Warning: The NCBI web site requires JavaScript to function. more...
Generate a file for use with external citation management software.
A lysine-rich region in Dot1p is crucial for direct interaction with H2B ubiquitylation and high level methylation of H3K79.
Oh S, Jeong K, Kim H, Kwon CS, Lee D.
Biochem Biophys Res Commun. 2010 Sep 3;399(4):512-7. Epub 2010 Aug 3.
Related citations
Nonprocessive methylation by Dot1 leads to functional redundancy of histone H3K79 methylation states.
Frederiks F, Tzouros M, Oudgenoeg G, van Welsem T, Fornerod M, Krijgsveld J, van Leeuwen F.
Nat Struct Mol Biol. 2008 Jun;15(6):550-7. Epub 2008 May 30.
UV sensitive mutations in histone H3 in Saccharomyces cerevisiae that alter specific K79 methylation states genetically act through distinct DNA repair pathways.
Evans ML, Bostelman LJ, Albrecht AM, Keller AM, Strande NT, Thompson JS.
Curr Genet. 2008 May;53(5):259-74. Epub 2008 Mar 8.
Interplay of chromatin modifiers on a short basic patch of histone H4 tail defines the boundary of telomeric heterochromatin.
Altaf M, Utley RT, Lacoste N, Tan S, Briggs SD, Côté J.
Mol Cell. 2007 Dec 28;28(6):1002-14.
Disruptor of telomeric silencing-1 is a chromatin-specific histone H3 methyltransferase.
Lacoste N, Utley RT, Hunter JM, Poirier GG, Côte J.
J Biol Chem. 2002 Aug 23;277(34):30421-4. Epub 2002 Jul 3.
Dot1p modulates silencing in yeast by methylation of the nucleosome core.
van Leeuwen F, Gafken PR, Gottschling DE.
Cell. 2002 Jun 14;109(6):745-56.
Lysine methylation within the globular domain of histone H3 by Dot1 is important for telomeric silencing and Sir protein association.
Ng HH, Feng Q, Wang H, Erdjument-Bromage H, Tempst P, Zhang Y, Struhl K.
Genes Dev. 2002 Jun 15;16(12):1518-27.
Filters: Manage Filters
Your browsing activity is empty.
Activity recording is turned off.
Turn recording back on