Heterochromatin and tri-methylated lysine 20 of histone H4 in animals

被引:209
作者
Kourmouli, N
Jeppesen, P
Mahadevhaiah, S
Burgoyne, P
Wu, R
Gilbert, DM
Bongiorni, S
Prantera, G
Fanti, L
Pimpinelli, S
Shi, W
Fundele, R
Singh, PB [1 ]
机构
[1] Roslin Inst, Div Gene Express & Dev, Nucl Reprogramming Lab, Roslin EH25 9PS, Midlothian, Scotland
[2] Natl Inst Med Res, Lab Dev Genet, London NW7 1AA, England
[3] SUNY Upstate Med Univ, Dept Biochem & Mol Biol, Syracuse, NY 13210 USA
[4] Univ Tuscia, Dipartimento Agrobiol & Agrochim, I-01100 Viterbo, Italy
[5] Univ Roma La Sapienza, Dipartimento Genet & Biol Mol, I-00185 Rome, Italy
[6] Uppsala Univ, Dept Genet & Dev, S-75236 Uppsala, Sweden
关键词
heterochromatin; epigenetics; histone code;
D O I
10.1242/jcs.01238
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tri-methylated lysine 20 on histone H4 (Me(3)K20H4) is a marker of constitutive heterochromatin in murine interphase and metaphase cells. Heterochromatin marked by Me(3)K20H4 replicates late during S phase of the cell cycle. Serum starvation increases the number of cells that exhibit high levels of Me(3)K20H4 at constitutive heterochromatin. Me(3)K20H4 is also present at the centromeric heterochromatin of most meiotic chromosomes during spermatogenesis and at the pseudoautosomal region, as well as at some telomeres. It is not present on the XY-body. During murine embryogenesis the maternal pronucleus contains Me(3)K20H4; Me(3)K20H4 is absent from the paternal pronucleus. On Drosophila polytene chromosomes Me(3)K20H4 is present in a 'punctate pattern' at many chromosomal bands, including the chromocenter. In coccids it is present on the facultatively heterochromatinised paternal chromosome set. We also present evidence that Me(3)K20H4 is dependent upon H3-specific Suv(3)9 histone methyltransferase activity, suggesting that there may be 'epigenetic cross-talk' between histones H3 and H4.
引用
收藏
页码:2491 / 2501
页数:11
相关论文
共 54 条
[1]   Embryonic inheritance of the chromatin organisation of the imprinted H19 domain in mouse spermatozoa [J].
Banerjee, S ;
Singh, PB ;
Rasberry, C ;
Cattanach, BM .
MECHANISMS OF DEVELOPMENT, 2000, 90 (02) :217-226
[2]   Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain [J].
Bannister, AJ ;
Zegerman, P ;
Partridge, JF ;
Miska, EA ;
Thomas, JO ;
Allshire, RC ;
Kouzarides, T .
NATURE, 2001, 410 (6824) :120-124
[3]   A MORPHOLOGICAL DISTINCTION BETWEEN NEURONES OF THE MALE AND FEMALE, AND THE BEHAVIOUR OF THE NUCLEOLAR SATELLITE DURING ACCELERATED NUCLEOPROTEIN SYNTHESIS [J].
BARR, ML ;
BERTRAM, EG .
NATURE, 1949, 163 (4148) :676-677
[4]   Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes [J].
Boggs, BA ;
Cheung, P ;
Heard, E ;
Spector, DL ;
Chinault, AC ;
Allis, CD .
NATURE GENETICS, 2002, 30 (01) :73-76
[5]  
Bongiorni S, 1999, GENETICS, V151, P1471
[6]  
Bongiorni S, 2001, DEVELOPMENT, V128, P3809
[7]   Dynamic organization of DNA replication in one-cell mouse embryos: Relationship to transcriptional activation [J].
BouniolBaly, C ;
Nguyen, E ;
Besombes, D ;
Debey, P .
EXPERIMENTAL CELL RESEARCH, 1997, 236 (01) :201-211
[8]   HETEROCHROMATIC CHROMOSOMES IN COCCIDS - PROCESS OF HETEROCHROMATIZATION + FUNCTION OF HETEROCHROMATIN IN COCCID INSECTS ARE REVIEWED [J].
BROWN, SW ;
NUR, U .
SCIENCE, 1964, 145 (362) :130-&
[9]   HETEROCHROMATIN [J].
BROWN, SW .
SCIENCE, 1966, 151 (3709) :417-+
[10]   Chromatin of the Barr body: histone and non-histone proteins associated with or excluded from the inactive X chromosome [J].
Chadwick, BP ;
Willard, HF .
HUMAN MOLECULAR GENETICS, 2003, 12 (17) :2167-2178