Heterochromatin, HP1 and methylation at lysine 9 of histone H3 in animals - PubMed (original) (raw)
doi: 10.1007/s00412-002-0182-8.
Rebecca Aucott, Shantha K Mahadevaiah, Paul S Burgoyne, Neville Huskisson, Silvia Bongiorni, Giorgio Prantera, Laura Fanti, Sergio Pimpinelli, Rong Wu, David M Gilbert, Wei Shi, Reinald Fundele, Harris Morrison, Peter Jeppesen, Prim B Singh
Affiliations
- PMID: 12068920
- DOI: 10.1007/s00412-002-0182-8
Heterochromatin, HP1 and methylation at lysine 9 of histone H3 in animals
Ian G Cowell et al. Chromosoma. 2002 Mar.
Abstract
We show that methylated lysine 9 of histone H3 (Me9H3) is a marker of heterochromatin in divergent animal species. It localises to both constitutive and facultative heterochromatin and replicates late in S-phase of the cell cycle. Significantly, Me9H3 is enriched in the inactive mammalian X chromosome (Xi) in female cells, as well as in the XY body during meiosis in the male, and forms a G-band pattern along the arms of the autosomes. Me9H3 is a constituent of imprinted chromosomes that are repressed. The paternal and maternal pronuclei in one-cell mouse embryos show a striking non-equivalence in Me9H3: the paternal pronucleus contains no immunocytologically detectable Me9H3. The levels of Me9H3 on the parental chromosomes only become equivalent after the two-cell stage. Finally, we provide evidence that Me9H3 is neither necessary nor sufficient for localisation of heterochromatin protein 1 (HP1) to chromosomal DNA.
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