Literature DB >> 6379904

Human renin gene is on chromosome 1.

J M Chirgwin, I M Schaefer, P S Rotwein, N Piccini, K W Gross, S L Naylor.   

Abstract

DNA sequences encoding kidney renin were localized to region p21----qter of human chromosome 1 by Southern blot analysis of mouse-human somatic cell hybrids with a cloned human renin DNA probe. The renin gene may be a member of a chromosome 1 linkage group which is conserved in mouse and man. Available evidence suggests this gene is present in one copy per haploid genome. Thus those renin-like molecules detected immunologically in tissues other than the kidney (such as brain, placenta, uterus, pituitary, vasculature, and adrenal) may be derived from this single gene. Since renin messenger RNA in human kidney is about 1550 nucleotides long, reported molecular weights in excess of 45,000 for circulating renin represent posttranslational or postsecretory modifications of the polypeptide.

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Year:  1984        PMID: 6379904     DOI: 10.1007/bf01535637

Source DB:  PubMed          Journal:  Somat Cell Mol Genet        ISSN: 0740-7750


  11 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

3.  Assignment by in situ hybridization of the angiotensinogen gene to chromosome band 1q4, the same region as the human renin gene.

Authors:  I Gaillard-Sanchez; M G Mattei; E Clauser; P Corvol
Journal:  Hum Genet       Date:  1990-03       Impact factor: 4.132

4.  Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma.

Authors:  K H Buetow; J C Murray; J L Israel; W T London; M Smith; M Kew; V Blanquet; C Brechot; A Redeker; S Govindarajah
Journal:  Proc Natl Acad Sci U S A       Date:  1989-11       Impact factor: 11.205

5.  Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression.

Authors:  N C Dracopoli; P Harnett; S J Bale; B Z Stanger; M A Tucker; D E Housman; R F Kefford
Journal:  Proc Natl Acad Sci U S A       Date:  1989-06       Impact factor: 11.205

6.  Mouse serum amyloid P-component (SAP) levels controlled by a locus on chromosome 1.

Authors:  R F Mortensen; P T Le; B A Taylor
Journal:  Immunogenetics       Date:  1985       Impact factor: 2.846

7.  Human renin gene: structure and sequence analysis.

Authors:  P M Hobart; M Fogliano; B A O'Connor; I M Schaefer; J M Chirgwin
Journal:  Proc Natl Acad Sci U S A       Date:  1984-08       Impact factor: 11.205

8.  Association of a new chromosomal deletion [del(1)(q32q42)] with diaphragmatic hernia: assignment of a human ferritin gene.

Authors:  H Youssoufian; P Chance; C M Tuck-Muller; E W Jabs
Journal:  Hum Genet       Date:  1988-03       Impact factor: 4.132

9.  Close physical linkage of the murine Ren-1 and Ren-2 loci.

Authors:  K J Abel; K W Gross
Journal:  Nucleic Acids Res       Date:  1988-03-25       Impact factor: 16.971

10.  Linkage of genes for laminin B1 and B2 subunits on chromosome 1 in mouse.

Authors:  R W Elliott; D Barlow; B L Hogan
Journal:  In Vitro Cell Dev Biol       Date:  1985-08
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