Literature DB >> 7683677

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

W Jiang1, P M Sadler, N A Jenkins, D J Gilbert, N G Copeland, J S Bond.   

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.

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Year:  1993        PMID: 7683677

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  10 in total

1.  Activation of the epithelial sodium channel by the metalloprotease meprin β subunit.

Authors:  Agustin Garcia-Caballero; Susan S Ishmael; Yan Dang; Daniel Gillie; Judith S Bond; Sharon L Milgram; M Jackson Stutts
Journal:  Channels (Austin)       Date:  2011-01-01       Impact factor: 2.581

2.  Renal release of N-acetyl-seryl-aspartyl-lysyl-proline is part of an antifibrotic peptidergic system in the kidney.

Authors:  Cesar A Romero; Nitin Kumar; Pablo Nakagawa; Morel E Worou; Tang-Dong Liao; Edward L Peterson; Oscar A Carretero
Journal:  Am J Physiol Renal Physiol       Date:  2018-11-07

Review 3.  The astacin family of metalloendopeptidases.

Authors:  J S Bond; R J Beynon
Journal:  Protein Sci       Date:  1995-07       Impact factor: 6.725

Review 4.  Natural selection on the peptide-binding regions of major histocompatibility complex molecules.

Authors:  A L Hughes; M K Hughes
Journal:  Immunogenetics       Date:  1995       Impact factor: 2.846

5.  To be there when the picture is being painted.

Authors:  Judith S Bond
Journal:  J Biol Chem       Date:  2020-11-20       Impact factor: 5.157

6.  Identification of Mep1a as a susceptibility gene for atherosclerosis in mice.

Authors:  Andrew T Grainger; Nathanael Pilar; Jun Li; Mei-Hua Chen; Ashley M Abramson; Christoph Becker-Pauly; Weibin Shi
Journal:  Genetics       Date:  2021-12-10       Impact factor: 4.402

7.  PEBP2 alpha B/mouse AML1 consists of multiple isoforms that possess differential transactivation potentials.

Authors:  S C Bae; E Ogawa; M Maruyama; H Oka; M Satake; K Shigesada; N A Jenkins; D J Gilbert; N G Copeland; Y Ito
Journal:  Mol Cell Biol       Date:  1994-05       Impact factor: 4.272

Review 8.  Meprins, membrane-bound and secreted astacin metalloproteinases.

Authors:  Erwin E Sterchi; Walter Stöcker; Judith S Bond
Journal:  Mol Aspects Med       Date:  2008-08-22

9.  Characterization of the soluble, secreted form of urinary meprin.

Authors:  R J Beynon; S Oliver; D H Robertson
Journal:  Biochem J       Date:  1996-04-15       Impact factor: 3.857

Review 10.  The metalloproteases meprin α and meprin β: unique enzymes in inflammation, neurodegeneration, cancer and fibrosis.

Authors:  Claudia Broder; Christoph Becker-Pauly
Journal:  Biochem J       Date:  2013-03-01       Impact factor: 3.857

  10 in total

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