XB-ART-1746
DNA Repair (Amst)
2005 Jul 12;47:760-72. doi: 10.1016/j.dnarep.2005.02.007.
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Xenopus CENP-A assembly into chromatin requires base excision repair proteins.
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CENP-A is an essential histone H3 variant found in all eukaryotes examined to date. To begin to determine how CENP-A is assembled into chromatin, we developed a binding assay using sperm chromatin in cell-free extract derived from Xenopus eggs. Our data suggest that the catalytic activities of an unidentified deoxycytidine deaminase and UNG2, a uracil DNA glycosylase, are involved in CENP-A assembly. In support of this model, inhibiting deoxycytidine deaminase with zebularine, or uracil DNA glycosylase with Ugi, uracil or UTP results in a lack of detectable CENP-A on sperm DNA. Conversely, inducing DNA damage increases the level of CENP-A detected on sperm chromatin. Our data suggest that base excision repair may be involved in assembly of this histone H3 variant.
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Species referenced: Xenopus laevis
Genes referenced: ccno cenpa