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PICKLE is a CHD subfamily II ATP-dependent chromatin remodeling factor

机译:PICKLE是CHD亚家族II ATP依赖的染色质重塑因子

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PICKLE plays a critical role in repression of genes that regulate development identity in Arabidopsis thaliana. PICKLE codes for a putative ATP-dependent chromatin remodeler that exhibits sequence similarity to members of subfamily II of animal CHD remodelers, which includes remodelers such as CHD3/Mi-2 that also restrict expression of developmental regulators. Whereas animal CHD3 remodelers are a component of the Mi-2/NuRD complex that promotes histone deacetylation, PICKLE promotes trimethylation of histone H3 lysine 27 suggesting that it acts via a distinct epigenetic pathway. Here, we examine whether PICKLE is also a member of a multisubunit complex and characterize the biochemical properties of recombinant PICKLE protein. Phylogenetic analysis indicates that PICKLE-related proteins in plants share a common ancestor with members of subfamily II of animal CHD remodelers. Biochemical characterization of PICKLE in planta, however, reveals that PICKLE primarily exists as a monomer. Recombinant PICKLE protein is an ATPase that is stimulated by ssDNA and mononucleosomes and binds to both naked DNA and mononucleosomes. Furthermore, recombinant PICKLE exhibits ATP-dependent chromatin remodeling activity. These studies demonstrate that subfamily II CHD proteins in plants, such as PICKLE, retain ATP-dependent chromatin remodeling activity but act through a mechanism that does not involve the ubiquitous Mi-2/NuRD complex. ? 2012 Elsevier B.V.
机译:泡菜在抑制拟南芥中调节发育特性的基因中起关键作用。 PICKLE编码一个假定的ATP依赖的染色质重塑剂,其与动物CHD重塑剂的亚家族II的成员表现出序列相似性,其中包括CHD3 / Mi-2等重塑剂,它们也限制了发育调节因子的表达。动物CHD3重塑剂是Mi-2 / NuRD复合物的一个组成部分,可促进组蛋白去乙酰化,而PICKLE则可促进组蛋白H3赖氨酸27的三甲基化,表明它通过独特的表观遗传途径起作用。在这里,我们检查PICKLE是否也是多亚基复合物的成员,并表征重组PICKLE蛋白的生化特性。系统发育分析表明,植物中与PICKLE相关的蛋白与动物CHD重塑剂的亚家族II的成员具有相同的祖先。但是,植物中PICKLE的生化特性表明,PICKLE主要以单体形式存在。重组PICKLE蛋白是一种ssDNA和单核小体刺激的ATPase,可与裸DNA和单核小体结合。此外,重组PICKLE表现出ATP依赖的染色质重塑活性。这些研究表明,植物中的亚家族II CHD蛋白(例如PICKLE)保留了ATP依赖的染色质重塑活性,但通过不涉及普遍存在的Mi-2 / NuRD复合物的机制起作用。 ? 2012年Elsevier B.V.

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