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未剪接的人尿激酶聚腺苷酸加尾RNA的鉴定及一级序列

Identification and primary sequence of an unspliced human urokinase poly(A)+ RNA.

作者信息

Verde P, Stoppelli M P, Galeffi P, Di Nocera P, Blasi F

出版信息

Proc Natl Acad Sci U S A. 1984 Aug;81(15):4727-31. doi: 10.1073/pnas.81.15.4727.

Abstract

Human urokinase cDNA clones have been identified from a cDNA library prepared from total RNA of human fibroblasts transformed by simian virus 40 [Okayama, H. & Berg, P. (1983) Mol. Cell. Biol. 3, 280-289]. Synthetic oligonucleotides, corresponding to urokinase protein sequence, were used as probes. The cloned cDNA covers most of the coding sequence and the entire 3' untranslated region. The nucleotide sequence of one of the clones identifies this as a copy of a partially spliced polyadenylylated precursor to urokinase mRNA. The introns separate functionally different domains of the enzyme. Human urokinase mRNA has been identified by RNA blot and its size was estimated at 2500 nucleotides.

摘要

已从由猿猴病毒40转化的人成纤维细胞的总RNA制备的cDNA文库中鉴定出人类尿激酶cDNA克隆[冈山,H.和伯格,P.(1983年)《分子细胞生物学》3,280 - 289]。对应于尿激酶蛋白质序列的合成寡核苷酸被用作探针。克隆的cDNA覆盖了大部分编码序列和整个3'非翻译区。其中一个克隆的核苷酸序列表明它是尿激酶mRNA部分剪接的聚腺苷酸化前体的一个拷贝。内含子分隔了该酶功能不同的结构域。通过RNA印迹法鉴定出了人类尿激酶mRNA,其大小估计为2500个核苷酸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dedf/391563/317979ca5dda/pnas00616-0121-a.jpg

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