_2_9_22_1 doi: 10.1016/j.molcel.2009.11.020 – ident: e_1_2_9_34_1 doi: 10.1101/cshperspect.a012286 – ident: e_1_2_9_55_1 doi: 10.1002/j.1460-2075.1995.tb07199.x – ident: e_1_2_9_68_1 doi: 10.1007/s00709-009-0042-y – ident: e_1_2_9_46_1 doi: 10.3410/B4-16 – ident: e_1_2_9_82_1 doi: 10.1371/journal.pone.0022463 – ident: e_1_2_9_102_1 doi: 10.1093/bioinformatics/btr026 – ident: e_1_2_9_29_1 doi: 10.1016/S0925-4773(03)00181-3 – ident: e_1_2_9_30_1 doi: 10.3389/fpls.2017.01235 – ident: e_1_2_9_69_1 doi: 10.1111/nph.15690 – ident: e_1_2_9_111_1 doi: 10.1242/dev.095034 – ident: e_1_2_9_112_1 doi: 10.1073/pnas.0906498106 – ident: e_1_2_9_58_1 doi: 10.1007/s00441-011-1145-2 – ident: e_1_2_9_20_1 doi: 10.1105/tpc.110.081059 – ident: e_1_2_9_23_1 doi: 10.1080/07391102.2011.10508593 – start-page: 174 volume-title: ImageJ User & Developer Conference year: 2008 ident: e_1_2_9_32_1 – ident: e_1_2_9_91_1 doi: 10.1093/jxb/erw373 – ident: e_1_2_9_53_1 doi: 10.1105/tpc.114.134494 – ident: e_1_2_9_104_1 doi: 10.1186/1742-4690-10-55 – ident: e_1_2_9_31_1 doi: 10.1093/humrep/der176 – ident: e_1_2_9_125_1 doi: 10.1126/science.1090095 – ident: e_1_2_9_59_1 doi: 10.1073/pnas.1900084116 – ident: e_1_2_9_100_1 doi: 10.1101/gad.286404 – ident: e_1_2_9_118_1 doi: 10.1007/978-1-4939-2444-8_10 – ident: e_1_2_9_128_1 doi: 10.1016/j.phytochem.2014.01.015 – ident: e_1_2_9_37_1 doi: 10.1091/mbc.e04-02-0116 – ident: e_1_2_9_75_1 doi: 10.1371/journal.pone.0045966 – ident: e_1_2_9_105_1 doi: 10.1093/emboj/cdf322 – volume: 45 start-page: 2757 year: 2017 ident: e_1_2_9_66_1 article-title: Active 5 splice sites regulate the biogenesis efficiency of Arabidopsis microRNAs derived from intron‐containing genes publication-title: Nucleic Acids Res. – ident: e_1_2_9_86_1 doi: 10.1016/j.biocel.2009.11.018 – ident: e_1_2_9_136_1 doi: 10.1016/0022-2836(88)90312-9 – ident: e_1_2_9_6_1 doi: 10.1186/gb-2012-13-3-r17 – ident: e_1_2_9_12_1 doi: 10.1080/07352689.2011.645431 – ident: e_1_2_9_76_1 doi: 10.1016/j.jprot.2013.07.010 – ident: e_1_2_9_132_1 doi: 10.1016/j.pbi.2010.10.003 – ident: e_1_2_9_13_1 doi: 10.1042/BST0330433 – ident: e_1_2_9_64_1 doi: 10.1016/j.tibs.2005.07.006 – ident: e_1_2_9_47_1 doi: 10.1242/dev.042721 – ident: e_1_2_9_90_1 doi: 10.1104/pp.105.065649 |
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In recent years, research has increasingly focused on the key role of post‐transcriptional regulation of messenger ribonucleoprotein (mRNP) function... In recent years, research has increasingly focused on the key role of post‐transcriptional regulation of messenger ribonucleoprotein (mRNP) function and... In recent years, research has increasingly focused on the key role of post-transcriptional regulation of messenger ribonucleoprotein (mRNP) function and... SUMMARYIn recent years, research has increasingly focused on the key role of post‐transcriptional regulation of messenger ribonucleoprotein (mRNP) function and... |
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SubjectTerms | cajal bodies Chemical composition Complexity Cytoplasm Cytoplasm - metabolism cytoplasmic bodies Gene expression gene expression regulation Gene Expression Regulation, Plant Gene regulation Larix - metabolism Larix decidua Life cycles messenger RNA Microscopic analysis mRNP Original Plant Proteins - metabolism Polyadenylation Proteins P‐bodies Ribonucleic acid ribonucleoproteins Ribonucleoproteins - metabolism RIP‐seq RNA RNA, Messenger - metabolism RNA, Plant - metabolism RNA, Small Cytoplasmic - metabolism RNA-binding protein RNA-Binding Proteins - metabolism Sm proteins spliceosomes Spliceosomes - metabolism Splicing stress granules Transcription |
Title | Core spliceosomal Sm proteins as constituents of cytoplasmic mRNPs in plants |
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