Csankovszki Györgyi, McDonel Patrick, Meyer Barbara J
Howard Hughes Medical Institute and Department of Molecular and Cell Biology, University of California, Berkeley, CA 94720-3204, USA.
Science. 2004 Feb 20;303(5661):1182-5. doi: 10.1126/science.1092938.
To achieve X-chromosome dosage compensation, organisms must distinguish X chromosomes from autosomes. We identified multiple, cis-acting regions that recruit the Caenorhabditis elegans dosage compensation complex (DCC) through a search for regions of X that bind the complex when detached from X. The DCC normally assembles along the entire X chromosome, but not all detached regions recruit the complex, despite having genes known to be dosage compensated on the native X. Thus, the DCC binds first to recruitment sites, then spreads to neighboring X regions to accomplish chromosome-wide gene repression. From a large chromosomal domain, we defined a 793-base pair fragment that functions in vivo as an X-recognition element to recruit the DCC.
为实现X染色体剂量补偿,生物体必须区分X染色体和常染色体。我们通过寻找X染色体上与剂量补偿复合体(DCC)分离时仍能结合该复合体的区域,鉴定出多个顺式作用区域,这些区域可招募秀丽隐杆线虫的剂量补偿复合体。DCC通常沿整个X染色体组装,但并非所有分离区域都能招募该复合体,尽管这些区域含有已知在天然X染色体上受剂量补偿的基因。因此,DCC首先结合到招募位点,然后扩散到相邻的X区域以实现全染色体范围的基因抑制。从一个大的染色体结构域中,我们定义了一个793个碱基对的片段,该片段在体内作为X识别元件发挥作用,以招募DCC。