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哺乳动物细胞中的自发突变率:不同生长速率和表型滞后的影响。

Spontaneous mutation rates in mammalian cells: effect of differential growth rates and phenotypic lag.

作者信息

Rudd C J, Daston D S, Caspary W J

机构信息

Cellular and Genetic Toxicology Department, SRI International, Menlo Park, California 94025.

出版信息

Genetics. 1990 Oct;126(2):435-42. doi: 10.1093/genetics/126.2.435.

Abstract

We calculated a spontaneous rate of 26-37 x 10(-6) mutations per cell division for L5178Y MOLY (mouse lymphoma) cells at the thymidine kinase locus (tk+/(-)----tk-/-) using a procedure that isolated and segregated cells during expression. This rate was 50 times higher than when cells expressed the mutant phenotype in suspension. The higher mutation rates obtained with the in situ procedure suggest that many of the mutants, whether expressed or unexpressed, grew more slowly than wild-type cells prior to selection with trifluorothymidine (TFT), implying that the slow growth phenotype is expressed earlier than the TFTr (TFT-resistant) phenotype. The loss of mutants was not restricted to cells forming small colonies; the mutation rate for cells forming large colonies was more than ten times higher using the in situ procedure. In this new procedure, the cells expressed spontaneous mutations while growing in semisolid medium for up to 3 days without TFT. Mutants were then selected in situ by adding an overlay of TFT and the visible colonies were analyzed after 11 days. Cells with spontaneous mutations at the tk locus required approximately 30 hr for the more rapidly expressing cells with new mutations to be detected. Most of the TFTr colonies selected after 60 hr of growth in semisolid medium represented independent mutations that had accumulated during the first 30 hr.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们使用一种在表达过程中分离和分选细胞的方法,计算出L5178Y MOLY(小鼠淋巴瘤)细胞在胸苷激酶基因座(tk+/(-)----tk-/-)处每细胞分裂的自发突变率为26 - 37×10(-6)。该速率比细胞在悬浮液中表达突变表型时高50倍。原位方法获得的较高突变率表明,许多突变体,无论是否表达,在使用三氟胸苷(TFT)选择之前,其生长速度都比野生型细胞慢,这意味着缓慢生长表型比TFTr(TFT抗性)表型更早表达。突变体的损失并不局限于形成小菌落的细胞;使用原位方法时,形成大菌落的细胞的突变率高出十倍以上。在这个新方法中,细胞在不含TFT的半固体培养基中生长长达3天的过程中表达自发突变。然后通过添加TFT覆盖层原位选择突变体,并在11天后分析可见菌落。在tk基因座处有自发突变的细胞,对于新突变表达较快的细胞,大约需要30小时才能检测到。在半固体培养基中生长60小时后选择的大多数TFTr菌落代表在最初30小时内积累的独立突变。(摘要截断于250字)

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