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染色体分离常常与小鼠细胞中隐性突变的表达相关。

Chromosome segregation is frequently associated with the expression of recessive mutations in mouse cells.

作者信息

Eves E M, Farber R A

出版信息

Proc Natl Acad Sci U S A. 1981 Mar;78(3):1768-72. doi: 10.1073/pnas.78.3.1768.

Abstract

The genes coding for adenosine kinase (ADK; ATP:adenosine 5'-phosphotransferase, EC 2.7.1.20) and esterase-10 (ES-10; carboxylesterase, carboxylic-ester hydrolase, EC 3.1.1.1) are both located on chromosome 14 in the mouse. The near-diploid mouse cell line CAK is heterozygous for two electrophoretic variants of ES-10. Recessive Adk- mutants of CAK have been isolated and analyzed for Es-10 phenotype and karyotypic abnormalities. Two classes of mutants were found with approximatley equal frequencies: those that remained heterozygous in the expression of Es-10 and those that expressed only one Es-10 allele. Of the mutants that lacked one form of ES-10, approximately half were missing most or all of one copy of chromosome 14; the other contained two copies of 14, frequently in the form of an isochromosome. There were no abnormalities of this chromosome found among the mutants that were Es-10 heterozygotes. These results suggest that the expression of an autosomal recessive mutation in near-diploid mouse cells is frequently associated with events that result in the segregation of a physically linked marker and part or all of a chromosome.

摘要

编码腺苷激酶(ADK;ATP:腺苷5'-磷酸转移酶,EC 2.7.1.20)和酯酶-10(ES-10;羧酸酯酶,羧酸酯水解酶,EC 3.1.1.1)的基因都位于小鼠的14号染色体上。近二倍体小鼠细胞系CAK对于ES-10的两种电泳变体是杂合的。已分离出CAK的隐性Adk-突变体,并分析其Es-10表型和核型异常。发现了两类频率大致相等的突变体:一类在Es-10表达中保持杂合状态,另一类只表达一个Es-10等位基因。在缺乏一种ES-10形式的突变体中,大约一半缺失了一条14号染色体的大部分或全部;另一半含有两条14号染色体,通常以等臂染色体的形式存在。在Es-10杂合子的突变体中未发现这条染色体的异常。这些结果表明,近二倍体小鼠细胞中常染色体隐性突变的表达常与导致物理连锁标记以及部分或全部染色体分离的事件相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05a1/319215/e42f768e6496/pnas00654-0483-a.jpg

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