Unknown

Dataset Information

0

An ERG (ets-related gene)-associated histone methyltransferase interacts with histone deacetylases 1/2 and transcription co-repressors mSin3A/B.


ABSTRACT: Covalent modifications of histone tails play important roles in gene transcription and silencing. We recently identified an ERG ( ets -related gene)-associated protein with a SET (suppressor of variegation, enhancer of zest and trithorax) domain (ESET) that was found to have the activity of a histone H3-specific methyltransferase. In the present study, we investigated the interaction of ESET with other chromatin remodelling factors. We show that ESET histone methyltransferase associates with histone deacetylase 1 (HDAC1) and HDAC2, and that ESET also interacts with the transcription co-repressors mSin3A and mSin3B. Deletion analysis of ESET reveals that an N-terminal region containing a tudor domain is responsible for interaction with mSin3A/B and association with HDAC1/2, and that truncation of ESET enhances its binding to mSin3. When bound to a promoter, ESET represses the transcription of a downstream luciferase reporter gene. This repression by ESET is independent of its histone methyltransferase activity, but correlates with its binding to the mSin3 co-repressors. In addition, the repression can be partially reversed by treatment with the HDAC inhibitor trichostatin A. Taken together, these data suggest that ESET histone methyltransferase can form a large, multi-protein complex(es) with mSin3A/B co-repressors and HDAC1/2 that participates in multiple pathways of transcriptional repression.

SUBMITTER: Yang L 

PROVIDER: S-EPMC1223118 | biostudies-other | 2003 Feb

REPOSITORIES: biostudies-other

Similar Datasets

| S-EPMC5349888 | biostudies-literature
| S-EPMC4934896 | biostudies-literature
| S-EPMC2077898 | biostudies-literature
| S-EPMC7165421 | biostudies-literature
| S-EPMC6614369 | biostudies-literature
| S-EPMC8968219 | biostudies-literature
| S-EPMC5518989 | biostudies-literature
| S-EPMC3633699 | biostudies-literature
| S-EPMC3557088 | biostudies-literature
| S-EPMC4152371 | biostudies-literature