Global analysis of trans-splicing in Drosophila
Precursor mRNA (pre-mRNA) splicing can join exons contained on either a single pre-mRNA (cis) or on separate pre-mRNAs (trans). It is exceedingly rare to have trans-splicing between protein-coding exons and has been demonstrated for only two Drosophila genes: mod(mdg4) and lola. It has also been sug...
Saved in:
Published in | Proceedings of the National Academy of Sciences - PNAS Vol. 107; no. 29; pp. 12975 - 12979 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
National Academy of Sciences
20.07.2010
National Acad Sciences |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Precursor mRNA (pre-mRNA) splicing can join exons contained on either a single pre-mRNA (cis) or on separate pre-mRNAs (trans). It is exceedingly rare to have trans-splicing between protein-coding exons and has been demonstrated for only two Drosophila genes: mod(mdg4) and lola. It has also been suggested that trans-splicing is a mechanism for the generation of chimeric RNA products containing sequence from multiple distant genomic sites. Because most high-throughput approaches cannot distinguish cis- and transsplicing events, the extent to which trans-splicing occurs between protein-coding exons in any organism is unknown. Here, we used paired-end deep sequencing of mRNA to identify genes that undergo trans-splicing in Drosophila interspecies hybrids. We did not observe credible evidence for the existence of chimeric RNAs generated by trans-splicing of RNAs transcribed from distant genomic loci. Rather, our data suggest that experimental artifacts are the source of most, if not all, apparent chimeric RNA products. We did, however, identify 80 genes that appear to undergo trans-splicing between homologous alleles and can be classified into three categories based on their organization: (i) genes with multiple 3' terminal exons, (ii) genes with multiple first exons, and (iii) genes with very large introns, often containing other genes. Our results suggest that trans-splicing between homologous alleles occurs more commonly in Drosophila than previously believed and may facilitate expression of architecturally complex genes. |
---|---|
AbstractList | Precursor mRNA (pre-mRNA) splicing can join exons contained on either a single pre-mRNA (cis) or on separate pre-mRNAs (trans). It is exceedingly rare to have trans-splicing between protein-coding exons and has been demonstrated for only two Drosophila genes: mod(mdg4) and lola. It has also been suggested that trans-splicing is a mechanism for the generation of chimeric RNA products containing sequence from multiple distant genomic sites. Because most high-throughput approaches cannot distinguish cis- and trans-splicing events, the extent to which trans-splicing occurs between protein-coding exons in any organism is unknown. Here, we used paired-end deep sequencing of mRNA to identify genes that undergo trans-splicing in Drosophila interspecies hybrids. We did not observe credible evidence for the existence of chimeric RNAs generated by trans-splicing of RNAs transcribed from distant genomic loci. Rather, our data suggest that experimental artifacts are the source of most, if not all, apparent chimeric RNA products. We did, however, identify 80 genes that appear to undergo trans-splicing between homologous alleles and can be classified into three categories based on their organization: (i) genes with multiple 3' terminal exons, (ii) genes with multiple first exons, and (iii) genes with very large introns, often containing other genes. Our results suggest that trans-splicing between homologous alleles occurs more commonly in Drosophila than previously believed and may facilitate expression of architecturally complex genes. [PUBLICATION ABSTRACT] Precursor mRNA (pre-mRNA) splicing can join exons contained