An epigenetically mediated double negative cascade from EFD to HB21 regulates anther development

Epigenetic modifications are crucial for plant development. EFD ( E xine F ormation D efect) encodes a SAM-dependent methyltransferase that is essential for the pollen wall pattern formation and male fertility in Arabidopsis. In this study, we find that the expression of DRM2 , a de novo DNA methylt...

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Published inNature communications Vol. 15; no. 1; pp. 7796 - 12
Main Authors Zhang, Cheng, Xiong, Ao-Tong, Ren, Meng-Yi, Zhao, Yan-Yun, Huang, Min-Jia, Huang, Long-Cheng, Zhang, Zheng, Wang, Yun, Zheng, Quan-Quan, Fan, Jing, Guan, Jing-Jing, Yang, Zhong-Nan
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 06.09.2024
Nature Publishing Group
Nature Portfolio
Subjects
14
14/19
631/449/1659
631/449/2491
631/449/2679/1743
Arabidopsis - genetics
Arabidopsis - growth & development
Arabidopsis - metabolism
Arabidopsis Proteins - genetics
Arabidopsis Proteins - metabolism
Dehiscence
Deoxyribonucleic acid
DNA
DNA Methylation
DNA methyltransferase
Epigenesis, Genetic
Epigenetics
Fertility
Flowers - genetics
Flowers - growth & development
Gene expression
Gene Expression Regulation, Plant
Genetic analysis
Histones
Humanities and Social Sciences
Methyltransferases - genetics
Methyltransferases - metabolism
multidisciplinary
Mutation
Pattern formation
Plant reproductive structures
Plants, Genetically Modified
Pollen
Pollen - genetics
Pollen - growth & development
Pollen - metabolism
Science
Science (multidisciplinary)
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Abstract Epigenetic modifications are crucial for plant development. EFD ( E xine F ormation D efect) encodes a SAM-dependent methyltransferase that is essential for the pollen wall pattern formation and male fertility in Arabidopsis. In this study, we find that the expression of DRM2 , a de novo DNA methyltransferase in plants, complements for the defects in efd , suggesting its potential de novo DNA methyltransferase activity. Genetic analysis indicates that EFD functions through HB21 , as the knockout of HB21 fully restores fertility in efd mutants. DNA methylation and histone modification analyses reveal that EFD represses the transcription of HB21 through epigenetic mechanisms. Additionally, we demonstrate that HB21 directly represses the expression of genes crucial for pollen formation and anther dehiscence, including CalS5 , RPG1/SWEET8 , CYP703A2 and NST2 . Collectively, our findings unveil a double negative regulatory cascade mediated by epigenetic modifications that coordinates anther development, offering insights into the epigenetic regulation of this process. Epigenetic modifications are crucial for plant development. Here, the authors find an epigenetically mediated double negative cascade for pollen formation and anther dehiscence, offering new insights into epigenetic regulation of anther development.
AbstractList Abstract Epigenetic modifications are crucial for plant development. EFD ( E xine F ormation D efect) encodes a SAM-dependent methyltransferase that is essential for the pollen wall pattern formation and male fertility in Arabidopsis. In this study, we find that the expression of DRM2, a de novo DNA methyltransferase in plants, complements for the defects in efd, suggesting its potential de novo DNA methyltransferase activity. Genetic analysis indicates that EFD functions through HB21, as the knockout of HB21 fully restores fertility in efd mutants. DNA methylation and histone modification analyses reveal that EFD represses the transcription of HB21 through epigenetic mechanisms. Additionally, we demonstrate that HB21 directly represses the expression of genes crucial for pollen formation and anther dehiscence, including CalS5, RPG1/SWEET8, CYP703A2 and NST2. Collectively, our findings unveil a double negative regulatory cascade mediated by epigenetic modifications that coordinates anther development, offering insights into the epigenetic regulation of this process.
Epigenetic modifications are crucial for plant development. EFD ( E xine F ormation D efect) encodes a SAM-dependent methyltransferase that is essential for the pollen wall pattern formation and male fertility in Arabidopsis. In this study, we find that the expression of DRM2 , a de novo DNA methyltransferase in plants, complements for the defects in efd , suggesting its potential de novo DNA methyltransferase activity. Genetic analysis indicates that EFD functions through HB21 , as the knockout of HB21 fully restores fertility in efd mutants. DNA methylation and histone modification analyses reveal that EFD represses the transcription of HB21 through epigenetic mechanisms. Additionally, we demonstrate that HB21 directly represses the expression of genes crucial for pollen formation and anther dehiscence, including CalS5 , RPG1/SWEET8 , CYP703A2 and NST2 . Collectively, our findings unveil a double negative regulatory cascade mediated by epigenetic modifications that coordinates anther development, offering insights into the epigenetic regulation of this process. Epigenetic modifications are crucial for plant development. Here, the authors find an epigenetically mediated double negative cascade for pollen formation and anther dehiscence, offering new insights into epigenetic regulation of anther development.
