Literature DB >> 7135161

The BrdU content of DNA is decreased during reversal of inhibition of myogenesis by deoxycytidine.

W E Wright.   

Abstract

The mechanism by which 5-bromodeoxyuridine (BrdU) inhibits cell differentiation is unresolved. The ability of deoxycytidine to reverse the inhibition of myogenesis produced by BrdU has been cited as evidence that the inhibition is not a direct result of the incorporation of BrdU into cellular DNA. In contrast to previous work, the present study demonstrates a direct correlation between the effects of deoxycytidine on myogenic cells and a reduction in the substitution of BrdU for thymidine in the DNA. Further-more, the reversal occurs at the same degree of BrdU substitution (20-30%) as is required to inhibit myogenesis when cells are grown in BrdU alone or with deoxycytidine in a medium that prevents the conversion of deoxycytidine to thymidine. The effects of deoxycytidine thus do not support a mechanism of action of BrdU in myogenic cells independent of its effects on DNA.

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Year:  1982        PMID: 7135161     DOI: 10.1007/bf01542850

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


  3 in total

1.  Regulation of telomerase activity in immortal cell lines.

Authors:  S E Holt; W E Wright; J W Shay
Journal:  Mol Cell Biol       Date:  1996-06       Impact factor: 4.272

2.  The amplified expression of factors regulating myogenesis in L6 myoblasts.

Authors:  W E Wright
Journal:  J Cell Biol       Date:  1985-01       Impact factor: 10.539

3.  Regulation of rat myosin light-chain synthesis in heterokaryons between 5-bromodeoxyuridine-blocked rat myoblasts and differentiated chick myocytes.

Authors:  W E Wright; J Aronoff
Journal:  J Cell Biol       Date:  1983-06       Impact factor: 10.539

  3 in total

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