on either a single pre-mRNA (cis) or on separate pre-mRNAs (trans). It is exceedingly rare to have trans-splicing between protein-coding exons and has been demonstrated for only two Drosophila genes: mod(mdg4) and lola. It has also been suggested that trans-splicing is a mechanism for the generation of chimeric RNA products containing sequence from multiple distant genomic sites. Because most high-throughput approaches cannot distinguish cis- and trans-splicing events, the extent to which trans-splicing occurs between protein-coding exons in any organism is unknown. Here, we used paired-end deep sequencing of mRNA to identify genes that undergo trans-splicing in Drosophila interspecies hybrids. We did not observe credible evidence for the existence of chimeric RNAs generated by trans-splicing of RNAs transcribed from distant genomic loci. Rather, our data suggest that experimental artifacts are the source of most, if not all, apparent chimeric RNA products. We did, however, identify 80 genes that appear to undergo trans-splicing between homologous alleles and can be classified into three categories based on their organization: (i) genes with multiple 3' terminal exons, (ii) genes with multiple first exons, and (iii) genes with very large introns, often containing other genes. Our results suggest that trans-splicing between homologous alleles occurs more commonly in Drosophila than previously believed and may facilitate expression of architecturally complex genes. Precursor mRNA (pre-mRNA) splicing can join exons contained on either a single pre-mRNA (cis) or on separate pre-mRNAs (trans). It is exceedingly rare to have trans-splicing between protein-coding exons and has been demonstrated for only two Drosophila genes: mod(mdg4) and lola. It has also been suggested that trans-splicing is a mechanism for the generation of chimeric RNA products containing sequence from multiple distant genomic sites. Because most high-throughput approaches cannot distinguish cis- and transsplicing events, the extent to which trans-splicing occurs between protein-coding exons in any organism is unknown. Here, we used paired-end deep sequencing of mRNA to identify genes that undergo trans-splicing in Drosophila interspecies hybrids. We did not observe credible evidence for the existence of chimeric RNAs generated by trans-splicing of RNAs transcribed from distant genomic loci. Rather, our data suggest that experimental artifacts are the source of most, if not all, apparent chimeric RNA products. We did, however, identify 80 genes that appear to undergo trans-splicing between homologous alleles and can be classified into three categories based on their organization: (i) genes with multiple 3' terminal exons, (ii) genes with multiple first exons, and (iii) genes with very large introns, often containing other genes. Our results suggest that trans-splicing between homologous alleles occurs more commonly in Drosophila than previously believed and may facilitate expression of architecturally complex genes. Precursor mRNA (pre-mRNA) splicing can join exons contained on either a single pre-mRNA (cis) or on separate pre-mRNAs (trans). It is exceedingly rare to have trans-splicing between protein-coding exons and has been demonstrated for only two Drosophila genes: mod(mdg4) and lola. It has also been suggested that trans-splicing is a mechanism for the generation of chimeric RNA products containing sequence from multiple distant genomic sites. Because most high-throughput approaches cannot distinguish cis- and trans-splicing events, the extent to which trans-splicing occurs between protein-coding exons in any organism is unknown. Here, we used paired-end deep sequencing of mRNA to identify genes that undergo trans-splicing in Drosophila interspecies hybrids. We did not observe credible evidence for