Epigenetic modifications are crucial for plant development. EFD (Exine Formation Defect) encodes a SAM-dependent methyltransferase that is essential for the pollen wall pattern formation and male fertility in Arabidopsis. In this study, we find that the expression of DRM2, a de novo DNA methyltransferase in plants, complements for the defects in efd, suggesting its potential de novo DNA methyltransferase activity. Genetic analysis indicates that EFD functions through HB21, as the knockout of HB21 fully restores fertility in efd mutants. DNA methylation and histone modification analyses reveal that EFD represses the transcription of HB21 through epigenetic mechanisms. Additionally, we demonstrate that HB21 directly represses the expression of genes crucial for pollen formation and anther dehiscence, including CalS5, RPG1/SWEET8, CYP703A2 and NST2. Collectively, our findings unveil a double negative regulatory cascade mediated by epigenetic modifications that coordinates anther development, offering insights into the epigenetic regulation of this process.Epigenetic modifications are crucial for plant development. EFD (Exine Formation Defect) encodes a SAM-dependent methyltransferase that is essential for the pollen wall pattern formation and male fertility in Arabidopsis. In this study, we find that the expression of DRM2, a de novo DNA methyltransferase in plants, complements for the defects in efd, suggesting its potential de novo DNA methyltransferase activity. Genetic analysis indicates that EFD functions through HB21, as the knockout of HB21 fully restores fertility in efd mutants. DNA methylation and histone modification analyses reveal that EFD represses the transcription of HB21 through epigenetic mechanisms. Additionally, we demonstrate that HB21 directly represses the expression of genes crucial for pollen formation and anther dehiscence, including CalS5, RPG1/SWEET8, CYP703A2 and NST2. Collectively, our findings unveil a double negative regulatory cascade mediated by epigenetic modifications that coordinates anther development, offering insights into the epigenetic regulation of this process.
Epigenetic modifications are crucial for plant development. EFD (Exine Formation Defect) encodes a SAM-dependent methyltransferase that is essential for the pollen wall pattern formation and male fertility in Arabidopsis. In this study, we find that the expression of DRM2, a de novo DNA methyltransferase in plants, complements for the defects in efd, suggesting its potential de novo DNA methyltransferase activity. Genetic analysis indicates that EFD functions through HB21, as the knockout of HB21 fully restores fertility in efd mutants. DNA methylation and histone modification analyses reveal that EFD represses the transcription of HB21 through epigenetic mechanisms. Additionally, we demonstrate that HB21 directly represses the expression of genes crucial for pollen formation and anther dehiscence, including CalS5, RPG1/SWEET8, CYP703A2 and NST2. Collectively, our findings unveil a double negative regulatory cascade mediated by epigenetic modifications that coordinates anther development, offering insights into the epigenetic regulation of this process.
Epigenetic modifications are crucial for plant development. EFD (ExineFormationDefect) encodes a SAM-dependent methyltransferase that is essential for the pollen wall pattern formation and male fertility in Arabidopsis. In this study, we find that the expression of DRM2, a de novo DNA methyltransferase in plants, complements for the defects in efd, suggesting its potential de novo DNA methyltransferase activity. Genetic analysis indicates that EFD functions through HB21, as the knockout of HB21 fully restores fertility in efd mutants. DNA methylation and histone modification analyses reveal that EFD represses the transcription of HB21 through epigenetic mechanisms. Additionally, we demonstrate that HB21 directly represses the expression of genes crucial for pollen formation and anther dehiscence, including CalS5, RPG1/SWEET8, CYP703A2 and NST2. Collectively, our findings unveil a double negative regulatory cascade mediated by epigenetic modifications that coordinates anther development, offering insights into the epigenetic regulation of this process.Epigenetic modifications are crucial for plant development. Here, the authors find an epigenetically mediated double negative cascade for pollen formation and anther dehiscence, offering new insights into epigenetic regulation of anther development.
ArticleNumber 7796
Author Ren, Meng-Yi
Zhao, Yan-Yun
Zhang, Zheng
Xiong, Ao-Tong
Yang, Zhong-Nan
Zhang, Cheng
Huang, Long-Cheng
Zheng, Quan-Quan
Huang, Min-Jia
Wang, Yun
Fan, Jing
Guan, Jing-Jing
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/39242635$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1016/j.tcb.2008.02.005
