MBD3L1 and MBD3L2, two new proteins homologous to the methyl-CpG-binding proteins MBD2 and MBD3:: Characterization of MBD3L1 as a testis-specific transcriptional repressor

被引:33
作者
Jiang, CL
Jin, SG
Lee, DH
Lan, ZJ
Xu, XP
O'Connor, TR
Szabó, PE
Mann, JR
Cooney, AJ
Pfeifer, GP [1 ]
机构
[1] City Hope Natl Med Ctr, Beckman Res Inst, Dept Biol, Duarte, CA 91010 USA
[2] Baylor Coll Med, Dept Mol & Cellular Biol, Houston, TX 77030 USA
关键词
methyl CpG binding proteins; spermatogenesis; repressor; DNA methylation; testis;
D O I
10.1006/geno.2002.7001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Methylation of cytosines at CpG dinucleotides is essential for mammalian development. MeCP2, MBD1, MBD2, MBD3, and MBD4 comprise a family of proteins that contain a methyl-CpG binding domain (MBD). Except for MBD4, these proteins are involved in gene silencing imposed by methylated DNA. We have identified a human gene that codes for a protein that is 42% identical to MBD3 and 38% identical to MBD2 but lacks the methyl-CpG binding domain. The recombinant protein does not bind to methylated DNA in vitro. The corresponding mouse Mbd3L1 gene was also cloned. The MBD3L1 gene is expressed specifically in testis. During spermatogenesis, expression of MBD3L1 is observed only in round spermatids, suggesting a role for the gene product in the postmeiotic stages of male germ cell development. The MBD3L1 protein is localized to discrete areas in the nucleus and contains an N-terminal transcriptional repression domain. This repression is independent of histone deacetylase inhibition. A homologue of MBD3L1, MBD3L2, was also identified and cloned. Expression of MBD3L2 was found in germ cell tumors and some somatic tissues. These novel proteins may function as counterparts of MBD2 and/or MBD3 in developmental stage-specific transcriptional repression.
引用
收藏
页码:621 / 629
页数:9
相关论文
共 32 条
[1]   Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer [J].
Baylin, SB ;
Esteller, M ;
Rountree, MR ;
Bachman, KE ;
Schuebel, K ;
Herman, JG .
HUMAN MOLECULAR GENETICS, 2001, 10 (07) :687-692
[2]  
BELLVE AR, 1993, METHOD ENZYMOL, V225, P84
[3]   Creation of genomic methylation patterns [J].
Bestor, TH ;
Tycko, B .
NATURE GENETICS, 1996, 12 (04) :363-367
[4]   GENE NUMBER, NOISE-REDUCTION AND BIOLOGICAL COMPLEXITY [J].
BIRD, AP .
TRENDS IN GENETICS, 1995, 11 (03) :94-100
[5]   The minimal repression domain of MBD2b overlaps with the methyl-CpG-binding domain and binds directly to Sin3A [J].
Boeke, J ;
Ammerpohl, O ;
Kegel, S ;
Moehren, U ;
Renkawitz, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (45) :34963-34967
[6]   Packaging paternal chromosomes with protamine [J].
Braun, RE .
NATURE GENETICS, 2001, 28 (01) :10-12
[7]   Genes on human chromosome 19 show extreme divergence from the mouse orthologs and a high GC content [J].
Castresana, J .
NUCLEIC ACIDS RESEARCH, 2002, 30 (08) :1751-1756
[8]   DNA METHYLATION AND GENE ACTIVITY [J].
CEDAR, H .
CELL, 1988, 53 (01) :3-4
[9]   HYPERACETYLATION OF HISTONE H-4 PROMOTES CHROMATIN DECONDENSATION PRIOR TO HISTONE REPLACEMENT BY PROTAMINES DURING SPERMATOGENESIS IN RAINBOW-TROUT [J].
CHRISTENSEN, ME ;
RATTNER, JB ;
DIXON, GH .
NUCLEIC ACIDS RESEARCH, 1984, 12 (11) :4575-4592
[10]   A component of the transcriptional repressor MeCP1 shares a motif with DNA methyltransferase and HRX proteins [J].
Cross, SH ;
Meehan, RR ;
Nan, XS ;
Bird, A .
NATURE GENETICS, 1997, 16 (03) :256-259