Institut für allgemeine Mikrobiologie, Altenbergrain 21, CH-3013, Bern, Switzerland.
Curr Genet. 1980 Feb;1(2):89-95. doi: 10.1007/BF00446954.
Gene conversion and postmeiotic segregation patterns have been analysed at 14 mutant sites of sup3, sup8 and sup9 including 5 alleles with a strong marker effect on recombination frequencies in two-factor crosses. The total frequency of gene conversion and postmeiotic segregation tetrads is fairly constant within each gene, but may vary from one gene to another. About 97% of the conversion events are coconversions spanning the whole sup gene. Postmeiotic segregations are usually quite rare. None of the marker-effect alleles has an increased rate of hybrid DNA formation at the allele considered, as judged from the frequency of gene conversion and postmeiotic segregation in one-factor crosses. At least two of them, sup3-e and sup9-e, are associated with a high frequency of postmeiotic segregation indicating a poor repair of the corresponding base-pair mismatches. This is also observed in a two-factor cross and can account for the marker effect on recombination frequencies. The properties of a third marker effect allele, sup3-e,r10, are best explained by a higher probability of single site conversions as opposed to coconversions in two-factor crosses involving the mutant site r10.
已分析了 sup3、sup8 和 sup9 的 14 个突变位点的基因转换和减数分裂后分离模式,其中包括 5 个等位基因,它们在双因子杂交中对重组频率具有强烈的标记效应。在每个基因内,基因转换和减数分裂后四分体的总频率相当恒定,但可能因基因而异。大约 97%的转换事件是跨越整个 sup 基因的共转换。减数分裂后分离通常非常罕见。从单因子杂交中基因转换和减数分裂后分离的频率来看,没有一个标记效应等位基因在考虑的等位基因中具有增加杂种 DNA 形成的速率。至少其中两个,sup3-e 和 sup9-e,与减数分裂后分离的高频率相关,表明相应碱基对错配的修复不良。在双因子杂交中也观察到这种情况,这可以解释对重组频率的标记效应。第三个标记效应等位基因 sup3-e,r10 的特性最好通过在涉及突变位点 r10 的双因子杂交中,与共转换相比,单一位点转换的概率更高来解释。