Evidence map›Paper›PMID 12556482›Full record

ArticleMolecular and cellular biology2003

Targeted disruption of the meprin beta gene in mice leads to underrepresentation of knockout mice and changes in renal gene expression profiles.

Lourdes P Norman, Weiping Jiang, Xiaoli Han, Thomas L Saunders, Judith S Bond

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 62 citations in OpenAlex.

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  8. To be there when the picture is being painted.The Journal of biological chemistry · 2020
    Article
  9. Meprin β induces activities of A disintegrin and metalloproteinases 9, 10, and 17 by specific prodomain cleavage.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  10. Tethering soluble meprin α in an enzyme complex to the cell surface affects IBD-associated genes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  11. Proteases: History, discovery, and roles in health and disease.The Journal of biological chemistry · 2019
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Lourdes P NormanDepartment of Biochemistry and Molecular Biology, The Pennsylvania State University, Hershey, Pennsylvania 17033-0850, USA.
Weiping Jiang
Xiaoli Han
Thomas L Saunders
Judith S Bond
Pennsylvania State University · USUniversity of Michigan–Ann Arbor · US

Funding

MEPRINS-METALLOPROTEINSASES OF THE KIDNEY AND INTESTINER01DK019691 · NIDDK · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI BOND, JUDITH S · 1986 to 2010
$3.1M
CANDIDATE GENE FOR DIABETIC NEPHROPATHY--MEPRIN BETAR01DK054625 · NIDDK · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI BOND, JUDITH S · 1998 to 2002
$278k
SPECIFICITY OF RNA TRANSPORT IN VITROR01CA040145 · NCI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI CLAWSON, GARY A · 1985 to 2000
$224k
MEPRINS - METALLOPROTEINASES OF THE KIDNEY AND INTESTINER56DK019691 · NIDDK · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI BOND, JUDITH S · 2005 to 2005
$73k
INTRACELLULAR PROTEIN CATABOLISM IN DIABETES MELLITUSR37DK019691 · NIDDK · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI BOND, JUDITH S · 1989 to 1996
–
NCI NIH HHS CA40145NIDDK NIH HHS DK19691NIDDK NIH HHS DK54625NIDDK NIH HHS R01 DK019691NIDDK NIH HHS R56 DK019691
6 · The paper itself

Abstract

Meprins are multidomain zinc metalloproteases that are highly expressed in mammalian kidney and intestinal brush border membranes and in leukocytes and certain cancer cells. Mature meprins are oligomers of evolutionarily related, separately encoded alpha and/or beta subunits. Homooligomers of meprin alpha are secreted; oligomers containing meprin beta are plasma membrane associated. Meprin substrates include bioactive peptides and extracellular matrix proteins. Meprins have been implicated in cancer and intestinal inflammation. Additionally, meprin beta is a candidate gene for diabetic nephropathy. To elucidate in vivo functions of these metalloproteases, meprin beta null mice were generated by targeted disruption of the meprin beta gene on mouse chromosome 18q12. Analyses of meprin beta knockout mice indicated that (i) 50% fewer null mice are born than the Mendelian distribution predicts, (ii) null mice that survive develop normally and are viable and fertile, (iii) meprin beta knockout mice lack membrane-associated meprin alpha in kidney and intestine, and (iv) null mice have changes in renal gene expression profiles compared to wild-type mice as assessed by microarray analyses. Thus, disruption of the meprin beta allele in mice affects embryonic viability, birth weight, renal gene expression profiles, and the distribution of meprin alpha in kidney and intestine.

Indexed as

AnimalsAnimals, NewbornBirth WeightBody WeightFemaleFetal DeathGene Expression ProfilingIntestinesKidneyMaleMetalloendopeptidasesMiceMice, KnockoutOligonucleotide Array Sequence AnalysisRNA, Messengermeprin Ameprin BMetalloendopeptidasesRNA, Messenger

Identifiers

PMID12556482
PMCPMC141138
OpenAlexW2142454070

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.