Jepsen K, Hermanson O, Onami T M, Gleiberman A S, Lunyak V, McEvilly R J, Kurokawa R, Kumar V, Liu F, Seto E, Hedrick S M, Mandel G, Glass C K, Rose D W, Rosenfeld M G
Howard Hughes Medical Institute, Department of Biology, University of California, San Diego, La Jolla 92093, USA.
Cell. 2000 Sep 15;102(6):753-63. doi: 10.1016/s0092-8674(00)00064-7.
Transcriptional repression plays crucial roles in diverse aspects of metazoan development, implying critical regulatory roles for corepressors such as N-CoR and SMRT. Altered patterns of transcription in tissues and cells derived from N-CoR gene-deleted mice and the resulting block at specific points in CNS, erythrocyte, and thymocyte development indicated that N-CoR was a required component of short-term active repression by nuclear receptors and MAD and of a subset of long-term repression events mediated by REST/NRSF. Unexpectedly, N-CoR and a specific deacetylase were also required for transcriptional activation of one class of retinoic acid response element. Together, these findings suggest that specific combinations of corepressors and histone deacetylases mediate the gene-specific actions of DNA-bound repressors in development of multiple organ systems.
转录抑制在多细胞动物发育的各个方面发挥着关键作用,这意味着诸如N-CoR和SMRT等共抑制因子具有重要的调节作用。源自N-CoR基因缺失小鼠的组织和细胞中的转录模式改变以及在中枢神经系统、红细胞和胸腺细胞发育的特定阶段出现的阻滞表明,N-CoR是核受体和MAD介导的短期活性抑制以及REST/NRSF介导的一部分长期抑制事件所必需的组成部分。出乎意料的是,一类视黄酸反应元件的转录激活也需要N-CoR和一种特定的脱乙酰酶。这些发现共同表明,共抑制因子和组蛋白脱乙酰酶的特定组合介导了DNA结合阻遏物在多个器官系统发育中的基因特异性作用。