Histone H4 lysine 20 monomethylation promotes transcriptional repression by L3MBTL1
Autor: | Piernicola Boccuni, Xinyang Zhao, Nadia Gurvich, Donal MacGrogan, Stephen D. Nimer, Nagesh Kalakonda, J C Rice, Y Miyata, Wolfgang Fischle, J Zhang, Ruben Hoya-Arias, Jennifer K. Sims |
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Rok vydání: | 2008 |
Předmět: |
Cancer Research
Transcription Genetic Chromosomal Proteins Non-Histone Repressor Plasma protein binding Methylation Article Histone H4 Histones Genetics Humans Molecular Biology Psychological repression Regulation of gene expression Binding Sites biology Lysine Tumor Suppressor Proteins Cell Cycle Histone-Lysine N-Methyltransferase Chromatin Neoplasm Proteins Repressor Proteins Histone Biochemistry Gene Expression Regulation biology.protein K562 Cells Protein Binding |
Zdroj: | Oncogene. 27(31) |
ISSN: | 1476-5594 |
Popis: | Lethal 3 malignant brain tumor 1 (L3MBTL1), a homolog of the Drosophila polycomb tumor suppressor l(3)mbt, contains three tandem MBT repeats (3xMBT) that are critical for transcriptional repression. We recently reported that the 3xMBT repeats interact with mono- and dimethylated lysines in the amino termini of histones H4 and H1b to promote methylation-dependent chromatin compaction. Using a series of histone peptides, we now show that the recognition of mono- and dimethylated lysines in histones H3, H4 and H1.4 (but not their trimethylated or unmodified counterparts) by 3xMBT occurs in the context of a basic environment, requiring a conserved aspartic acid (D355) in the second MBT repeat. Despite the broad range of in vitro binding, the chromatin association of L3MBTL1 mirrors the progressive accumulation of H4K20 monomethylation during the cell cycle. Furthermore, transcriptional repression by L3MBTL1 is enhanced by the H4K20 monomethyltransferase PR-SET7 (to which it binds) but not SUV420H1 (an H4K20 trimethylase) or G9a (an H3K9 dimethylase) and knockdown of PR-SET7 decreases H4K20me1 levels and the chromatin association of L3MBTL1. Our studies identify the importance of H4K20 monomethylation and of PR-SET7 for L3MBTL1 function. |
Databáze: | OpenAIRE |
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