Literature DB >> 4000280

Expression of c-mos proto-oncogene transcripts in mouse tissues.

F Propst, G F Vande Woude.   

Abstract

Valuable information about proto-oncogenes and their physiological function has been obtained by studying their expression in normal cells. However, expression of the c-mos gene, the cellular homologue of the transforming gene of Moloney murine sarcoma virus, has not been detected in normal mouse cells or tissues. The conservation of the c-mos open reading frame strongly indicates that the gene must function during some portion of the animal life cycle, and other lines of evidence suggested to us that the c-mos proto-oncogene may be expressed at very low levels in normal tissues. We have used a sensitive S1 nuclease assay to screen RNA preparations from mouse tissues and describe here the detection of c-mos-related transcripts especially in mouse embryos, testes and ovaries. The transcripts found in testis RNA are estimated to be approximately 1.7 kilobases (kb) long by Northern analysis. S1 analysis demonstrated that the entire mos open reading frame is present. In contrast, we detect approximately 1.4-kb transcripts in ovary RNA and at least two major transcripts, approximately 2.3 and approximately 1.3 kb, in embryo RNA. The latter transcripts have in common sequences of at least 1 kb, representing most of the c-mos open reading frame. The variation in size of the mos transcript in different tissues suggests a novel regulatory mechanism for the expression of this proto-oncogene.

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Year:  1985        PMID: 4000280     DOI: 10.1038/315516a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  43 in total

1.  Identification of a negative regulatory element that inhibits c-mos transcription in somatic cells.

Authors:  S S Zinkel; S K Pal; J Szeberényi; G M Cooper
Journal:  Mol Cell Biol       Date:  1992-05       Impact factor: 4.272

2.  c-mos expression in mouse oocytes is controlled by initiator-related sequences immediately downstream of the transcription initiation site.

Authors:  S K Pal; S S Zinkel; A A Kiessling; G M Cooper
Journal:  Mol Cell Biol       Date:  1991-10       Impact factor: 4.272

3.  The repressor sequence upstream of c-mos acts neither as polyadenylation site nor as transcription termination region.

Authors:  F A van der Hoorn; B Neupert
Journal:  Nucleic Acids Res       Date:  1986-11-25       Impact factor: 16.971

4.  Nucleoside triphosphate-dependent DNA-binding properties of mos protein.

Authors:  A Seth; E Priel; G F Vande Woude
Journal:  Proc Natl Acad Sci U S A       Date:  1987-06       Impact factor: 11.205

5.  Two proto-oncogenes implicated in mammary carcinogenesis, int-1 and int-2, are independently regulated during mouse development.

Authors:  A Jakobovits; G M Shackleford; H E Varmus; G R Martin
Journal:  Proc Natl Acad Sci U S A       Date:  1986-10       Impact factor: 11.205

6.  Expression of growth-associated genes in various tissues of the fetal and adult rat.

Authors:  K J Soprano; D R Soprano; S Cosenza; T Owen
Journal:  Mol Cell Biochem       Date:  1987-05       Impact factor: 3.396

7.  The molecular biology of chromosome alterations in myelogenous leukemia.

Authors:  H A Drabkin
Journal:  West J Med       Date:  1985-12

8.  Expression of cellular protooncogenes in the mouse male germ line: a distinctive 2.4-kilobase pim-1 transcript is expressed in haploid postmeiotic cells.

Authors:  V Sorrentino; M D McKinney; M Giorgi; R Geremia; E Fleissner
Journal:  Proc Natl Acad Sci U S A       Date:  1988-04       Impact factor: 11.205

9.  In vitro growth rate of placental fibroblasts is developmentally regulated.

Authors:  M E Fant
Journal:  J Clin Invest       Date:  1991-11       Impact factor: 14.808

10.  Distinct developmental patterns of c-mos protooncogene expression in female and male mouse germ cells.

Authors:  G L Mutter; D J Wolgemuth
Journal:  Proc Natl Acad Sci U S A       Date:  1987-08       Impact factor: 11.205

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