首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Some C. elegans class B synthetic multivulva proteins encode a conserved LIN-35 Rb-containing complex distinct from a NuRD-like complex
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Some C. elegans class B synthetic multivulva proteins encode a conserved LIN-35 Rb-containing complex distinct from a NuRD-like complex

机译:某些秀丽隐杆线虫B类合成多外阴蛋白编码不同于NURD样复合物的保守的含LIN-35 Rb的复合物

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The Caenorhabditis elegans synthetic muitivulva (synMuv) genes act redundantly to antagonize the specification of vulval cell fates, which are promoted by an RTK/Ras pathway. At least 26 synMuv genes have been genetically identified, several of which encode proteins with homologs that act in chromatin remodeling or transcriptional repression. Here we report the molecular characterization of two synMuv genes, lin-37 and lin-54. We show that lin-37 and lin-54 encode proteins in a complex with at least seven synMuv proteins, including LIN-35, the only C elegans homolog of the mammalian tumor suppressor Rb. Biochemical analyses of mutants suggest that LIN-9, LIN-53, and LIN-54 are required for the stable formation of this complex. This complex is distinct from a second complex of synMuv proteins with a composition similar to that of the mammalian Nucleosome Remodeling and Deacetylase complex. The class B synMuv complex we identified is evolutionarily conserved and likely functions in transcriptional repression and developmental regulation.
机译:秀丽隐杆线虫合成粘液(synMuv)基因多余地对抗由RTK / Ras途径促进的外阴细胞命运的规范。遗传上已经鉴定出至少26个synMuv基因,其中几个编码具有在染色质重塑或转录抑制中起作用的同系物的蛋白质。在这里,我们报告了两个synMuv基因lin-37和lin-54的分子表征。我们显示lin-37和lin-54编码与至少七个synMuv蛋白(包括LIN-35,哺乳动物肿瘤抑制因子Rb的唯一C elegans同源物)形成的复合物中的蛋白。突变体的生化分析表明,LIN-9,LIN-53和LIN-54是稳定形成此复合物所必需的。该复合物不同于synMuv蛋白的第二种复合物,其组成类似于哺乳动物的核小体重塑和脱乙酰酶复合物。我们确定的B类synMuv复合物在进化上是保守的,并且可能在转录抑制和发育调控中起作用。

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