Thomm M
Institut für Allgemeine Mikrobiologie, Christian-Albrechts-Universität zu Kiel, Germany.
FEMS Microbiol Rev. 1996 May;18(2-3):159-71. doi: 10.1111/j.1574-6976.1996.tb00234.x.
Archaeal RNA polymerases show a weak ability in vitro to bind to promoter DNA and/or to initiate transcription with low activity independent of upstream regulatory DNA sequences. Active transcription in vitro and in vivo, however, depends strictly on a TATA box resembling the TATA box of eucaryal polII promoters. This TATA box is recognized by a polypeptide related to eucaryal TATA-binding protein (TBP) that was formerly designated aTFB. Template competition studies showed that this archaeal TATA-binding protein (aTBP) is stably sequestered at the promoter by interaction with the second archaeal transcription factor, aTFA, which is related to eucaryal transcription factor IIB (TFIIB). The association of archaeal TFIIB (aTFIIB) with the aTBP-promoter complex leads to template commitment, indicating that aTFIIB recruits archaeal RNA polymerase to the preinitiation complex. These analyses suggest the following order for assembly of transcription factors on the archaeal promoter: aTBP, aTFIIB, RNA polymerase, and provide evidence for a common molecular mechanism of transcription initiation by eucaryal RNA polymerase II and archaeal RNA polymerases. The sequence of the genes encoding aTBP and aTFIIB (TFB) showed all the characteristics conserved in their eucaryal counterparts. The degree of sequence similarity between archaeal and eucaryal transcription factors is between 27 to 35% for TFIIB and between 36 to 41% for TBP. The findings discussed here indicate that TBP and TFIIB perform analogous functions in Archaea and Eucarya and show that four essential components of archaeal and eucaryal transcriptional machineries. RNA polymerase, TATA box, TBP and TFIIB are homologous.
古细菌RNA聚合酶在体外与启动子DNA结合的能力较弱,和/或在不依赖上游调控DNA序列的情况下以低活性起始转录。然而,体外和体内的活性转录严格依赖于一个类似于真核生物聚合酶II启动子的TATA框。这个TATA框由一种与真核生物TATA结合蛋白(TBP)相关的多肽识别,该多肽以前被命名为aTFB。模板竞争研究表明,这种古细菌TATA结合蛋白(aTBP)通过与第二种古细菌转录因子aTFA相互作用而稳定地结合在启动子上,aTFA与真核生物转录因子IIB(TFIIB)相关。古细菌TFIIB(aTFIIB)与aTBP-启动子复合物的结合导致模板确定,表明aTFIIB将古细菌RNA聚合酶招募到预起始复合物中。这些分析表明转录因子在古细菌启动子上的组装顺序如下:aTBP、aTFIIB、RNA聚合酶,并为真核生物RNA聚合酶II和古细菌RNA聚合酶转录起始的共同分子机制提供了证据。编码aTBP和aTFIIB(TFB)的基因序列显示出其在真核生物对应物中保守的所有特征。古细菌和真核生物转录因子之间的序列相似程度,TFIIB为27%至35%,TBP为36%至41%。这里讨论的发现表明,TBP和TFIIB在古细菌和真核生物中发挥类似功能,并表明古细菌和真核生物转录机制的四个基本组成部分,RNA聚合酶、TATA框、TBP和TFIIB是同源的。