Donahue T F, Daves R S, Lucchini G, Fink G R
Cell. 1983 Jan;32(1):89-98. doi: 10.1016/0092-8674(83)90499-3.
We have made deletions of the HIS4 5' noncoding region in vitro and inserted these deletions into the yeast genome by transformation. Deletions that extend from -588 to -235 have no detectable effects on either promoter or regulatory functions. Deletions that extend to -138 affect promoter function, but are still regulated by the general control of amino acid biosynthesis. A deletion that extends to -136 cannot derepress HIS4 mRNA in response to the general control. This deletion removes all copies of the sequence 5'-TGACTC-3', which appears at positions -194, -182 and -138 in strains without the deletion. The importance of at least one copy of this repeat for regulation of HIS4 is shown by the reappearance of this sequence in revertants of the -136 deletion that have regained the regulatory response. The fact that deletion of this sequence leads to the inability to derepress suggests that HIS4 is under positive control.
我们在体外对HIS4 5'非编码区进行了缺失操作,并通过转化将这些缺失片段插入酵母基因组。从-588延伸至-235的缺失对启动子或调控功能均无可检测到的影响。延伸至-138的缺失影响启动子功能,但仍受氨基酸生物合成的一般调控。延伸至-136的缺失无法响应一般调控而解除对HIS4 mRNA的抑制。该缺失去除了序列5'-TGACTC-3'的所有拷贝,在未缺失的菌株中,该序列出现在-194、-182和-138位置。在已恢复调控响应的-136缺失回复子中该序列的重现表明,该重复序列的至少一个拷贝对于HIS4的调控至关重要。该序列缺失导致无法解除抑制这一事实表明,HIS4受到正调控。