Literature DB >> 6581543

Expression of recessive Aprt- mutations in mouse CAK cells resulting from chromosome loss and duplication.

E M Eves, R A Farber.   

Abstract

Karyotypes of recessive mutants at the autosomal adenine phosphoribosyltransferase (Aprt) locus in a clone of the near-diploid mouse CAK cell line have been analyzed. The Aprt located on chromosome 8. One copy of chromosome 8 was morphologically abnormal in the parental clone (CAK-B3-Toyr13) from which Aprt- mutants were isolated. Among 22 mutants, there were ten in which one copy of chromosome 8 had been lost. Four of these were monosomic, and in the others duplication of the remaining homolog had occurred. These findings indicate that newly induced recessive mutations in cultured mammalian cells can be expressed as the result of loss of one chromosome carrying a wild-type allele with or without duplication of the homolog carrying the mutant allele. Loss and duplication would not be detected in cell lines lacking morphologically marked chromosomes.

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Year:  1983        PMID: 6581543     DOI: 10.1007/bf01539479

Source DB:  PubMed          Journal:  Somatic Cell Genet        ISSN: 0098-0366


  6 in total

1.  Mutations in human lymphocytes commonly involve gene duplication and resemble those seen in cancer cels.

Authors:  D R Turner; S A Grist; M Janatipour; A A Morley
Journal:  Proc Natl Acad Sci U S A       Date:  1988-05       Impact factor: 11.205

2.  Adenosine kinase deficiency in tritiated deoxyadenosine-resistant mouse S49 lymphoma cell lines.

Authors:  K J Sastry; C Huang; T S Chan
Journal:  Biochem Genet       Date:  1987-12       Impact factor: 1.890

Review 3.  Somatic cell fusion as a source of genetic rearrangement leading to metastatic variants.

Authors:  L Larizza; V Schirrmacher
Journal:  Cancer Metastasis Rev       Date:  1984       Impact factor: 9.264

4.  Measurements of the frequency of human erythrocytes with gene expression loss phenotypes at the glycophorin A locus.

Authors:  R G Langlois; W L Bigbee; R H Jensen
Journal:  Hum Genet       Date:  1986-12       Impact factor: 4.132

5.  Uniparental disomy as a mechanism for human genetic disease.

Authors:  J E Spence; R G Perciaccante; G M Greig; H F Willard; D H Ledbetter; J F Hejtmancik; M S Pollack; W E O'Brien; A L Beaudet
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

6.  The TP53 tumour suppressor gene in colorectal carcinomas. I. Genetic alterations on chromosome 17.

Authors:  G I Meling; R A Lothe; A L Børresen; C Graue; S Hauge; O P Clausen; T O Rognum
Journal:  Br J Cancer       Date:  1993-01       Impact factor: 7.640

  6 in total

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