Morgan B A, Johnson W A, Hirsh J
EMBO J. 1986 Dec 1;5(12):3335-42. doi: 10.1002/j.1460-2075.1986.tb04648.x.
The dopa decarboxylase gene (Ddc) of Drosophila melanogaster is expressed in the hypoderm and the nervous system and promoter elements mediating differential expression in these tissues have been identified (Scholnick et al., 1986). Here we report an additional mode of regulation; the unique primary transcript of the Ddc gene is spliced to form mRNAs in these two tissues which differ by a single internal exon. In vitro mutagenesis and P-element-mediated transformation were employed to manipulate the tissue-specific expression of these RNAs. This approach demonstrated that regulated splicing rather than differential stability causes the tissue-specific expression of these RNAs and allowed the identification of Ddc enzyme isoforms encoded by each mRNA. The Ddc enzyme in the central nervous system differs from the hypodermal Ddc protein by the addition of 33-35 amino acids on the N terminus.
黑腹果蝇的多巴脱羧酶基因(Ddc)在皮下组织和神经系统中表达,并且已经鉴定出介导这些组织中差异表达的启动子元件(Scholnick等人,1986年)。在此我们报告一种额外的调控模式;Ddc基因独特的初级转录本在这两个组织中剪接形成mRNA,它们仅相差一个内部外显子。采用体外诱变和P元素介导的转化来操纵这些RNA的组织特异性表达。该方法表明,调控剪接而非差异稳定性导致了这些RNA的组织特异性表达,并使得鉴定出每种mRNA编码的Ddc酶同工型成为可能。中枢神经系统中的Ddc酶与皮下Ddc蛋白的不同之处在于其N端额外添加了33 - 35个氨基酸。