Zic4, a zinc-finger transcription factor, is expressed in the developing mouse nervous system

被引:35
作者
Gaston-Massuet, C
Henderson, DJ
Greene, NDE
Copp, AJ
机构
[1] UCL, Inst Child Hlth, Neural Dev Unit, London WC1N 1EH, England
[2] Univ Newcastle Upon Tyne, Inst Human Genet, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
基金
英国惠康基金;
关键词
Zic genes; gene expression; neural development; mouse embryo; zine-finger transcription factor; neural tube;
D O I
10.1002/dvdy.20417
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
Zic genes comprise a family of transcription factors, characterized by the presence of a zinc-finger domain containing two cysteines and two histidines (C2-112). Whereas the embryonic expression patterns of Zic1,2, 3, and 5 have been described in detail, Zic4 has not yet received close attention. We studied the expression of Zic4 by in situ hybridization during mouse embryogenesis. Zic4 mRNA was first detected at low intensity at embryonic day (E) 9 and, by E10.5, expression was up-regulated in the dorsal midline of the forebrain with a strong, expanded expression domain at the boundary between the diencephalon and telencephalon, the septum, and the lamina terminalis. The choroid plexus of the third ventricle expresses Zic4, as does the dorsal part of the spinal neural tube, excluding the roof plate. The dorsal sclerotome and the dorsomedial lip of the dermomyotome also express Zic4 whereas dorsal root ganglia are negative, At E12.5, Zic4 continues to be expressed in the midline of the forebrain and in the dorsal spinal neural tube. Postnatally, Zic4 is expressed in the granule cells of the postnatal day 2 cerebellum, and in the periventricular thalamus and anterior end of the superior colliculus. We conclude that Zic4 has an expression pattern distinct from, but partly overlapping with, other members of the Zic gene family. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:1110 / 1115
页数:6
相关论文
共 28 条
[1]   Zic2 controls cerebellar development in cooperation with Zic1 [J].
Aruga, J ;
Inoue, T ;
Hoshino, J ;
Mikoshiba, K .
JOURNAL OF NEUROSCIENCE, 2002, 22 (01) :218-225
[2]  
Aruga J, 1998, J NEUROSCI, V18, P284
[3]  
ARUGA J, 1994, J NEUROCHEM, V63, P1880
[4]   Identification and characterization of Zic4, a new member of the mouse Zic gene family [J].
Aruga, J ;
Yozu, A ;
Hayashizaki, Y ;
Okazaki, Y ;
Chapman, VM ;
Mikoshiba, K .
GENE, 1996, 172 (02) :291-294
[5]   The mouse Zic gene family - Homologues of the Drosophila pair-rule gene odd-paired [J].
Aruga, J ;
Nagai, T ;
Tokuyama, T ;
Hayashizaki, Y ;
Okazaki, Y ;
Chapman, VM ;
Mikoshiba, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (02) :1043-1047
[6]  
BREITSCHOPF H, 1992, ACTA NEUROPATHOL, V84, P581
[7]   Holoprosencephaly due to mutations in ZIC2:: alanine tract expansion mutations may be caused by parental somatic recombination [J].
Brown, LY ;
Odent, S ;
David, V ;
Blayau, M ;
Dubourg, C ;
Apacik, C ;
Delgado, MA ;
Ha, BD ;
Reynolds, JF ;
Sommer, A ;
Wieczorek, D ;
Brown, SA ;
Muenke, M .
HUMAN MOLECULAR GENETICS, 2001, 10 (08) :791-796
[8]   Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired [J].
Brown, SA ;
Warburton, D ;
Brown, LY ;
Yu, CY ;
Roeder, ER ;
Stengel-Rutkowski, S ;
Hennekam, RCM ;
Muenke, M .
NATURE GENETICS, 1998, 20 (02) :180-183
[9]   The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locus [J].
Carrel, T ;
Purandare, SM ;
Harrison, W ;
Elder, F ;
Fox, T ;
Casey, B ;
Herman, GE .
HUMAN MOLECULAR GENETICS, 2000, 9 (13) :1937-1942
[10]  
Christ B, 1998, ANAT EMBRYOL, V197, P1