Characterization of mouse Dach2, a homologue of Drosophila dachshund

被引:42
作者
Davis, RJ
Shen, WP
Sandler, YI
Heanue, TA
Mardon, G
机构
[1] Baylor Coll Med, Dept Pathol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Neurosci, Houston, TX 77030 USA
[3] Natl Inst Med Res, Dept Dev Neurobiol, London NW7 1AA, England
[4] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[5] Baylor Coll Med, Dept Ophthalmol, Houston, TX 77030 USA
[6] Baylor Coll Med, Program Dev Biol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
Dach1; Dach2; dachshund; eye; brain; limb; development;
D O I
10.1016/S0925-4773(01)00307-0
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Drosophila genes eyeless, eyes absent, sine oculis and dachshund cooperate as components of a network to control retinal determination. Vertebrate homologues of these genes have been identified and implicated in the control of cell fate. We present the cloning and characterization of mouse Dach2, a homologue of dachshund. In situ hybridization studies demonstrate Dach2 expression in embryonic nervous tissues, sensory organs and limbs. This pattern is similar to mouse Dach1, suggesting a partially redundant role for these genes during development. In addition, we determine that Dach2 expression in the forebrain of Pax6 mutants and dermamyotome of Pax3 mutants is not detectably altered. Finally, genetic mapping experiments place mouse Dach2 on the X chromosome between Xist and Esx1. The identification of human DACH2 sequences at Xq21 suggests a possible role for this gene in Allan-Herndon syndrome, Miles-Carpenter syndrome, X-linked cleft palate and/or Megalocornea. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:169 / 179
页数:11
相关论文
共 60 条
[1]   ALLAN-HERNDON-DUDLEY SYNDROME - CLINICAL AND LINKAGE STUDIES ON A 2ND FAMILY [J].
BIALER, MG ;
LAWRENCE, L ;
STEVENSON, RE ;
SILVERBERG, G ;
WILLIAMS, MK ;
ARENA, JF ;
LUBS, HA ;
SCHWARTZ, CE .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 43 (1-2) :491-497
[2]   THE EYES ABSENT GENE - GENETIC-CONTROL OF CELL-SURVIVAL AND DIFFERENTIATION IN THE DEVELOPING DROSOPHILA EYE [J].
BONINI, NM ;
LEISERSON, WM ;
BENZER, S .
CELL, 1993, 72 (03) :379-395
[3]  
Bonini NM, 1997, DEVELOPMENT, V124, P4819
[4]   EYA4, a novel vertebrate gene related to Drosophila eyes absent [J].
Borsani, G ;
DeGrandi, A ;
Ballabio, A ;
Bulfone, A ;
Bernard, L ;
Banfi, S ;
Gattuso, C ;
Mariani, M ;
Dixon, M ;
Donnai, D ;
Metcalfe, K ;
Winter, R ;
Robertson, M ;
Axton, R ;
Brown, A ;
van Heyningen, V ;
Hanson, I .
HUMAN MOLECULAR GENETICS, 1999, 8 (01) :11-23
[5]   Expression pattern of cSix3, a member of the Six/sine oculis family of transcription factors [J].
Bovolenta, P ;
Mallamaci, A ;
Puelles, L ;
Boncinelli, E .
MECHANISMS OF DEVELOPMENT, 1998, 70 (1-2) :201-203
[6]  
Caubit X, 1999, DEV DYNAM, V214, P66, DOI 10.1002/(SICI)1097-0177(199901)214:1<66::AID-DVDY7>3.0.CO
[7]  
2-7
[8]   X-LINKED MEGALOCORNEA - CLOSE LINKAGE TO DXS87 AND DXS94 [J].
CHEN, JD ;
MACKEY, D ;
FULLER, H ;
SERRAVALLE, S ;
OLSSON, J ;
DENTON, MJ .
HUMAN GENETICS, 1989, 83 (03) :292-294
[9]   Dachshund and eyes absent proteins form a complex and function synergistically to induce ectopic eye development in Drosophila [J].
Chen, R ;
Amoui, M ;
Zhang, ZH ;
Mardon, G .
CELL, 1997, 91 (07) :893-903
[10]  
Chen R, 1999, DEVELOPMENT, V126, P935