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编码大鼠鸟氨酸转氨甲酰酶的cDNA的分子克隆。

Molecular cloning of the cDNA coding for rat ornithine transcarbamoylase.

作者信息

Horwich A L, Kraus J P, Williams K, Kalousek F, Konigsberg W, Rosenberg L E

出版信息

Proc Natl Acad Sci U S A. 1983 Jul;80(14):4258-62. doi: 10.1073/pnas.80.14.4258.

Abstract

Ornithine transcarbamoylase is a mitochondrial matrix enzyme composed of three identical subunits encoded on the X chromosome. The subunit is synthesized on cytoplasmic polysomes as a precursor that is cleaved during transport into mitochondria. We report here the isolation and characterization of cDNA clones containing sequences corresponding to the mRNA encoding the ornithine transcarbamoylase subunit. cDNA was synthesized using rat liver mRNA enriched by polysome immunoadsorption for the low-abundance messenger species encoding the enzyme subunit. After insertion of cDNA into plasmid pBR322 and cloning in Escherichia coli, identification of the desired plasmids was accomplished by (i) differential colony hybridization using cDNA probes synthesized from mRNA of various tissues; (ii) differential blot hybridization using cDNA probes synthesized from mRNA enriched for or depleted of the ornithine transcarbamoylase message; (iii) hybrid-selected translation assays; and (iv) most definitively, structural analysis, which matched 25 consecutive amino acid residues determined by sequential Edman analysis of the carboxyl-terminal portion of the purified enzyme subunit with coding sequence present in the insert of one of the plasmids.

摘要

鸟氨酸转氨甲酰酶是一种线粒体基质酶,由位于X染色体上的三个相同亚基组成。该亚基在细胞质多核糖体上以前体形式合成,在前体转运至线粒体的过程中被切割。我们在此报告含有与编码鸟氨酸转氨甲酰酶亚基的mRNA相对应序列的cDNA克隆的分离和特性。使用通过多核糖体免疫吸附富集的大鼠肝脏mRNA合成cDNA,该mRNA用于编码该酶亚基的低丰度信使物种。将cDNA插入质粒pBR322并在大肠杆菌中克隆后,通过以下方法鉴定所需质粒:(i) 使用从各种组织的mRNA合成的cDNA探针进行差异菌落杂交;(ii) 使用从富含或缺乏鸟氨酸转氨甲酰酶信息的mRNA合成的cDNA探针进行差异印迹杂交;(iii) 杂交选择翻译分析;以及(iv) 最具决定性的结构分析,该分析将通过对纯化酶亚基的羧基末端部分进行顺序埃德曼分析确定的25个连续氨基酸残基与其中一个质粒插入片段中存在的编码序列进行匹配。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e14c/384016/cfa3c9e0a861/pnas00640-0074-a.jpg

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