Patterning of the third pharyngeal pouch into thymus/parathyroid by Six and Eya1

被引:97
作者
Zou, Dan
Silvius, Derek
Davenport, Julie
Grifone, Raphaelle
Maire, Pascal
Xu, Pin-Xian [1 ]
机构
[1] McLaughlin Res Inst Biomed Sci, Great Falls, MT 59405 USA
[2] Univ Paris 05, CNRS, INSERM 567, Inst Cochin,UMR 8104,24 Rue faubourg St Jacques, F-75014 Paris, France
关键词
Sixl1; Six4; third pharyngeal pouch; patterning; thymus; parathyroid; Eya1; Pax; Hoxa3; Fox; Tbx1; Fgf8; Wnt5b;
D O I
10.1016/j.ydbio.2005.12.015
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Previous studies have suggested a role of the homeodomain Six family proteins in patterning the developing vertebrate head that involves appropriate segmentation of three tissue layers, the endoderm, the paraxial mesoderm and the neural crest cells; however, the developmental programs and mechanisms by which the Six genes act in the pharyngeal endoderm remain largely unknown. Here, we examined their roles in pharyngeal pouch development. Six1(-/-) mice lack thymus and parathyroid and analysis of Six1(-/-) third pouch endoderm demonstrated that the patterning of the third pouch into thymus/parathyroid primordia is initiated. However, the endodermal cells of the thymus/parathyroid rudiments fail to maintain the expression of the parathyroid-specific gene Gcm2 and the thymus-specific gene Foxn1 and subsequently undergo abnormal apoptosis, leading to a complete disappearance of organ primordia by E 12.5. This thus defines the thymus/parathyroid defects present in the Six1 mutant. Analyses of the thymus/parathyroid development in Six1(-/-);Six4(-/-) double mutant show that both Six1 and Six4 act synergistically to control morphogenetic movements of early thymus/parathyroid tissues, and the threshold of Six1/Six4 appears to be crucial for the regulation of the organ primordia-specific gene expression. Previous studies in flies and mice suggested that Eya and Six genes may function downstream of Pax genes. Our data clearly show that Eya1 and Six1 expression in the pouches does not require Pax1/Pax9 function, suggesting that they may function independently from Pax1/Pax9. In contrast, Pax1 expression in all pharyngeal pouches requires both Eya1 and Six1 function. Moreover, we show that the expression of Tbx1, Fgf8 and Wnt5b in the pouch endoderm was normal in Six1(-/-) embryos and slightly reduced in Siy1(-/-); Six4(-/-) double mutant, but was largely reduced in Eya1(-/-) embryos. These results indicate that Eya I appears to be upstream of very early events in the initiation of thymus/parathyroid organogenesis, while Six genes appear to act in an early differentiation step during thymus/parathyroid morphogenesis. Together, these analyses establish an essential role for Eya1 and Six genes in patterning the third pouch into organ-specific primordia. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:499 / 512
页数:14
相关论文
共 73 条
[1]   Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1 [J].
Abdelhak, S ;
Kalatzis, V ;
Heilig, R ;
Compain, S ;
Samson, D ;
Vincent, C ;
LeviAcobas, F ;
Cruaud, C ;
LeMerrer, M ;
Mathieu, M ;
Konig, R ;
Vigneron, J ;
Weissenbach, J ;
Petit, C ;
Weil, D .
HUMAN MOLECULAR GENETICS, 1997, 6 (13) :2247-2255
[2]   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
[3]  
Abu-Issa R, 2002, DEVELOPMENT, V129, P4613
[4]   Wnt glycoproteins regulate the expression of FoxNI, the gene defective in nude mice [J].
Balciunaite, G ;
Keller, MP ;
Balciunaite, E ;
Piali, L ;
Zuklys, S ;
Mathieu, YD ;
Gill, J ;
Boyd, R ;
Sussman, DJ ;
Holländer, GA .
NATURE IMMUNOLOGY, 2002, 3 (11) :1102-1108
[5]   The nu gene acts cell-autonomously and is required for differentiation of thymic epithelial progenitors [J].
Blackburn, CC ;
Augustine, CL ;
Li, R ;
Harvey, RP ;
Malin, MA ;
Boyd, RL ;
Miller, JFAP ;
Morahan, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (12) :5742-5746
[6]  
BODMER R, 1993, DEVELOPMENT, V118, P719
[7]   Molecular effects of Eya1 domain mutations causing organ defects in BOR syndrome [J].
Buller, C ;
Xu, X ;
Marquis, V ;
Schwanke, R ;
Xu, PX .
HUMAN MOLECULAR GENETICS, 2001, 10 (24) :2775-2781
[8]   PHENOTYPIC MANIFESTATIONS OF BRANCHIOOTORENAL SYNDROME [J].
CHEN, A ;
FRANCIS, M ;
NI, L ;
CREMERS, CWRJ ;
KIMBERLING, WJ ;
SATO, Y ;
PHELPS, PD ;
BELLMAN, SC ;
WAGNER, MJ ;
PEMBREY, M ;
SMITH, RJH .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 58 (04) :365-370
[9]   Dachshund and eyes absent proteins form a complex and function synergistically to induce ectopic eye development in Drosophila [J].
Chen, R ;
Amoui, M ;
Zhang, ZH ;
Mardon, G .
CELL, 1997, 91 (07) :893-903
[10]   An essential role for Fgfs in endodermal pouch formation influences later craniofacial skeletal patterning [J].
Crump, JG ;
Maves, L ;
Lawson, ND ;
Weinstein, BM ;
Kimmel, CB .
DEVELOPMENT, 2004, 131 (22) :5703-5716