10.1007/s004970050158
10.3109/10520296909063335
10.1104/pp.113.214940
10.1016/j.febslet.2012.06.026
10.1104/pp.108.118026
10.1016/j.cell.2005.12.034
10.1007/s00425-014-2199-7
10.1104/pp.105.063461
10.1111/j.1365-313X.2004.02169.x
10.1104/pp.18.00219
10.1016/j.molp.2021.03.001
10.1105/tpc.015800
10.1007/s00497-012-0208-1
10.3389/fpls.2022.878693
10.1186/s13059-022-02768-x
10.1111/jipb.12901
10.1105/tpc.18.00584
10.1038/s41586-022-05171-5
10.1038/s41588-017-0008-5
10.1104/pp.111.184853
10.1016/j.pbi.2014.10.003
10.1186/s12870-017-1185-1
10.1073/pnas.1613199114
10.1146/annurev.arplant.043008.091939
10.1111/j.1365-313X.2007.03254.x
10.1371/journal.pbio.0050129
10.1105/tpc.113.113340
10.1093/plcell/koac136
10.1038/ng1929
10.1016/j.pbi.2015.11.010
10.1104/pp.19.00576
10.1016/S0960-9822(02)00925-9
10.1007/s11434-016-1062-6
10.1038/nrm2763
10.1038/nsmb.2735
10.1016/j.cell.2010.09.050
10.1016/j.cub.2003.11.052
10.1016/j.pbi.2011.01.001
10.1016/j.tplants.2007.08.003
10.1016/S0167-4781(98)00119-5
10.1126/science.1059745
10.1016/j.pbi.2008.07.004
10.1105/tpc.105.031716
10.1111/nph.12788
10.1016/j.molp.2020.08.005
10.1093/jxb/err014
10.1038/nsmb840
10.1105/tpc.105.036004
10.1111/nph.14132
10.1002/pld3.100
10.1371/journal.pgen.1007397
10.1111/tpj.12694
10.1038/nrg3683
10.1038/nrg2719
10.1016/S0022-2836(03)00506-0
10.1093/plcell/koab060
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References Li (CR50) 2013; 25
Bowler (CR58) 2004; 39
Chan (CR36) 1998; 1442
Zhang (CR56) 2007; 52
Xu (CR46) 2019; 181
Edlund, Swanson, Preuss (CR14) 2004; 16
Matzke, Mosher (CR1) 2014; 15
Walker (CR6) 2018; 50
Zhang (CR7) 2007; 5
Zheng, Chen (CR8) 2011; 14
Zilberman (CR37) 2008; 11
Li (CR11) 2021; 14
Mitsuda (CR22) 2005; 17
Hu (CR17) 2014; 203
Zilberman (CR39) 2007; 39
Lindroth (CR18) 2001; 292
Sun (CR25) 2013; 26
Xu (CR15) 2016; 61
Liu (CR41) 2010; 61
Xiao, Wagner (CR33) 2015; 23
Ye (CR35) 2022; 609
Mallory, Bartel, Bartel (CR47) 2005; 17
Henriksson (CR30) 2005; 139
Roodbarkelari, Groot (CR28) 2017; 213
Miao (CR29) 2018; 30
Gehring (CR38) 2006; 124
Yang (CR54) 2022; 13
Huang, Sun (CR12) 2022; 34
Xue (CR52) 2020; 13
Rosenfeld, Alon (CR48) 2003; 329
Cao, Jacobsen (CR3) 2002; 12
Kohler, Villar (CR9) 2008; 18
Zhao (CR10) 2022; 23
Simon, Kingston (CR31) 2009; 10
Law, Jacobsen (CR2) 2010; 11
Gu (CR19) 2014; 80
Shu (CR34) 2019; 3
Yang (CR44) 2013; 162
Goldberg, Beals, Sanders (CR13) 1993; 5
Wang (CR45) 2017; 17
Alexander (CR55) 1969; 44
Cao (CR4) 2003; 13
Forderer, Zhou, Turck (CR32) 2016; 29
Gonzalez-Grandio (CR27) 2017; 114
Wilson (CR16) 2011; 62
Shoval, Alon (CR49) 2010; 143
Chang (CR42) 2020; 62
Chang (CR24) 2012; 158
Renzaglia, Lopez, Johnson (CR53) 2015; 241
Sanders (CR21) 1999; 11
Lorincz (CR40) 2004; 11
Yao (CR57) 2018; 14
Ariel (CR26) 2007; 12
Kim (CR43) 2012; 586
Wang (CR20) 2018; 178
Guan (CR23) 2008; 147
Stroud (CR5) 2014; 21
Jiang (CR51) 2021; 33
MA Matzke (52114_CR1) 2014; 15
ZB Zhang (52114_CR56) 2007; 52
X Zhang (52114_CR7) 2007; 5
YN Chang (52114_CR42) 2020; 62
A Jiang (52114_CR51) 2021; 33
HS Chang (52114_CR24) 2012; 158
X Cao (52114_CR3) 2002; 12
T Xu (52114_CR15) 2016; 61
K Wang (52114_CR20) 2018; 178
Z Li (52114_CR50) 2013; 25
AC Mallory (52114_CR47) 2005; 17
Z Li (52114_CR11) 2021; 14
X Huang (52114_CR12) 2022; 34
B Wang (52114_CR45) 2017; 17
MX Sun (52114_CR25) 2013; 26
R Ye (52114_CR35) 2022; 609
N Rosenfeld (52114_CR48) 2003; 329
H Stroud (52114_CR5) 2014; 21
F Roodbarkelari (52114_CR28) 2017; 213
JA Law (52114_CR2) 2010; 11
ZA Wilson (52114_CR16) 2011; 62
C Liu (52114_CR41) 2010; 61
E Henriksson (52114_CR30) 2005; 139
B Zheng (52114_CR8) 2011; 14
KS Renzaglia (52114_CR53) 2015; 241
A Forderer (52114_CR32) 2016; 29
C Kohler (52114_CR9) 2008; 18
AF Edlund (52114_CR14) 2004; 16
JN Gu (52114_CR19) 2014; 80
JA Simon (52114_CR31) 2009; 10
J Walker (52114_CR6) 2018; 50
L Zhao (52114_CR10) 2022; 23
MC Lorincz (52114_CR40) 2004; 11
XF Xu (52114_CR46) 2019; 181
PM Sanders (52114_CR21) 1999; 11
ZQ Miao (52114_CR29) 2018; 30
RB Goldberg (52114_CR13) 1993; 5
M Gehring (52114_CR38) 2006; 124
O Shoval (52114_CR49) 2010; 143
JS Xue (52114_CR52) 2020; 13
X Yao (52114_CR57) 2018; 14
RL Chan (52114_CR36) 1998; 1442
E Gonzalez-Grandio (52114_CR27) 2017; 114
C Bowler (52114_CR58) 2004; 39
N Mitsuda (52114_CR22) 2005; 17
J Xiao (52114_CR33) 2015; 23
D Zilberman (52114_CR39) 2007; 39
J Hu (52114_CR17) 2014; 203
J Shu (52114_CR34) 2019; 3
YF Guan (52114_CR23) 2008; 147
MP Alexander (52114_CR55) 1969; 44
JY Kim (52114_CR43) 2012; 586
NY Yang (52114_CR54) 2022; 13
J Yang (52114_CR44) 2013; 162
X Cao (52114_CR4) 2003; 13
FD Ariel (52114_CR26) 2007; 12
D Zilberman (52114_CR37) 2008; 11
AM Lindroth (52114_CR18) 2001; 292
References_xml – volume: 18
  start-page: 236
  year: 2008
  end-page: 243
  ident: CR9
  article-title: Programming of gene expression by Polycomb group proteins
  publication-title: Trends Cell Biol.
