首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >INOSITOL MUTANTS OF SACCHAROMYCES CEREVISIAE: MAPPING THE ino1 LOCUS AND CHARACTERIZING ALLELES OF THE ino1, ino2 AND ino4 LOCI
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INOSITOL MUTANTS OF SACCHAROMYCES CEREVISIAE: MAPPING THE ino1 LOCUS AND CHARACTERIZING ALLELES OF THE ino1, ino2 AND ino4 LOCI

机译:酿酒酵母的肌苷突变:映射ino1基因座并表征ino1,ino2和ino4 LOCI等位基因

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An extensive genetic analysis of inositol auxotrophic mutants of yeast is reported. The analysis includes newly isolated mutants, as well as those previously reported (Culbertson and Henry 1975). Approximately 70% of all inositol auxotrophs isolated are shown to be alleles of the ino1 locus, the structural gene for inositol-1-phosphate synthase, the major enzyme involved in inositol biosynthesis. Alleles of two other loci, ino2 and ino4 , comprise 9% of total mutants, with the remainder representing unique loci or complementation groups. The ino1 locus was mapped by trisomic analysis with an n + 1 disomic strain constructed with complementing alleles at this locus. The ino1 locus is shown to be located between ura2 (11.1 cm) and cdc6 (21.8 cm) on chromosome X . An extended map of chromosome X of yeast is presented. Unlike most yeast loci, but similar to the his1 locus, the ino1 locus lacks allelic representatives that are suppressible by known suppressors. This finding suggests that premature termination of translation of the ino1 gene product may be incompatible with cell viability.
机译:据报道对酵母的肌醇营养缺陷型突变体进行了广泛的遗传分析。分析包括新分离的突变体,以及以前报道的突变体(Culbertson和Henry 1975)。分离出的所有肌醇营养缺陷型中大约70%被证明是ino1基因座的等位基因,ino1基因是肌醇-1-磷酸合酶的结构基因,肌醇-1-磷酸合酶是肌醇生物合成中涉及的主要酶。另外两个基因座ino2和ino4的等位基因占总突变体的9%,其余代表独特的基因座或互补基团。通过三体组分析,用在该基因座处互补等位基因构建的n + 1二体组菌株对ino1基因座进行作图。已显示ino1基因座位于X染色体上的ura2(11.1 cm)和cdc6(21.8 cm)之间。给出了酵母X染色体的延伸图。与大多数酵母基因座不同,但与his1基因座相似,ino1基因座缺少可被已知抑制子抑制的等位基因代表。这一发现表明,ino1基因产物翻译的过早终止可能与细胞活力不兼容。

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