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两个不连锁的果蝇甘油醛-3-磷酸脱氢酶基因的结构

Structure of two unlinked Drosophila melanogaster glyceraldehyde-3-phosphate dehydrogenase genes.

作者信息

Tso J Y, Sun X H, Wu R

出版信息

J Biol Chem. 1985 Jul 5;260(13):8220-8.

PMID:2989282
Abstract

Two Drosophila genes that code for the enzyme glyceraldehyde-3-phosphate dehydrogenase (Gapdh) have been isolated and their structures determined by DNA sequence analysis. The two genes, Gadph-1 and Gapdh-2, are homologous to each other in their coding regions but differ entirely in the 5' and 3' flanking regions. Both genes are functionally expressed in adult flies as determined by Northern blot analysis using gene-specific probes. Gapdh-1 is mapped by in situ hybridization at position 43E-F on the right arm of the second chromosome and Gapdh-2 at position 13F on the left arm of the X chromosome. Transcription initiation sites as well as polyadenylation sites for both Gapdh transcripts have also been determined. Gapdh-1 lacks a sequence homologous to the TATA box in its -30-base pair region that is characteristic of many RNA polymerase II transcribed promoters. In contrast, Gapdh-2 contains a consensus TATA box sequence as well as a CAAT box in its promoter region. Furthermore, a sequence element ATTTGCAT (dc) and nontandem multiple direct repeats have been found in the -35 to -155-base pair 5' flanking region. Other than the intron located in the 5' noncoding region of Gapdh-2, both genes lack intervening sequences.

摘要

已分离出两个编码甘油醛-3-磷酸脱氢酶(Gapdh)的果蝇基因,并通过DNA序列分析确定了它们的结构。这两个基因,Gadph-1和Gapdh-2,在编码区域彼此同源,但在5'和3'侧翼区域完全不同。使用基因特异性探针通过Northern印迹分析确定,这两个基因在成年果蝇中均有功能表达。通过原位杂交将Gapdh-1定位在第二条染色体右臂的43E-F位置,将Gapdh-2定位在X染色体左臂的13F位置。还确定了两种Gapdh转录本的转录起始位点以及聚腺苷酸化位点。Gapdh-1在其-30碱基对区域缺乏与许多RNA聚合酶II转录启动子特有的TATA盒同源的序列。相比之下,Gapdh-2在其启动子区域包含一个共有TATA盒序列以及一个CAAT盒。此外,在-35至-155碱基对的5'侧翼区域发现了一个序列元件ATTTGCAT(dc)和非串联多个直接重复序列。除了位于Gapdh-2的5'非编码区域的内含子外,这两个基因都没有间隔序列。

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