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Genomic Study of RNA Polymerase II and III SNAPc-Bound Promoters Reveals a Gene Transcribed by Both Enzymes and a Broad Use of Common Activators

机译:RNA聚合酶II和III SNAPc结合启动子的基因组研究揭示了一种既被酶又被广泛使用的普通激活因子转录的基因。

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摘要

SNAPc is one of a few basal transcription factors used by both RNA polymerase (pol) II and pol III. To define the set of active SNAPc-dependent promoters in human cells, we have localized genome-wide four SNAPc subunits, GTF2B (TFIIB), BRF2, pol II, and pol III. Among some seventy loci occupied by SNAPc and other factors, including pol II snRNA genes, pol III genes with type 3 promoters, and a few un-annotated loci, most are primarily occupied by either pol II and GTF2B, or pol III and BRF2. A notable exception is the RPPH1 gene, which is occupied by significant amounts of both polymerases. We show that the large majority of SNAPc-dependent promoters recruit POU2F1 and/or ZNF143 on their enhancer region, and a subset also recruits GABP, a factor newly implicated in SNAPc-dependent transcription. These activators associate with pol II and III promoters in G1 slightly before the polymerase, and ZNF143 is required for efficient transcription initiation complex assembly. The results characterize a set of genes with unique properties and establish that polymerase specificity is not absolute in vivo.
机译:SNAPc是RNA聚合酶(pol)II和pol III均使用的几种基础转录因子之一。为了定义人类细胞中依赖于SNAPc的启动子集,我们已经定位了全基因组的四个SNAPc亚基,即GTF2B(TFIIB),BRF2,pol II和pol III。在SNAPc和其他因素所占据的大约70个基因座中,包括pol II snRNA基因,具有3型启动子的pol III基因和一些未注释的基因座,大多数主要被pol II和GTF2B或pol III和BRF2占据。 RPPH1基因是一个明显的例外,该基因被大量的两种聚合酶占据。我们显示,大多数SNAPc依赖型启动子在其增强子区域上募集POU2F1和/或ZNF143,还有一个子集还募集了GABP,这是一种新的与SNAPc依赖型转录有关的因子。这些活化剂在聚合酶之前不久就与G1中的pol II和III启动子结合,而ZNF143是高效转录起始复合物组装所必需的。结果表征了一组具有独特特性的基因,并证明聚合酶特异性在体内不是绝对的。

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