Kargaran Parisa K, Yasaei Hemad, Anjomani-Virmouni Sara, Mangiapane Giovanna, Slijepcevic Predrag
Division of Biosciences, Department of Life Sciences, College of Health and Life Sciences, Brunel University London, Uxbridge, UK.
Genes Chromosomes Cancer. 2016 Nov;55(11):864-76. doi: 10.1002/gcc.22386. Epub 2016 Jul 26.
Telomeres are specialized structures responsible for the chromosome end protection. Previous studies have revealed that defective BRCA1 may lead to elevated telomere fusions and accelerated telomere shortening. In addition, BRCA1 associates with promyelocytic leukemia (PML) bodies in alternative lengthening of telomeres (ALTs) positive cells. We report here elevated recombination rates at telomeres in cells from human BRCA1 mutation carriers and in mouse embryonic stem cells lacking both copies of functional Brca1. An increased recombination rate at telomeres is one of the signs of ALT. To investigate this possibility further we employed the C-circle assay that identifies ALT unequivocally. Our results revealed elevated levels of ALT activity in Brca1 defective mouse cells. Similar results were obtained when the same cells were assayed for the presence of another ALT marker, namely the frequency of PML bodies. These results suggest that BRCA1 may act as a repressor of ALT. © 2016 The Authors Genes, Chromosomes & Cancer Published by Wiley Periodicals, Inc.
端粒是负责染色体末端保护的特殊结构。先前的研究表明,有缺陷的BRCA1可能导致端粒融合增加和端粒加速缩短。此外,在端粒替代延长(ALT)阳性细胞中,BRCA1与早幼粒细胞白血病(PML)小体相关联。我们在此报告,在人类BRCA1突变携带者的细胞以及缺乏功能性Brca1两个拷贝的小鼠胚胎干细胞中,端粒处的重组率升高。端粒处重组率增加是ALT的标志之一。为了进一步研究这种可能性,我们采用了能明确识别ALT的C环检测法。我们的结果显示,Brca1缺陷小鼠细胞中的ALT活性水平升高。当对相同细胞检测另一种ALT标志物(即PML小体的频率)时,也获得了类似结果。这些结果表明,BRCA1可能作为ALT的抑制因子。© 2016作者 基因、染色体与癌症 由威利期刊公司出版