DNA single-strand break repair and spinocerebellar ataxia

Article Abstract:

The author reviews the publications on DNA single-strand break repair. The topics of interest include the studies of relationship between mutations in putative human DNA single-strand break repair and hereditary spinocerebellar ataxia, and the links between neurodegenerative disorders and spinocerebellar ataxia.

author: Caldecott, Keith W.
Cerebellar ataxia, Causes of, Gene mutations, Gene mutation

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XRCC1 stimulates human polynucleotide kinase activity at damaged DNA termini and accelerates DNA single-strand break repair

Article Abstract:

The mammalian DNA single-strand break repair is mediated by XRCC1 protein by interacting with human polynucleotide kinase and DNA polymerase-beta and DNA ligase III. Data indicate that XRCC1 interaction with polynucleotide kinase stimulates DNA kinase and DNA phosphatase activities.

author: Zhang, Hong, Whitehouse, Claire J., Taylor, Richard M., Thstlethwaite, Angela, Karimi-Busheri, Feridoun, Lasko, Dana D., Weinfeld, Michael, Caldecott, Keith W.
Canada, Protein kinases

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Molecular basis of phosphorylation-induced activation of the NADPH oxidase

Article Abstract:

Research has been conducted on cytoplasmic p40-p47-p67 (super)phox complex. The results of structural and biochemical data demonstrate that phosphorylation of p47 (super)phox activates molecular switch which relieves inhibitory intramolecular interaction.

author: Groemping, Yvonne, Lapouge, Karine, Smerdon, Stephen J., Rittinger, Katrin
Oxidases, Phosphorylation

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subjects list: United Kingdom, Analysis, Physiological aspects, Genetic aspects, DNA repair, Cells (Biology), Cells, Cell research, Cytological research
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