Literature DB >> 6493270

Preferential repair of nuclear matrix associated DNA in xeroderma pigmentosum complementation group C.

L H Mullenders, A C van Kesteren, C J Bussmann, A A van Zeeland, A T Natarajan.   

Abstract

The distribution of ultraviolet-induced DNA repair patches in the genome of xeroderma pigmentosum cells of complementation group C was investigated by determining the molecular weight distribution of repair labeled DNA and prelabeled DNA in alkaline sucrose gradients after treatment with the dimerspecific endonuclease V of bacteriophage T4. The results were consistent with the data reported by Mansbridge and Hanawalt (1983) and suggest that DNA-repair synthesis in xeroderma pigmentosum cells of complementation group C occurs in localized regions of the genome. Analysis of the spatial distribution of ultraviolet-induced repair patches in DNA loops attached to the nuclear matrix revealed that in xeroderma pigmentosum cells of complementation group C repair patches are preferentially situated near the attachment sites of DNA loops at the nuclear matrix. In normal human fibroblasts we observed no enrichment of repair-labeled DNA at the nuclear matrix and repair patches appeared to be distributed randomly along the DNA loops. The enrichment of repair-labeled DNA at the nuclear matrix in xeroderma pigmentosum cells of complementation group C may indicate that the residual DNA-repair synthesis in these cells occurs preferentially in transcribing regions of the genome.

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Year:  1984        PMID: 6493270     DOI: 10.1016/0165-7992(84)90014-9

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  15 in total

Review 1.  Evolutionary consequences of nonrandom damage and repair of chromatin domains.

Authors:  T Boulikas
Journal:  J Mol Evol       Date:  1992-08       Impact factor: 2.395

Review 2.  RNA polymerase between lesion bypass and DNA repair.

Authors:  Alexandra M Deaconescu
Journal:  Cell Mol Life Sci       Date:  2013-06-27       Impact factor: 9.261

3.  DNA repair in the metallothionein gene increases with transcriptional activation.

Authors:  D S Okumoto; V A Bohr
Journal:  Nucleic Acids Res       Date:  1987-12-10       Impact factor: 16.971

4.  Xeroderma pigmentosum complementation group C cells remove pyrimidine dimers selectively from the transcribed strand of active genes.

Authors:  J Venema; A van Hoffen; V Karcagi; A T Natarajan; A A van Zeeland; L H Mullenders
Journal:  Mol Cell Biol       Date:  1991-08       Impact factor: 4.272

5.  Recruitment of damaged DNA to the nuclear matrix in hamster cells following ultraviolet irradiation.

Authors:  D R Koehler; P C Hanawalt
Journal:  Nucleic Acids Res       Date:  1996-08-01       Impact factor: 16.971

6.  Repair of single-stranded DNA nicks, gaps, and loops in mammalian cells.

Authors:  D Ayares; D Ganea; L Chekuri; C R Campbell; R Kucherlapati
Journal:  Mol Cell Biol       Date:  1987-05       Impact factor: 4.272

7.  Differential repair of DNA damage in the human metallothionein gene family.

Authors:  S A Leadon; M M Snowden
Journal:  Mol Cell Biol       Date:  1988-12       Impact factor: 4.272

Review 8.  The nuclear matrix--its role in the spatial organization and replication of eukaryotic DNA.

Authors:  H M van der Velden; F Wanka
Journal:  Mol Biol Rep       Date:  1987       Impact factor: 2.316

Review 9.  Drug resistance and DNA repair.

Authors:  M Fox; J J Roberts
Journal:  Cancer Metastasis Rev       Date:  1987       Impact factor: 9.264

10.  RAD7 gene of Saccharomyces cerevisiae: transcripts, nucleotide sequence analysis, and functional relationship between the RAD7 and RAD23 gene products.

Authors:  G Perozzi; S Prakash
Journal:  Mol Cell Biol       Date:  1986-05       Impact factor: 4.272

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