Nagarajan P, Onami T M, Rajagopalan S, Kania S, Donnell R, Venkatachalam S
Department of Biochemistry and Cellular and Molecular Biology, University of Tennessee, Knoxville, TN 37996, USA.
Oncogene. 2009 Feb 26;28(8):1053-62. doi: 10.1038/onc.2008.440. Epub 2009 Jan 12.
The chromodomain helicase DNA-binding proteins (CHDs) are known to affect transcription through their ability to remodel chromatin and modulate histone deacetylation. In an effort to understand the functional role of the CHD2 in mammals, we have generated a Chd2 mutant mouse model. Remarkably, the Chd2 protein appears to play a critical role in the development, hematopoiesis and tumor suppression. The Chd2 heterozygous mutant mice exhibit increased extramedullary hematopoiesis and susceptibility to lymphomas. At the cellular level, Chd2 mutants are defective in hematopoietic stem cell differentiation, accumulate higher levels of the chromatin-associated DNA damage response mediator, gamma H2AX, and exhibit an aberrant DNA damage response after X-ray irradiation. Our data suggest a direct role for the chromatin remodeling protein in DNA damage signaling and genome stability maintenance.
已知染色体结构域解旋酶DNA结合蛋白(CHDs)通过其重塑染色质和调节组蛋白去乙酰化的能力来影响转录。为了了解CHD2在哺乳动物中的功能作用,我们构建了一个Chd2突变小鼠模型。值得注意的是,Chd2蛋白似乎在发育、造血和肿瘤抑制中起关键作用。Chd2杂合突变小鼠表现出髓外造血增加和对淋巴瘤的易感性。在细胞水平上,Chd2突变体在造血干细胞分化方面存在缺陷,积累了更高水平的与染色质相关的DNA损伤反应介质γH2AX,并在X射线照射后表现出异常的DNA损伤反应。我们的数据表明这种染色质重塑蛋白在DNA损伤信号传导和基因组稳定性维持中起直接作用。