Munson L M, Stormo G D, Niece R L, Reznikoff W S
J Mol Biol. 1984 Aug 25;177(4):663-83. doi: 10.1016/0022-2836(84)90043-3.
Sixteen single point mutations near the beginning of the lacZ gene have been isolated and their effect on lacZ expression has been measured. Five mutations were obtained that alter a potential stem-and-loop structure in the messenger RNA that masks the initiation codons. Formation of this stem-and-loop is a result of transcription of DNA sequences introduced during the cloning of the lac regulatory region. The mutations isolated were then moved into a background that deleted this structure. Analysis of these mutations indicated that the secondary structure inhibited lacZ expression 5.8-fold and that either single point mutations or a 9 base-pair deletion could relieve this inhibition completely. In addition, it was found that an A to C transversion in the first base following the initiation codon (in the absence of the inhibitory secondary structure) decreases lacZ expression almost twofold, whereas C to U transitions in the next two positions have negligible effects. Mutations were also obtained that either increase or decrease the length of the Shine-Dalgarno sequence. The effects of these mutations were studied in the presence or absence of the secondary structure that involves the two initiation codons. It was found that when translation initiation was inhibited by the secondary structure, increasing the length of the Shine-Dalgarno sequence increased lacZ expression 2.8-fold and decreasing the length of this sequence reduced lacZ expression 12-fold. When translation initiation was not inhibited by the secondary structure, increasing the length of the Shine-Dalgarno sequence had no effect and decreasing the length of this sequence only reduced lacZ expression sixfold. The mechanistic implications of these results are discussed. Two initiation codons are located in the beginning of the lacZ gene, 7 and 13 bases from the Shine-Dalgarno sequence. NH2-terminal sequence analysis indicated that the majority of the protein synthesized initiate at the first initiation codon in the wild-type lacZ gene (in agreement with results reported previously by J. L. Brown and his colleagues). Upon introduction of sequences that result in a change in the mRNA secondary structure, both initiation codons are used in almost equal amounts. Three mutations and two pseudorevertants were obtained, which are located in the first initiation codon. It was found that when the first initiation codon is changed from AUG to GUG, translation initiation is decreased tenfold at that codon.(ABSTRACT TRUNCATED AT 400 WORDS)
已分离出16个位于lacZ基因起始处附近的单点突变,并测定了它们对lacZ表达的影响。获得了5个突变,这些突变改变了掩盖起始密码子的信使RNA中的一个潜在茎环结构。这种茎环的形成是克隆lac调控区时引入的DNA序列转录的结果。然后将分离出的突变转移到删除了该结构的背景中。对这些突变的分析表明,二级结构抑制lacZ表达5.8倍,单点突变或9个碱基对的缺失都可以完全解除这种抑制。此外,还发现起始密码子后的第一个碱基由A颠换为C(在没有抑制性二级结构的情况下)会使lacZ表达降低近两倍,而接下来两个位置的C到U转换的影响可忽略不计。还获得了增加或减少Shine-Dalgarno序列长度的突变。在存在或不存在涉及两个起始密码子的二级结构的情况下研究了这些突变的影响。发现当翻译起始被二级结构抑制时,增加Shine-Dalgarno序列的长度会使lacZ表达增加2.8倍,而减少该序列的长度会使lacZ表达降低12倍。当翻译起始不受二级结构抑制时,增加Shine-Dalgarno序列的长度没有影响,而减少该序列的长度仅使lacZ表达降低6倍。讨论了这些结果的机制意义。两个起始密码子位于lacZ基因的起始处,距离Shine-Dalgarno序列7个和13个碱基。氨基末端序列分析表明,野生型lacZ基因中合成的大多数蛋白质在第一个起始密码子处起始(与J.L.布朗及其同事先前报道的结果一致)。引入导致mRNA二级结构改变的序列后,两个起始密码子的使用量几乎相等。获得了三个突变和两个假回复突变,它们位于第一个起始密码子处。发现当第一个起始密码子从AUG变为GUG时,该密码子处的翻译起始降低了10倍。