the existence of chimeric RNAs generated by trans-splicing of RNAs transcribed from distant genomic loci. Rather, our data suggest that experimental artifacts are the source of most, if not all, apparent chimeric RNA products. We did, however, identify 80 genes that appear to undergo trans-splicing between homologous alleles and can be classified into three categories based on their organization: (i) genes with multiple 3' terminal exons, (ii) genes with multiple first exons, and (iii) genes with very large introns, often containing other genes. Our results suggest that trans-splicing between homologous alleles occurs more commonly in Drosophila than previously believed and may facilitate expression of architecturally complex genes.Precursor mRNA (pre-mRNA) splicing can join exons contained on either a single pre-mRNA (cis) or on separate pre-mRNAs (trans). It is exceedingly rare to have trans-splicing between protein-coding exons and has been demonstrated for only two Drosophila genes: mod(mdg4) and lola. It has also been suggested that trans-splicing is a mechanism for the generation of chimeric RNA products containing sequence from multiple distant genomic sites. Because most high-throughput approaches cannot distinguish cis- and trans-splicing events, the extent to which trans-splicing occurs between protein-coding exons in any organism is unknown. Here, we used paired-end deep sequencing of mRNA to identify genes that undergo trans-splicing in Drosophila interspecies hybrids. We did not observe credible evidence for the existence of chimeric RNAs generated by trans-splicing of RNAs transcribed from distant genomic loci. Rather, our data suggest that experimental artifacts are the source of most, if not all, apparent chimeric RNA products. We did, however, identify 80 genes that appear to undergo trans-splicing between homologous alleles and can be classified into three categories based on their organization: (i) genes with multiple 3' terminal exons, (ii) genes with multiple first exons, and (iii) genes with very large introns, often containing other genes. Our results suggest that trans-splicing between homologous alleles occurs more commonly in Drosophila than previously believed and may facilitate expression of architecturally complex genes. Precursor mRNA (pre-mRNA) splicing can join exons contained on either a single pre-mRNA ( cis ) or on separate pre-mRNAs ( trans ). It is exceedingly rare to have trans -splicing between protein-coding exons and has been demonstrated for only two Drosophila genes: mod(mdg4) and lola . It has also been suggested that trans -splicing is a mechanism for the generation of chimeric RNA products containing sequence from multiple distant genomic sites. Because most high-throughput approaches cannot distinguish cis - and trans -splicing events, the extent to which trans -splicing occurs between protein-coding exons in any organism is unknown. Here, we used paired-end deep sequencing of mRNA to identify genes that undergo trans -splicing in Drosophila interspecies hybrids. We did not observe credible evidence for the existence of chimeric RNAs generated by trans -splicing of RNAs transcribed from distant genomic loci. Rather, our data suggest that experimental artifacts are the source of most, if not all, apparent chimeric RNA products. We did, however, identify 80 genes that appear to undergo trans -splicing between homologous alleles and can be classified into three categories based on their organization: ( i ) genes with multiple 3′ terminal exons, ( ii ) genes with multiple first exons, and ( iii ) genes with very large introns, often containing other genes. Our results suggest that trans -splicing between homologous alleles occurs more commonly in Drosophila than previously believed and may facilitate expression of architecturally complex genes. |
