Dlx5, the mouse homologue of the human-imprinted DLX5 gene, is biallelically expressed in the mouse brain

被引:33
作者
Kimura, MI
Kazuki, Y
Kashiwagi, A
Kai, Y
Abe, S
Barbieri, O
Levi, G
Oshimura, M
机构
[1] Tottori Univ, Grad Sch Med Sci, Inst Regenerat Med & Biofunct, Yonago, Tottori 6838503, Japan
[2] Tottori Univ, Fac Med, Lab Anim Res Ctr, Yonago, Tottori 683, Japan
[3] Univ Genoa, CBA, IST, Dept Oncol Biol & Genet,Transgenic Unit, I-16132 Genoa, Italy
[4] Museum Natl Hist Nat, CNRS, UMR5166, F-75231 Paris 05, France
关键词
DLX5; Dlx5; imprinting; brain; mouse chromosome 6; maternally expressed gene;
D O I
10.1007/s10038-004-0139-2
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The mouse Dlx5 gene encodes a distal-less-related DNA-binding homeobox protein first expressed during early embryonic development in anterior regions of mouse embryo and is located on chromosome 6, which is the syntenic region to the human chromosome 7q21-q31 imprinting cluster. Recently, its human homologue, DLX5, was identified to be imprinted and maternally expressed, at least in normal human lymphoblasts and in brain tissues. In our study, we analyzed the imprinting status of mouse Dlx5 by RT-PCR, first in the F1 of a reciprocal cross between two different mouse strains, and second in heterozygous Dlx5 mutant mice. Both approaches revealed that mouse Dlx5 followed a biallelic pattern of expression in brain tissue and in testis. Our findings suggest that the Dlx5 gene escapes genomic imprinting, at least in mice of certain genetic backgrounds.
引用
收藏
页码:273 / 277
页数:5
相关论文
共 11 条
[1]  
Acampora D, 1999, DEVELOPMENT, V126, P3795
[2]  
Depew MJ, 1999, DEVELOPMENT, V126, P3831
[3]   Strain-dependent developmental relaxation of imprinting of an endogenous mouse gene, Kvlqt1 [J].
Jiang, S ;
Hemann, MA ;
Lee, MP ;
Feinberg, AP .
GENOMICS, 1998, 53 (03) :395-399
[4]  
Kugoh H, 1999, DNA Res, V6, P165, DOI 10.1093/dnares/6.3.165
[5]   A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome [J].
Meguro, M ;
Kashiwagi, A ;
Mitsuya, K ;
Nakao, M ;
Kondo, I ;
Saitoh, S ;
Oshimura, M .
NATURE GENETICS, 2001, 28 (01) :19-20
[6]   Mouse model of split hand/foot malformation type I [J].
Merlo, GR ;
Paleari, L ;
Mantero, S ;
Genova, F ;
Beverdam, A ;
Palmisano, GL ;
Barbieri, O ;
Levi, G .
GENESIS, 2002, 33 (02) :97-101
[7]   A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids [J].
Okita, C ;
Meguro, M ;
Hoshiya, H ;
Haruta, M ;
Sakamoto, YK ;
Oshimura, M .
GENOMICS, 2003, 81 (06) :556-559
[8]   Stage-specific expression of Dix-5 during osteoblast differentiation: Involvement in regulation of osteocalcin gene expression [J].
Ryoo, HM ;
Hoffmann, HM ;
Beumer, T ;
Frenkel, B ;
Towler, DA ;
Stein, GS ;
Stein, JL ;
vanWijnen, AJ ;
Lian, JB .
MOLECULAR ENDOCRINOLOGY, 1997, 11 (11) :1681-1694
[9]   ORTHOPEDIA, A NOVEL HOMEOBOX-CONTAINING GENE EXPRESSED IN THE DEVELOPING CNS OF BOTH MOUSE AND DROSOPHILA [J].
SIMEONE, A ;
DAPICE, MR ;
NIGRO, V ;
CASANOVA, J ;
GRAZIANI, F ;
ACAMPORA, D ;
AVANTAGGIATO, V .
NEURON, 1994, 13 (01) :83-101
[10]   CLONING AND CHARACTERIZATION OF 2 MEMBERS OF THE VERTEBRATE DLX GENE FAMILY [J].
SIMEONE, A ;
ACAMPORA, D ;
PANNESE, M ;
DESPOSITO, M ;
STORNAIUOLO, A ;
GULISANO, M ;
MALLAMACI, A ;
KASTURY, K ;
DRUCK, T ;
HUEBNER, K ;
BONCINELLI, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (06) :2250-2254