O'Donnell J M, McLean J R, Reynolds E R
Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA 15213.
Dev Genet. 1989;10(3):273-86. doi: 10.1002/dvg.1020100316.
Punch (Pu), the gene encoding the pterin biosynthetic enzyme GTP cyclohydrolase in Drosophila, is a complex locus. Mutations fall into several complementation classes that correspond to classes of mutants with distinct morphological and protein phenotypes. Two of these classes are developmentally specific, with mutants in each having defects in discrete subsets of the known functions of the locus. Defined functions of the locus include a role in embryonic nuclear divisions using initially a maternal Pu product, the synthesis of pterin cofactors that are required for catecholamine biosynthesis beginning in late embryogenesis, and the production of pterin-screening pigments in the developing adult eye. Mutant phenotypes include an interruption in synchronous nuclear divisions in precellular blastoderm embryos, a segment pattern phenotype in late embryos, failure to pigment and cross-link embryonic cuticular structures and failure to synthesize red eye pigments. Molecular analysis reveals that the locus is large, a minimum of 29 kb as defined by Southern mapping of Pu mutants. This region is transcriptionally extremely active, encoding at least 16 developmentally regulated transcripts. One transcript has been shown to be responsible for the production of the adult eye GTP cyclohydrolase on the basis of developmental profile, location with respect to the mapping of eye-specific Pu mutants, absence in eye-specific mutants, and hybrid-selection in vitro translation experiments. Several other transcripts are candidates for Pu vital functions, as suggested by their pattern of expression and their derivation from regions to which lethal Pu mutations map.
Punch(Pu)基因在果蝇中编码蝶呤生物合成酶GTP环化水解酶,是一个复杂的基因座。突变分为几个互补类,这些互补类对应于具有不同形态和蛋白质表型的突变体类别。其中两类具有发育特异性,每类中的突变体在该基因座已知功能的离散子集中存在缺陷。该基因座的明确功能包括:最初利用母体Pu产物在胚胎核分裂中发挥作用;从胚胎后期开始,合成儿茶酚胺生物合成所需的蝶呤辅因子;在发育中的成虫眼中产生蝶呤筛选色素。突变体表型包括:细胞前期胚盘胚胎中同步核分裂的中断;晚期胚胎中的节段模式表型;胚胎表皮结构色素沉着和交联失败;红眼色素合成失败。分子分析表明,该基因座很大,根据Pu突变体的Southern定位,至少有29 kb。该区域转录活性极高,编码至少16种受发育调控的转录本。根据发育谱、与眼特异性Pu突变体定位的关系、在眼特异性突变体中的缺失以及体外杂交选择翻译实验,已证明一种转录本负责成虫眼GTP环化水解酶的产生。根据其表达模式以及它们来自致死性Pu突变所定位的区域,其他几种转录本是Pu重要功能的候选者。