Author | Maniatis, Tom Duff, Michael O. Graveley, Brenton R. Eipper-Mains, Jodi McManus, C. Joel |
Author_xml | – sequence: 1 givenname: C. Joel surname: McManus fullname: McManus, C. Joel – sequence: 2 givenname: Michael O. surname: Duff fullname: Duff, Michael O. – sequence: 3 givenname: Jodi surname: Eipper-Mains fullname: Eipper-Mains, Jodi – sequence: 4 givenname: Brenton R. surname: Graveley fullname: Graveley, Brenton R. – sequence: 5 givenname: Tom surname: Maniatis fullname: Maniatis, Tom |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/20615941$$D View this record in MEDLINE/PubMed |
BookMark | eNqFkjtvFDEUhS0URDaBmgo0ooFmsr5-u4mEAiSRItFAbXm8nsQrrz2MZ5Hy7_FolyxJESpbvt89vo9zgo5STh6ht4DPAEu6HJIt9YYlV6I-vEALwBpawTQ-QguMiWwVI-wYnZSyxhhrrvArdEywAK4ZLNDyMubOxsYmG-9LKE3um2m0qbRliMGFdNuE1HwZc8nDXYj2NXrZ21j8m_15in5--_rj4qq9-X55ffH5pnWcwtQKZTlZaUtwrcR5zplT1GnhKe2kXpEa6ZSkijLRYa3BYsc4kw4YWN3Lnp6i853usO02fuV8qlVFM4xhY8d7k20wjyMp3Jnb_NsQDVVPV4GPe4Ex_9r6MplNKM7HaJPP22IkZ1xUmPyfpGyeHJ41Pz1LgiKcAQXgFf3wBF3n7ViHXIwQDISu26vQ-3-bfOju73oqsNwBri6gjL5_QACb2QBmNoA5GKBm8CcZLkx2CnmeUojP5DX7UubA4RdZB2qAaDm39G6HrMuUx0OxXGJVDUf_AKI-xhs |
CitedBy_id | crossref_primary_10_1002_jez_b_22542 crossref_primary_10_1002_wrna_71 crossref_primary_10_1093_nargab_lqab074 crossref_primary_10_1186_1471_2105_12_270 crossref_primary_10_1517_17460441_2012_660145 crossref_primary_10_1038_s41598_020_73077_1 crossref_primary_10_1093_nar_gku643 crossref_primary_10_1534_genetics_113_153544 crossref_primary_10_3390_biology13120994 crossref_primary_10_1093_gbe_evw025 crossref_primary_10_1101_gad_258863_115 crossref_primary_10_1155_2018_3178789 crossref_primary_10_3389_fvets_2021_742593 crossref_primary_10_1371_journal_pone_0033947 crossref_primary_10_1007_s40484_016_0069_y crossref_primary_10_1371_journal_pone_0079703 crossref_primary_10_1371_journal_pone_0028213 crossref_primary_10_4161_rna_27866 crossref_primary_10_1371_journal_pcbi_1004325 crossref_primary_10_1093_nar_gku1199 crossref_primary_10_1371_journal_pone_0021022 crossref_primary_10_26508_lsa_202201793 crossref_primary_10_1186_1471_2164_12_552 crossref_primary_10_3390_genes9010040 crossref_primary_10_1093_nar_gkw032 crossref_primary_10_1371_journal_pcbi_1006158 crossref_primary_10_1186_s13059_015_0777_z crossref_primary_10_1093_bioinformatics_bts216 crossref_primary_10_1371_journal_pgen_1011241 crossref_primary_10_1111_pbi_14296 crossref_primary_10_1134_S1607672924601021 crossref_primary_10_1261_rna_066225_118 crossref_primary_10_1002_wrna_1294 crossref_primary_10_1038_nbt_2890 crossref_primary_10_1038_cr_2013_86 crossref_primary_10_1038_nrg_2016_46 crossref_primary_10_18632_oncotarget_8917 crossref_primary_10_1261_rna_029751_111 crossref_primary_10_1038_nprot_2014_121 crossref_primary_10_1093_nar_gkz1025 crossref_primary_10_1016_j_cub_2011_01_032 crossref_primary_10_1002_wrna_1427 crossref_primary_10_1186_1471_2164_13_429 crossref_primary_10_1002_wrna_1626 crossref_primary_10_1101_gr_130062_111 crossref_primary_10_3390_epigenomes3030014 crossref_primary_10_1016_j_jgg_2020_04_005 crossref_primary_10_1534_g3_115_018937 crossref_primary_10_1002_wrna_1187 crossref_primary_10_1186_s12859_018_2589_0 crossref_primary_10_1101_gr_107854_110 crossref_primary_10_1016_j_ygeno_2011_05_005 crossref_primary_10_1098_rsob_170150 crossref_primary_10_1261_rna_079623_123 crossref_primary_10_1146_annurev_genom_090413_025448 crossref_primary_10_1126_sciadv_abn9458 crossref_primary_10_1186_1745_6150_7_11 crossref_primary_10_1101_gr_159483_113 crossref_primary_10_1016_j_celrep_2014_10_062 crossref_primary_10_1134_S0006297914130021 crossref_primary_10_3389_fgene_2019_00176 crossref_primary_10_1093_nar_gkad623 crossref_primary_10_1093_nar_gky716 crossref_primary_10_1101_gr_161521_113 crossref_primary_10_1093_nar_gkw1127 crossref_primary_10_1016_j_conbuildmat_2022_130209 crossref_primary_10_1016_j_cub_2011_01_025 crossref_primary_10_1038_ncomms9734 crossref_primary_10_4161_rna_24570 crossref_primary_10_1016_j_molcel_2013_01_031 crossref_primary_10_1093_nar_gkv1013 crossref_primary_10_3390_cells10020297 crossref_primary_10_1038_nrg2934 crossref_primary_10_1007_s11427_019_1609_6 crossref_primary_10_1158_2159_8290_CD_12_0042 crossref_primary_10_1038_nbt_4259 crossref_primary_10_1146_annurev_ecolsys_110411_160513 |
