Huang Der-Hwa, Chang Yuh-Long, Yang Chih-Chao, Pan I-Ching, King Balas
Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan 115, Republic of China.
Mol Cell Biol. 2002 Sep;22(17):6261-71. doi: 10.1128/MCB.22.17.6261-6271.2002.
The Polycomb (Pc) group (Pc-G) of repressors is essential for transcriptional silencing of homeotic genes that determine the axial development of metazoan animals. It is generally believed that the multimeric complexes formed by these proteins nucleate certain chromatin structures to silence promoter activity upon binding to Pc-G response elements (PRE). Little is known, however, about the molecular mechanism involved in sequence-specific binding of these complexes. Here, we show that an immunoaffinity-purified Pc protein complex contains a DNA binding activity specific to the (GA)n motif in a PRE from the bithoraxoid region. We found that this activity can be attributed primarily to the large protein isoform encoded by pipsqueak (psq) instead of to the well-characterized GAGA factor. The functional relevance of psq to the silencing mechanism is strongly supported by its synergistic interactions with a subset of Pc-G that cause misexpression of homeotic genes.
多梳(Pc)抑制因子家族(Pc-G)对于决定后生动物轴向发育的同源异型基因的转录沉默至关重要。一般认为,这些蛋白质形成的多聚体复合物在与Pc-G反应元件(PRE)结合时,会促使某些染色质结构形成,从而使启动子活性沉默。然而,对于这些复合物序列特异性结合所涉及的分子机制却知之甚少。在此,我们表明,免疫亲和纯化的Pc蛋白复合物含有一种对来自双胸区PRE中的(GA)n基序具有特异性的DNA结合活性。我们发现,这种活性主要归因于由“小不点儿”(psq)编码的大蛋白异构体,而非特征明确的GAGA因子。psq与导致同源异型基因错误表达的Pc-G子集的协同相互作用,有力地支持了psq与沉默机制的功能相关性。