Termolino Pasquale, Cremona Gaetana, Consiglio Maria Federica, Conicella Clara
CNR, National Research Council of Italy, Institute of Biosciences and Bioresources, Research Division Portici, Via Università 133, 80055, Portici, Italy.
Chromosoma. 2016 Jun;125(2):301-8. doi: 10.1007/s00412-016-0574-9. Epub 2016 Jan 22.
Genome architecture is shaped by gene-rich and repeat-rich regions also known as euchromatin and heterochromatin, respectively. Under normal conditions, the repeat-containing regions undergo little or no meiotic crossover (CO) recombination. COs within repeats are risky for the genome integrity. Indeed, they can promote non-allelic homologous recombination (NAHR) resulting in deleterious genomic rearrangements associated with diseases in humans. The assembly of heterochromatin is driven by the combinatorial action of many factors including histones, their modifications, and DNA methylation. In this review, we discuss current knowledge dealing with the epigenetic signatures of the major repeat regions where COs are suppressed. Then we describe mutants for epiregulators of heterochromatin in different organisms to find out how chromatin structure influences the CO rate and distribution.
基因组结构由富含基因和富含重复序列的区域塑造,这两个区域分别也被称为常染色质和异染色质。在正常情况下,含有重复序列的区域很少或不发生减数分裂交叉(CO)重组。重复序列内的CO对基因组完整性有风险。事实上,它们可促进非等位基因同源重组(NAHR),导致与人类疾病相关的有害基因组重排。异染色质的组装由包括组蛋白、其修饰和DNA甲基化在内的多种因素的组合作用驱动。在本综述中,我们讨论了关于主要重复区域表观遗传特征的现有知识,在这些区域CO被抑制。然后我们描述了不同生物体中异染色质表观调控因子的突变体,以了解染色质结构如何影响CO速率和分布。