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来自致瘤性人成纤维细胞的编码转化敏感原肌球蛋白同工型3的cDNA的克隆与鉴定

Cloning and characterization of a cDNA encoding transformation-sensitive tropomyosin isoform 3 from tumorigenic human fibroblasts.

作者信息

Lin C S, Leavitt J

机构信息

Armand Hammer Cancer Research Center, Linus Pauling Institute of Science and Medicine, Palo Alto, California 94306.

出版信息

Mol Cell Biol. 1988 Jan;8(1):160-8. doi: 10.1128/mcb.8.1.160-168.1988.

DOI:10.1128/mcb.8.1.160-168.1988
PMID:3336357
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC363096/
Abstract

We isolated a cDNA clone from the tumorigenic human fibroblast cell line HuT-14 that contains the entire protein coding region of tropomyosin isoform 3 (Tm3) and 781 base pairs of 5'- and 3'-untranslated sequences. Tm3, despite its apparent smaller molecular weight than Tm1 in two-dimensional gels, has the same peptide length as Tm1 (284 amino acids) and shares 83% homology with Tm1. Tm3 cDNA hybridized to an abundant mRNA of 1.3 kilobases in fetal muscle and cardiac muscle, suggesting that Tm3 is related to an alpha fast-tropomyosin. The first 188 amino acids of Tm3 are identical to those of rat or rabbit skeletal muscle alpha-tropomyosin, and the last 71 amino acids differ from those of rat smooth muscle alpha-tropomyosin by only 1 residue. Tm3 therefore appears to be encoded by the same gene that encodes the fast skeletal muscle alpha-tropomyosin and the smooth muscle alpha-tropomyosin via an alternative RNA-splicing mechanism. In contrast to Tm4 and Tm5, Tm3 has a small gene family, with, at best, only one pseudogene.

摘要

我们从致瘤性人成纤维细胞系HuT-14中分离出一个cDNA克隆,它包含原肌球蛋白异构体3(Tm3)的完整蛋白质编码区以及781个碱基对的5'-和3'-非翻译序列。在二维凝胶中,Tm3尽管其表观分子量比Tm1小,但它与Tm1具有相同的肽长度(284个氨基酸),并且与Tm1有83%的同源性。Tm3 cDNA与胎儿肌肉和心肌中一种丰富的1.3千碱基的mRNA杂交,这表明Tm3与α快原肌球蛋白相关。Tm3的前188个氨基酸与大鼠或兔骨骼肌α-原肌球蛋白的相同,而最后71个氨基酸与大鼠平滑肌α-原肌球蛋白的仅相差1个残基。因此,Tm3似乎是由通过可变RNA剪接机制编码快速骨骼肌α-原肌球蛋白和平滑肌α-原肌球蛋白的同一个基因所编码。与Tm4和Tm5不同,Tm3有一个小的基因家族,最多只有一个假基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac4/363096/0cd3a021058e/molcellb00061-0189-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac4/363096/892950583228/molcellb00061-0183-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac4/363096/350caabf3320/molcellb00061-0186-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac4/363096/f045d2ee7818/molcellb00061-0186-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac4/363096/f6646a66f5cd/molcellb00061-0186-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac4/363096/0cd3a021058e/molcellb00061-0189-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac4/363096/892950583228/molcellb00061-0183-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac4/363096/350caabf3320/molcellb00061-0186-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac4/363096/f045d2ee7818/molcellb00061-0186-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac4/363096/f6646a66f5cd/molcellb00061-0186-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cac4/363096/0cd3a021058e/molcellb00061-0189-a.jpg

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本文引用的文献

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Biochem J. 1948;43(2):271-9. doi: 10.1042/bj0430271.
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Expression of a variant form of actin and additional polypeptide changes following chemical-induced in vitro neoplastic transformation of human fibroblasts.
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Binding of pEL98 protein, an S100-related calcium-binding protein, to nonmuscle tropomyosin.pEL98蛋白(一种与S100相关的钙结合蛋白)与非肌肉原肌球蛋白的结合。
J Cell Biol. 1994 Mar;124(5):757-68. doi: 10.1083/jcb.124.5.757.
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