Krox-20 patterns the hindbrain through both cell autonomous and non cell-autonomous mechanisms

被引:93
作者
Giudicelli, F [1 ]
Taillebourg, E [1 ]
Charnay, P [1 ]
Gilardi-Hebenstreit, P [1 ]
机构
[1] Ecole Normale Super, INSERM, U368, F-75230 Paris 05, France
关键词
hindbrain; rhombomere; segmentation; Krox-20; Hox; Eph; kreisler;
D O I
10.1101/gad.189801
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Krox-20 gene encodes a zinc finger transcription factor, which has been shown previously, by targeted inactivation in the mouse, to be required for the development of rhombomeres (r) 3 and 5 in the segmented embryonic hindbrain. In the present work, Krox-20 was expressed ectopically in the developing chick hindbrain by use of electroporation. We demonstrate that Krox-20 expression is sufficient to confer odd-numbered rhombomere characteristics to r2, r4, and r6 cells, presumably in a cell-autonomous manner. Therefore, Krox-20, appears as the major determinant of odd-numbered identity within the hindbrain. In addition, we provide evidence for the existence of a non cell-autonomous autoactivation mechanism allowing recruitment of Krox-20-positive cells from even-numbered territories by neighboring Krox-20-expressing cells. On the basis of these observations, we propose that Krox-20 regulates multiple, intertwined steps in segmental patterning: Initial activation of Krox-20 in a few cells leads to the segregation, homogenization, and possibly expansion of territories to which Krox-20 in addition confers an odd-numbered identity.
引用
收藏
页码:567 / 580
页数:14
相关论文
共 53 条
[31]   Control of cell behaviour by signalling through Eph receptors and ephrins [J].
Mellitzer, G ;
Xu, QL ;
Wilkinson, DG .
CURRENT OPINION IN NEUROBIOLOGY, 2000, 10 (03) :400-408
[32]   Eph receptors and ephrins restrict cell intermingling and communication [J].
Mellitzer, G ;
Xu, QL ;
Wilkinson, DG .
NATURE, 1999, 400 (6739) :77-81
[33]   IRES-dependent second gene expression is significantly lower than cap-dependent first gene expression in a bicistronic vector [J].
Mizuguchi, H ;
Xu, ZL ;
Ishii-Watabe, A ;
Uchida, E ;
Hayakawa, T .
MOLECULAR THERAPY, 2000, 1 (04) :376-382
[34]  
MURPHY P, 1991, DEVELOPMENT, V111, P61
[35]  
NIETO MA, 1991, DEVELOPMENT, P59
[36]  
Nonchev S, 1996, DEVELOPMENT, V122, P543
[37]  
PRINCE V, 1994, DEVELOPMENT, V120, P911
[38]  
SAJJADI FG, 1993, ONCOGENE, V8, P1807
[39]   How to build a vertebrate hindbrain. Lessons from genetics [J].
Schneider-Maunoury, S ;
Gilardi-Hebenstreit, P ;
Charnay, P .
COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE III-SCIENCES DE LA VIE-LIFE SCIENCES, 1998, 321 (10) :819-834
[40]   DISRUPTION OF KROX-20 RESULTS IN ALTERATION OF RHOMBOMERE-3 AND RHOMBOMERE-5 IN THE DEVELOPING HINDBRAIN [J].
SCHNEIDERMAUNOURY, S ;
TOPILKO, P ;
SEITANIDOU, T ;
LEVI, G ;
COHENTANNOUDJI, M ;
POURNIN, S ;
BABINET, C ;
CHARNAY, P .
CELL, 1993, 75 (06) :1199-1214