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Items: 1 to 20 of 338

1.

The conserved bromo-adjacent homology domain of yeast Orc1 functions in the selection of DNA replication origins within chromatin.

Müller P, Park S, Shor E, Huebert DJ, Warren CL, Ansari AZ, Weinreich M, Eaton ML, MacAlpine DM, Fox CA.

Genes Dev. 2010 Jul 1;24(13):1418-33. doi: 10.1101/gad.1906410.

2.

The BAH domain facilitates the ability of human Orc1 protein to activate replication origins in vivo.

Noguchi K, Vassilev A, Ghosh S, Yates JL, DePamphilis ML.

EMBO J. 2006 Nov 15;25(22):5372-82. Epub 2006 Oct 26.

3.

Specific binding of eukaryotic ORC to DNA replication origins depends on highly conserved basic residues.

Kawakami H, Ohashi E, Kanamoto S, Tsurimoto T, Katayama T.

Sci Rep. 2015 Oct 12;5:14929. doi: 10.1038/srep14929.

4.

Concerted interaction between origin recognition complex (ORC), nucleosomes and replication origin DNA ensures stable ORC-origin binding.

Hizume K, Yagura M, Araki H.

Genes Cells. 2013 Sep;18(9):764-79. doi: 10.1111/gtc.12073. Epub 2013 Jun 24.

5.

A Link between ORC-origin binding mechanisms and origin activation time revealed in budding yeast.

Hoggard T, Shor E, Müller CA, Nieduszynski CA, Fox CA.

PLoS Genet. 2013;9(9):e1003798. doi: 10.1371/journal.pgen.1003798. Epub 2013 Sep 12.

6.

Phylogenetic conservation and homology modeling help reveal a novel domain within the budding yeast heterochromatin protein Sir1.

Hou Z, Danzer JR, Mendoza L, Bose ME, Müller U, Williams B, Fox CA.

Mol Cell Biol. 2009 Feb;29(3):687-702. doi: 10.1128/MCB.00202-08. Epub 2008 Nov 24.

7.
8.

The BAH domain of ORC1 links H4K20me2 to DNA replication licensing and Meier-Gorlin syndrome.

Kuo AJ, Song J, Cheung P, Ishibe-Murakami S, Yamazoe S, Chen JK, Patel DJ, Gozani O.

Nature. 2012 Mar 7;484(7392):115-9. doi: 10.1038/nature10956.

9.

The origin recognition complex interacts with a subset of metabolic genes tightly linked to origins of replication.

Shor E, Warren CL, Tietjen J, Hou Z, Müller U, Alborelli I, Gohard FH, Yemm AI, Borisov L, Broach JR, Weinreich M, Nieduszynski CA, Ansari AZ, Fox CA.

PLoS Genet. 2009 Dec;5(12):e1000755. doi: 10.1371/journal.pgen.1000755. Epub 2009 Dec 4.

10.
11.

RNAP-II molecules participate in the anchoring of the ORC to rDNA replication origins.

Mayan MD.

PLoS One. 2013;8(1):e53405. doi: 10.1371/journal.pone.0053405. Epub 2013 Jan 4.

12.

High-resolution analysis of four efficient yeast replication origins reveals new insights into the ORC and putative MCM binding elements.

Chang F, May CD, Hoggard T, Miller J, Fox CA, Weinreich M.

Nucleic Acids Res. 2011 Aug;39(15):6523-35. doi: 10.1093/nar/gkr301. Epub 2011 May 9.

13.

Diversity of eukaryotic DNA replication origins revealed by genome-wide analysis of chromatin structure.

Berbenetz NM, Nislow C, Brown GW.

PLoS Genet. 2010 Sep 2;6(9):e1001092. doi: 10.1371/journal.pgen.1001092.

14.
16.

Human origin recognition complex binds preferentially to G-quadruplex-preferable RNA and single-stranded DNA.

Hoshina S, Yura K, Teranishi H, Kiyasu N, Tominaga A, Kadoma H, Nakatsuka A, Kunichika T, Obuse C, Waga S.

J Biol Chem. 2013 Oct 18;288(42):30161-71. doi: 10.1074/jbc.M113.492504. Epub 2013 Sep 3.

17.
18.

Forced binding of the origin of replication complex to chromosomal sites in Drosophila S2 cells creates an origin of replication.

Crevel G, Cotterill S.

J Cell Sci. 2012 Feb 15;125(Pt 4):965-72. doi: 10.1242/jcs.094409. Epub 2012 Mar 15.

19.

Origin replication complex binding, nucleosome depletion patterns, and a primary sequence motif can predict origins of replication in a genome with epigenetic centromeres.

Tsai HJ, Baller JA, Liachko I, Koren A, Burrack LS, Hickman MA, Thevandavakkam MA, Rusche LN, Berman J.

MBio. 2014 Sep 2;5(5):e01703-14. doi: 10.1128/mBio.01703-14.

20.

Transcriptional silencing functions of the yeast protein Orc1/Sir3 subfunctionalized after gene duplication.

Hickman MA, Rusche LN.

Proc Natl Acad Sci U S A. 2010 Nov 9;107(45):19384-9. doi: 10.1073/pnas.1006436107. Epub 2010 Oct 25.

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