  doi: 10.1016/j.tcb.2008.02.005
– volume: 11
  start-page: 297
  year: 1999
  end-page: 322
  ident: CR21
  article-title: Anther developmental defects in Arabidopsis thaliana male-sterile mutants
  publication-title: Sex. Plant Reprod.
  doi: 10.1007/s004970050158
– volume: 44
  start-page: 117
  year: 1969
  end-page: 122
  ident: CR55
  article-title: Differential staining of aborted and nonaborted pollen
  publication-title: Stain Technol.
  doi: 10.3109/10520296909063335
– volume: 162
  start-page: 720
  year: 2013
  end-page: 731
  ident: CR44
  article-title: AUXIN RESPONSE FACTOR17 is essential for pollen wall pattern formation in Arabidopsis
  publication-title: Plant Physiol.
  doi: 10.1104/pp.113.214940
– volume: 586
  start-page: 3159
  year: 2012
  end-page: 3165
  ident: CR43
  article-title: H3K27 methylation and H3S28 phosphorylation-dependent transcriptional regulation by INHAT subunit SET/TAF-Ibeta
  publication-title: FEBS Lett.
  doi: 10.1016/j.febslet.2012.06.026
– volume: 147
  start-page: 852
  year: 2008
  end-page: 863
  ident: CR23
  article-title: RUPTURED POLLEN GRAIN1, a member of the MtN3/saliva gene family, is crucial for exine pattern formation and cell integrity of microspores in Arabidopsis
  publication-title: Plant Physiol.
  doi: 10.1104/pp.108.118026
– volume: 124
  start-page: 495
  year: 2006
  end-page: 506
  ident: CR38
  article-title: DEMETER DNA glycosylase establishes MEDEA polycomb gene self-imprinting by allele-specific demethylation
  publication-title: Cell
  doi: 10.1016/j.cell.2005.12.034
– volume: 241
  start-page: 615
  year: 2015
  end-page: 627
  ident: CR53
  article-title: Callose is integral to the development of permanent tetrads in the liverwort Sphaerocarpos
  publication-title: Planta
  doi: 10.1007/s00425-014-2199-7
– volume: 139
  start-page: 509
  year: 2005
  end-page: 518
  ident: CR30
  article-title: Homeodomain leucine zipper class I genes in Arabidopsis. Expression patterns and phylogenetic relationships
  publication-title: Plant Physiol.
  doi: 10.1104/pp.105.063461
– volume: 39
  start-page: 776
  year: 2004
  end-page: 789
  ident: CR58
  article-title: Chromatin techniques for plant cells
  publication-title: Plant J.
  doi: 10.1111/j.1365-313X.2004.02169.x
– volume: 178
  start-page: 283
  year: 2018
  end-page: 294
  ident: CR20
  article-title: The regulation of sporopollenin biosynthesis genes for rapid pollen wall formation
  publication-title: Plant Physiol.
  doi: 10.1104/pp.18.00219
– volume: 14
  start-page: 732
  year: 2021
  end-page: 747
  ident: CR11
  article-title: JASMONATE-ZIM DOMAIN proteins engage Polycomb chromatin modifiers to modulate Jasmonate signaling in Arabidopsis
  publication-title: Mol. Plant
  doi: 10.1016/j.molp.2021.03.001
– volume: 16
  start-page: S84
  year: 2004
  end-page: S97
  ident: CR14
  article-title: Pollen and stigma structure and function: the role of diversity in pollination
  publication-title: Plant Cell
  doi: 10.1105/tpc.015800
– volume: 26
  start-page: 83
  year: 2013
  end-page: 91
  ident: CR25
  article-title: Arabidopsis RPG1 is important for primexine deposition and functions redundantly with RPG2 for plant fertility at the late reproductive stage
  publication-title: Plant Reprod.
  doi: 10.1007/s00497-012-0208-1
– volume: 13
  start-page: 878693
  year: 2022
  ident: CR54
  article-title: Documenting the sporangium development of the polypodiales fern pteris multifida
  publication-title: Front. Plant Sci.
  doi: 10.3389/fpls.2022.878693
– volume: 23
  year: 2022
  ident: CR10
  article-title: DNA methylation underpins the epigenomic landscape regulating genome transcription in Arabidopsis
  publication-title: Genome Biol.
  doi: 10.1186/s13059-022-02768-x
– volume: 62
  start-page: 563
  year: 2020
  end-page: 580
  ident: CR42
  article-title: Epigenetic regulation in plant abiotic stress responses
  publication-title: J. Integr. Plant Biol.
  doi: 10.1111/jipb.12901
– volume: 30
  start-page: 2761
  year: 2018
  end-page: 2778
  ident: CR29
  article-title: HOMEOBOX PROTEIN52 mediates the crosstalk between ethylene and auxin signaling during primary root elongation by modulating auxin transport-related gene expression
  publication-title: Plant Cell
  doi: 10.1105/tpc.18.00584
– volume: 609
  start-page: 986
  year: 2022
  end-page: 993
  ident: CR35
  article-title: Glucose-driven TOR-FIE-PRC2 signalling controls plant development
  publication-title: Nature
  doi: 10.1038/s41586-022-05171-5
– volume: 50
  start-page: 130
  year: 2018
  end-page: 137
  ident: CR6
  article-title: Sexual-lineage-specific DNA methylation regulates meiosis in Arabidopsis
  publication-title: Nat. Genet.
