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大豆球蛋白A2B1a亚基编码DNA的克隆与结构分析。

Cloning and structural analysis of DNA encoding an A2B1a subunit of glycinin.

作者信息

Marco Y A, Thanh V H, Tumer N E, Scallon B J, Nielsen N C

出版信息

J Biol Chem. 1984 Nov 10;259(21):13436-41.

PMID:6092376
Abstract

The partial DNA sequence of a glycinin gene in a genomic clone and a homologous cDNA clone were determined. They have nearly identical nucleotide sequences and encode the basic polypeptide and part of the acidic polypeptide for an A2B1a glycinin subunit. The protein primary structure deduced from the DNA sequence is in close agreement with the amino acid sequence of the subunit determined chemically and confirms assignment of part of the amino acid sequence in the basic component where we were able to establish an overlap using conventional approaches. The coding part of the basic subunit is interrupted by a 625-base pair A + T-rich intron whose boundaries correlate with the established consensus sequences for the exon-intron junctions. Comparison of the nucleotide sequence of the basic subunit of pea legumin gene with that of the gene for A2B1a subunit reveals 70% homology in coding regions, although there is considerably less in the 3'-flanking regions.

摘要

测定了基因组克隆和同源cDNA克隆中大豆球蛋白基因的部分DNA序列。它们具有几乎相同的核苷酸序列,编码A2B1a大豆球蛋白亚基的碱性多肽和部分酸性多肽。从DNA序列推导的蛋白质一级结构与化学测定的亚基氨基酸序列高度一致,并证实了我们能够使用传统方法建立重叠的碱性组分中部分氨基酸序列的归属。碱性亚基的编码部分被一个625个碱基对的富含A+T的内含子打断,其边界与已建立的外显子-内含子连接的共有序列相关。豌豆豆球蛋白基因碱性亚基的核苷酸序列与A2B1a亚基基因的核苷酸序列比较显示,编码区有70%的同源性,尽管3'侧翼区的同源性要低得多。

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