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Closely related proteins MBD2 and MBD3 play distinctive but interacting roles in mouse development

机译:密切相关的蛋白质MBD2和MBD3在小鼠发育中发挥独特但相互作用的作用

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摘要

MBD2 and MBD3 are closely related proteins with consensus methyl-CpG binding domains. MBD2 is a transcriptional repressor that specifically binds to methylated DNA and is a component of the MeCP1 protein complex. In contrast, MBD3 fails to bind methylated DNA in murine cells, and is a component of the Mi-2/NuRD corepressor complex. We show by gene targeting that the two proteins are not functionally redundant in mice, as Mbd3(−/−) mice die during early embryogenesis, whereas Mbd2(−/−) mice are viable and fertile. Maternal behavior of Mbd2(−/−) mice is however defective and, at the molecular level, Mbd2(−/−) mice lack a component of MeCP1. Mbd2-mutant cells fail to fully silence transcription from exogenous methylated templates, but inappropriate activation of endogenous imprinted genes or retroviral sequences was not detected. Despite their differences, Mbd3 and Mbd2 interact genetically suggesting a functional relationship. Genetic and biochemical data together favor the view that MBD3 is a key component of the Mi-2/NuRD corepressor complex, whereas MBD2 may be one of several factors that can recruit this complex to DNA.
机译:MBD2和MBD3是具有共有甲基CpG结合域的密切相关的蛋白质。 MBD2是特异性结合甲基化DNA的转录阻遏物,是MeCP1蛋白复合物的组成部分。相比之下,MBD3不能结合鼠细胞中的甲基化DNA,并且是Mi-2 / NuRD核心加压复合物的组成部分。我们通过基因定位显示,这两种蛋白质在小鼠中并不是功能上多余的,因为Mbd3(-/-)小鼠在早期胚胎发生过程中死亡,而Mbd2(-/-)小鼠却是活的和肥沃的。但是,Mbd2(-/-)小鼠的母亲行为是有缺陷的,并且在分子水平上,Mbd2(-/-)小鼠缺乏MeCP1的成分。 Mbd2突变细胞无法完全沉默外源甲基化模板的转录,但未检测到内源性印迹基因或逆转录病毒序列的不适当激活。尽管它们之间存在差异,但Mbd3和Mbd2在基因上相互作用,提示功能相关。遗传和生化数据共同支持这样一种观点,即MBD3是Mi-2 / NuRD核心表达复合物的关键成分,而MBD2可能是可以将该复合物募集到DNA的几种因素之一。

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