  doi: 10.1038/s41588-017-0008-5
– volume: 158
  start-page: 264
  year: 2012
  end-page: 272
  ident: CR24
  article-title: No primexine and plasma membrane undulation is essential for primexine deposition and plasma membrane undulation during microsporogenesis in Arabidopsis
  publication-title: Plant Physiol.
  doi: 10.1104/pp.111.184853
– volume: 23
  start-page: 15
  year: 2015
  end-page: 24
  ident: CR33
  article-title: Polycomb repression in the regulation of growth and development in Arabidopsis
  publication-title: Curr. Opin. Plant Biol.
  doi: 10.1016/j.pbi.2014.10.003
– volume: 17
  year: 2017
  ident: CR45
  article-title: Fine regulation of ARF17 for anther development and pollen formation
  publication-title: BMC Plant Biol.
  doi: 10.1186/s12870-017-1185-1
– volume: 114
  start-page: E245
  year: 2017
  end-page: E254
  ident: CR27
  article-title: Abscisic acid signaling is controlled by a BRANCHED1/HD-ZIP I cascade in Arabidopsis axillary buds
  publication-title: Proc. Natl Acad. Sci. USA
  doi: 10.1073/pnas.1613199114
– volume: 61
  start-page: 395
  year: 2010
  end-page: 420
  ident: CR41
  article-title: Histone methylation in higher plants
  publication-title: Annu. Rev. Plant Biol.
  doi: 10.1146/annurev.arplant.043008.091939
– volume: 52
  start-page: 528
  year: 2007
  end-page: 538
  ident: CR56
  article-title: Transcription factor AtMYB103 is required for anther development by regulating tapetum development, callose dissolution and exine formation in Arabidopsis
  publication-title: Plant J.
  doi: 10.1111/j.1365-313X.2007.03254.x
– volume: 5
  start-page: e129
  year: 2007
  ident: CR7
  article-title: Whole-genome analysis of histone H3 lysine 27 trimethylation in Arabidopsis
  publication-title: PLoS Biol.
  doi: 10.1371/journal.pbio.0050129
– volume: 25
  start-page: 3311
  year: 2013
  end-page: 3328
  ident: CR50
  article-title: Ethylene-insensitive3 is a senescence-associated gene that accelerates age-dependent leaf senescence by directly repressing miR164 transcription in Arabidopsis
  publication-title: Plant Cell
  doi: 10.1105/tpc.113.113340
– volume: 34
  start-page: 2989
  year: 2022
  end-page: 3005
  ident: CR12
  article-title: H3K27 methylation regulates the fate of two cell lineages in male gametophytes
  publication-title: Plant Cell
  doi: 10.1093/plcell/koac136
– volume: 39
  start-page: 61
  year: 2007
  end-page: 69
  ident: CR39
  article-title: Genome-wide analysis of Arabidopsis thaliana DNA methylation uncovers an interdependence between methylation and transcription
  publication-title: Nat. Genet.
  doi: 10.1038/ng1929
– volume: 29
  start-page: 169
  year: 2016
  end-page: 178
  ident: CR32
  article-title: The age of multiplexity: recruitment and interactions of Polycomb complexes in plants
  publication-title: Curr. Opin. Plant Biol.
  doi: 10.1016/j.pbi.2015.11.010
– volume: 181
  start-page: 645
  year: 2019
  end-page: 655
  ident: CR46
  article-title: AUXIN RESPONSE FACTOR17 directly regulates MYB108 for anther dehiscence
  publication-title: Plant Physiol.
  doi: 10.1104/pp.19.00576
– volume: 12
  start-page: 1138
  year: 2002
  end-page: 1144
  ident: CR3
  article-title: Role of the arabidopsis DRM methyltransferases in de novo DNA methylation and gene silencing
  publication-title: Curr. Biol.
  doi: 10.1016/S0960-9822(02)00925-9
– volume: 61
  start-page: 832
  year: 2016
  end-page: 837
  ident: CR15
  article-title: Pollen wall pattern in Arabidopsis
  publication-title: Sci. Bull.
  doi: 10.1007/s11434-016-1062-6
– volume: 10
  start-page: 697
  year: 2009
  end-page: 708
  ident: CR31
  article-title: Mechanisms of polycomb gene silencing: knowns and unknowns
  publication-title: Nat. Rev. Mol. Cell Biol.
  doi: 10.1038/nrm2763
– volume: 21
  start-page: 64
  year: 2014
  end-page: 72
  ident: CR5
  article-title: Non-CG methylation patterns shape the epigenetic landscape in Arabidopsis
  publication-title: Nat. Struct. Mol. Biol.
  doi: 10.1038/nsmb.2735
– volume: 143
  start-page: 326
  year: 2010
  end-page: e1
  ident: CR49
  article-title: SnapShot: network motifs
  publication-title: Cell
  doi: 10.1016/j.cell.2010.09.050
– volume: 13
  start-page: 2212
  year: 2003
  end-page: 2217
  ident: CR4
  article-title: Role of the DRM and CMT3 methyltransferases in RNA-directed DNA methylation
  publication-title: Curr. Biol.
  doi: 10.1016/j.cub.2003.11.052
– volume: 5
  start-page: 1217
  year: 1993
  end-page: 1229
  ident: CR13
  article-title: Anther development: basic principles and practical applications
  publication-title: Plant Cell
– volume: 14
  start-page: 123
  year: 2011
  end-page: 129
  ident: CR8
  article-title: Dynamics of histone H3 lysine 27 trimethylation in plant development
  publication-title: Curr. Opin. Plant Biol.
