Mouse Eya genes are expressed during limb tendon development and encode a transcriptional activation function

被引:145
作者
Xu, PX
Cheng, J
Epstein, JA
Maas, RL
机构
[1] HARVARD UNIV, SCH MED,BRIGHAM & WOMENS HOSP,DEPT MED,DIV GENET, BOSTON, MA 02115 USA
[2] HOWARD HUGHES MED INST, BOSTON, MA 02115 USA
关键词
eyes absent; Splotch; tendon patterning; transcription factor;
D O I
10.1073/pnas.94.22.11974
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Vertebrate limb tendons are derived from connective cells of the lateral plate mesoderm, Some of the developmental steps leading to the formation of vertebrate limb tendons have been previously identified; however, the molecular mechanisms responsible for tendinous patterning and maintenance during embryogenesis are largely unknown, The eyes absent (eya) gene of Drosophila encodes a novel nuclear protein of unknown molecular function, Here we show that Eya1 and Eya2, two mouse homologues of Drosophila eya, are expressed initially during limb development in connective tissue precursor cells, Later in limb development, Eya1 and Eya2 expression is associated with cell condensations that form different sets of limb tendons, Eya1 expression is largely restricted to flexor tendons, while Eya2 is expressed in the extensor tendons and ligaments of the phalangeal elements of the limb. These data suggest that Eya genes participate in the patterning of the distal tendons of the limb, To investigate the molecular functions of the Eya gene products, we have analyzed whether the highly divergent PST (proline-serine-threonine)-rich N-terminal regions of Eya1-3 function as transactivation domains, Our results demonstrate that Ega gene products can act as transcriptional activators, and they support a role for this molecular function in connective tissue patterning.
引用
收藏
页码:11974 / 11979
页数:6
相关论文
共 32 条
[1]   A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family [J].
Abdelhak, S ;
Kalatzis, V ;
Heilig, R ;
Compain, S ;
Samson, D ;
Vincent, C ;
Weil, D ;
Cruaud, C ;
Sahly, I ;
Leibovici, M ;
BitnerGlindzicz, M ;
Francis, M ;
Lacombe, D ;
Vigneron, J ;
Charachon, R ;
Boven, K ;
Bedbeder, P ;
VanRegemorter, N ;
Weissenbach, J ;
Petit, C .
NATURE GENETICS, 1997, 15 (02) :157-164
[2]  
BOBER E, 1994, DEVELOPMENT, V120, P603
[3]   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
[4]   AN EXPERIMENTAL-ANALYSIS OF THE DEVELOPMENTAL CAPACITIES OF DISTAL PARTS OF AVIAN LEG BUDS [J].
BRAND, B ;
CHRIST, B ;
JACOB, HJ .
AMERICAN JOURNAL OF ANATOMY, 1985, 173 (04) :321-340
[5]  
BUTLER J, 1988, DEVELOPMENT, V102, P763
[6]  
CHEVALLIER A, 1977, J EMBRYOL EXP MORPH, V41, P245
[7]   ON THE ROLE OF THE CONNECTIVE-TISSUE IN THE PATTERNING OF THE CHICK LIMB MUSCULATURE [J].
CHEVALLIER, A ;
KIENY, M .
WILHELM ROUXS ARCHIVES OF DEVELOPMENTAL BIOLOGY, 1982, 191 (04) :277-280
[8]   SPLOTCH (SP2H), A MUTATION AFFECTING DEVELOPMENT OF THE MOUSE NEURAL-TUBE, SHOWS A DELETION WITHIN THE PAIRED HOMEODOMAIN OF PAX-3 [J].
EPSTEIN, DJ ;
VEKEMANS, M ;
GROS, P .
CELL, 1991, 67 (04) :767-774
[9]   Pax3 modulates expression of the c-Met receptor during limb muscle development [J].
Epstein, JA ;
Shapiro, DN ;
Cheng, J ;
Lam, PYP ;
Maas, RL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (09) :4213-4218
[10]   PAX6 GENE DOSAGE EFFECT IN A FAMILY WITH CONGENITAL CATARACTS, ANIRIDIA, ANOPHTHALMIA AND CENTRAL-NERVOUS-SYSTEM DEFECTS [J].
GLASER, T ;
JEPEAL, L ;
EDWARDS, JG ;
YOUNG, SR ;
FAVOR, J ;
MAAS, RL .
NATURE GENETICS, 1994, 7 (04) :463-471