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钙调神经磷酸酶催化亚基的人类基因的染色体定位。

Chromosomal mapping of the human genes for the calmodulin-dependent protein phosphatase (calcineurin) catalytic subunit.

作者信息

Giri P R, Higuchi S, Kincaid R L

机构信息

Section on Immunology, National Institute on Alcohol Abuse and Alcoholism, Rockville, MD 20852.

出版信息

Biochem Biophys Res Commun. 1991 Nov 27;181(1):252-8. doi: 10.1016/s0006-291x(05)81410-x.

Abstract

Multiple catalytic subunits of the Ca2+ and calmodulin (CaM)-dependent protein phosphatase (PrP) ("calcineurin" or PrP-2B) are derived from at least two structural genes, type 1 ("calcineurin A alpha") and type 2 ("calcineurin A beta "), each of which can produce alternatively spliced transcripts. To examine the possible linkage of these genes, we analyzed genomic DNA from human/hamster hybrid cell lines using probes of 122 base pairs that were designed to bind selectively to exon 3 of the open reading frame. In this region, the nucleotide sequence of the type 2 murine cDNA that we cloned was greater than 99% identical to the type 2 human cDNA but only 78% identical to the type 1 human cDNA. Hybridization to Southern blots containing DNA from all human chromosomes showed that gene 1 was found on chromosome 4, whereas gene 2 segregated to chromosome 10. These data suggest that expression of the two calcineurin genes is not physically linked.

摘要

钙离子和钙调蛋白(CaM)依赖性蛋白磷酸酶(PrP)(“钙调神经磷酸酶”或PrP - 2B)的多个催化亚基源自至少两个结构基因,1型(“钙调神经磷酸酶Aα”)和2型(“钙调神经磷酸酶Aβ”),每个基因都可以产生可变剪接的转录本。为了研究这些基因可能的连锁关系,我们使用设计用于选择性结合开放阅读框外显子3的122个碱基对的探针,分析了人/仓鼠杂交细胞系的基因组DNA。在该区域,我们克隆的2型小鼠cDNA的核苷酸序列与2型人cDNA的同源性大于99%,但与1型人cDNA的同源性仅为78%。与包含来自所有人染色体的DNA的Southern印迹杂交表明,基因1位于4号染色体上,而基因2分离到10号染色体上。这些数据表明,两种钙调神经磷酸酶基因的表达在物理上没有连锁关系。

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