Ishiguro Akira, Kassavetis George A
Division of Biological Sciences and Center for Molecular Genetics, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0634, USA.
FEBS Lett. 2003 Jul 31;548(1-3):33-6. doi: 10.1016/s0014-5793(03)00724-5.
The Saccharomyces cerevisiae RPR1 gene encodes the RNA subunit of its RNase P, which processes RNA polymerase (pol) III primary transcripts. RPR1, which is transcribed by pol III, has been isolated as a multicopy suppressor of a specific small internal deletion (amino acids 253-269) in the Bdp1 subunit of transcription factor TFIIIB, the core pol III transcription factor. The selective effect of this Bdp1 deletion on RPR1 transcription has been analyzed in vitro. It is shown that TFIIIC-dependent assembly of TFIIIB on the RPR1 promoter is specifically sensitive to this Bdp1 deletion, leading to gene-specifically defective single-round and multiple-round transcription.
酿酒酵母RPR1基因编码其核糖核酸酶P的RNA亚基,该亚基负责加工RNA聚合酶(pol)III的初级转录本。由pol III转录的RPR1已作为转录因子TFIIIB(核心pol III转录因子)的Bdp1亚基中特定小内部缺失(氨基酸253 - 269)的多拷贝抑制子被分离出来。已在体外分析了这种Bdp1缺失对RPR1转录的选择性影响。结果表明,TFIIIC依赖的TFIIIB在RPR1启动子上的组装对这种Bdp1缺失特别敏感,导致基因特异性的单轮和多轮转录缺陷。