Hovemann B, Richter S, Walldorf U, Cziepluch C
Zentrum für Molekulare Biologie Heidelberg (ZMBH), Universität Heidelberg.
Nucleic Acids Res. 1988 Apr 25;16(8):3175-94. doi: 10.1093/nar/16.8.3175.
We have characterized two previously cloned genes, F1 and F2 (1) that code for elongation factor EF - 1 alpha of Drosophila melanogaster. Genomic Southern blot hybridization revealed that they are the only gene copies present. We isolated cDNA clones of both transcripts from embryonal and pupal stage of development that cover the entire transcription unit. The 5' ends of both genes have been determined by primer extension and for F1 also by RNA sequencing. These start sites have been shown to be used consistently during development. Comparison of cDNA and genomic sequences revealed that EF - 1 alpha,F1 consists of two and EF - 1 alpha,F2 of five exons. The two described elongation factor genes exhibit several regions of strong sequence conservation when compared to five recently cloned eucaryotic elongation factors.
我们已经鉴定了两个先前克隆的基因,F1和F2(1),它们编码果蝇的延伸因子EF-1α。基因组Southern印迹杂交显示它们是仅有的基因拷贝。我们从胚胎和蛹发育阶段分离出了这两种转录本的cDNA克隆,这些克隆覆盖了整个转录单元。通过引物延伸确定了两个基因的5'端,对于F1还通过RNA测序确定了其5'端。这些起始位点在发育过程中一直被使用。cDNA和基因组序列的比较显示,EF-1α,F1由两个外显子组成,EF-1α,F2由五个外显子组成。与最近克隆的五个真核延伸因子相比,这两个已描述的延伸因子基因表现出几个高度保守的序列区域。