Identification of Epha4 enhancer required for segmental expression and the regulation by Mesp2

被引:59
作者
Nakajima, Yoshiro
Morimoto, Mitsuru
Takahashi, Yuki
Koseki, Haruhiko
Saga, Yumiko
机构
[1] Natl Inst Genet, Div Mammalian Dev, Mishima, Shizuoka 4118540, Japan
[2] RIKEN, Div Dev Genet, RCAI, Yokohama Inst,Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
来源
DEVELOPMENT | 2006年 / 133卷 / 13期
关键词
Mesp2; Epha4; somitogenesis; segmental border; Mox1; mouse;
D O I
10.1242/dev.02422
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Somites provide the basic body plan for metameric axial structures in vertebrates, and establish the segmental features through the sequential gene expression in the presomitic mesoderm (PSM). A crucial protein for segment border formation is the bHLH transcription factor Mesp2, the expression of which is restricted to the anterior PSM. A gene candidate that is activated by Mesp2 is Epha4, as its expression pattern resembles Mesp2 and is absent in Mesp2- null embryos. We have analyzed the enhancer region of Epha4, which is responsible for its expression in the anterior PSM, and identified an E-box containing region. Subsequent transgenic and transient luciferase analyses successfully determined that the presence of repeated E-box sequences is a minimum essential requirement for the expression in the anterior PSM. We also show that Mesp2 directly binds to the enhancer sequence of Epha4. Furthermore, the forced expression of Mesp2 in somitic cells results in the activation of Epha4 and repression of the caudal gene Uncx4.1, which may trigger the events leading to the formation of abnormal somites and rostralized vertebra. In addition, ectopic Mesp2 expression induces abnormally epithelialized structures, which support to the idea that Mesp2 induces the formation of segmental borders by activating genes that play roles in cellular epithelialization.
引用
收藏
页码:2517 / 2525
页数:9
相关论文
共 34 条
[1]   The transcription factor Sox9 is degraded by the ubiquitin-proteasome system and stabilized by a mutation in a ubiquitin-target site [J].
Akiyama, H ;
Kamitani, T ;
Yang, XH ;
Kandyil, R ;
Bridgewater, LC ;
Fellous, M ;
Mori-Akiyama, Y ;
de Crombrugghe, B .
MATRIX BIOLOGY, 2005, 23 (08) :499-505
[2]   Segmentation in vertebrates: clock and gradient finally joined [J].
Aulehla, A ;
Herrmann, BG .
GENES & DEVELOPMENT, 2004, 18 (17) :2060-2067
[3]   Eph/Ephrin signaling regulates the mesenchymal-to-epithelial transition of the paraxial mesoderm during somite morphogenesis [J].
Barrios, A ;
Poole, RJ ;
Durbin, L ;
Brennan, C ;
Holder, N ;
Wilson, SW .
CURRENT BIOLOGY, 2003, 13 (18) :1571-1582
[4]   Oscillations, clocks and segmentation [J].
Bessho, Y ;
Kageyama, R .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2003, 13 (04) :379-384
[5]   The T-box transcription factor Tbx18 maintains the separation of anterior and posterior somite compartments [J].
Bussen, M ;
Petry, M ;
Schuster-Gossler, K ;
Leitges, M ;
Gossler, A ;
Kispert, A .
GENES & DEVELOPMENT, 2004, 18 (10) :1209-1221
[6]   EDhA4 is required for cell adhesion and rhombomere-boundary formation in the zebrafish [J].
Cooke, JE ;
Kemp, HA ;
Moens, CB .
CURRENT BIOLOGY, 2005, 15 (06) :536-542
[7]  
Denetclaw WF, 2000, DEVELOPMENT, V127, P893
[8]   EphA4 (Sek1) receptor tyrosine kinase is required for the development of the corticospinal tract [J].
Dottori, M ;
Hartley, L ;
Galea, M ;
Paxinos, G ;
Polizzotto, M ;
Kilpatrick, T ;
Bartlett, PF ;
Murphy, M ;
Köntgen, F ;
Boyd, AW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :13248-13253
[9]   Eph signaling is required for segmentation and differentiation of the somites [J].
Durbin, L ;
Brennan, C ;
Shiomi, K ;
Cooke, J ;
Barrios, A ;
Shanmugalingam, S ;
Guthrie, B ;
Lindberg, R ;
Holder, N .
GENES & DEVELOPMENT, 1998, 12 (19) :3096-3109
[10]   A SIMPLE AND RAPID METHOD FOR GENERATING A DELETION BY PCR [J].
IMAI, Y ;
MATSUSHIMA, Y ;
SUGIMURA, T ;
TERADA, M .
NUCLEIC ACIDS RESEARCH, 1991, 19 (10) :2785-2785