Literature DB >> 14522075

Genomic structure and expression of the mouse ESET gene encoding an ERG-associated histone methyltransferase with a SET domain.

Michael L Blackburn1, Howard A Chansky, Anna Zielinska-Kwiatkowska, Yoshito Matsui, Liu Yang.   

Abstract

ESET (ERG-associated protein with a SET domain, also called SETDB1) is a novel histone methyltransferase that catalyzes methylation of histone H3-lysine 9 (H3-K9). Here we describe the genomic structure and expression of the mouse ESET gene that gives rise to ESET protein and its alternative splicing product. ESET is a 36-kb single copy gene and full-length ESET transcript consisting of 22 exons. The splicing variant retains only the first 12 exons and thus lacks sequences encoding the methyl CpG-binding domain and the catalytic SET domain. The U2 type conserved GT/AG consensus sequence is present at all of the splicing junctions within the ESET gene. The transcription initiation site of the ESET gene was determined by 5'-RACE experiment and by primer extension. The 5'-flanking sequence of the ESET gene does not contain the consensus TATA box. Instead, this ESET promoter region has features such as SP1-binding sites that are typical of housekeeping genes. The ESET promoter was functionally active when tested in transfection and luciferase assay. Full-length ESET transcript appears to be ubiquitously expressed. While the SET domain-deficient splicing variant is present in immortalized cell lines, it is undetectable by RT-PCR in the majority of normal mouse tissues.

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Year:  2003        PMID: 14522075     DOI: 10.1016/s0167-4781(03)00155-6

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  18 in total

1.  Setdb1-mediated histone H3K9 hypermethylation in neurons worsens the neurological phenotype of Mecp2-deficient mice.

Authors:  Yan Jiang; Anouch Matevossian; Yin Guo; Schahram Akbarian
Journal:  Neuropharmacology       Date:  2010-09-30       Impact factor: 5.250

2.  The oncogenic TLS-ERG fusion protein exerts different effects in hematopoietic cells and fibroblasts.

Authors:  Junhui Zou; Hitoshi Ichikawa; Michael L Blackburn; Hsien-Ming Hu; Anna Zielinska-Kwiatkowska; Qi Mei; Gerald J Roth; Howard A Chansky; Liu Yang
Journal:  Mol Cell Biol       Date:  2005-07       Impact factor: 4.272

3.  ESET histone methyltransferase is essential to hypertrophic differentiation of growth plate chondrocytes and formation of epiphyseal plates.

Authors:  Liu Yang; Kevin A Lawson; Colin J Teteak; Junhui Zou; Jacques Hacquebord; David Patterson; Andrew C Ghatan; Qi Mei; Anna Zielinska-Kwiatkowska; Steven D Bain; Russell J Fernandes; Howard A Chansky
Journal:  Dev Biol       Date:  2013-05-04       Impact factor: 3.582

4.  H3K9MTase G9a is essential for the differentiation and growth of tenocytes in vitro.

Authors:  Satoshi Wada; Hisashi Ideno; Akemi Shimada; Taichi Kamiunten; Yoshiki Nakamura; Kazuhisa Nakashima; Hiroshi Kimura; Yoichi Shinkai; Makoto Tachibana; Akira Nifuji
Journal:  Histochem Cell Biol       Date:  2015-03-27       Impact factor: 4.304

5.  Mesenchyme-specific knockout of ESET histone methyltransferase causes ectopic hypertrophy and terminal differentiation of articular chondrocytes.

Authors:  Kevin A Lawson; Colin J Teteak; Junhui Zou; Jacques Hacquebord; Andrew Ghatan; Anna Zielinska-Kwiatkowska; Russell J Fernandes; Howard A Chansky; Liu Yang
Journal:  J Biol Chem       Date:  2013-09-20       Impact factor: 5.157

6.  Systematic genetic interaction studies identify histone demethylase Utx as potential target for ameliorating Huntington's disease.

Authors:  Wan Song; Nóra Zsindely; Anikó Faragó; J Lawrence Marsh; László Bodai
Journal:  Hum Mol Genet       Date:  2018-02-15       Impact factor: 6.150

7.  ESET/SETDB1 gene expression and histone H3 (K9) trimethylation in Huntington's disease.

Authors:  Hoon Ryu; Junghee Lee; Sean W Hagerty; Byoung Yul Soh; Sara E McAlpin; Kerry A Cormier; Karen M Smith; Robert J Ferrante
Journal:  Proc Natl Acad Sci U S A       Date:  2006-12-01       Impact factor: 11.205

8.  Coordinated expression of H3K9 histone methyltransferases during tooth development in mice.

Authors:  Taichi Kamiunten; Hisashi Ideno; Akemi Shimada; Yoshiki Nakamura; Hiroshi Kimura; Kazuhisa Nakashima; Akira Nifuji
Journal:  Histochem Cell Biol       Date:  2014-10-08       Impact factor: 4.304

9.  Akt/PKB interacts with the histone H3 methyltransferase SETDB1 and coordinates to silence gene expression.

Authors:  Haidong Gao; Zhigang Yu; Dongsong Bi; Liyu Jiang; Yazhou Cui; Jingzhong Sun; Rong Ma
Journal:  Mol Cell Biochem       Date:  2007-06-19       Impact factor: 3.396

10.  ERG-associated protein with SET domain (ESET)-Oct4 interaction regulates pluripotency and represses the trophectoderm lineage.

Authors:  Leng-Siew Yeap; Katsuhiko Hayashi; M Azim Surani
Journal:  Epigenetics Chromatin       Date:  2009-10-07       Impact factor: 4.954

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