Pattatucci A M, Otteson D C, Kaufman T C
Howard Hughes Medical Institute, Indiana University, Bloomington 47405.
Genetics. 1991 Oct;129(2):423-41. doi: 10.1093/genetics/129.2.423.
We have undertaken a developmental genetic analysis of the homeotic gene Sex combs reduced (Scr) of Drosophila melanogaster by examining embryonic and adult phenotypes of mutations affecting Scr gene function. Molecular mapping of Scr breakpoint lesions has defined a segment of greater than 70 kb of DNA necessary for proper Scr gene function. This region is split by the fushi tarazu (ftz) gene, with lesions affecting embryonic Scr function molecularly mapping to the region proximal (5') to ftz and those exhibiting polyphasic semilethality predominantly mapping distal (3') to ftz. Gain-of-function mutations are associated with genomic rearrangements and map throughout the Scr locus. Our analysis has revealed that the Scr locus encompasses genetic elements that are responsible for functions in both the embryonic and larval to adult periods of development. From these studies, we conclude that Scr is a complex genetic locus with an extensive regulatory region that directs functions required for normal head and thoracic development in both the embryo and the adult and that the regulation of Scr during these two periods is distinct.
我们通过研究影响果蝇黑腹果蝇同源异型基因性梳减少(Scr)功能的突变的胚胎和成虫表型,对该基因进行了发育遗传学分析。Scr断点损伤的分子图谱确定了一段大于70 kb的DNA片段,这是Scr基因正常功能所必需的。该区域被腹节基因(ftz)分割,影响胚胎Scr功能的损伤在分子水平上定位于ftz近端(5')区域,而表现出多相半致死性的损伤主要定位于ftz远端(3')区域。功能获得性突变与基因组重排相关,并定位于整个Scr基因座。我们的分析表明,Scr基因座包含负责胚胎期以及幼虫到成虫发育期功能的遗传元件。从这些研究中,我们得出结论,Scr是一个复杂的遗传基因座,具有广泛的调控区域,该区域指导胚胎和成虫正常头部和胸部发育所需的功能,并且在这两个时期对Scr的调控是不同的。