| Literature DB >> 24981860 |
Edyta Marcon1, Zuyao Ni1, Shuye Pu2, Andrei L Turinsky2, Sandra Smiley Trimble3, Jonathan B Olsen3, Rosalind Silverman-Gavrila4, Lorelei Silverman-Gavrila5, Sadhna Phanse1, Hongbo Guo1, Guoqing Zhong1, Xinghua Guo1, Peter Young1, Swneke Bailey6, Denitza Roudeva3, Dorothy Zhao3, Johannes Hewel1, Joyce Li1, Susanne Gräslund7, Marcin Paduch8, Anthony A Kossiakoff8, Mathieu Lupien9, Andrew Emili10, Shoshana J Wodak11, Jack Greenblatt12.
Abstract
Chromatin regulation is driven by multicomponent protein complexes, which form functional modules. Deciphering the components of these modules and their interactions is central to understanding the molecular pathways these proteins are regulating, their functions, and their relation to both normal development and disease. We describe the use of affinity purifications of tagged human proteins coupled with mass spectrometry to generate a protein-protein interaction map encompassing known and predicted chromatin-related proteins. On the basis of 1,394 successful purifications of 293 proteins, we report a high-confidence (85% precision) network involving 11,464 protein-protein interactions among 1,738 different human proteins, grouped into 164 often overlapping protein complexes with a particular focus on the family of JmjC-containing lysine demethylases, their partners, and their roles in chromatin remodeling. We show that RCCD1 is a partner of histone H3K36 demethylase KDM8 and demonstrate that both are important for cell-cycle-regulated transcriptional repression in centromeric regions and accurate mitotic division.Entities:
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Year: 2014 PMID: 24981860 DOI: 10.1016/j.celrep.2014.05.050
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423