Cites_doi | 10.1534/genetics.107.070938 10.1073/pnas.151268698 10.1186/gb-2009-10-3-r25 10.1038/35059000 10.1016/j.ygeno.2005.12.013 10.1101/gad.1137303 10.1126/science.1156725 10.1007/s00239-008-9187-0 10.1016/S0168-9525(01)02499-4 10.1093/nar/23.11.2049 10.1038/nature08390 10.1038/nature06341 10.1016/S0092-8674(85)80112-4 10.1016/S0092-8674(85)80111-2 10.1534/genetics.103.020842 10.1038/nmeth.1417 10.1016/0092-8674(86)90617-3 10.1101/gr.102491.109 10.1038/nature08452 10.1016/S1097-2765(02)00578-6 10.1002/jez.1400210204 10.1038/ng2049 10.1101/gr.100677.109 |
ContentType | Journal Article |
Copyright | Copyright National Academy of Sciences Jul 20, 2010 |
Copyright_xml | – notice: Copyright National Academy of Sciences Jul 20, 2010 |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7QG 7QL 7QP 7QR 7SN 7SS 7T5 7TK 7TM 7TO 7U9 8FD C1K FR3 H94 M7N P64 RC3 7S9 L.6 7X8 5PM |
DOI | 10.1073/pnas.1007586107 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Animal Behavior Abstracts Bacteriology Abstracts (Microbiology B) Calcium & Calcified Tissue Abstracts Chemoreception Abstracts Ecology Abstracts Entomology Abstracts (Full archive) Immunology Abstracts Neurosciences Abstracts Nucleic Acids Abstracts Oncogenes and Growth Factors Abstracts Virology and AIDS Abstracts Technology Research Database Environmental Sciences and Pollution Management Engineering Research Database AIDS and Cancer Research Abstracts Algology Mycology and Protozoology Abstracts (Microbiology C) Biotechnology and BioEngineering Abstracts Genetics Abstracts AGRICOLA AGRICOLA - Academic MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Virology and AIDS Abstracts Oncogenes and Growth Factors Abstracts Technology Research Database Nucleic Acids Abstracts Ecology Abstracts Neurosciences Abstracts Biotechnology and BioEngineering Abstracts Environmental Sciences and Pollution Management Entomology Abstracts Genetics Abstracts Animal Behavior Abstracts Bacteriology Abstracts (Microbiology B) Algology Mycology and Protozoology Abstracts (Microbiology C) AIDS and Cancer Research Abstracts Chemoreception Abstracts Immunology Abstracts Engineering Research Database Calcium & Calcified Tissue Abstracts AGRICOLA AGRICOLA - Academic MEDLINE - Academic |
DatabaseTitleList | Virology and AIDS Abstracts AGRICOLA Entomology Abstracts MEDLINE - Academic MEDLINE CrossRef |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Sciences (General) |
EISSN | 1091-6490 |
EndPage | 12979 |
ExternalDocumentID | PMC2919919 2090170551 20615941 10_1073_pnas_1007586107 107_29_12975 25708649 |
Genre | Journal Article Research Support, N.I.H., Extramural Feature |
GrantInformation_xml | – fundername: NIGMS NIH HHS grantid: R01 GM062516 – fundername: NIGMS NIH HHS grantid: GM062516 |
GroupedDBID | --- -DZ -~X .55 0R~ 123 29P 2AX 2FS 2WC 4.4 53G 5RE 5VS 85S AACGO AAFWJ AANCE AAYJJ ABBHK ABOCM ABPLY ABPPZ ABTLG ABXSQ ABZEH ACGOD ACHIC ACIWK ACNCT ACPRK ADQXQ ADULT ADXHL AENEX AEUPB AEXZC AFFNX AFOSN AFRAH ALMA_UNASSIGNED_HOLDINGS AQVQM AS~ BKOMP CS3 D0L DCCCD DIK DU5 E3Z EBS EJD F5P FRP GX1 H13 HH5 HQ3 HTVGU HYE IPSME JAAYA JBMMH JENOY JHFFW JKQEH JLS JLXEF JPM JSG JST KQ8 L7B LU7 MVM N9A N~3 O9- OK1 P-O PNE PQQKQ R.V RHI RNA RNS RPM RXW SA0 SJN TAE TN5 UKR W8F WH7 WOQ WOW X7M XSW Y6R YBH YKV YSK ZCA ~02 ~KM - 02 0R 1AW 55 AAPBV ABFLS ABPTK ADACO ADZLD AJYGW AS ASUFR DNJUQ DOOOF DWIUU DZ F20 JSODD KM PQEST RHF VQA X XHC ZA5 AAYXX CITATION CGR CUY CVF ECM EIF NPM VXZ YIF YIN 7QG 7QL 7QP 7QR 7SN 7SS 7T5 7TK 7TM 7TO 7U9 8FD C1K FR3 H94 M7N P64 RC3 7S9 L.6 7X8 5PM |
