Department of Medical and Molecular Genetics, Division of Reproductive and Child Health, Institute of Biomedical Research, University of Birmingham, B15 2TT Edgbaston, Birmingham, UK.
Curr Opin Genet Dev. 2010 Oct;20(5):533-40. doi: 10.1016/j.gde.2010.06.004. Epub 2010 Jul 2.
The traditional model of transcription initiation nucleated by the TFIID complex has suffered significant erosion in the last decade. The discovery of cell-specific paralogs of TFIID subunits and a variety of complexes that replace TFIID in transcription initiation of protein coding genes have been paralleled by the description of diverse core promoter sequences. These observations suggest an additional level of regulation of developmental and tissue-specific gene expression at the core promoter level. Recent work suggests that this regulation may function through specific roles of distinct TBP-type factors and TBP-associated factors (TAFs), however the picture emerging is still far from complete. Here we summarize the proposed models of transcription initiation by alternative initiation complexes in distinct stages of developmental specialization during vertebrate ontogeny.
在过去的十年中,由 TFIID 复合物引发的转录起始的传统模型受到了重大冲击。TFIID 亚基的细胞特异性同源物以及各种可替代蛋白编码基因转录起始中 TFIID 的复合物的发现,与不同核心启动子序列的描述相平行。这些观察结果表明,在核心启动子水平上存在另一种调节发育和组织特异性基因表达的机制。最近的研究表明,这种调节可能通过不同的 TBP 型因子和 TBP 相关因子 (TAFs) 的特定作用来发挥功能,然而,目前的情况仍然远未完全清楚。在这里,我们总结了在脊椎动物个体发生过程中不同发育特化阶段,通过替代起始复合物进行转录起始的模型。