  doi: 10.1016/j.pbi.2011.01.001
– volume: 12
  start-page: 419
  year: 2007
  end-page: 426
  ident: CR26
  article-title: The true story of the HD-Zip family
  publication-title: Trends Plant Sci.
  doi: 10.1016/j.tplants.2007.08.003
– volume: 1442
  start-page: 1
  year: 1998
  end-page: 19
  ident: CR36
  article-title: Homeoboxes in plant development
  publication-title: Biochim. Biophys. Acta
  doi: 10.1016/S0167-4781(98)00119-5
– volume: 292
  start-page: 2077
  year: 2001
  end-page: 2080
  ident: CR18
  article-title: Requirement of CHROMOMETHYLASE3 for maintenance of CpXpG methylation
  publication-title: Science
  doi: 10.1126/science.1059745
– volume: 11
  start-page: 554
  year: 2008
  end-page: 559
  ident: CR37
  article-title: The evolving functions of DNA methylation
  publication-title: Curr. Opin. Plant Biol.
  doi: 10.1016/j.pbi.2008.07.004
– volume: 17
  start-page: 1360
  year: 2005
  end-page: 1375
  ident: CR47
  article-title: MicroRNA-directed regulation of Arabidopsis AUXIN RESPONSE FACTOR17 is essential for proper development and modulates expression of early auxin response genes
  publication-title: Plant Cell
  doi: 10.1105/tpc.105.031716
– volume: 203
  start-page: 140
  year: 2014
  end-page: 154
  ident: CR17
  article-title: The Arabidopsis Exine Formation Defect (EFD) gene is required for primexine patterning and is critical for pollen fertility
  publication-title: New Phytol.
  doi: 10.1111/nph.12788
– volume: 13
  start-page: 1644
  year: 2020
  end-page: 1653
  ident: CR52
  article-title: Phenylpropanoid derivatives are essential components of sporopollenin in vascular plants
  publication-title: Mol. Plant
  doi: 10.1016/j.molp.2020.08.005
– volume: 62
  start-page: 1633
  year: 2011
  end-page: 1649
  ident: CR16
  article-title: The final split: the regulation of anther dehiscence
  publication-title: J. Exp. Bot.
  doi: 10.1093/jxb/err014
– volume: 11
  start-page: 1068
  year: 2004
  end-page: 1075
  ident: CR40
  article-title: Intragenic DNA methylation alters chromatin structure and elongation efficiency in mammalian cells
  publication-title: Nat. Struct. Mol. Biol.
  doi: 10.1038/nsmb840
– volume: 17
  start-page: 2993
  year: 2005
  end-page: 3006
  ident: CR22
  article-title: The NAC transcription factors NST1 and NST2 of Arabidopsis regulate secondary wall thickenings and are required for anther dehiscence
  publication-title: Plant Cell
  doi: 10.1105/tpc.105.036004
– volume: 213
  start-page: 95
  year: 2017
  end-page: 104
  ident: CR28
  article-title: Regulatory function of homeodomain-leucine zipper (HD-ZIP) family proteins during embryogenesis
  publication-title: New Phytol.
  doi: 10.1111/nph.14132
– volume: 3
  start-page: e00100
  year: 2019
  ident: CR34
  article-title: Genome-wide occupancy of histone H3K27 methyltransferases CURLY LEAF and SWINGER in Arabidopsis seedlings
  publication-title: Plant Direct
  doi: 10.1002/pld3.100
– volume: 14
  start-page: e1007397
  year: 2018
  ident: CR57
  article-title: Auxin production in diploid microsporocytes is necessary and sufficient for early stages of pollen development
  publication-title: PLoS Genet.
  doi: 10.1371/journal.pgen.1007397
– volume: 80
  start-page: 1005
  year: 2014
  end-page: 1013
  ident: CR19
  article-title: DYT1 directly regulates the expression of TDF1 for tapetum development and pollen wall formation in Arabidopsis
  publication-title: Plant J.
  doi: 10.1111/tpj.12694
– volume: 15
  start-page: 394
  year: 2014
  end-page: 408
  ident: CR1
  article-title: RNA-directed DNA methylation: an epigenetic pathway of increasing complexity
  publication-title: Nat. Rev. Genet
  doi: 10.1038/nrg3683
– volume: 11
  start-page: 204
  year: 2010
  end-page: 220
  ident: CR2
  article-title: Establishing, maintaining and modifying DNA methylation patterns in plants and animals
  publication-title: Nat. Rev. Genet
  doi: 10.1038/nrg2719
– volume: 329
  start-page: 645
  year: 2003
  end-page: 654
  ident: CR48
  article-title: Response delays and the structure of transcription networks
  publication-title: J. Mol. Biol.
  doi: 10.1016/S0022-2836(03)00506-0
– volume: 33
  start-page: 1506
  year: 2021
  end-page: 1529
  ident: CR51
  article-title: The PIF1-miR408-PLANTACYANIN repression cascade regulates light-dependent seed germination
  publication-title: Plant Cell
  doi: 10.1093/plcell/koab060
– volume: 62
  start-page: 1633
  year: 2011
  ident: 52114_CR16
  publication-title: J. Exp. Bot.
  doi: 10.1093/jxb/err014
– volume: 11
  start-page: 1068
  year: 2004
  ident: 52114_CR40
  publication-title: Nat. Struct. Mol. Biol.
