Ercan Sevinc, Lieb Jason D
Department of Biology and Carolina Center for the Genome Sciences, CB #3280, 406 Fordham Hall, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3280, USA.
Chromosome Res. 2009;17(2):215-27. doi: 10.1007/s10577-008-9011-0.
The C. elegans dosage compensation complex (DCC) reduces transcript levels from each of the two hermaphrodite X chromosomes to equalize X-linked gene expression to that of XO males. Several of the proteins that comprise the DCC are homologous to subunits of the evolutionarily conserved condensin complexes, which in most organisms function in mitotic and meiotic chromosome condensation. These include the DCC subunits MIX-1 and DPY-27, which belong to the structural maintenance of chromosomes (SMC) family of proteins. Several of the C. elegans DCC subunits also perform double duty as members of the canonical meiotic and mitotic condensin complexes. Here, we review what is known about the C. elegans DCC and how study of this model might shed light on general mechanisms of domain-scale transcriptional regulation. We discuss how condensin-like complexes may be targeted to specific chromosomal locations for performance of their functions.
秀丽隐杆线虫剂量补偿复合体(DCC)降低两条雌雄同体X染色体上每条染色体的转录水平,以使X连锁基因的表达与XO雄性的表达相等。构成DCC的几种蛋白质与进化上保守的凝聚素复合体的亚基同源,在大多数生物体中,凝聚素复合体在有丝分裂和减数分裂染色体凝聚中起作用。这些包括DCC亚基MIX-1和DPY-27,它们属于染色体结构维持(SMC)蛋白家族。秀丽隐杆线虫的几个DCC亚基还作为经典减数分裂和有丝分裂凝聚素复合体的成员发挥双重作用。在这里,我们综述了关于秀丽隐杆线虫DCC的已知信息,以及对该模型的研究如何可能揭示结构域尺度转录调控的一般机制。我们讨论了凝聚素样复合体如何可能被靶向到特定的染色体位置以执行其功能。