Conservation of the MORF4 related gene family:: identification of a new chromo domain subfamily and novel protein motif

被引:82
作者
Bertram, MJ
Pereira-Smith, OM
机构
[1] Univ Alabama Birmingham, Dept Med, Div Endocrinol, Ctr Aging, Birmingham, AL 35209 USA
[2] Baylor Coll Med, Dept Cell Biol, Div Mol Virol, Roy M & Phyllis Gough Huffington Ctr Aging, Houston, TX 77030 USA
关键词
Mrg-15; Msl-3; senescence; histone acetylation; chromatin remodeling;
D O I
10.1016/S0378-1119(01)00372-9
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
The seven member, human MORF4 related gene (MRG) family was recently identified based on the ability of Mortality factor on chromosome 4 (MORF4) to induce replicative senescence in immortal cell lines assigned to complementation group B (Bertram et al., 1999, Mel. Cell Biol. 19, 1;179- 1485). Initial computer based similarity searches identified human retinoblastoma binding protein 1 (RBP-1), Drosophila melanognster male specific lethal-3 (Msl-3), S, pombe altered polarity-13 (Alp13) and S. cerevisiae Eaf3p, a component of the yeast NuA4 HAT complex (Galarneau et al,, 2000. Mel. Cell 5, 927-937), as having similarity to the human MRG protein family. This suggested that the MRG family might be found in multiple species, and analysis of other homologs would provide functional and evolutionary insights into this gene family. Here, we report that MRG family members are present in twenty-three species based on molecular assays and sequence similarity searches. The new family members were divided into two groups based on similarity to the predominant human MRC family members, MRG15 and MRGX. The family members similar to MRC 15 define a new, highly conserved subsection of the chrome domain superfamily. Additionally, conservation in the C-terminal two thirds of all the MRG family members and the Drosophila and human MSL-3 proteins defines a new protein domain, the MRG domain. These results indicate a highly conserved role for the MRG family in transcriptional regulation via chromatin remodeling by histone acetylation. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:111 / 121
页数:11
相关论文
共 40 条
[1]
NuA4, an essential transcription adaptor/histone H4 acetyltransferase complex containing Esa1p and the ATM-related cofactor Tra1p [J].
Allard, S ;
Utley, RT ;
Savard, J ;
Clarke, A ;
Grant, P ;
Brandl, CJ ;
Pillus, L ;
Workman, JL ;
Côté, J .
EMBO JOURNAL, 1999, 18 (18) :5108-5119
[2]
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]
[Anonymous], 2000, PHYLIP (Phylogeny Inference Package)
[4]
Structure of the chromatin binding (chromo) domain from mouse modifier protein 1 [J].
Ball, LJ ;
Murzina, NV ;
Broadhurst, RW ;
Raine, ARC ;
Archer, SJ ;
Stott, FJ ;
Murzin, AG ;
Singh, PB ;
Domaille, PJ ;
Laue, ED .
EMBO JOURNAL, 1997, 16 (09) :2473-2481
[5]
Bateman A, 2004, NUCLEIC ACIDS RES, V32, pD138, DOI [10.1093/nar/gkp985, 10.1093/nar/gkh121, 10.1093/nar/gkr1065]
[6]
Bertram MJ, 1999, MOL CELL BIOL, V19, P1479
[7]
The structure of mouse HP1 suggests a unique mode of single peptide recognition by the shadow chrome domain dimer [J].
Brasher, SV ;
Smith, BO ;
Fogh, RH ;
Nietlispach, D ;
Thiru, A ;
Nielsen, PR ;
Broadhurst, RW ;
Ball, LJ ;
Murzina, NV ;
Laue, ED .
EMBO JOURNAL, 2000, 19 (07) :1587-1597
[8]
CAO J, 2000, HUMAN BREAST CARCINO
[9]
Recognition of an epitope of a breast cancer antigen by human antibody [J].
Cao, JN ;
Gao, TW ;
Giuliano, AE ;
Irie, RF .
BREAST CANCER RESEARCH AND TREATMENT, 1999, 53 (03) :279-290
[10]
The Drosophila Fab-7 chromosomal element conveys epigenetic inheritance during mitosis and meiosis [J].
Cavalli, G ;
Paro, R .
CELL, 1998, 93 (04) :505-518