ID | FETCH-LOGICAL-c531t-68a52d9a20490ce554c83c96e33b79d29a2b8738346b0991a0c4547c141a9f7f3 |
ISSN | 0027-8424 1091-6490 |
IngestDate | Thu Aug 21 13:48:35 EDT 2025 Fri Jul 11 12:40:56 EDT 2025 Fri Jul 11 10:08:46 EDT 2025 Fri Jul 11 12:20:37 EDT 2025 Mon Jun 30 08:10:17 EDT 2025 Wed Feb 19 02:32:07 EST 2025 Tue Jul 01 00:46:56 EDT 2025 Thu Apr 24 22:55:39 EDT 2025 Wed Nov 11 00:30:48 EST 2020 Thu May 29 08:40:45 EDT 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 29 |
Language | English |
License | Freely available online through the PNAS open access option. |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c531t-68a52d9a20490ce554c83c96e33b79d29a2b8738346b0991a0c4547c141a9f7f3 |
Notes | SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 Communicated by Tom Maniatis, Columbia University Medical Center, New York, NY, June 8, 2010 (received for review April 20, 2010) Author contributions: C.J.M. and B.R.G. designed research; C.J.M. performed research; C.J.M., M.O.D., and J.E.-M. contributed new reagents/analytic tools; C.J.M., M.O.D., and B.R.G. analyzed data; and C.J.M. and B.R.G. wrote the paper. |
OpenAccessLink | http://doi.org/10.1073/pnas.1007586107 |
PMID | 20615941 |
PQID | 664169073 |
PQPubID | 42026 |
PageCount | 5 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_2919919 pubmed_primary_20615941 proquest_miscellaneous_754562912 crossref_primary_10_1073_pnas_1007586107 pnas_primary_107_29_12975 proquest_journals_664169073 proquest_miscellaneous_734000909 jstor_primary_25708649 proquest_miscellaneous_1825413115 crossref_citationtrail_10_1073_pnas_1007586107 |
ProviderPackageCode | RNA PNE CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2010-07-20 |
PublicationDateYYYYMMDD | 2010-07-20 |
PublicationDate_xml | – month: 07 year: 2010 text: 2010-07-20 day: 20 |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States – name: Washington |
PublicationTitle | Proceedings of the National Academy of Sciences - PNAS |
PublicationTitleAlternate | Proc Natl Acad Sci U S A |
PublicationYear | 2010 |
Publisher | National Academy of Sciences National Acad Sciences |
Publisher_xml | – name: National Academy of Sciences – name: National Acad Sciences |
References | Tasic B (e_1_3_4_11_2) 2002; 10 McManus CJ (e_1_3_4_23_2) 2010; 20 Li H (e_1_3_4_15_2) 2008; 321 Clark AG (e_1_3_4_21_2) 2007; 450 Zhang G (e_1_3_4_13_2) 2010; 20 Ozsolak F (e_1_3_4_19_2) 2009; 461 Sutton RE (e_1_3_4_3_2) 1986; 47 Solnick D (e_1_3_4_2_2) 1985; 42 Horiuchi T (e_1_3_4_7_2) 2003; 17 Langmead B (e_1_3_4_22_2) 2009; 10 Li X (e_1_3_4_12_2) 2009; 68 Nilsen TW (e_1_3_4_4_2) 2001; 17 Gingeras TR (e_1_3_4_8_2) 2009; 461 Cocquet J (e_1_3_4_9_2) 2006; 88 Dorn R (e_1_3_4_5_2) 2001; 98 Chintapalli VR (e_1_3_4_16_2) 2007; 39 Robertson HM (e_1_3_4_18_2) 2007; 176 Gabler M (e_1_3_4_14_2) 2005; 169 Metz CW (e_1_3_4_17_2) 1916; 21 Mamanova L (e_1_3_4_20_2) 2010; 7 Labrador M (e_1_3_4_6_2) 2001; 409 Odelberg SJ (e_1_3_4_10_2) 1995; 23 Konarska MM (e_1_3_4_1_2) 1985; 42 Proc Natl Acad Sci U S A. 2013 May 7;110(19):7958 |
References_xml | – volume: 176 start-page: 1351 year: 2007 ident: e_1_3_4_18_2 article-title: The bursicon gene in mosquitoes: An unusual example of mRNA trans-splicing publication-title: Genetics doi: 10.1534/genetics.107.070938 – volume: 98 start-page: 9724 year: 2001 ident: e_1_3_4_5_2 article-title: Transgene analysis proves mRNA trans-splicing at the complex mod(mdg4) locus in Drosophila publication-title: Proc Natl Acad Sci USA doi: 10.1073/pnas.151268698 – volume: 10 start-page: R25 year: 2009 ident: e_1_3_4_22_2 article-title: Ultrafast and memory-efficient alignment of short DNA sequences