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组蛋白macroH2A1亚型的发育和组织表达模式。

Developmental and tissue expression patterns of histone macroH2A1 subtypes.

作者信息

Pehrson J R, Costanzi C, Dharia C

机构信息

Department of Animal Biology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia 19104-6048, USA.

出版信息

J Cell Biochem. 1997 Apr;65(1):107-13. doi: 10.1002/(sici)1097-4644(199704)65:1<107::aid-jcb11>3.0.co;2-h.

Abstract

MacroH2A is a novel nucleosomal core histone that contains a large nonhistone region and a region that closely resembles a full length histone H2A. We have cloned a cDNA that contains the entire coding region of macroH2A1.2, one of the two identified subtypes of macroH2A1. MacroH2A1.2 was found to differ from the other known subtype, macroH2A1.1, in a single segment of the nonhistone region. MacroH2A1 specific antibodies revealed relatively high levels of both subtypes in adult liver and kidney. MacroH2A1.1 was much lower in fetal liver and kidney in comparison to their adult counterparts, and was not detected in adult thymus and testis, tissues with active cell division and differentiation. Both subtypes were present at very low levels or absent from mouse embryonic stem cells maintained in an undifferentiated state by growth in the presence of leukemia inhibitory factor. MacroH2A1.2 increased when the embryonic stem cells were induced to differentiate in vitro, while macroH2A1.1 remained undetectable. These results support the idea that macroH2A1.1 and macroH2A1.2 are functionally distinct, and suggest that changes in their expression may play a role in developmentally regulated changes in chromatin structure and function.

摘要

巨H2A是一种新型核小体核心组蛋白,它包含一个大的非组蛋白区域和一个与全长组蛋白H2A非常相似的区域。我们克隆了一个包含巨H2A1.2完整编码区的cDNA,巨H2A1.2是已鉴定的巨H2A1的两种亚型之一。发现巨H2A1.2在非组蛋白区域的单个片段上与另一种已知亚型巨H2A1.1不同。巨H2A1特异性抗体显示,在成年肝脏和肾脏中,这两种亚型的水平相对较高。与成年肝脏和肾脏相比,胎儿肝脏和肾脏中的巨H2A1.1水平要低得多,并且在成年胸腺和睾丸(具有活跃细胞分裂和分化的组织)中未检测到。在白血病抑制因子存在下生长以维持未分化状态的小鼠胚胎干细胞中,这两种亚型的水平都非常低或不存在。当胚胎干细胞在体外被诱导分化时,巨H2A1.2增加,而巨H2A1.1仍未检测到。这些结果支持了巨H2A1.1和巨H2A1.2在功能上不同的观点,并表明它们表达的变化可能在染色质结构和功能的发育调控变化中起作用。

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