Wutz Anton, Gribnau Joost
Research Institute of Molecular Pathology, Dr. Bohr-Gasse 7, 1030 Vienna, Austria.
Curr Opin Genet Dev. 2007 Oct;17(5):387-93. doi: 10.1016/j.gde.2007.08.001. Epub 2007 Sep 14.
Random inactivation of one of the two female X chromosomes establishes dosage compensation between XY males and XX females in placental mammals. X inactivation is controlled by the X inactivation center (Xic). Recent advances in genome sequencing show that the Xic has evolved from an ancestral vertebrate gene cluster in placental mammals and has undergone separate rearrangements in marsupials. The Xic ensures that all but one X chromosome per diploid genome are inactivated. Which chromosome remains active is randomly chosen. Pairing of Xic loci on the two X chromosomes and alternate states of the X chromosomes before inactivation have recently been implicated in the mechanism of random choice. Chromosome-wide silencing is then initiated by the noncoding Xist RNA, which evolved with the mammalian Xic and covers the inactive X chromosome.
在胎盘哺乳动物中,两条雌性X染色体中的一条随机失活,从而在XY雄性和XX雌性之间建立剂量补偿。X染色体失活由X染色体失活中心(Xic)控制。基因组测序的最新进展表明,Xic是从胎盘哺乳动物的一个祖先脊椎动物基因簇进化而来的,并且在有袋类动物中经历了单独的重排。Xic确保每个二倍体基因组中除一条X染色体外的所有X染色体均失活。哪条染色体保持活跃是随机选择的。两条X染色体上Xic位点的配对以及失活前X染色体的交替状态最近被认为与随机选择机制有关。然后,由非编码Xist RNA启动全染色体范围的沉默,Xist RNA与哺乳动物Xic一起进化,并覆盖失活的X染色体。