to the human genome publication-title: Genome Biol doi: 10.1186/gb-2009-10-3-r25 – volume: 409 start-page: 1000 year: 2001 ident: e_1_3_4_6_2 article-title: Protein encoding by both DNA strands publication-title: Nature doi: 10.1038/35059000 – volume: 88 start-page: 127 year: 2006 ident: e_1_3_4_9_2 article-title: Reverse transcriptase template switching and false alternative transcripts publication-title: Genomics doi: 10.1016/j.ygeno.2005.12.013 – volume: 17 start-page: 2496 year: 2003 ident: e_1_3_4_7_2 article-title: Alternative trans-splicing of constant and variable exons of a Drosophila axon guidance gene, lola publication-title: Genes Dev doi: 10.1101/gad.1137303 – volume: 321 start-page: 1357 year: 2008 ident: e_1_3_4_15_2 article-title: A neoplastic gene fusion mimics trans-splicing of RNAs in normal human cells publication-title: Science doi: 10.1126/science.1156725 – volume: 68 start-page: 56 year: 2009 ident: e_1_3_4_12_2 article-title: Short homologous sequences are strongly associated with the generation of chimeric RNAs in eukaryotes publication-title: J Mol Evol doi: 10.1007/s00239-008-9187-0 – volume: 17 start-page: 678 year: 2001 ident: e_1_3_4_4_2 article-title: Evolutionary origin of SL-addition trans-splicing: Still an enigma publication-title: Trends Genet doi: 10.1016/S0168-9525(01)02499-4 – volume: 23 start-page: 2049 year: 1995 ident: e_1_3_4_10_2 article-title: Template-switching during DNA synthesis by Thermus aquaticus DNA polymerase I publication-title: Nucleic Acids Res doi: 10.1093/nar/23.11.2049 – volume: 461 start-page: 814 year: 2009 ident: e_1_3_4_19_2 article-title: Direct RNA sequencing publication-title: Nature doi: 10.1038/nature08390 – volume: 450 start-page: 203 year: 2007 ident: e_1_3_4_21_2 article-title: Evolution of genes and genomes on the Drosophila phylogeny publication-title: Nature doi: 10.1038/nature06341 – volume: 42 start-page: 165 year: 1985 ident: e_1_3_4_1_2 article-title: Trans splicing of mRNA precursors in vitro publication-title: Cell doi: 10.1016/S0092-8674(85)80112-4 – volume: 42 start-page: 157 year: 1985 ident: e_1_3_4_2_2 article-title: Trans splicing of mRNA precursors publication-title: Cell doi: 10.1016/S0092-8674(85)80111-2 – volume: 169 start-page: 723 year: 2005 ident: e_1_3_4_14_2 article-title: Trans-splicing of the mod(mdg4) complex locus is conserved between the distantly related species Drosophila melanogaster and D. virilis publication-title: Genetics doi: 10.1534/genetics.103.020842 – volume: 7 start-page: 130 year: 2010 ident: e_1_3_4_20_2 article-title: FRT-seq: Amplification-free, strand-specific transcriptome sequencing publication-title: Nat Methods doi: 10.1038/nmeth.1417 – volume: 47 start-page: 527 year: 1986 ident: e_1_3_4_3_2 article-title: Evidence for trans splicing in trypanosomes publication-title: Cell doi: 10.1016/0092-8674(86)90617-3 – volume: 20 start-page: 816 year: 2010 ident: e_1_3_4_23_2 article-title: Regulatory divergence in Drosophila revealed by mRNA-seq publication-title: Genome Res doi: 10.1101/gr.102491.109 – volume: 461 start-page: 206 year: 2009 ident: e_1_3_4_8_2 article-title: Implications of chimaeric non-co-linear transcripts publication-title: Nature doi: 10.1038/nature08452 – volume: 10 start-page: 21 year: 2002 ident: e_1_3_4_11_2 article-title: Promoter choice determines splice site selection in protocadherin alpha and gamma pre-mRNA splicing publication-title: Mol Cell doi: 10.1016/S1097-2765(02)00578-6 – volume: 21 start-page: 213 year: 1916 ident: e_1_3_4_17_2 article-title: Chromosome studies on the Diptera II. The paired association of chromosomes in the Diptera and its significance publication-title: J Exp Zool doi: 10.1002/jez.1400210204 – volume: 39 start-page: 715 year: 2007 ident: e_1_3_4_16_2 article-title: Using FlyAtlas to identify better Drosophila melanogaster models of human disease publication-title: Nat Genet doi: 10.1038/ng2049 – volume: 20 start-page: 646 year: 2010 ident: e_1_3_4_13_2 article-title: Deep RNA sequencing at single base-pair resolution reveals high complexity of the rice transcriptome publication-title: Genome Res doi: 10.1101/gr.100677.109 – reference: - Proc Natl Acad Sci U S A. 2013 May 7;110(19):7958 |
