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酿酒酵母减数分裂过程中基因转换、非串联重复处的不等交换和错配。

Gene conversion, unequal crossing-over and mispairing at a non-tandem duplication during meiosis of Saccharomyces cerevisiae.

作者信息

Maloney D H, Fogel S

机构信息

Department of Genetics, University of California, Berkeley 94720.

出版信息

Curr Genet. 1987;12(1):1-7. doi: 10.1007/BF00420720.

Abstract

We have developed a novel system to examine conversion, exchange and mispairing involving a non-tandem duplication of the ade8 locus in yeast by monitoring the segregation of heterozygous markers between the duplicated sequence. Plasmid Yrp17 carries the yeast selectable markers URA3+ and TRP1+. Yrp17 derivatives with a 4 kb insert carrying ade8-18 were used to clone the mutations trp1-1 and ura3-1 by gap repair. Integrants of the resulting plasmids at the Ade8 locus were crossed to yield diploid hybrids with a non-tandem duplication of Ade8 and heterozygosity for the plasmid markers between the duplicated sequences. 1192 complete, unselected asci were analyzed and 270 exhibiting recombination of the markers contributed by the plasmid were analyzed by Southern transfers to detect changes in plasmid sequences. Twenty-seven tetrads had unequal homologous exchanges and five had unequal sister-chromatid exchanges. Seven tetrads carry an additional copy of the integrated plasmid and ten are missing one. We propose that these two classes represent conversions of the entire 11 kb plasmid, which occur after misalignment and formation of an unpaired loop. Mispairing is a frequent event, and occurs in approximately fifty percent of all meioses. The system described provides a means to determine the meiotic rules of conversion, exchange and pairing for duplicated DNA sequences.

摘要

我们开发了一种新型系统,通过监测重复序列之间杂合标记的分离,来检测酵母中ade8基因座非串联重复所涉及的转换、交换和错配。质粒Yrp17携带酵母选择标记URA3+和TRP1+。携带ade8-18的4 kb插入片段的Yrp17衍生物用于通过缺口修复克隆trp1-1和ura3-1突变。将所得质粒在Ade8基因座的整合体进行杂交,以产生具有Ade8非串联重复且重复序列之间的质粒标记为杂合的二倍体杂种。分析了1192个完整的、未选择的子囊,并通过Southern印迹分析了270个表现出质粒贡献的标记重组的子囊,以检测质粒序列的变化。27个四分体有不等位同源交换,5个有不等位姐妹染色单体交换。7个四分体携带整合质粒的额外拷贝,10个缺少一个。我们认为这两类代表了整个11 kb质粒的转换,它们发生在未对齐和形成未配对环之后。错配是一个常见事件,大约在所有减数分裂的50%中发生。所描述的系统提供了一种确定重复DNA序列减数分裂转换、交换和配对规则的方法。

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