Hue K K, Bechhofer D H
Department of Biochemistry, Mount Sinai School of Medicine, New York, New York 10029.
J Bacteriol. 1992 Sep;174(18):5860-8. doi: 10.1128/jb.174.18.5860-5868.1992.
The erythromycin resistance gene ermD, which encodes an rRNA methylase protein, has an unusually long leader region (354 nucleotides). Previously, a single promoter-proximal leader peptide coding sequence was recognized from the nucleotide sequence, and erythromycin-induced ribosome stalling in this sequence was proposed to be required for the induction of methylase translation. We characterized spontaneously occurring and in vitro-constructed leader region mutations in an effort to understand the function of various segments of the long ermD leader region. A second leader peptide coding sequence was identified, and the location of insertion and point mutations that expressed ermD methylase constitutively suggested that translation of the second leader peptide is controlled by ribosome stalling in the first leader peptide. From Northern RNA blot analysis of ermD transcription, it appears that regulation of ermD expression is not by transcriptional attenuation.
编码一种rRNA甲基化酶蛋白的红霉素抗性基因ermD具有异常长的前导区(354个核苷酸)。以前,从核苷酸序列中识别出一个单一的启动子近端前导肽编码序列,并且有人提出在该序列中红霉素诱导的核糖体停滞是甲基化酶翻译诱导所必需的。我们对自发产生的和体外构建的前导区突变进行了表征,以了解长ermD前导区各个片段的功能。鉴定出了第二个前导肽编码序列,组成型表达ermD甲基化酶的插入和点突变的位置表明,第二个前导肽的翻译受第一个前导肽中的核糖体停滞控制。从ermD转录的Northern RNA印迹分析来看,ermD表达的调控似乎不是通过转录衰减实现的。