Weiffenbach B, Rogers D T, Haber J E, Zoller M, Russell D W, Smith M
Proc Natl Acad Sci U S A. 1983 Jun;80(11):3401-5. doi: 10.1073/pnas.80.11.3401.
Several cis-acting mutations that prevent homothallic mating type conversions in Saccharomyces cerevisiae have been examined. Deletions within the mating type (MAT) locus were obtained by selecting for survivors among homothallic MAT alpha cells carrying the rad52 mutation. The survivors were unable to switch mating type, even in RAD+ derivatives. The deletions varied in size from fewer than 50 to more than 750 base pairs. All of the deletions removed a Hha I site at the border between the alpha-specific sequences (Y alpha) and the adjacent Z region. We also examined several spontaneous inc mutations that prevent MAT switching. Two of these mutations were cloned in recombinant DNA plasmids and their sequences were determined. The MAT alpha-inc 3-7 mutation proved to have an altered Hha I site at the Y alpha/Z border, by virtue of a single base pair substitution G . C leads to A . T in the second base pair of the Z region (Z2). Restriction fragment analysis showed that two other independently isolated strains with MAT alpha-inc mutations had altered the same Hha I site. The MAT a-inc 4-28 mutation contains a single base pair substitution C . G leads to T . A at position Z6. A base pair difference at position Z11 in two MATa strains does not affect MATa conversions. We conclude that the region near the Y/Z border is essential for the efficient switching of MAT alleles and constitutes an enzyme recognition site for a specific nucleolytic cleavage of MAT DNA.
已对酿酒酵母中几种阻止同宗配合型转换的顺式作用突变进行了研究。通过在携带rad52突变的同宗配合MATα细胞中筛选存活菌株,获得了交配型(MAT)位点内的缺失。这些存活菌株即使在RAD+衍生物中也无法转换交配型。缺失的大小从少于50个碱基对到超过750个碱基对不等。所有缺失都去除了α特异性序列(Yα)与相邻Z区域边界处的一个Hha I位点。我们还研究了几种阻止MAT转换的自发inc突变。其中两个突变被克隆到重组DNA质粒中并测定了其序列。MATα-inc 3-7突变被证明在Yα/Z边界处有一个改变的Hha I位点,这是由于Z区域(Z2)第二个碱基对中的一个碱基对替换G.C变为A.T所致。限制性片段分析表明,另外两个独立分离的具有MATα-inc突变的菌株也改变了同一个Hha I位点。MAT a-inc 4-28突变在Z6位置含有一个碱基对替换C.G变为T.A。两个MATa菌株在Z11位置的碱基对差异不影响MATa转换。我们得出结论,Y/Z边界附近的区域对于MAT等位基因的有效转换至关重要,并且构成了MAT DNA特异性核酸裂解的酶识别位点。