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CRY1基因的分子克隆与分析:一个酵母核糖体蛋白基因

Molecular cloning and analysis of the CRY1 gene: a yeast ribosomal protein gene.

作者信息

Larkin J C, Woolford J L

出版信息

Nucleic Acids Res. 1983 Jan 25;11(2):403-20. doi: 10.1093/nar/11.2.403.

Abstract

Using cloned DNA from the vicinity of the yeast mating type locus (MAT) as a probe, the wild type allele of the cryptopleurine resistance gene CRY1 has been isolated by the technique of chromosome walking and has been shown to be identical to the gene for ribosomal protein 59. A recessive cryR1 allele has also been cloned, using the integration excision method. The genetic distance from MAT to CRY1 is 2.2 cM, while the physical distance is 21 kb, giving a ratio of about 10 kb/cM for this interval. The phenotypic expression of both plasmid borne alleles of the gene can be detected in vivo. The use of this gene as a hybridization probe to examine RNA processing defects in the rna 2, rna 3, rna 4, rna 8, and rna 11 mutants is also discussed.

摘要

以酵母交配型基因座(MAT)附近的克隆DNA为探针,通过染色体步移技术分离出了隐品碱抗性基因CRY1的野生型等位基因,并已证明它与核糖体蛋白59的基因相同。还利用整合切除法克隆了一个隐性cryR1等位基因。从MAT到CRY1的遗传距离为2.2厘摩,而物理距离为21千碱基对,该区间的比值约为10千碱基对/厘摩。该基因的两个质粒携带等位基因的表型表达均可在体内检测到。还讨论了使用该基因作为杂交探针来检测rna 2、rna 3、rna 4、rna 8和rna 11突变体中的RNA加工缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ac0/325722/154e4532d205/nar00347-0176-a.jpg

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