Storto Patrick Daniel, King Robert Charles
Department of Evolutionary Biology, Northwestern University, 60201, Evanston, IL, USA.
Rouxs Arch Dev Biol. 1987 Apr;196(4):210-221. doi: 10.1007/BF00376345.
This paper describes the ovarian pathologies observed when 108 different heteroallelic combinations were made involving 17 independent mutations at the ovarian tumor (otu) locus. Most of the mutant phenotypes can be explained as graded responses by individual germ cells to different levels of functionally active otu gene product (OGP) synthesized by the mutant cells themselves. The lowest and highest levels of OGP appear to be produced by otu and otu , respectively. In most heteroallelic ovaries the alleles have additive effects, and hybrid germ cells reach a developmental stage more advanced than the "weaker" homozygote but less advanced than the "stronger" homozygote. However, examples of both positive and negative complementation also have been found, and these suggest that the products encoded by different mutant alleles can combine to form dimers or multimers which may be superior or inferior to the homodimers. In flies homozygous for otu most ovarioles contain tumors, but some germ cells are able to develop further than those in otu homozygotes. This suggests that, while otu produces intermediate levels of OGP, it also produces a second product (which otu cannot make) that is utilized at the period in oogenesis when development in cells homozygous for otu is blocked. When otu is combined with any one of eight specific alleles, it allows oocyte/nurse cell syncytia to differentiate that can complete development and undergo embryogenesis, if fertilized. The endopolyploid nurse cells of these hybrids have giant polytene chromosomes, and the presence of GPCs in functionally active, germ-line derived cells provides an interesting new system for experimental study. Analysis of the characteristic ovarian pathologies produced by flies of different genotypes leads to the conclusion that the products of the otu gene are utilized during at least six different periods in Drosophila oogenesis.
本文描述了在卵巢肿瘤(otu)位点的17个独立突变形成108种不同的杂合等位基因组合时所观察到的卵巢病理情况。大多数突变表型可解释为单个生殖细胞对突变细胞自身合成的不同功能活性水平的otu基因产物(OGP)的分级反应。OGP的最低和最高水平似乎分别由otu 和otu 产生。在大多数杂合等位基因的卵巢中,等位基因具有加性效应,杂种生殖细胞达到的发育阶段比“较弱”的纯合子更高级,但比“较强”的纯合子更低级。然而,也发现了正互补和负互补的例子,这表明不同突变等位基因编码的产物可以结合形成二聚体或多聚体,可能优于或劣于同型二聚体。在otu 纯合的果蝇中,大多数卵巢小管含有肿瘤,但一些生殖细胞比otu 纯合子中的生殖细胞能进一步发育。这表明,虽然otu 产生中等水平的OGP,但它也产生一种otu 不能产生的第二种产物,该产物在卵子发生期被利用,此时otu 纯合细胞的发育被阻断。当otu 与八个特定等位基因中的任何一个组合时,它允许卵母细胞/滋养细胞合胞体分化,如果受精,这些合胞体可以完成发育并进行胚胎发生。这些杂种的内多倍体滋养细胞具有巨大的多线染色体,功能活跃的、源自生殖系的细胞中存在GPCs为实验研究提供了一个有趣的新系统。对不同基因型果蝇产生的特征性卵巢病理情况的分析得出结论,otu 基因的产物在果蝇卵子发生的至少六个不同时期被利用。