Literature DB >> 3986183

Distribution of 5-methyldeoxycytidine in products of staphylococcal nuclease digestion of nuclei and purified DNA.

F G Barr, M B Kastan, M W Lieberman.   

Abstract

We have compared the distribution of 5-methyldeoxycytidine (m5dC) between staphylococcal nuclease (SN) sensitive and resistant regions of human diploid fibroblast chromatin to the corresponding distribution in purified DNA. After SN digestion of fibroblast nuclei or purified DNA, nuclease-resistant products were separated from sensitive products by perchloric acid or ethanol precipitation; the radioactively labeled nucleosides were then fractionated by high-performance liquid chromatography and quantitated. Our results indicate that m5dC is preferentially associated with SN-resistant regions of both chromatin and purified DNA. The magnitudes of these preferences in fibroblast chromatin and DNA are similar; we find that the enrichment of m5dC content in SN-resistant fractions of nuclei and DNA relative to the corresponding sensitive fractions is approximately 2-3-fold. Therefore, highly methylated regions of DNA have an intrinsic resistance to digestion by SN that is of sufficient magnitude to explain the high degree of nuclease resistance of chromatin containing highly methylated DNA.

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Year:  1985        PMID: 3986183     DOI: 10.1021/bi00327a021

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  3 in total

1.  Structural analysis of a carcinogen-induced genomic rearrangement event.

Authors:  F G Barr; R J Davis; L Eichenfield; B S Emanuel
Journal:  Proc Natl Acad Sci U S A       Date:  1992-02-01       Impact factor: 11.205

2.  Analysis of the rearrangements associated with carcinogen-induced activation of the hamster thymidine kinase gene.

Authors:  F G Barr; S Rajagopalan; M W Lieberman
Journal:  Nucleic Acids Res       Date:  1990-01-11       Impact factor: 16.971

3.  Genomic hypomethylation and far-5' sequence alterations are associated with carcinogen-induced activation of the hamster thymidine kinase gene.

Authors:  F G Barr; S Rajagopalan; C A MacArthur; M W Lieberman
Journal:  Mol Cell Biol       Date:  1986-09       Impact factor: 4.272

  3 in total

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