Home LiteratureArticle Details
PMID: 15681608 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

PR-Set7-dependent methylation of histone H4 Lys 20 functions in repression of gene expression and is essential for mitosis.

Genes & development ·Vol. 19 ·No. 4 ·2005-02-15 ·Pages 431-5

Karachentsev D, Sarma K, Reinberg D, Steward R

Abstract

The histone methyl transferase PR-Set7 mediates histone H4 Lys 20 methylation, a mark of constitutive and facultative heterochromatin. We isolated a null mutation in Drosophila PR-Set7 that suppresses position effect variegation, indicating that PR-Set7 indeed functions in silencing general gene expression. In PR-Set7 larval leg and eye discs, the number of cells is lower than normal, and the DNA content in these cells is significantly increased. These data show that PR-Set7-dependent methylation is essential for the process of mitosis. The methylation mark is highly stable and is maintained even in the absence of PR-Set7 protein.

MeSH Terms
Animals Blotting, Western Drosophila Drosophila Proteins/physiology Gene Silencing/physiology Histone-Lysine N-Methyltransferase/physiology Histones/chemistry,metabolism Lysine/metabolism Methylation Mitosis/physiology
Chemicals
Drosophila Proteins Histones Histone-Lysine N-Methyltransferase PR-Set7 protein, Drosophila Lysine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Karachentsev Dmitry
Waksman Institute, Department of Molecular Biology and Biochemistry, New Jersey Cancer Center, Rutgers University, Piscataway, New Jersey 08854-8020, USA.
Sarma Kavitha
Reinberg Danny
Steward Ruth
References (17)
17 references, click to expand
  1. SET domain proteins modulate chromatin domains in eu- and heterochromatin.
    Cell Mol Life Sci. 1998 Jan;54(1):80-93 PMID: 9487389
  2. Crystal structure of the nucleosome core particle at 2.8 A resolution.
    Nature. 1997 Sep 18;389(6648):251-60 PMID: 9305837
  3. Silencing at Drosophila telomeres: nuclear organization and chromatin structure play critical roles.
    EMBO J. 1999 Jul 1;18(13):3724-35 PMID: 10393187
  4. Methylation of histone H4 lysine 20 controls recruitment of Crb2 to sites of DNA damage.
    Cell. 2004 Nov 24;119(5):603-14 PMID: 15550243
  5. Methylation of histone H3 at lysine 4 is highly conserved and correlates with transcriptionally active nuclei in Tetrahymena.
    Proc Natl Acad Sci U S A. 1999 Dec 21;96(26):14967-72 PMID: 10611321
  6. The language of covalent histone modifications.
    Nature. 2000 Jan 6;403(6765):41-5 PMID: 10638745
  7. P-TEFb kinase recruitment and function at heat shock loci.
    Genes Dev. 2000 Apr 1;14(7):792-803 PMID: 10766736
  8. Transcription regulation by histone methylation: interplay between different covalent modifications of the core histone tails.
    Genes Dev. 2001 Sep 15;15(18):2343-60 PMID: 11562345
  9. Code of silence.
    Nature. 2001 Nov 15;414(6861):258-61 PMID: 11713509
  10. Central role of Drosophila SU(VAR)3-9 in histone H3-K9 methylation and heterochromatic gene silencing.
    EMBO J. 2002 Mar 1;21(5):1121-31 PMID: 11867540
  11. PR-Set7 is a nucleosome-specific methyltransferase that modifies lysine 20 of histone H4 and is associated with silent chromatin.
    Mol Cell. 2002 Jun;9(6):1201-13 PMID: 12086618
  12. Purification and functional characterization of SET8, a nucleosomal histone H4-lysine 20-specific methyltransferase.
    Curr Biol. 2002 Jul 9;12(13):1086-99 PMID: 12121615
  13. Mitotic-specific methylation of histone H4 Lys 20 follows increased PR-Set7 expression and its localization to mitotic chromosomes.
    Genes Dev. 2002 Sep 1;16(17):2225-30 PMID: 12208845
  14. A silencing pathway to induce H3-K9 and H4-K20 trimethylation at constitutive heterochromatin.
    Genes Dev. 2004 Jun 1;18(11):1251-62 PMID: 15145825
  15. A switch in mitotic histone H4 lysine 20 methylation status is linked to M phase defects upon loss of HCF-1.
    Mol Cell. 2004 Jun 18;14(6):713-25 PMID: 15200950
  16. Dissociation of the dorsal-cactus complex and phosphorylation of the dorsal protein correlate with the nuclear localization of dorsal.
    J Cell Biol. 1993 Nov;123(3):523-34 PMID: 8227123
  17. Characterization of sequences associated with position-effect variegation at pericentric sites in Drosophila heterochromatin.
    Chromosoma. 1998 Nov;107(5):277-85 PMID: 9880760
Article Info
Journal
Genes & development
Abbr.
Genes Dev
ISSN
0890-9369
Published
2005-02-15
Epub
2005-00-28
Pages
431-5
Language
English
Region
United States
NLM ID
8711660
PMCID
PMC548943
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com