Rowland O, Segall J
Department of Biochemistry, University of Toronto, Ontario, Canada.
J Biol Chem. 1996 May 17;271(20):12103-10. doi: 10.1074/jbc.271.20.12103.
Transcription factor (TF) IIIA, which contains nine zinc finger motifs, binds to the internal control region of the 5S RNA gene as the first step in the assembly of a multifactor complex that promotes accurate initiation of transcription by RNA polymerase III. We have monitored the interaction of wild-type and truncated forms of yeast TFIIIA with the 5 S RNA gene. The DNase I footprints obtained with full-length TFIIIA and a polypeptide containing the amino-terminal five zinc fingers (TF5) were indistinguishable, extending from nucleotides +64 to +99 of the 5 S RNA gene. This suggests that fingers 6 through 9 of yeast TFIIIA are not in tight association with DNA. The DNase I footprint obtained with a polypeptide containing the amino-terminal four zinc fingers (TF4) was 14 base pairs shorter than that of TF5, extending from nucleotides +78 to +99 on the nontranscribed strand and from nucleotides +79 to +98 on the transcribed strand of the 5 S RNA gene. Protection provided by a polypeptide containing the first three zinc fingers (TF3) was similar to that provided by TF4, with the exception that protection on the nontranscribed strand ended at nucleotide +80, rather than nucleotide +78. Methylation protection analysis indicated that finger 5 makes major groove contacts with guanines +73 and +74. The amino-terminal four zinc fingers make contacts that span the internal control region, which extends from nucleotides +81 to +94 of the 5 S RNA gene, with finger 4 appearing to contact guanine +82. Measurements of the apparent Kd values of the TFIIIA.DNA complexes indicated that the amino-terminal three zinc fingers of TFIIIA have a binding energy that is similar to that of the full-length protein.
转录因子IIIA(TFIIIA)含有九个锌指基序,它与5S RNA基因的内部控制区结合,这是促进RNA聚合酶III精确起始转录的多因子复合物组装的第一步。我们监测了野生型和截短形式的酵母TFIIIA与5S RNA基因的相互作用。用全长TFIIIA和含有氨基末端五个锌指的多肽(TF5)获得的DNase I足迹无法区分,从5S RNA基因的核苷酸+64延伸到+99。这表明酵母TFIIIA的第6至9个锌指与DNA没有紧密结合。用含有氨基末端四个锌指的多肽(TF4)获得的DNase I足迹比TF5的短14个碱基对,从5S RNA基因非转录链上的核苷酸+78延伸到+99,从转录链上的核苷酸+79延伸到+98。含有前三个锌指的多肽(TF3)提供的保护与TF4提供的保护相似,不同之处在于非转录链上的保护在核苷酸+80处结束,而不是核苷酸+78。甲基化保护分析表明,锌指5与鸟嘌呤+73和+74形成大沟接触。氨基末端四个锌指形成的接触跨越内部控制区,该区域从5S RNA基因的核苷酸+81延伸到+94,锌指4似乎与鸟嘌呤+82接触。TFIIIA-DNA复合物表观解离常数(Kd)值的测量表明,TFIIIA的氨基末端三个锌指具有与全长蛋白相似的结合能。