首页> 美国卫生研究院文献>Nucleic Acids Research >Cloning of eukaryotic protein synthesis initiation factor genes: isolation and characterization of cDNA clones encoding factor eIF-4A.
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Cloning of eukaryotic protein synthesis initiation factor genes: isolation and characterization of cDNA clones encoding factor eIF-4A.

机译:真核蛋白合成起始因子基因的克隆:编码因子eIF-4A的cDNA克隆的分离和鉴定。

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摘要

Monoclonal antibodies directed against rabbit reticulocyte protein synthesis initiation factor 4A (eIF-4A) were used to isolate mouse cDNA clones expressing eIF-4A protein sequences in E. coli. The identity of cDNA clones encoding eIF-4A sequences was confirmed by hybrid-selected translation and peptide mapping of the translation product. Analysis of the mRNA coding for eIF-4A from mouse liver and HeLa cells by Northern hybridization revealed two discrete mRNA species of approximately 2000 and 1600 nucleotides in length. The existence of two mRNAs in mouse and HeLa cells encoding eIF-4A was confirmed by cDNA sequencing.
机译:针对兔网织细胞蛋白合成起始因子4A(eIF-4A)的单克隆抗体被用于分离在大肠杆菌中表达eIF-4A蛋白序列的小鼠cDNA克隆。通过杂合选择的翻译和翻译产物的肽图确定了编码eIF-4A序列的cDNA克隆的身份。通过Northern杂交对编码来自小鼠肝脏和HeLa细胞的eIF-4A的mRNA的分析揭示了两个离散的mRNA种类,长度分别约为2000和1600个核苷酸。通过cDNA测序证实了在编码eIF-4A的小鼠和HeLa细胞中存在两个mRNA。

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