SSID | ssj0009580 |
Score | 2.3117864 |
Snippet | Precursor mRNA (pre-mRNA) splicing can join exons contained on either a single pre-mRNA (cis) or on separate pre-mRNAs (trans). It is exceedingly rare to have... Precursor mRNA (pre-mRNA) splicing can join exons contained on either a single pre-mRNA ( cis ) or on separate pre-mRNAs ( trans ). It is exceedingly rare to... Precursor mRNA (pre-mRNA) splicing can join exons contained on either a single pre-mRNA ( cis ) or on separate pre-mRNAs ( trans ). It is exceedingly rare to... |
SourceID | pubmedcentral proquest pubmed crossref pnas jstor |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 12975 |
SubjectTerms | alleles Animals Base Sequence Biological Sciences chimerism Drosophila Drosophila melanogaster - genetics Drosophila Proteins - genetics Exons Gene expression Genes Genes, Insect - genetics Genetics Genomes high-throughput nucleotide sequencing Hybridity Hybrids Insects introns loci Messenger RNA Models, Genetic Proteins Reproducibility of Results Reverse Transcriptase Polymerase Chain Reaction Ribonucleic acid RNA RNA - genetics RNA precursors RNA, Messenger - genetics RNA, Messenger - metabolism Sequence Analysis, DNA Sequencing Trans splicing Trans-Splicing - genetics Transcription Factors - genetics |
Title | Global analysis of trans-splicing in Drosophila |
URI | https://www.jstor.org/stable/25708649 http://www.pnas.org/content/107/29/12975.abstract https://www.ncbi.nlm.nih.gov/pubmed/20615941 https://www.proquest.com/docview/664169073 https://www.proquest.com/docview/1825413115 https://www.proquest.com/docview/734000909 https://www.proquest.com/docview/754562912 https://pubmed.ncbi.nlm.nih.gov/PMC2919919 |
Volume | 107 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3da9swEBdZ97KXsW7r5nYbHuyhIziNJUWyHsu6UQLJymihb0aWZRYoTsjHy_rP986SP1KSsu3FJPZZFrqT7k66-x0hXwwrlJacR7HOODooMKVoTiOemaLILSgcU6F9TsXlDR_fjm57vftudsk6G5g_O_NK_oercA_4ilmy_8DZplG4Ab-Bv3AFDsP1r3jsAPv7ugMsskbdE63wVNpnq1wsq1IFszvdNUSvGsW1qsMEpvW-4HmbZeKn_qof9a-mbc3iiZnocuPQCQb98dw2cRoXGwfz6MPx-z8Hjc0-WyzsMppov8M9nuezNvpHYwEMV_Qa8aJAJn8NujsSeJguIzpsAzae6G13KaagHrlLoG6WYlcB18uc3wpxK2uMKcAdNY3_1U4dAIsWFi4u9aoKARklom52G1gb6_clgqtn5DkFH4PVWz0NYnPi8pd8P2tcKMnOHrW9ZdK4qFaEygWiXW7L4-jbjjlz_Yq89H5IeO6E6pD0bPmaHNYDGJ56OPKvb8iZk7KwlrJwXoTbUhbOyrCVsrfk5sf362-XkS-zERlYgNeRSPSI5kpTPAQ2FuxLkzCjhGUskyqn8CRLJEsYFxn4E7EeGkSBMzGPtSpkwY7IQTkv7XsS5swWAgxem4BbP8rzJBcjXWhhWJ6ANlMBGdQjlRqPQY-lUO7SKhZCshRHLW2HNiCnzQsLB7-yn_SoGvqGruZvQIKKtH1fplSllUAF5KRmUOon9ioVguPhsWQB-dw8hVUXj9J0aecb-CxurFRIVQEJ99BIxlGMhuoJEvRfqIppQN45oWh7j76G4nFA5Ja4NASIC7_9pJz9rvDhoUFgkzreNyAn5EU7bT-Qg_VyYz-Cab3OPlVT4AG_Q8ty |
linkProvider | National Library of Medicine |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Global+analysis+of+trans-splicing+in+Drosophila&rft.jtitle=Proceedings+of+the+National+Academy+of+Sciences+-+PNAS&rft.au=McManus%2C+C.+Joel&rft.au=Duff%2C+Michael+O.&rft.au=Eipper-Mains%2C+Jodi&rft.au=Graveley%2C+Brenton+R.&rft.date=2010-07-20&rft.pub=National+Academy+of+Sciences&rft.issn=0027-8424&rft.volume=107&rft.issue=29&rft.spage=12975&rft.epage=12979&rft_id=info:doi/10.1073%2Fpnas.1007586107&rft.externalDocID=25708649 |
thumbnail_m | http://utb.summon.serialssolutions.com/2.0.0/image/custom?url=http%3A%2F%2Fwww.pnas.org%2Fcontent%2F107%2F29.cover.gif |
thumbnail_s | http://utb.summon.serialssolutions.com/2.0.0/image/custom?url=http%3A%2F%2Fwww.pnas.org%2Fcontent%2F107%2F29.cover.gif |