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小鼠meprin Aα亚基的组织特异性表达及染色体定位

Tissue-specific expression and chromosomal localization of the alpha subunit of mouse meprin A.

作者信息

Jiang W, Sadler P M, Jenkins N A, Gilbert D J, Copeland N G, Bond J S

机构信息

Department of Biochemistry, Virginia Polytechnic Institute and State University, Blacksburg 24061-0308.

出版信息

J Biol Chem. 1993 May 15;268(14):10380-5.

PMID:7683677
Abstract

Meprins, membrane-bound oligomeric metalloendopeptidases, contain alpha and/or beta subunits. Their activities have been found in the mouse and rat kidney. The cloned cDNA for the mouse alpha subunit of meprin A (EC cloned cDNA for the mouse alpha subunit of meprin A (EC 3.4.24.18) was used here to survey mRNA expression in kidney of different mouse strains and in various tissues of mice and rats. A single message of 3.6 kilobases was found in kidney of random bred (ICR) and inbred mice (C57BL/6, DBA/2) that contain high meprin A activity and in Sprague-Dawley rat kidney. The alpha subunit message was undetectable in the kidney of C3H/He and CBA mice, inbred strains that do not express meprin A activity. Therefore, meprin A activity in the kidney of mouse strains correlates with the amount of alpha subunit mRNA present. The 3.6-kilobase mRNA meprin alpha subunit message was also detected in the small intestine of the rat but not in mice. No message was detected in brain, heart, skeletal muscle, liver, lung, or spleen of mice or rats. Polymerase chain reaction amplification or Southern blot analysis of genomic DNA revealed that the gene for the alpha subunit is present in all mouse strains as well as in human, monkey, rat, mouse, dog, cow, rabbit, and chicken, but it was not detected in yeast. There is one gene copy present in the mouse genome. The gene was localized to mouse chromosome 17 centromeric to the major histocompatibility complex (H-2) by the interspecific backcrossing method. The localization of this allele to Mep-1, the gene previously found to regulate the expression of meprin A activity in mice, supports the proposal that Mep-1 is the structural gene for the alpha subunit.

摘要

膜联寡聚金属内肽酶美普明含有α和/或β亚基。已在小鼠和大鼠肾脏中发现它们的活性。本文使用克隆的小鼠美普明Aα亚基(EC 3.4.24.18)的cDNA来检测不同小鼠品系的肾脏以及小鼠和大鼠的各种组织中的mRNA表达。在具有高美普明A活性的随机繁殖(ICR)和近交系小鼠(C57BL/6、DBA/2)的肾脏以及斯普拉格-道利大鼠肾脏中发现了一条3.6千碱基的单一信使RNA。在不表达美普明A活性的近交系C3H/He和CBA小鼠的肾脏中未检测到α亚基信使RNA。因此,小鼠品系肾脏中的美普明A活性与存在的α亚基mRNA量相关。在大鼠小肠中也检测到了3.6千碱基的mRNA美普明α亚基信使RNA,但在小鼠中未检测到。在小鼠或大鼠的脑、心、骨骼肌、肝、肺或脾中未检测到信使RNA。基因组DNA的聚合酶链反应扩增或Southern印迹分析表明,α亚基基因存在于所有小鼠品系以及人、猴、大鼠、小鼠、狗、牛、兔和鸡中,但在酵母中未检测到。小鼠基因组中存在一个基因拷贝。通过种间回交法将该基因定位到小鼠第17号染色体上,位于主要组织相容性复合体(H-2)的着丝粒附近。该等位基因定位于Mep-1,先前发现该基因可调节小鼠中美普明A活性的表达,这支持了Mep-1是α亚基结构基因的提议。

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