Department of Neurobiology, Harvard Medical School, Boston, MA 02115, USA.
Science. 2012 Aug 3;337(6094):599-602. doi: 10.1126/science.1221592. Epub 2012 Jul 5.
Eukaryotic circadian clocks are built on transcriptional feedback loops. In mammals, the PERIOD (PER) and CRYPTOCHROME (CRY) proteins accumulate, form a large nuclear complex (PER complex), and repress their own transcription. We found that mouse PER complexes included RNA helicases DDX5 and DHX9, active RNA polymerase II large subunit, Per and Cry pre-mRNAs, and SETX, a helicase that promotes transcriptional termination. During circadian negative feedback, RNA polymerase II accumulated near termination sites on Per and Cry genes but not on control genes. Recruitment of PER complexes to the elongating polymerase at Per and Cry termination sites inhibited SETX action, impeding RNA polymerase II release and thereby repressing transcriptional reinitiation. Circadian clock negative feedback thus includes direct control of transcriptional termination.
真核生物的生物钟是建立在转录反馈环上的。在哺乳动物中,PERIOD(PER)和 CRYPTOCHROME(CRY)蛋白积累,形成一个大型核复合物(PER 复合物),并抑制自身的转录。我们发现,小鼠 PER 复合物包括 RNA 解旋酶 DDX5 和 DHX9、活性 RNA 聚合酶 II 大亚基、Per 和 Cry 前体 mRNA,以及 SETX,一种促进转录终止的解旋酶。在生物钟负反馈过程中,RNA 聚合酶 II 在前体 mRNA 基因的终止位点附近积累,但在对照基因上则没有。PER 复合物在 Per 和 Cry 终止位点招募到延伸中的聚合酶,抑制 SETX 的作用,阻碍 RNA 聚合酶 II 的释放,从而抑制转录的重新起始。因此,生物钟负反馈包括对转录终止的直接控制。