  doi: 10.1038/nsmb840
– volume: 241
  start-page: 615
  year: 2015
  ident: 52114_CR53
  publication-title: Planta
  doi: 10.1007/s00425-014-2199-7
– volume: 609
  start-page: 986
  year: 2022
  ident: 52114_CR35
  publication-title: Nature
  doi: 10.1038/s41586-022-05171-5
– volume: 12
  start-page: 1138
  year: 2002
  ident: 52114_CR3
  publication-title: Curr. Biol.
  doi: 10.1016/S0960-9822(02)00925-9
– volume: 39
  start-page: 61
  year: 2007
  ident: 52114_CR39
  publication-title: Nat. Genet.
  doi: 10.1038/ng1929
– volume: 5
  start-page: 1217
  year: 1993
  ident: 52114_CR13
  publication-title: Plant Cell
– volume: 11
  start-page: 204
  year: 2010
  ident: 52114_CR2
  publication-title: Nat. Rev. Genet
  doi: 10.1038/nrg2719
– volume: 13
  start-page: 2212
  year: 2003
  ident: 52114_CR4
  publication-title: Curr. Biol.
  doi: 10.1016/j.cub.2003.11.052
– volume: 39
  start-page: 776
  year: 2004
  ident: 52114_CR58
  publication-title: Plant J.
  doi: 10.1111/j.1365-313X.2004.02169.x
– volume: 11
  start-page: 297
  year: 1999
  ident: 52114_CR21
  publication-title: Sex. Plant Reprod.
  doi: 10.1007/s004970050158
– volume: 52
  start-page: 528
  year: 2007
  ident: 52114_CR56
  publication-title: Plant J.
  doi: 10.1111/j.1365-313X.2007.03254.x
– volume: 17
  start-page: 2993
  year: 2005
  ident: 52114_CR22
  publication-title: Plant Cell
  doi: 10.1105/tpc.105.036004
– volume: 213
  start-page: 95
  year: 2017
  ident: 52114_CR28
  publication-title: New Phytol.
  doi: 10.1111/nph.14132
– volume: 329
  start-page: 645
  year: 2003
  ident: 52114_CR48
  publication-title: J. Mol. Biol.
  doi: 10.1016/S0022-2836(03)00506-0
– volume: 12
  start-page: 419
  year: 2007
  ident: 52114_CR26
  publication-title: Trends Plant Sci.
  doi: 10.1016/j.tplants.2007.08.003
– volume: 143
  start-page: 326
  year: 2010
  ident: 52114_CR49
  publication-title: Cell
  doi: 10.1016/j.cell.2010.09.050
– volume: 158
  start-page: 264
  year: 2012
  ident: 52114_CR24
  publication-title: Plant Physiol.
  doi: 10.1104/pp.111.184853
– volume: 124
  start-page: 495
  year: 2006
  ident: 52114_CR38
  publication-title: Cell
  doi: 10.1016/j.cell.2005.12.034
– volume: 25
  start-page: 3311
  year: 2013
  ident: 52114_CR50
  publication-title: Plant Cell
  doi: 10.1105/tpc.113.113340
– volume: 11
  start-page: 554
  year: 2008
  ident: 52114_CR37
  publication-title: Curr. Opin. Plant Biol.
  doi: 10.1016/j.pbi.2008.07.004
– volume: 178
  start-page: 283
  year: 2018
  ident: 52114_CR20
  publication-title: Plant Physiol.
  doi: 10.1104/pp.18.00219
– volume: 14
  start-page: 732
  year: 2021
  ident: 52114_CR11
  publication-title: Mol. Plant
  doi: 10.1016/j.molp.2021.03.001
– volume: 1442
  start-page: 1
  year: 1998
  ident: 52114_CR36
  publication-title: Biochim. Biophys. Acta
  doi: 10.1016/S0167-4781(98)00119-5
– volume: 586
  start-page: 3159
  year: 2012
  ident: 52114_CR43
  publication-title: FEBS Lett.
  doi: 10.1016/j.febslet.2012.06.026
– volume: 33
  start-page: 1506
  year: 2021
  ident: 52114_CR51
  publication-title: Plant Cell
  doi: 10.1093/plcell/koab060
– volume: 26
  start-page: 83
  year: 2013
  ident: 52114_CR25
  publication-title: Plant Reprod.
  doi: 10.1007/s00497-012-0208-1
– volume: 23
  start-page: 15
  year: 2015
  ident: 52114_CR33
  publication-title: Curr. Opin. Plant Biol.
  doi: 10.1016/j.pbi.2014.10.003
– volume: 21
  start-page: 64
  year: 2014
  ident: 52114_CR5
  publication-title: Nat. Struct. Mol. Biol.
  doi: 10.1038/nsmb.2735
– volume: 292
  start-page: 2077
  year: 2001
  ident: 52114_CR18
  publication-title: Science
  doi: 10.1126/science.1059745
– volume: 29
  start-page: 169
  year: 2016
  ident: 52114_CR32
  publication-title: Curr. Opin. Plant Biol.
  doi: 10.1016/j.pbi.2015.11.010
– volume: 147
  start-page: 852
  year: 2008
  ident: 52114_CR23
  publication-title: Plant Physiol.
  doi: 10.1104/pp.108.118026
– volume: 30
  start-page: 2761
  year: 2018
  ident: 52114_CR29
  publication-title: Plant Cell
  doi: 10.1105/tpc.18.00584
– volume: 5
  start-page: e129
  year: 2007
  ident: 52114_CR7
  publication-title: PLoS Biol.
  doi: 10.1371/journal.pbio.0050129
– volume: 23
  year: 2022
  ident: 52114_CR10
  publication-title: Genome Biol.
  doi: 10.1186/s13059-022-02768-x
– volume: 61
  start-page: 395
  year: 2010
  ident: 52114_CR41
  publication-title: Annu. Rev. Plant Biol.
