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酿酒酵母HIS2基因处发生基因转换的重组热点分析。

Analysis of a recombination hotspot for gene conversion occurring at the HIS2 gene of Saccharomyces cerevisiae.

作者信息

Malone R E, Kim S, Bullard S A, Lundquist S, Hutchings-Crow L, Cramton S, Lutfiyya L, Lee J

机构信息

Department of Biological Sciences, University of Iowa, Iowa City 52242.

出版信息

Genetics. 1994 May;137(1):5-18. doi: 10.1093/genetics/137.1.5.

Abstract

The properties of gene conversion as measured in fungi that generate asci containing all the products of meiosis imply that meiotic recombination initiates at specific sites. The HIS2 gene of Saccharomyces cerevisiae displays a high frequency of gene conversion, indicating that it is a recombination hotspot. The HIS2 gene was cloned and sequenced, and the cloned DNA was used to make several different types of alterations in the yeast chromosome by transformation; these alterations were used to determine the location of the sequences necessary for the high levels of meiotic conversion observed at HIS2. Previous work indicated that the gene conversion polarity gradient is high at the 3' end of the gene, and that the promoter of the gene is not necessary for the high frequency of conversion observed. Data presented here suggest that at least some of the sequences necessary for high levels of conversion at HIS2 are located over 700 bp downstream of the end of the coding region, extend over (at least) several hundred base pairs, and may be quite complex, perhaps involving chromatin structure. Additional data indicate that multiple single base heterologies within a 1-kb interval contribute little to the frequency of gene conversion. This contrasts with other reports about the role of heterologies at the MAT locus.

摘要

在能产生包含减数分裂所有产物的子囊的真菌中所测定的基因转换特性表明,减数分裂重组起始于特定位点。酿酒酵母的HIS2基因显示出高频率的基因转换,这表明它是一个重组热点。对HIS2基因进行了克隆和测序,并通过转化利用克隆的DNA在酵母染色体上进行了几种不同类型的改变;这些改变被用于确定在HIS2观察到的高水平减数分裂转换所必需的序列的位置。先前的研究表明,基因转换极性梯度在基因的3'端较高,并且观察到的高频率转换并不需要该基因的启动子。此处给出的数据表明,HIS2高水平转换所必需的至少一些序列位于编码区末端下游700 bp以上,延伸(至少)几百个碱基对,并且可能相当复杂,也许涉及染色质结构。其他数据表明,1 kb间隔内的多个单碱基异源对基因转换频率贡献不大。这与关于MAT位点异源作用的其他报道形成对比。

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