Phosphorylation of histone H3 at Thr3 is part of a combinatorial pattern that marks and configures mitotic chromatin

被引:48
作者
Markaki, Yolanda [1 ]
Christogianni, Anastasia [1 ]
Politou, Anastasia S. [2 ]
Georgatos, Spyros D. [1 ]
机构
[1] Univ Ioannina, Sch Med, Biol Lab, GR-45110 Ioannina, Greece
[2] Univ Ioannina, Sch Med, Biol Chem Lab, Stem Cell & Chromatin Grp, GR-45110 Ioannina, Greece
关键词
Chromatin; Histones; Phosphorylation; MITOSIS-SPECIFIC PHOSPHORYLATION; CHROMOSOME CONDENSATION; CENTROMERIC CHROMATIN; MASS-SPECTROMETRY; AURORA-B; KINASE; HETEROCHROMATIN; METHYLATION; BINDING; HASPIN;
D O I
10.1242/jcs.043810
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have previously shown that histone H3 is transiently phosphorylated at Thr3 during mitosis. Extending these studies, we now report that phosphorylated Thr3 is always in cis to trimethylated Lys4 and dimethylated Arg8, forming a new type of combinatorial modification, which we have termed PMM. PMM-marked chromatin emerges at multiple, peripheral sites of the prophase nucleus, then forms distinct clusters at the centric regions of metaphase chromosomes, and finally spreads (as it wanes) to the distal areas of segregating chromatids. The characteristic prophase pattern can be reproduced by expressing ectopically the kinase haspin at interphase, suggesting that the formation of the PMM signature does not require a pre-existing mitotic environment. On the other hand, the 'dissolution' and displacement of PMM clusters from a centric to distal position can be induced by partial dephosphorylation or chromosome unravelling, indicating that these changes reflect the regulated grouping and scrambling of PMM subdomains during cell division. Formation of PMM is prevented by haspin knockdown and leads to delayed exit from mitosis. However, PMM-negative cells do not exhibit major chromosomal defects, suggesting that the local structures formed by PMM chromatin may serve as a 'licensing system' that allows quick clearance through the metaphase-anaphase checkpoint.
引用
收藏
页码:2809 / 2819
页数:11
相关论文
共 33 条
[1]   Deciphering the transcriptional histone acetylation code for a human gene [J].
Agalioti, T ;
Chen, GY ;
Thanos, D .
CELL, 2002, 111 (03) :381-392
[2]   Role of histone tails in chromatin folding revealed by a mesoscopic oligonucleosome model [J].
Arya, Gaurav ;
Schlick, Tamar .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (44) :16236-16241
[3]   A bivalent chromatin structure marks key developmental genes in embryonic stem cells [J].
Bernstein, BE ;
Mikkelsen, TS ;
Xie, XH ;
Kamal, M ;
Huebert, DJ ;
Cuff, J ;
Fry, B ;
Meissner, A ;
Wernig, M ;
Plath, K ;
Jaenisch, R ;
Wagschal, A ;
Feil, R ;
Schreiber, SL ;
Lander, ES .
CELL, 2006, 125 (02) :315-326
[4]   Conserved organization of centromeric chromatin in flies and humans [J].
Blower, MD ;
Sullivan, BA ;
Karpen, GH .
DEVELOPMENTAL CELL, 2002, 2 (03) :319-330
[5]   The role of Drosophila CID in kinetochore formation, cell-cycle progression and heterochromatin interactions [J].
Blower, MD ;
Karpen, GH .
NATURE CELL BIOLOGY, 2001, 3 (08) :730-739
[6]   Signaling to chromatin through histone modifications [J].
Cheung, P ;
Allis, CD ;
Sassone-Corsi, P .
CELL, 2000, 103 (02) :263-271
[7]   Rapid phosphorylation of histone H2A.X following ionotropic glutamate receptor activation [J].
Crowe, Samantha L. ;
Movsesyan, Vilen A. ;
Jorgensen, Timothy J. ;
Kondratyev, Alexei .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2006, 23 (09) :2351-2361
[8]   The kinase haspin is required for mitotic histone H3 Thr 3 phosphorylation and normal metaphase chromosome alignment [J].
Dai, J ;
Sultan, S ;
Taylor, SS ;
Higgins, JMG .
GENES & DEVELOPMENT, 2005, 19 (04) :472-488
[9]   Regulation of mitotic chromosome cohesion by Haspin and Aurora B [J].
Dai, Jun ;
Sullivan, Beth A. ;
Higgins, Jonathan M. G. .
DEVELOPMENTAL CELL, 2006, 11 (05) :741-750
[10]   Core histone N-termini play an essential role in mitotic chromosome condensation [J].
de la Barre, AE ;
Gerson, V ;
Gout, S ;
Creaven, M ;
Allis, CD ;
Dimitrov, S .
EMBO JOURNAL, 2000, 19 (03) :379-391