首页> 外文期刊>Molecular and Cellular Biology >Proximal sequence element-binding transcription factor (PTF) is a multisubunit complex required for transcription of both RNA polymerase II- and RNA polymerase III-dependent small nuclear RNA genes.
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Proximal sequence element-binding transcription factor (PTF) is a multisubunit complex required for transcription of both RNA polymerase II- and RNA polymerase III-dependent small nuclear RNA genes.

机译:近端序列元件结合转录因子(PTF)是转录RNA聚合酶II和依赖RNA聚合酶III的小核RNA基因所需的一个多亚基复合物。

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The proximal sequence element (PSE), found in both RNA polymerase II (Pol II)- and RNA Pol III-transcribed small nuclear RNA (snRNA) genes, is specifically bound by the PSE-binding transcription factor (PTF). We have purified PTF to near homogeneity from HeLa cell extracts by using a combination of conventional and affinity chromatographic methods. Purified PTF is composed of four polypeptides with apparent molecular masses of 180, 55, 45, and 44 kDa. A combination of preparative electrophoretic mobility shift and sodium dodecyl sulfate-polyacrylamide gel electrophoresis analyses has conclusively identified these four polypeptides as subunits of human PTF, while UV cross-linking experiments demonstrate that the largest subunit of PTF is in close contact with the PSE. The purified PTF activates transcription from promoters of both Pol II- and Pol III-transcribed snRNA genes in a PSE-dependent manner. In addition, we have investigated factor requirements in transcription of Pol III-dependent snRNA genes. We show that in extracts that have been depleted of TATA-binding protein (TBP) and associated factors, recombinant TBP restores transcription from U6 and 7SK promoters but not from the VAI promoter, whereas the highly purified TBP-TBP-associated factor complex TFIIIB restores transcription from the VAI but not the U6 or 7SK promoter. Furthermore, by complementation of heat-treated extracts lacking TFIIIC activity, we show that TFIIIC1 is required for transcription of both the 7SK and VAI genes, whereas TFIIIC2 is required only for transcription of the VAI gene. From these observations, we conclude (i) that PTF and TFIIIC2 function as gene-specific as gene-specific factors for PSE-and B-box-containing Pol III genes, respectively, (ii) that the form of TBP used by class III genes with upstream promoter elements differs from the from used by class III genes with internal promoters, and (iii) that TFIIIC1 is required for both internal and external Pol III promoters.
机译:在RNA聚合酶II(Pol II)和RNA Pol III转录的小核RNA(snRNA)基因中都发现了近端序列元件(PSE),它被PSE结合转录因子(PTF)特异性结合。通过使用常规色谱和亲和色谱方法的组合,我们已经从HeLa细胞提取物中纯化了近乎同质的PTF。纯化的PTF由四种表观分子量为180、55、45和44 kDa的多肽组成。制备性电泳迁移率变动与十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析相结合,已最终确定这四种多肽为人PTF的亚基,而UV交联实验表明PTF的最大亚基与PSE紧密接触。纯化的PTF以PSE依赖性方式激活Pol II和Pol III转录的snRNA基因启动子的转录。此外,我们已经调查了依赖于Pol III的snRNA基因转录的因子要求。我们显示出在已经耗尽TATA结合蛋白(TBP)和相关因子的提取物中,重组TBP恢复了U6和7SK启动子的转录,而不是VAI启动子,而高度纯化的TBP-TBP相关因子复合物TFIIIB恢复了从VAI转录,但不是U6或7SK启动子。此外,通过补充缺乏TFIIIC活性的热处理提取物,我们显示TFIIIC1是7SK和VAI基因转录所必需的,而TFIIIC2仅是VAI基因的转录所必需的。从这些观察中,我们得出结论:(i)PTF和TFIIIC2分别作为含PSE和B-box的Pol III基因的基因特异性因子,作为基因特异性因子,(ii)III类使用的TBP形式具有上游启动子元件的基因不同于具有内部启动子的III类基因所使用的基因,(iii)内部和外部Pol III启动子都需要TFIIIC1。

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