  doi: 10.1146/annurev.arplant.043008.091939
– volume: 10
  start-page: 697
  year: 2009
  ident: 52114_CR31
  publication-title: Nat. Rev. Mol. Cell Biol.
  doi: 10.1038/nrm2763
– volume: 50
  start-page: 130
  year: 2018
  ident: 52114_CR6
  publication-title: Nat. Genet.
  doi: 10.1038/s41588-017-0008-5
– volume: 15
  start-page: 394
  year: 2014
  ident: 52114_CR1
  publication-title: Nat. Rev. Genet
  doi: 10.1038/nrg3683
– volume: 13
  start-page: 1644
  year: 2020
  ident: 52114_CR52
  publication-title: Mol. Plant
  doi: 10.1016/j.molp.2020.08.005
– volume: 181
  start-page: 645
  year: 2019
  ident: 52114_CR46
  publication-title: Plant Physiol.
  doi: 10.1104/pp.19.00576
– volume: 17
  start-page: 1360
  year: 2005
  ident: 52114_CR47
  publication-title: Plant Cell
  doi: 10.1105/tpc.105.031716
– volume: 13
  start-page: 878693
  year: 2022
  ident: 52114_CR54
  publication-title: Front. Plant Sci.
  doi: 10.3389/fpls.2022.878693
– volume: 80
  start-page: 1005
  year: 2014
  ident: 52114_CR19
  publication-title: Plant J.
  doi: 10.1111/tpj.12694
– volume: 62
  start-page: 563
  year: 2020
  ident: 52114_CR42
  publication-title: J. Integr. Plant Biol.
  doi: 10.1111/jipb.12901
– volume: 162
  start-page: 720
  year: 2013
  ident: 52114_CR44
  publication-title: Plant Physiol.
  doi: 10.1104/pp.113.214940
– volume: 139
  start-page: 509
  year: 2005
  ident: 52114_CR30
  publication-title: Plant Physiol.
  doi: 10.1104/pp.105.063461
– volume: 44
  start-page: 117
  year: 1969
  ident: 52114_CR55
  publication-title: Stain Technol.
  doi: 10.3109/10520296909063335
– volume: 14
  start-page: e1007397
  year: 2018
  ident: 52114_CR57
  publication-title: PLoS Genet.
  doi: 10.1371/journal.pgen.1007397
– volume: 61
  start-page: 832
  year: 2016
  ident: 52114_CR15
  publication-title: Sci. Bull.
  doi: 10.1007/s11434-016-1062-6
– volume: 114
  start-page: E245
  year: 2017
  ident: 52114_CR27
  publication-title: Proc. Natl Acad. Sci. USA
  doi: 10.1073/pnas.1613199114
– volume: 3
  start-page: e00100
  year: 2019
  ident: 52114_CR34
  publication-title: Plant Direct
  doi: 10.1002/pld3.100
– volume: 17
  year: 2017
  ident: 52114_CR45
  publication-title: BMC Plant Biol.
  doi: 10.1186/s12870-017-1185-1
– volume: 34
  start-page: 2989
  year: 2022
  ident: 52114_CR12
  publication-title: Plant Cell
  doi: 10.1093/plcell/koac136
– volume: 16
  start-page: S84
  year: 2004
  ident: 52114_CR14
  publication-title: Plant Cell
  doi: 10.1105/tpc.015800
– volume: 18
  start-page: 236
  year: 2008
  ident: 52114_CR9
  publication-title: Trends Cell Biol.
  doi: 10.1016/j.tcb.2008.02.005
– volume: 203
  start-page: 140
  year: 2014
  ident: 52114_CR17
  publication-title: New Phytol.
  doi: 10.1111/nph.12788
– volume: 14
  start-page: 123
  year: 2011
  ident: 52114_CR8
  publication-title: Curr. Opin. Plant Biol.
  doi: 10.1016/j.pbi.2011.01.001
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Snippet Epigenetic modifications are crucial for plant development. EFD ( E xine F ormation D efect) encodes a SAM-dependent methyltransferase that is essential for...
Epigenetic modifications are crucial for plant development. EFD (Exine Formation Defect) encodes a SAM-dependent methyltransferase that is essential for the...
Epigenetic modifications are crucial for plant development. EFD (ExineFormationDefect) encodes a SAM-dependent methyltransferase that is essential for the...
Abstract Epigenetic modifications are crucial for plant development. EFD ( E xine F ormation D efect) encodes a SAM-dependent methyltransferase that is...
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14/19
631/449/1659
631/449/2491
631/449/2679/1743
Arabidopsis - genetics
Arabidopsis - growth & development
Arabidopsis - metabolism
Arabidopsis Proteins - genetics
Arabidopsis Proteins - metabolism
Dehiscence
Deoxyribonucleic acid
DNA
DNA Methylation
DNA methyltransferase
Epigenesis, Genetic
Epigenetics
Fertility
Flowers - genetics
Flowers - growth & development
Gene expression
Gene Expression Regulation, Plant
Genetic analysis
Histones
Humanities and Social Sciences
Methyltransferases - genetics
Methyltransferases - metabolism
multidisciplinary
Mutation
Pattern formation
Plant reproductive structures
Plants, Genetically Modified
Pollen
Pollen - genetics
Pollen - growth & development
Pollen - metabolism
Science
Science (multidisciplinary)
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Title An epigenetically mediated double negative cascade from EFD to HB21 regulates anther development
URI https://link.springer.com/article/10.1038/s41467-024-52114-x
https://www.ncbi.nlm.nih.gov/pubmed/39242635
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