Hinnebusch A G, Fink G R
J Biol Chem. 1983 Apr 25;258(8):5238-47.
The HIS1 gene of Saccharomyces cerevisiae encodes ATP phosphoribosyltransferase, the first enzyme in the pathway of histidine biosynthesis. We have cloned this gene by complementation of a his1 auxotroph. The HIS1 coding region was localized within the cloned segment by assay of subcloned fragments for their ability to complement a his1 auxotroph. We determined the DNA sequence of the HIS1 region defined by this complementation test. S1 nuclease and exonuclease VII mapping of the 5' and 3' termini of HIS1 mRNA reveal considerable heterogeneity at both ends of the transcript, especially the 5' end which displays 13 different termini that span a 110-base pair region. Northern analysis shows that derepression of HIS1 enzyme activity under conditions of amino acid deprivation can be accounted for by an increase in the steady state level of HIS1 mRNA. There are no large differences between the relative levels of HIS1 mRNA molecules with different 5' termini in repressed and derepressed cells. In the DNA sequence upstream from the 5' termini of HIS1 mRNA we have found four closely related copies of a 9-base pair sequence. This sequence is also repeated in the 5' noncoding regions of HIS4, HIS3, and TRP5. Closely related sequences are not found flanking a number of other yeast genes, suggesting that the repeated sequence plays a role in the regulation of amino acid biosynthetic genes subject to the general amino acid control.
酿酒酵母的HIS1基因编码ATP磷酸核糖基转移酶,它是组氨酸生物合成途径中的第一个酶。我们通过对his1营养缺陷型进行互补克隆了该基因。通过检测亚克隆片段互补his1营养缺陷型的能力,将HIS1编码区定位在克隆片段内。我们测定了由这种互补试验确定的HIS1区域的DNA序列。对HIS1 mRNA 5'和3'末端进行S1核酸酶和外切核酸酶VII作图,结果显示转录本两端存在相当大的异质性,尤其是5'端,有13个不同的末端,跨越110个碱基对的区域。Northern分析表明,在氨基酸缺乏条件下HIS1酶活性的去阻遏可以由HIS1 mRNA稳态水平的增加来解释。在阻遏和去阻遏细胞中,具有不同5'末端的HIS1 mRNA分子的相对水平没有很大差异。在HIS1 mRNA 5'末端上游的DNA序列中,我们发现了一个9碱基对序列的四个紧密相关的拷贝。该序列也在HIS4、HIS3和TRP5的5'非编码区重复。在许多其他酵母基因的侧翼未发现紧密相关的序列,这表明该重复序列在受一般氨基酸控制的氨基酸生物合成基因的调控中起作用。