Temporal association of ORCA/LRWD1 to late-firing origins during G1 dictates heterochromatin replication and organization

Yating Wang, Abid Khan, Anna B. Marks, Owen K. Smith, Sumanprava Giri, Yo Chuen Lin, Rachel Creager, David M. MacAlpine, Kannanganattu V. Prasanth, Mirit I. Aladjem, Supriya G. Prasanth

Research output: Contribution to journalArticlepeer-review


DNA replication requires the recruitment of a prereplication complex facilitated by Origin Recognition Complex (ORC) onto the chromatin during G1 phase of the cell cycle. The ORC-associated protein (ORCA/LRWD1) stabilizes ORC on chromatin. Here, we evaluated the genome-wide distribution of ORCA using ChIP-seq during specific time points of G1. ORCA binding sites on the G1 chromatin are dynamic and temporally regulated. ORCA association to specific genomic sites decreases as the cells progressed towards S-phase. The majority of the ORCA-bound sites represent replication origins that also associate with the repressive chromatin marks H3K9me3 and methylated-CpGs, consistent with ORCA-bound origins initiating DNA replication late in S-phase. Further, ORCA directly associates with the repressive marks and interacts with the enzymes that catalyze these marks. Regions that associate with both ORCA and H3K9me3, exhibit diminished H3K9methylation in ORCA-depleted cells, suggesting a role for ORCA in recruiting the H3K9me3 mark at certain genomic loci. Similarly, DNA methylation is altered at ORCA-occupied sites in cells lacking ORCA. Furthermore, repressive chromatinmarks influence ORCA's binding on chromatin. We propose that ORCA coordinates with the histone and DNA methylationmachinery to establish a repressive chromatin environment at a subset of origins, which primes them for late replication.

Original languageEnglish (US)
Pages (from-to)2490-2502
Number of pages13
JournalNucleic acids research
Issue number5
StatePublished - Mar 17 2017

ASJC Scopus subject areas

  • Genetics


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