Nagoshi R N, Gelbart W M
Department of Cellular and Developmental Biology, Harvard University, Cambridge, Massachusetts 02138.
Genetics. 1987 Nov;117(3):487-502. doi: 10.1093/genetics/117.3.487.
The Ace locus in Drosophila melanogaster is known to be the structural gene for acetylcholinesterase. Ace is located in a region of chromosome arm 3R which has been subjected to intensive genetic and molecular analysis. Previous deletion mapping studies have identified a 40-kb region within which the Ace gene resides. This report focuses on the further localization of Ace within this 40-kb interval. Within this region, selective fine structure recombinational analysis was employed to localize three recessive Ace lethals relative to unselected restriction site variations. These three mutations fall into a segment of 7 kb within the Ace interval. Fine structure recombinational analysis was also used to confirm that the Ace phenotype of one deletion, Df(3R)AceHD1, co-segregated with the molecular deletion. This deletion does not fully remove Ace activity, but it behaves as a recessive Ace lethal. Df(3R)AceHD1 is the most distal Ace lesion identified and indicates that the Ace locus must extend at least 16 kb. Several poly(A)transcripts are detectable in the region defined by the Ace lesions. The position and extent of the Ace locus, as well as the types of transcripts found, is consistent with the recent findings which identified Torpedo-AChE homologous cDNA sequences in this region.
已知果蝇中的Ace基因座是乙酰胆碱酯酶的结构基因。Ace位于3R染色体臂的一个区域,该区域已经进行了深入的遗传和分子分析。先前的缺失定位研究确定了Ace基因所在的一个40kb区域。本报告重点关注Ace在这个40kb区间内的进一步定位。在该区域内,采用选择性精细结构重组分析来确定三个隐性Ace致死突变相对于未选择的限制性位点变异的位置。这三个突变位于Ace区间内一段7kb的区域。精细结构重组分析还用于确认一个缺失Df(3R)AceHD1的Ace表型与分子缺失共分离。这个缺失并没有完全消除Ace活性,但它表现为隐性Ace致死突变。Df(3R)AceHD1是已确定最远的Ace损伤,表明Ace基因座必须至少延伸16kb。在由Ace损伤定义的区域中可检测到几种多聚腺苷酸化转录本。Ace基因座的位置和范围,以及所发现的转录本类型,与最近在该区域鉴定出Torpedo - AChE同源cDNA序列的研究结果一致。