Lindahl L, Archer R, Zengel J M
Cell. 1983 May;33(1):241-8. doi: 10.1016/0092-8674(83)90353-7.
Previous studies have shown that ribosomal protein L4 specifically inhibits the expression of its own operon, the 11-gene S10 operon. To elucidate the mechanism for this regulation, we have examined the effect of protein L4 on transcription of the S10 operon. Hybridization and gel electrophoresis studies indicate that in the presence of excess L4 only RNA molecules about 140 bases long are transcribed from the S10 operon. These short RNA molecules contain the leader, but not structural gene, sequences. Our results suggest that protein L4 stimulates premature termination (attenuation) of transcription about 30 bases upstream from the start of the first structural gene of the S10 operon. The attenuation appears to be independent of the regulation of translation of the operon. We suggest that attenuation of transcription plays a primary role in the autogenous regulation of the S10 operon.
先前的研究表明,核糖体蛋白L4能特异性抑制其自身操纵子(由11个基因组成的S10操纵子)的表达。为阐明这种调控机制,我们研究了蛋白L4对S10操纵子转录的影响。杂交和凝胶电泳研究表明,在存在过量L4的情况下,S10操纵子仅转录出约140个碱基长的RNA分子。这些短RNA分子包含前导序列,但不包含结构基因序列。我们的结果表明,蛋白L4在S10操纵子第一个结构基因起始上游约30个碱基处刺激转录的提前终止(衰减)。这种衰减似乎与操纵子的翻译调控无关。我们认为转录衰减在S10操纵子的自身调控中起主要作用。