PoplarV1, Main, Exploration, bibRecord, 002911

Splice variant of the SND1 transcription factor is a dominant negative of SND1 members and their regulation in Populus trichocarpa.

Identifieur interne : 002911 ( Main/Exploration ); précédent : 002910; suivant : 002912

Splice variant of the SND1 transcription factor is a dominant negative of SND1 members and their regulation in Populus trichocarpa.

Auteurs : Quanzi Li [États-Unis] ; Ying-Chung Lin ; Ying-Hsuan Sun ; Jian Song ; Hao Chen ; Xing-Hai Zhang ; Ronald R. Sederoff ; Vincent L. Chiang

Source :

Proceedings of the National Academy of Sciences of the United States of America [ 1091-6490 ] ; 2012.

RBID : pubmed:22915581

Descripteurs français

English descriptors

KwdEn :
- Blotting, Western (MeSH), Cloning, Molecular (MeSH), DNA Primers (genetics), Dimerization (MeSH), Electrophoresis, Polyacrylamide Gel (MeSH), Gene Regulatory Networks (genetics), Homeostasis (physiology), Models, Biological (MeSH), Plasmids (genetics), Populus (genetics), Protein Isoforms (genetics), Protein Transport (MeSH), Real-Time Polymerase Chain Reaction (MeSH), Transcription Factors (genetics).
MESH :
- chemical , genetics : DNA Primers, Protein Isoforms, Transcription Factors.
- genetics : Gene Regulatory Networks, Plasmids, Populus.
- physiology : Homeostasis.
- Blotting, Western, Cloning, Molecular, Dimerization, Electrophoresis, Polyacrylamide Gel, Models, Biological, Protein Transport, Real-Time Polymerase Chain Reaction.

Abstract

Secondary Wall-Associated NAC Domain 1s (SND1s) are transcription factors (TFs) known to activate a cascade of TF and pathway genes affecting secondary cell wall biosynthesis (xylogenesis) in Arabidopsis and poplars. Elevated SND1 transcriptional activation leads to ectopic xylogenesis and stunted growth. Nothing is known about the upstream regulators of SND1. Here we report the discovery of a stem-differentiating xylem (SDX)-specific alternative SND1 splice variant, PtrSND1-A2(IR), that acts as a dominant negative of SND1 transcriptional network genes in Populus trichocarpa. PtrSND1-A2(IR) derives from PtrSND1-A2, one of the four fully spliced PtrSND1 gene family members (PtrSND1-A1, -A2, -B1, and -B2). Each full-size PtrSND1 activates its own gene, and all four full-size members activate a common MYB gene (PtrMYB021). PtrSND1-A2(IR) represses the expression of its PtrSND1 member genes and PtrMYB021. Repression of the autoregulation of a TF family by its only splice variant has not been previously reported in plants. PtrSND1-A2(IR) lacks DNA binding and transactivation abilities but retains dimerization capability. PtrSND1-A2(IR) is localized exclusively in cytoplasmic foci. In the presence of any full-size PtrSND1 member, PtrSND1-A2(IR) is translocated into the nucleus exclusively as a heterodimeric partner with full-size PtrSND1s. Our findings are consistent with a model in which the translocated PtrSND1-A2(IR) lacking DNA-binding and transactivating abilities can disrupt the function of full-size PtrSND1s, making them nonproductive through heterodimerization, and thereby modulating the SND1 transcriptional network. PtrSND1-A2(IR) may contribute to transcriptional homeostasis to avoid deleterious effects on xylogenesis and plant growth.

DOI: 10.1073/pnas.1212977109
PubMed: 22915581
PubMed Central: PMC3437841

Affiliations:

