Poeck B, Balles J, Pflugfelder G O
Theordor-Boveri-Institut (Biozentrum), Lehrstuhl für Genetik, Universität Würzburg, Germany.
Mol Gen Genet. 1993 Apr;238(3):325-32. doi: 10.1007/BF00291990.
The optomotor-blind gene of Drosophila melanogaster is large and genetically complex. Five partly independent complementation groups are uncovered by several viable and lethal mutations at the locus. At least 15 RNA signals have been detected by Northern blot analysis. One of them, T3, derived from a 75 kb primary transcript, has been proposed as the carrier of optomotor-blind function, based on the large size of its precursor and its tissue distribution. We here provide direct evidence that T3 is the optomotor-blind transcript. A facile and generally applicable selection scheme for the isolation of intragenic meiotic recombinants was applied to map two lethal optomotor-blind point mutations to exons of the T3 transcript. Amplification of mutant DNA by the polymerase chain reaction (PCR) and sequencing of the amplified exons revealed the presence of mutations that lead to truncation of the T3 open reading frame. The recombination rate observed in the optomoter-blind locus is within the range of rates that have been determined in a few other Drosophila loci.
果蝇的视动盲基因很大且遗传复杂。该位点的几个存活和致死突变揭示了五个部分独立的互补组。通过Northern印迹分析检测到至少15个RNA信号。其中一个信号T3来源于一个75 kb的初级转录本,基于其前体的大小及其组织分布,它被认为是视动盲功能的载体。我们在此提供直接证据表明T3是视动盲转录本。一种简便且普遍适用的用于分离基因内减数分裂重组体的选择方案被用于将两个致死性视动盲点突变定位到T3转录本的外显子上。通过聚合酶链反应(PCR)扩增突变DNA并对扩增的外显子进行测序,结果显示存在导致T3开放阅读框截短的突变。在视动盲位点观察到的重组率在其他一些果蝇位点所确定的速率范围内。