Liu H, Jang J K, Graham J, Nycz K, McKim K S
Waksman Institute and Department of Genetics, Rutgers University, Piscataway, New Jersey 08854-8020, USA.
Genetics. 2000 Apr;154(4):1735-46. doi: 10.1093/genetics/154.4.1735.
We have isolated two alleles of a previously unidentified meiotic recombination gene, mei-217. Genetic analysis of these mutants shows that mei-217 is a typical "precondition" gene. The phenotypes of the mutants are meiosis specific. The strongest allele has <10% of the normal level of crossing over, and the residual events are distributed abnormally. We have used double mutant analysis to position mei-217 in the meiotic recombination pathway. In general, mutations causing defects in the initiation of meiotic recombination are epistatic to mutations in mei-41 and spnB. These two mutations, however, are epistatic to mei-217, suggesting that recombination is initiated normally in mei-217 mutants. It is likely that mei-217 mutants are able to make Holliday junction intermediates but are defective in the production of crossovers. These phenotypes are most similar to mutants of the mei-218 gene. This is striking because mei-217 and mei-218 are part of the same transcription unit and are most likely produced from a dicistronic message.
我们分离出了一个先前未鉴定的减数分裂重组基因mei-217的两个等位基因。对这些突变体的遗传分析表明,mei-217是一个典型的“前提条件”基因。这些突变体的表型是减数分裂特异性的。最强的等位基因的交叉水平不到正常水平的10%,且剩余事件分布异常。我们利用双突变分析将mei-217定位在减数分裂重组途径中。一般来说,导致减数分裂重组起始缺陷的突变对mei-41和spnB中的突变是上位性的。然而,这两个突变对mei-217是上位性的,这表明在mei-217突变体中重组正常起始。mei-217突变体很可能能够形成霍利迪连接中间体,但在交叉产生方面存在缺陷。这些表型与mei-218基因的突变体最为相似。这很引人注目,因为mei-217和mei-218是同一转录单位的一部分,很可能由双顺反子信息产生。