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人及小鼠组织蛋白酶L原的完整核苷酸序列及推导的氨基酸序列。一种由成纤维细胞转化诱导产生的丰富转录本。

Complete nucleotide and deduced amino acid sequences of human and murine preprocathepsin L. An abundant transcript induced by transformation of fibroblasts.

作者信息

Joseph L J, Chang L C, Stamenkovich D, Sukhatme V P

机构信息

Howard Hughes Medical Institute, Department of Medicine, University of Chicago, Illinois 60637.

出版信息

J Clin Invest. 1988 May;81(5):1621-9. doi: 10.1172/JCI113497.

Abstract

Transfection of an activated rat oncogene into NIH3T3 fibroblasts leads to transformation and induction of a metastatic phenotype. To identify genes whose activation might mediate these processes, we used a differential screening strategy. A 1.5-kb transcript is induced fiftyfold, constitutes 1% of ras transformed cell messenger RNA (mRNA) and is the most abundantly induced message in these cells. Our sequence data shows that it encodes murine cathepsin L, a potent collagenolytic and elastinolytic lysosomal enzyme. The murine clone was used to isolate human cathepsin L complementary DNA (cDNA) clones. The complete nucleotide and deduced amino acid sequences of human and murine preprocathepsin L are presented and compared to other papain family cysteine proteinases. Northern analysis shows that both human and murine cathepsin L probes hybridize to a 1.5-kb transcript in several tissues, but also to a 4-kb transcript in human kidney. These clones will facilitate studies of the structure, expression, and function of cathepsin L, including its unexpected upregulation in transformation.

摘要

将一个激活的大鼠癌基因转染到NIH3T3成纤维细胞中会导致细胞转化并诱导转移表型。为了鉴定其激活可能介导这些过程的基因,我们采用了差异筛选策略。一种1.5kb的转录本被诱导了50倍,占ras转化细胞信使核糖核酸(mRNA)的1%,并且是这些细胞中诱导最丰富的信息。我们的序列数据表明它编码小鼠组织蛋白酶L,一种强大的胶原分解和弹性蛋白分解溶酶体酶。该小鼠克隆被用于分离人组织蛋白酶L互补DNA(cDNA)克隆。本文给出了人和小鼠前组织蛋白酶L的完整核苷酸和推导氨基酸序列,并与其他木瓜蛋白酶家族半胱氨酸蛋白酶进行了比较。Northern分析表明,人和小鼠组织蛋白酶L探针在多个组织中均与一个1.5kb的转录本杂交,但在人肾脏中还与一个4kb的转录本杂交。这些克隆将有助于对组织蛋白酶L的结构、表达和功能进行研究,包括其在转化过程中意外的上调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62c8/442598/67944786a663/jcinvest00099-0329-a.jpg

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