Literature DB >> 6838486

Studies on genetic variation in major urinary protein synthesis in mouse liver.

F G Berger.   

Abstract

A two- to fourfold difference in the relative rate of total major urinary protein (MUP) synthesis between C57BL/6J and C3H/HeJ female mice has been analyzed at the genetic and molecular levels. The C57BL/6J phenotype is dominant in F1 female progeny of a cross between the two strains. Quantitation of MUP mRNA levels indicates that the rate of synthesis variation does not reflect a change in the concentration of total MUP mRNA. In recombinant inbred strains derived from C57BL/6J and C3H/HeJ progenitors, the rate of synthesis difference segregates as a single genetic determinant that is not linked to the Mup-a locus on chromosome 4. The results suggest an unlinked locus that acts to alter total MUP synthesis without altering total MUP mRNA levels. Two models are proposed to describe the action of this locus, both of which imply some sort of posttranscriptional control of MUP synthesis.

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Year:  1983        PMID: 6838486     DOI: 10.1007/bf02395388

Source DB:  PubMed          Journal:  Biochem Genet        ISSN: 0006-2928            Impact factor:   1.890


  16 in total

Review 1.  Acid hydrolases as models of genetic control.

Authors:  K Paigen
Journal:  Annu Rev Genet       Date:  1979       Impact factor: 16.830

2.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.

Authors:  P W Rigby; M Dieckmann; C Rhodes; P Berg
Journal:  J Mol Biol       Date:  1977-06-15       Impact factor: 5.469

3.  MRNA-directed synthesis of catalytically active mouse beta-glucuronidase in Xenopus oocytes.

Authors:  C Labarca; K Paigen
Journal:  Proc Natl Acad Sci U S A       Date:  1977-10       Impact factor: 11.205

Review 4.  Recent developments in the molecular genetics of human hemoglobin.

Authors:  D J Weatherall; J B Clegg
Journal:  Cell       Date:  1979-03       Impact factor: 41.582

5.  The response of recombinant inbred strains of mice to bacterial lipopolysaccharides.

Authors:  J Watson; R Riblet; B A Taylor
Journal:  J Immunol       Date:  1977-06       Impact factor: 5.422

6.  Components of the major urinary protein complex of inbred mice: determination of NH2-terminal sequences and comparison with homologous components from wild mice.

Authors:  J S Finlayson; M Potter; C S Shinnick; O Smithies
Journal:  Biochem Genet       Date:  1974-04       Impact factor: 1.890

7.  Components of the major urinary protein complex in inbred mice: separation and peptide mapping.

Authors:  J S Finlayson; J F Mushinski; D M Hudson; M Potter
Journal:  Biochem Genet       Date:  1968-09       Impact factor: 1.890

8.  Recombinant-inbred strains. An aid to finding identity, linkage, and function of histocompatibility and other genes.

Authors:  D W Bailey
Journal:  Transplantation       Date:  1971-03       Impact factor: 4.939

9.  Multiple genes coding for the androgen-regulated major urinary proteins of the mouse.

Authors:  N D Hastie; W A Held; J J Toole
Journal:  Cell       Date:  1979-06       Impact factor: 41.582

10.  Regulation of mouse major urinary protein production by the Mup-A gene.

Authors:  P R Szoka; K Paigen
Journal:  Genetics       Date:  1978-11       Impact factor: 4.562

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  2 in total

1.  Proposed mechanistic description of dose-dependent BDE-47 urinary elimination in mice using a physiologically based pharmacokinetic model.

Authors:  Claude Emond; J Michael Sanders; Daniele Wikoff; Linda S Birnbaum
Journal:  Toxicol Appl Pharmacol       Date:  2013-09-19       Impact factor: 4.219

2.  Histidine decarboxylase phenotypes of inbred mouse strains: a regulatory locus (Hdc) determines kidney enzyme concentration.

Authors:  S A Martin; B A Taylor; T Watanabe; G Bulfield
Journal:  Biochem Genet       Date:  1984-04       Impact factor: 1.890

  2 in total

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