TY - JOUR
T1 - Tissue-specific expression and chromosomal localization of the α subunit of mouse meprin A
AU - Jiang, Weiping
AU - Sadler, Philip M.
AU - Jenkins, Nancy A.
AU - Gilbert, Debra J.
AU - Copeland, Neal G.
AU - Bond, Judith S.
N1 - Copyright:
Copyright 2004 Elsevier B.V., All rights reserved.
PY - 1993/5/15
Y1 - 1993/5/15
N2 - Meprins, membrane-bound oligomeric metalloendopeptidases, contain α and/or β subunits. Their activities have been found in the mouse and rat kidney. The cloned cDNA for the mouse α 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 α 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 α subunit mRNA present. The 3.6-kilobase mRNA meprin α 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 α 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 α subunit.
AB - Meprins, membrane-bound oligomeric metalloendopeptidases, contain α and/or β subunits. Their activities have been found in the mouse and rat kidney. The cloned cDNA for the mouse α 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 α 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 α subunit mRNA present. The 3.6-kilobase mRNA meprin α 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 α 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 α subunit.
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M3 - Article
C2 - 7683677
AN - SCOPUS:0027176126
SN - 0021-9258
VL - 268
SP - 10380
EP - 10385
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 14
ER -