Histone H2BK123 monoubiquitination is the critical determinant for H3K4 and H3K79 trimethylation by COMPASS and Dot1

被引:104
作者
Nakanishi, Shima [1 ]
Lee, Jung Shin [1 ]
Gardner, Kathryn E. [2 ]
Gardner, Jennifer M. [1 ]
Takahashi, Yoh-hei [1 ]
Chandrasekharan, Mahesh B. [3 ]
Sun, Zu-Wen [3 ]
Osley, Mary Ann [4 ]
Strahl, Brian D. [2 ]
Jaspersen, Sue L. [1 ,5 ]
Shilatifard, Ali [1 ]
机构
[1] Stowers Inst Med Res, Kansas City, MO 64110 USA
[2] Univ N Carolina, Dept Biochem & Biophys, Lineberger Comprehens Canc Ctr, Sch Med, Chapel Hill, NC 27599 USA
[3] Vanderbilt Univ, Dept Biochem, Vanderbilt Ingram Canc Ctr, Sch Med, Nashville, TN 37232 USA
[4] Dept Mol Genet & Microbiol, Albuquerque, NM 87131 USA
[5] Univ Kansas, Med Ctr, Dept Mol & Integrat Physiol, Kansas City, KS 66160 USA
基金
美国国家卫生研究院;
关键词
RNA-POLYMERASE-II; H2B UBIQUITYLATION; GENE-EXPRESSION; TRANSCRIPTIONAL ACTIVATION; METHYLATION; UBIQUITINATION; CHROMATIN; COMPLEX; RAD6; ELONGATION;
D O I
10.1083/jcb.200906005
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Histone H2B monoubiquitination by Rad6/Bre1 is required for the trimethylation of both histone H3K4 and H3K79 by COMPASS and Dot1 methyl-transferases, respectively. The dependency of methylation at H3K4 and H3K79 on the monoubiquitination of H2BK123 was recently challenged, and extragenic mutations in the strain background used for previous studies or epitopetagged proteins were suggested to be the sources of this discrepancy. In this study, we show that H3K4 and H3K79 methylation is solely dependent on H2B monoubiquitination regardless of any additional alteration to the H2B sequence or genome. Furthermore, we report that Y131, one of the yeast histone H2A/H2B shuffle strains widely used for the last decade in the field of chromatin and transcription biology, carries a wildtype copy of each of the HTA2 and HTB2 genes under the GAL1/10 promoter on chromosome II. Therefore, we generated the entire histone H2A and H2B alanine-scanning mutant strains in another background, which does not express wildtype histones.
引用
收藏
页码:371 / 377
页数:7
相关论文
共 24 条
[1]   Gene silencing -: Trans-histone regulatory pathway in chromatin [J].
Briggs, SD ;
Xiao, TJ ;
Sun, ZW ;
Caldwell, JA ;
Shabanowitz, J ;
Hunt, DF ;
Allis, CD ;
Strahl, BD .
NATURE, 2002, 418 (6897) :498-498
[2]   Methylation of histone H3 by COMPASS requires ubiquitination of histone H2B by Rad6 [J].
Dover, J ;
Schneider, J ;
Tawiah-Boateng, MA ;
Wood, A ;
Dean, K ;
Johnston, M ;
Shilatifard, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (32) :28368-28371
[3]   Methylation of H3 K4 and K79 is not strictly dependent on H2B K123 ubiquitylation [J].
Foster, Elinor R. ;
Downs, Jessica A. .
JOURNAL OF CELL BIOLOGY, 2009, 184 (05) :631-638
[4]   Transcriptional activation via sequential histone H2B ubiquitylation and deubiquitylation, mediated by SAGA-associated Ubp8 [J].
Henry, KW ;
Wyce, A ;
Lo, WS ;
Duggan, LJ ;
Emre, NCT ;
Kao, CF ;
Pillus, L ;
Shilatifard, A ;
Osley, MA ;
Berger, SL .
GENES & DEVELOPMENT, 2003, 17 (21) :2648-2663
[5]   A conserved RING finger protein required for histone H2B monoubiquitination and cell size control [J].
Hwang, WW ;
Venkatasubrahmanyam, S ;
Ianculescu, AG ;
Tong, A ;
Boone, C ;
Madhani, HD .
MOLECULAR CELL, 2003, 11 (01) :261-266
[6]   Rad6 plays a role in transcriptional activation through ubiquitylation of histone H2B [J].
Kao, CF ;
Hillyer, C ;
Tsukuda, T ;
Henry, K ;
Berger, S ;
Osley, MA .
GENES & DEVELOPMENT, 2004, 18 (02) :184-195
[7]   RAD6-Mediated Transcription-Coupled H2B Ubiquitylation Directly Stimulates H3K4 Methylation in Human Cells [J].
Kim, Jaehoon ;
Guermah, Mohamed ;
McGinty, Robert K. ;
Lee, Jung-Shin ;
Tang, Zhanyun ;
Milne, Thomas A. ;
Shilatifard, Ali ;
Muir, Tom W. ;
Roeder, Robert G. .
CELL, 2009, 137 (03) :459-471
[8]   CHROMATIN STRUCTURE - REPEATING UNIT OF HISTONES AND DNA [J].
KORNBERG, RD .
SCIENCE, 1974, 184 (4139) :868-871
[9]   Twenty-five years of the nucleosome, fundamental particle of the eukaryote chromosome [J].
Kornberg, RD ;
Lorch, YL .
CELL, 1999, 98 (03) :285-294
[10]   COMPASS, a histone H3 (lysine 4) methyltransferase required for telomeric silencing of gene expression [J].
Krogan, NJ ;
Dover, J ;
Khorrami, S ;
Greenblatt, JF ;
Schneider, J ;
Johnston, M ;
Shilatifard, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (13) :10753-10755