首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >SWI2/SNF2 chromatin remodeling ATPases overcome polycomb repression and control floral organ identity with the LEAFY and SEPALLATA3 transcription factors
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SWI2/SNF2 chromatin remodeling ATPases overcome polycomb repression and control floral organ identity with the LEAFY and SEPALLATA3 transcription factors

机译:SWI2 / SNF2染色质重塑ATPase克服了多梳抑制并利用LEAFY和SEPALLATA3转录因子控制花器官的身份

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摘要

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.
机译:花器官的图案由四类顺势调节器精确控制和执行。其中,B级和C级花卉顺势调节剂具有至关重要的意义,因为它们规定了雄性和雌性生殖器官。 B类基因APETALA3(AP3)和C类基因AGAMOUS(AG)的不当诱导会导致生殖适应性降低,并受到多梳阻抑作用的阻止。在花朵图案出现之初,需要克服多梳抑制,以诱导AP3和AG并形成生殖器官。我们显示SWI2 / SNF2染色质重塑ATP酶SPLAYED(SYD)和BRAHMA(BRM)对于花型图案以及AP3和AG的激活是多余的。 SWI2 / SNF2 ATPase在花朵发育过程中被募集到AP3和AG的调控区,并与两个B类和C类基因表达的直接转录激活因子LEAFY(LFY)和SEPALLATA3(SEP3)发生物理相互作用。 SYD和LFY与AP3和AG调控位点的关联在花朵图案形成过程中同时达到峰值,并且SYD与这些位点的结合在lfy和lfy sep3突变体中受损。这表明在正确的阶段和正确的细胞中,SWI2 / SNF2 ATPase募集到这些基因座的机制。 SYD和BRM充当三胸腺蛋白,花型中SYD和BRM的需求可以通过卷曲叶片(clf)突变体中多梳活性的部分丧失来克服,这意味着SWI2 / SNF2染色质重塑剂可以逆转多梳抑制。

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