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<front><div type="abstract" xml:lang="en">Secondary Wall-Associated NAC Domain 1s (SND1s) are transcription factors (TFs) known to activate a cascade of TF and pathway genes affecting secondary cell wall biosynthesis (xylogenesis) in Arabidopsis and poplars. Elevated SND1 transcriptional activation leads to ectopic xylogenesis and stunted growth. Nothing is known about the upstream regulators of SND1. Here we report the discovery of a stem-differentiating xylem (SDX)-specific alternative SND1 splice variant, PtrSND1-A2(IR), that acts as a dominant negative of SND1 transcriptional network genes in Populus trichocarpa. PtrSND1-A2(IR) derives from PtrSND1-A2, one of the four fully spliced PtrSND1 gene family members (PtrSND1-A1, -A2, -B1, and -B2). Each full-size PtrSND1 activates its own gene, and all four full-size members activate a common MYB gene (PtrMYB021). PtrSND1-A2(IR) represses the expression of its PtrSND1 member genes and PtrMYB021. Repression of the autoregulation of a TF family by its only splice variant has not been previously reported in plants. PtrSND1-A2(IR) lacks DNA binding and transactivation abilities but retains dimerization capability. PtrSND1-A2(IR) is localized exclusively in cytoplasmic foci. In the presence of any full-size PtrSND1 member, PtrSND1-A2(IR) is translocated into the nucleus exclusively as a heterodimeric partner with full-size PtrSND1s. Our findings are consistent with a model in which the translocated PtrSND1-A2(IR) lacking DNA-binding and transactivating abilities can disrupt the function of full-size PtrSND1s, making them nonproductive through heterodimerization, and thereby modulating the SND1 transcriptional network. PtrSND1-A2(IR) may contribute to transcriptional homeostasis to avoid deleterious effects on xylogenesis and plant growth.</div>
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<ReferenceList><Reference><Citation>Nature. 2000 Jun 1;405(6786):590-3</Citation>
<ArticleIdList><ArticleId IdType="pubmed">10850721</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Trends Biochem Sci. 2008 May;33(5):220-9</Citation>
<ArticleIdList><ArticleId IdType="pubmed">18406148</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Curr Opin Struct Biol. 2001 Feb;11(1):26-32</Citation>
<ArticleIdList><ArticleId IdType="pubmed">11179888</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Microbiol Mol Biol Rev. 2001 Dec;65(4):570-94, table of contents</Citation>
<ArticleIdList><ArticleId IdType="pubmed">11729264</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Cell Mol Life Sci. 2003 Apr;60(4):721-41</Citation>
<ArticleIdList><ArticleId IdType="pubmed">12785719</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Trends Cell Biol. 2003 Aug;13(8):410-8</Citation>
<ArticleIdList><ArticleId IdType="pubmed">12888293</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>EMBO Rep. 2004 Mar;5(3):297-303</Citation>
<ArticleIdList><ArticleId IdType="pubmed">15083810</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Nature. 1997 Apr 24;386(6627):779-87</Citation>
<ArticleIdList><ArticleId IdType="pubmed">9126736</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Annu Rev Immunol. 1998;16:569-92</Citation>
<ArticleIdList><ArticleId IdType="pubmed">9597142</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Genes Dev. 2005 Aug 15;19(16):1855-60</Citation>
<ArticleIdList><ArticleId IdType="pubmed">16103214</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Proc Natl Acad Sci U S A. 2006 Oct 3;103(40):14724-31</Citation>
<ArticleIdList><ArticleId IdType="pubmed">17003135</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant Cell. 2006 Nov;18(11):3158-70</Citation>
<ArticleIdList><ArticleId IdType="pubmed">17114348</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant J. 2007 Jun;50(6):1035-48</Citation>
<ArticleIdList><ArticleId IdType="pubmed">17565617</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant Cell. 2007 Sep;19(9):2776-92</Citation>
<ArticleIdList><ArticleId IdType="pubmed">17890373</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant J. 2008 Aug;55(4):652-64</Citation>
<ArticleIdList><ArticleId IdType="pubmed">18445131</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant J. 2009 Nov;60(4):649-65</Citation>
<ArticleIdList><ArticleId IdType="pubmed">19674407</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant Cell. 2009 Oct;21(10):3350-67</Citation>
<ArticleIdList><ArticleId IdType="pubmed">19820187</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant Physiol. 2010 Feb;152(2):1044-55</Citation>
<ArticleIdList><ArticleId IdType="pubmed">19965968</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant Cell. 2010 Apr;22(4):1249-63</Citation>
<ArticleIdList><ArticleId IdType="pubmed">20388856</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Curr Opin Plant Biol. 2010 Jun;13(3):299-304</Citation>
<ArticleIdList><ArticleId IdType="pubmed">20381410</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Nat Commun. 2011;2:303</Citation>
<ArticleIdList><ArticleId IdType="pubmed">21556057</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant J. 2011 Aug;67(3):499-512</Citation>
<ArticleIdList><ArticleId IdType="pubmed">21649762</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Trends Plant Sci. 2011 Oct;16(10):541-9</Citation>
<ArticleIdList><ArticleId IdType="pubmed">21723179</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant Physiol. 2011 Nov;157(3):1452-68</Citation>
<ArticleIdList><ArticleId IdType="pubmed">21908685</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant J. 2011 Dec;68(6):1104-14</Citation>
<ArticleIdList><ArticleId IdType="pubmed">21883551</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Proc Natl Acad Sci U S A. 2011 Dec 27;108(52):21253-8</Citation>
<ArticleIdList><ArticleId IdType="pubmed">22160716</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Mol Plant. 2012 Mar;5(2):297-303</Citation>
<ArticleIdList><ArticleId IdType="pubmed">22138968</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Trends Plant Sci. 2012 Jun;17(6):369-81</Citation>
<ArticleIdList><ArticleId IdType="pubmed">22445067</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Plant Cell. 2012 Jun;24(6):2427-42</Citation>
<ArticleIdList><ArticleId IdType="pubmed">22715042</ArticleId>
</ArticleIdList>
</Reference>
<Reference><Citation>Genes Dev. 2000 Dec 1;14(23):3024-36</Citation>
<ArticleIdList><ArticleId IdType="pubmed">11114891</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
</PubmedData>
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<name sortKey="Chiang, Vincent L" sort="Chiang, Vincent L" uniqKey="Chiang V" first="Vincent L" last="Chiang">Vincent L. Chiang</name>
<name sortKey="Lin, Ying Chung" sort="Lin, Ying Chung" uniqKey="Lin Y" first="Ying-Chung" last="Lin">Ying-Chung Lin</name>
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Splice variant of the SND1 transcription factor is a dominant negative of SND1 members and their regulation in Populus trichocarpa.

Splice variant of the SND1 transcription factor is a dominant negative of SND1 members and their regulation in Populus trichocarpa.

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