Suppr超能文献

SWI2/SNF2 染色质重塑 ATP 酶克服多梳抑制并与 LEAFY 和 SEPALLATA3 转录因子一起控制花器官的身份。

SWI2/SNF2 chromatin remodeling ATPases overcome polycomb repression and control floral organ identity with the LEAFY and SEPALLATA3 transcription factors.

机构信息

Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.

出版信息

Proc Natl Acad Sci U S A. 2012 Feb 28;109(9):3576-81. doi: 10.1073/pnas.1113409109. Epub 2012 Feb 9.

Abstract

Patterning of the floral organs is exquisitely controlled and executed by four classes of homeotic regulators. Among these, the class B and class C floral homeotic regulators are of central importance as they specify the male and female reproductive organs. Inappropriate induction of the class B gene APETALA3 (AP3) and the class C gene AGAMOUS (AG) causes reduced reproductive fitness and is prevented by polycomb repression. At the onset of flower patterning, polycomb repression needs to be overcome to allow induction of AP3 and AG and formation of the reproductive organs. We show that the SWI2/SNF2 chromatin-remodeling ATPases SPLAYED (SYD) and BRAHMA (BRM) are redundantly required for flower patterning and for the activation of AP3 and AG. The SWI2/SNF2 ATPases are recruited to the regulatory regions of AP3 and AG during flower development and physically interact with two direct transcriptional activators of class B and class C gene expression, LEAFY (LFY) and SEPALLATA3 (SEP3). SYD and LFY association with the AP3 and AG regulatory loci peaks at the same time during flower patterning, and SYD binding to these loci is compromised in lfy and lfy sep3 mutants. This suggests a mechanism for SWI2/SNF2 ATPase recruitment to these loci at the right stage and in the correct cells. SYD and BRM act as trithorax proteins, and the requirement for SYD and BRM in flower patterning can be overcome by partial loss of polycomb activity in curly leaf (clf) mutants, implicating the SWI2/SNF2 chromatin remodelers in reversal of polycomb repression.

摘要

花器官的模式形成是由四类同源异形调节因子精细控制和执行的。在这些调节因子中,B 类和 C 类花同源异形调节因子最为重要,因为它们决定了雄性和雌性生殖器官。B 类基因 APETALA3 (AP3) 和 C 类基因 AGAMOUS (AG) 的不当诱导会降低生殖适应性,并被多梳抑制所阻止。在花模式形成的开始时,需要克服多梳抑制,以允许 AP3 和 AG 的诱导和生殖器官的形成。我们表明,SWI2/SNF2 染色质重塑 ATP 酶 SPLAYED (SYD) 和 BRAHMA (BRM) 对于花模式形成以及 AP3 和 AG 的激活是冗余的。SWI2/SNF2 ATP 酶在花发育过程中被招募到 AP3 和 AG 的调节区域,并与 B 类和 C 类基因表达的两个直接转录激活因子 LEAFY (LFY) 和 SEPALLATA3 (SEP3) 物理相互作用。在花模式形成过程中,SYD 和 LFY 与 AP3 和 AG 调节位点的结合在同一时间达到峰值,并且在 lfy 和 lfy sep3 突变体中,SYD 与这些位点的结合受到损害。这表明了 SWI2/SNF2 ATP 酶在正确的阶段和正确的细胞中被招募到这些位点的机制。SYD 和 BRM 作为 trithorax 蛋白发挥作用,并且在 curly leaf (clf) 突变体中部分丧失多梳活性可以克服 SYD 和 BRM 在花模式形成中的作用,这表明 SWI2/SNF2 染色质重塑酶参与了多梳抑制的逆转。

相似文献

引用本文的文献

9
Reflections on the ABC model of flower development.关于花发育的 ABC 模型的思考。
Plant Cell. 2024 May 1;36(5):1334-1357. doi: 10.1093/plcell/koae044.

本文引用的文献

5
Inducible gene expression: diverse regulatory mechanisms.可诱导基因表达:多样化的调控机制。
Nat Rev Genet. 2010 Jun;11(6):426-37. doi: 10.1038/nrg2781. Epub 2010 Apr 27.
6
Seasonal and developmental timing of flowering.开花的季节性和发育时间。
Plant J. 2010 Mar;61(6):1001-13. doi: 10.1111/j.1365-313X.2010.04148.x.
7
Orchestration of floral initiation by APETALA1.APETALA1 对花起始的调控
Science. 2010 Apr 2;328(5974):85-9. doi: 10.1126/science.1185244.
9
Regulatory mechanisms for floral homeotic gene expression.花器官同源异形基因表达的调控机制。
Semin Cell Dev Biol. 2010 Feb;21(1):80-6. doi: 10.1016/j.semcdb.2009.11.012. Epub 2009 Nov 13.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验