Literature DB >> 17560546

Drosophila dSet2 functions in H3-K36 methylation and is required for development.

Marianne Stabell1, Jan Larsson, Reidunn B Aalen, Andrew Lambertsson.   

Abstract

Lysine methylation has important functions in biological processes that range from heterochromatin formation to transcription regulation. Here, we demonstrate that Drosophila dSet2 encodes a developmentally essential histone H3 lysine 36 (K36) methyltransferase. Larvae subjected to RNA interference-mediated (RNAi) suppression of dSet2 lack dSet2 expression and H3-K36 methylation, indicating that dSet2 is the sole enzyme responsible for this modification in Drosophila melanogaster. dSet2 RNAi blocks puparium formation and adult development, and causes partial (blister) separation of the dorsal and ventral wing epithelia, defects suggesting a failure of the ecdysone-controlled genetic program. A transheterozygous EcR null mutation/dSet2 RNAi combination produces a complete (balloon) separation of the wing surfaces, revealing a genetic interaction between EcR and dSet2. Using immunoprecipitation, we demonstrate that dSet2 associates with the hyperphosphorylated form of RNA polymerase II (RNAPII).

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Year:  2007        PMID: 17560546     DOI: 10.1016/j.bbrc.2007.05.189

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  20 in total

1.  Transcription-coupled methylation of histone H3 at lysine 36 regulates dosage compensation by enhancing recruitment of the MSL complex in Drosophila melanogaster.

Authors:  Oliver Bell; Thomas Conrad; Jop Kind; Christiane Wirbelauer; Asifa Akhtar; Dirk Schübeler
Journal:  Mol Cell Biol       Date:  2008-03-17       Impact factor: 4.272

2.  Localized H3K36 methylation states define histone H4K16 acetylation during transcriptional elongation in Drosophila.

Authors:  Oliver Bell; Christiane Wirbelauer; Marc Hild; Annette N D Scharf; Michaela Schwaiger; David M MacAlpine; Frédéric Zilbermann; Fred van Leeuwen; Stephen P Bell; Axel Imhof; Dan Garza; Antoine H F M Peters; Dirk Schübeler
Journal:  EMBO J       Date:  2007-11-15       Impact factor: 11.598

Review 3.  The Role of Nuclear Receptor-Binding SET Domain Family Histone Lysine Methyltransferases in Cancer.

Authors:  Richard L Bennett; Alok Swaroop; Catalina Troche; Jonathan D Licht
Journal:  Cold Spring Harb Perspect Med       Date:  2017-06-01       Impact factor: 6.915

Review 4.  Transcription-associated histone modifications and cryptic transcription.

Authors:  Michaela Smolle; Jerry L Workman
Journal:  Biochim Biophys Acta       Date:  2012-09-07

Review 5.  Set2 mediated H3 lysine 36 methylation: regulation of transcription elongation and implications in organismal development.

Authors:  Swaminathan Venkatesh; Jerry L Workman
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2013-02-01       Impact factor: 5.814

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.  The trithorax group proteins Kismet and ASH1 promote H3K36 dimethylation to counteract Polycomb group repression in Drosophila.

Authors:  Kristel M Dorighi; John W Tamkun
Journal:  Development       Date:  2013-09-04       Impact factor: 6.868

8.  Role for the nuclear receptor-binding SET domain protein 1 (NSD1) methyltransferase in coordinating lysine 36 methylation at histone 3 with RNA polymerase II function.

Authors:  Agda Karina Lucio-Eterovic; Melissa M Singh; Jeffrey E Gardner; Chendhore S Veerappan; Judd C Rice; Phillip B Carpenter
Journal:  Proc Natl Acad Sci U S A       Date:  2010-09-13       Impact factor: 11.205

9.  Ligand-independent requirements of steroid receptors EcR and USP for cell survival.

Authors:  A Mansilla; F A Martín; D Martín; A Ferrús
Journal:  Cell Death Differ       Date:  2015-08-07       Impact factor: 15.828

10.  Mining histone methyltransferases and demethylases from whole genome sequence.

Authors:  Parul Gulati; Surbhi Kohli; Ankita Narang; Vani Brahmachari
Journal:  J Biosci       Date:  2020       Impact factor: 1.826

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