Malone R E, Bullard S, Lundquist S, Kim S, Tarkowski T
Department of Biology, University of Iowa, Iowa City 52242.
Nature. 1992 Sep 10;359(6391):154-5. doi: 10.1038/359154a0.
Genetic recombination involves classical crossing-over and gene conversion (aberrant segregation). In fungi that produce an ascus containing four spores, a gene conversion event is manifested as 3:1 or 1:3 (or more rarely 4:0 or 0:4) segregations, in contrast to the normal mendelian 2:2 segregation. Polarity is one of the properties of gene conversion; in almost all cases the frequency of conversion exhibits a gradient across the gene monitored. The frequency of conversion is usually independent of the specific allele used as a marker, but dependent on its location. An interpretation of conversion polarity is that it is caused by the existence of specific initiation sites for meiotic recombination, located at the high end of the polarity gradient. Here we show that the polarity gradient for the HIS2 gene of Saccharomyces cerevisiae is high at the 3' end of the gene, implying that the promoter of HIS2 is not the initiation site.
基因重组涉及经典的交叉互换和基因转换(异常分离)。在产生含有四个孢子的子囊的真菌中,基因转换事件表现为3:1或1:3(或更罕见的4:0或0:4)的分离,这与正常的孟德尔2:2分离不同。极性是基因转换的特性之一;在几乎所有情况下,转换频率在被监测的基因上呈现出梯度变化。转换频率通常与用作标记的特定等位基因无关,但取决于其位置。对转换极性的一种解释是,它是由减数分裂重组的特定起始位点的存在引起的,这些位点位于极性梯度的高端。在这里,我们表明酿酒酵母HIS2基因的极性梯度在基因的3'端较高,这意味着HIS2的启动子不是起始位点。