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Genes Dev. 2013 Aug 1;27(15):1662-79. doi: 10.1101/gad.218966.113. Epub 2013 Jul 24.

Impaired replication elongation in Tetrahymena mutants deficient in histone H3 Lys 27 monomethylation.

Author information

1
Department of Pathology, University of Michigan, Ann Arbor, Michigan 48109, USA.

Abstract

Replication of nuclear DNA occurs in the context of chromatin and is influenced by histone modifications. In the ciliate Tetrahymena thermophila, we identified TXR1, encoding a histone methyltransferase. TXR1 deletion resulted in severe DNA replication stress, manifested by the accumulation of ssDNA, production of aberrant replication intermediates, and activation of robust DNA damage responses. Paired-end Illumina sequencing of ssDNA revealed intergenic regions, including replication origins, as hot spots for replication stress in ΔTXR1 cells. ΔTXR1 cells showed a deficiency in histone H3 Lys 27 monomethylation (H3K27me1), while ΔEZL2 cells, deleting a Drosophila E(z) homolog, were deficient in H3K27 di- and trimethylation, with no detectable replication stress. A point mutation in histone H3 at Lys 27 (H3 K27Q) mirrored the phenotype of ΔTXR1, corroborating H3K27me1 as a key player in DNA replication. Additionally, we demonstrated interactions between TXR1 and proliferating cell nuclear antigen (PCNA). These findings support a conserved pathway through which H3K27me1 facilitates replication elongation.

KEYWORDS:

H3 Lys 27 methylation; histone methyltransferase; replication elongation; replication origin; replication stress; ssDNA

PMID:
23884606
PMCID:
PMC3744725
DOI:
10.1101/gad.218966.113
[Indexed for MEDLINE]
Free PMC Article

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