Expression of Xenopus XlSALL4 during limb development and regeneration

被引:35
作者
Neff, AW
King, MW
Harty, MW
Nguyen, T
Calley, J
Smith, RC
Mescher, AL
机构
[1] Indiana Univ, Med Sci Program, Sch Med, Bloomington, IN 47405 USA
[2] IUPUI, Ctr Regenerat Biol & Med, Indianapolis, IN USA
[3] Indiana Univ, Sch Med, Terre Haute Ctr Med Educ, Terre Haute, IN USA
[4] Eli Lilly & Co, Lilly Res Labs, Div Eli Lilly, Biotechnol Discovery Res, Indianapolis, IN 46285 USA
关键词
Xenopus laevis; limb; development; regeneration; SALL4;
D O I
10.1002/dvdy.20363
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The multi-C2H2 zinc-finger domain containing transcriptional regulators of the spalt (SAL) family plays important developmental regulatory roles. In a competitive subtractive hybridization screen of genes expressed in Xenopus laevis hindlimb regeneration blastemas, we identified a SAL family member that, by phylogenetic analysis, falls in the same clade as human SALL4 and have designated it as XlSALL4. Mutations of human SALL4 have been linked to Okihiro syndrome, which includes preaxial (anterior) limb defects. The expression pattern of XlSALL4 transcripts during normal forelimb and hindlimb development and during hindlimb regeneration at the regeneration-competent and regeneration-incompetent stages is temporally and regionally dynamic. We show for the first time that a SAL family member (XlSALL4) is expressed at the right place and time to play a role regulating both digit identity along the anterior/posterior axis and epimorphic limb regeneration. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:356 / 367
页数:12
相关论文
共 74 条
[1]   Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family [J].
Al-Baradie, R ;
Yamada, K ;
St Hilaire, C ;
Chan, WM ;
Andrews, C ;
McIntosh, N ;
Nakano, M ;
Martonyi, EJ ;
Raymond, WR ;
Okumura, S ;
Okihiro, MM ;
Engle, EC .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (05) :1195-1199
[2]   A novel spalt gene expressed in branchial arches affects the ability of cranial neural crest cells to populate sensory ganglia [J].
Barembaum, Meyer ;
Bronner-Fraser, Marianne .
NEURON GLIA BIOLOGY, 2004, 1 :57-63
[3]   Regulation of spalt expression in the Drosophila wing blade in response to the decapentaplegic signaling pathway [J].
Barrio, R ;
de Celis, JF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (16) :6021-6026
[4]   Levels of Gli3 repressor correlate with Bmp4 expression and apoptosis during limb development [J].
Bastida, MF ;
Delgado, MD ;
Wang, BL ;
Fallon, JF ;
Fernandez-Teran, M ;
Ros, MA .
DEVELOPMENTAL DYNAMICS, 2004, 231 (01) :148-160
[5]   SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism -: art. no. e113 [J].
Borozdin, W ;
Boehm, D ;
Leipoldt, M ;
Wilhelm, C ;
Reardon, W ;
Clayton-Smith, J ;
Becker, K ;
Mühlendyck, H ;
Winter, R ;
Giray, Ö ;
Silan, F ;
Kohlhase, J .
JOURNAL OF MEDICAL GENETICS, 2004, 41 (09) :e113
[6]   Novel mutations in the gene SALL4 provide further evidence for acro-renal-ocular and Okihiro syndromes being allelic entities, and extend the phenotypic spectrum -: art. no. e102 [J].
Borozdin, W ;
Wright, MJ ;
Hennekam, RCM ;
Hannibal, MC ;
Crow, YJ ;
Neumann, TE ;
Kohlhase, J .
JOURNAL OF MEDICAL GENETICS, 2004, 41 (08)
[7]   Embryonic expression of the murine homologue of SALL1, the gene mutated in Townes-Brocks syndrome [J].
Buck, A ;
Kispert, A ;
Kohlhase, J .
MECHANISMS OF DEVELOPMENT, 2001, 104 (1-2) :143-146
[8]   Expression of three spalt (sal) gene homologues in zebrafish embryos [J].
Camp, E ;
Hope, R ;
Kortschak, RD ;
Cox, TC ;
Lardelli, M .
DEVELOPMENT GENES AND EVOLUTION, 2003, 213 (01) :35-43
[9]  
Carinato ME, 2000, DEV DYNAM, V217, P377, DOI 10.1002/(SICI)1097-0177(200004)217:4<377::AID-DVDY5>3.0.CO
[10]  
2-U