Rasooly R S
Department of Biology, St. John's University, Jamaica, New York 11439, USA.
Genetics. 1996 Dec;144(4):1725-34. doi: 10.1093/genetics/144.4.1725.
A new meiotic mutation, morewright (mwr) was identified by screening for new mutations that act as dominant enhancers of the dosage-sensitive Drosophila melanogaster female meiotic mutant, nodDTW.mwr is a recessive meiotic mutant, specifically impairing the segregation of nonexchange chromosomes. Cytological evidence suggests that the meiotic defect in mwr/mwr females is in homologue recognition because the chromosomes appear to be misaligned on an intact spindle. The mwr mutation was recovered during a screen of random P-element insertions on a chromosome with a single insertion located at 50C. The P-element insertion is a recessive female-sterile mutation. While excision of the P element from the mwr-bearing chromosome partially relieves the female sterility, the excisions retain the dominant nodDTW-enhancing activity. The mwr meiotic phenotype maps very close to the female-sterile P insertion. Thus the mwr locus appears to encode a function required for partner recognition in meiosis, although its relationship to the neighboring female-sterile mutation remains to be elucidated.
通过筛选作为剂量敏感型黑腹果蝇雌性减数分裂突变体nodDTW显性增强子的新突变,鉴定出一种新的减数分裂突变体morewright(mwr)。mwr是一种隐性减数分裂突变体,特别影响非交换染色体的分离。细胞学证据表明,mwr/mwr雌性的减数分裂缺陷在于同源染色体识别,因为染色体似乎在完整纺锤体上未正确排列。mwr突变是在对一条位于50C处有单个插入的染色体上的随机P元件插入进行筛选时发现的。P元件插入是一种隐性雌性不育突变。虽然从携带mwr的染色体上切除P元件可部分缓解雌性不育,但切除后的片段仍保留显性nodDTW增强活性。mwr减数分裂表型定位非常接近雌性不育P插入位点。因此,mwr基因座似乎编码减数分裂中伴侣识别所需的一种功能,尽管它与相邻雌性不育突变的关系仍有待阐明。