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人肝纤连蛋白cDNA克隆的分离与鉴定

Isolation and characterization of cDNA clones for human liver fibronectin.

作者信息

Umezawa K, Kornblihtt A R, Baralle F E

出版信息

FEBS Lett. 1985 Jul 1;186(1):31-4. doi: 10.1016/0014-5793(85)81333-8.

Abstract

Cellular and plasma fibronectin dimers are constituted by similar but not identical polypeptides. Their differences are the consequence of internal primary sequence variability due to alternative splicing in at least 2 regions (ED and IIICS) of the pre mRNAs [1-8]. A detailed analysis of human liver fibronectin mRNA in these regions was carried out by isolating cDNA clones and determining their nucleotide sequence. A novel type of IIICS segment (coding for 64 amino acids) was present in the two cDNA clones studied and, as expected from previous S1 mapping studies [6], the ED segment was absent in both.

摘要

细胞型和血浆型纤连蛋白二聚体由相似但并非完全相同的多肽组成。它们的差异是由于前体mRNA至少在两个区域(ED和IIICS)发生可变剪接导致内部一级序列变异性的结果[1-8]。通过分离cDNA克隆并确定其核苷酸序列,对这些区域的人肝纤连蛋白mRNA进行了详细分析。在所研究的两个cDNA克隆中存在一种新型的IIICS片段(编码64个氨基酸),并且正如先前S1作图研究[6]所预期的那样,两个克隆中均不存在ED片段。

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