单个染色质环两侧的两个基质附着区域之间的体内相互作用。
Interaction in vivo between the two matrix attachment regions flanking a single chromatin loop.
作者信息
Eivazova Elvira R, Gavrilov Aleksey, Pirozhkova Iryna, Petrov Andrei, Iarovaia Olga V, Razin Sergey V, Lipinski Marc, Vassetzky Yegor S
机构信息
Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN37232, USA.
出版信息
J Mol Biol. 2009 Mar 6;386(4):929-37. doi: 10.1016/j.jmb.2008.12.022. Epub 2008 Dec 14.
In interphase nuclei as in metaphase chromosomes, the genome is organized into topologically closed loop domains. Here, we have mapped the ends of the loop domain that contains the Ifng (interferon-gamma) gene in primary and cultured murine T-lymphocytes. To determine whether the ends of the loop are located in close proximity to each other in the nuclear space, the 3C (chromosome conformation capture) technique, which detects protein-mediated DNA-DNA interactions, was utilized. A strong interaction was demonstrated between the two ends of the loop, which were close enough to become cross-linked in vivo in the presence of paraformaldehyde. Chromatin immunoprecipitation combined with the 3C technique demonstrated that topoisomerase IIalpha and MeCP2, but not topoisomerase IIbeta, heterochromatin-associated protein HP1 or CTCF, were involved in this interaction. The present findings have important implications in terms of mechanisms of illegitimate recombination that can result in chromosomal translocations and deletions.
在间期细胞核中,如同在中期染色体中一样,基因组被组织成拓扑学上封闭的环状结构域。在此,我们已绘制出在原代和培养的小鼠T淋巴细胞中包含Ifng(干扰素γ)基因的环状结构域的末端。为了确定环状结构的末端在核空间中是否彼此紧密相邻,我们采用了检测蛋白质介导的DNA-DNA相互作用的3C(染色体构象捕获)技术。结果表明环状结构的两端之间存在强烈的相互作用,在多聚甲醛存在的情况下,它们在体内靠得足够近从而发生交联。染色质免疫沉淀结合3C技术表明,拓扑异构酶IIα和MeCP2参与了这种相互作用,而拓扑异构酶IIβ、异染色质相关蛋白HP1或CTCF未参与。目前的研究结果对于可能导致染色体易位和缺失的异常重组机制具有重要意义。