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卤虫异质性核糖核蛋白(hnRNP)蛋白质的互补DNA(cDNA)序列克隆:进化保守性的证据

Cloning of cDNA sequences for an Artemia salina hnRNP protein: evidence for conservation through evolution.

作者信息

Cruz-Alvarez M, Szer W, Pellicer A

出版信息

Nucleic Acids Res. 1985 Jun 11;13(11):3917-30. doi: 10.1093/nar/13.11.3917.

Abstract

A cDNA clone was isolated for Artemia salina protein HD40, a component of heterogenous nuclear ribonucleoproteins. Enriched Artemia 15S poly(A)+ RNA was used as a template and double-stranded cDNA sequences were inserted into the Pst I restriction endonuclease site of E. coli plasmid pBR322. Recombinant colonies were analyzed by positive hybrid selection of poly(A)+ RNA that directs the synthesis of protein HD40 in an in vitro assay. In vitro translation of the mRNA selected by recombinant clone 87HD yields a protein that is immunoprecipitated by anti-HD40 antibodies and that comigrates with authentic HD40 on gel electrophoresis. Partial proteolysis of protein HD40 and the in vitro translated product selected by clone 87HD produces the same peptide patterns. The size of the cloned insert is about 820 bp. The length of HD40 mRNA as determined by Northern blot analysis, is about 1500 nucleotides. Southern blot analysis performed with DNA of different species (plant, avian, mammal) shows cross-hybridizing bands when probed with clone 87HD DNA suggesting that the HD40 gene is evolutionarily conserved.

摘要

分离得到卤虫(Artemia salina)蛋白质HD40的一个cDNA克隆,HD40是不均一核核糖核蛋白的一个组分。用富集的卤虫15S多聚腺苷酸加尾(poly(A)+)RNA作为模板,双链cDNA序列被插入大肠杆菌质粒pBR322的Pst I限制性内切酶位点。通过对在体外分析中指导蛋白质HD40合成的多聚腺苷酸加尾RNA进行阳性杂交筛选来分析重组菌落。重组克隆87HD选择的mRNA的体外翻译产生一种蛋白质,该蛋白质能被抗HD40抗体免疫沉淀,并且在凝胶电泳上与天然HD40迁移一致。蛋白质HD40和克隆87HD选择的体外翻译产物的部分蛋白酶解产生相同的肽谱。克隆插入片段的大小约为820 bp。通过Northern印迹分析确定的HD40 mRNA的长度约为1500个核苷酸。用不同物种(植物、鸟类、哺乳动物)的DNA进行Southern印迹分析,当用克隆87HD DNA作为探针时显示出杂交带,这表明HD40基因在进化上是保守的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b59/341286/5f9fc41c276a/nar00305-0141-a.jpg

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