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首页> 外文期刊>Molecular and Cellular Biology >The Drosophila SNR1 (SNF5/INI1) Subunit Directs Essential Developmental Functions of the Brahma Chromatin Remodeling Complex
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The Drosophila SNR1 (SNF5/INI1) Subunit Directs Essential Developmental Functions of the Brahma Chromatin Remodeling Complex

机译:果蝇SNR1(SNF5 / INI1)亚基指导梵天染色质重塑复合体的基本发育功能。

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摘要

The Drosophila melanogaster Brahma (Brm) complex, a counterpart of the Saccharomyces cerevisiae SWI/SNF ATP-dependent chromatin remodeling complex, is important for proper development by maintaining specific gene expression patterns. The SNR1 subunit is strongly conserved with yeast SNF5 and mammalian INI1 and is required for full activity of the Brm complex. We identified a temperature-sensitive allele of snr1 caused by a single amino acid substitution in the conserved repeat 2 region, implicated in a variety of protein-protein interactions. Genetic analyses of snr1E1 reveal that it functions as an antimorph and that snr1 has critical roles in tissue patterning and growth control. Temperature shifts show that snr1 is continuously required, with essential functions in embryogenesis, pupal stages, and adults. Allele-specific genetic interactions between snr1E1 and mutations in genes encoding other members of the Brm complex suggest that snr1E1 mutant phenotypes result from reduced Brm complex function. Consistent with this view, SNR1E1 is stably associated with other components of the Brm complex at the restrictive temperature. SNR1 can establish direct contacts through the conserved repeat 2 region with the SET domain of the homeotic regulator Trithorax (TRX), and SNR1E1 is partially defective for functional TRX association. As truncating mutations of INI1 are strongly correlated with aggressive cancers, our results support the view that SNR1, and specifically the repeat 2 region, has a critical role in mediating cell growth control functions of the metazoan SWI/SNF complexes.
机译:果蝇(Srmcharomyces cerevisiae)SWI / SNF ATP依赖的染色质重塑复合物的对应物果蝇(Brm)复合物对维持特定基因表达模式对于正常发育至关重要。 SNR1亚基与酵母SNF5和哺乳动物INI1高度保守,是Brm复合物完全活性所必需的。我们确定了 snr1 的温度敏感等位基因,其由保守的重复2区中的单个氨基酸取代引起,涉及多种蛋白质-蛋白质相互作用。对 snr1 E1 的遗传分析表明,它起着抗变体的作用,并且 snr1 在组织构图和生长控制中具有关键作用。温度的变化表明, snr1 一直是必需的,在胚胎发生,p期和成年期都具有基本功能。 snr1 E1 与Brm复合体其他成员编码基因的突变之间的等位基因特异性遗传相互作用表明, snr1 E1 突变表型归因于Brm复杂功能降低。与该观点一致,SNR1 E1 在限定温度下与Brm配合物的其他成分稳定关联。 SNR1可以通过同源调节因子Trithorax(TRX)的SET域通过保守的重复2区建立直接接触,而SNR1 E1 在功能性TRX关联方面部分存在缺陷。由于 INI1 的截短突变与侵袭性癌症密切相关,因此我们的研究结果支持SNR1(特别是重复2区)在介导后生SWI / SNF细胞生长控制功能中起关键作用的观点。复合体。

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