Zebrafish blowout provides genetic evidence for Patched1-mediated negative regulation of Hedgehog signaling within the proximal optic vesicle of the vertebrate eye

被引:45
作者
Lee, Jiwoon
Willer, Jason R. [3 ]
Willer, Gregory B. [3 ]
Smith, Kierann [4 ]
Gregg, Ronald G. [3 ]
Gross, Jeffrey M. [1 ,2 ]
机构
[1] Univ Texas Austin, Sect Mol Cell & Dev Biol, Austin, TX 78712 USA
[2] Univ Texas Austin, Inst Neurosci, Austin, TX 78712 USA
[3] Univ Louisville, Dept Biochem & Mol Biol, Louisville, KY 40202 USA
[4] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
关键词
zebrafish; optic vesicle; coloboma; Hedgehog; patched1;
D O I
10.1016/j.ydbio.2008.03.035
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In this study, we have characterized the ocular defects in the recessive zebrafish mutant blowout that presents with a variably penetrant coloboma phenotype. blowout mutants develop unilateral or bilateral colobomas and as a result, the retina and retinal pigmented epithelium are not contained within the optic cup. Colobomas result from defects in optic stalk morphogenesis whereby the optic stalk extends into the retina and impedes the lateral edges of the choroid fissure from meeting and fusing. The expression domain of the proximal optic vesicle marker pax2a is expanded in blowout at the expense of the distal optic vesicle marker pax6, suggesting that the initial patterning of the optic vesicle into proximal and distal territories is disrupted in blowout. Later aspects of distal optic cup formation (i.e. retina development) are normal in blowout mutants, however. Positional cloning of blowout identified a nonsense mutation in patched1, a negative regulator of the Hedgehog pathway, as the underlying cause of the blowout phenotype. Expanded domains of expression of the Hedgehog target genes patched1 and patched2 were observed in blowout, consistent with a loss of Patched1 function and upregulation of Hedgehog pathway activity. Moreover, colobomas in blowout could be suppressed by pharmacologically inhibiting the Hedgehog pathway with cyclopamine, and maximal rescue occurred when embryos were exposed to cyclopamine between 5.5 and 13 hours post-fertilization. These observations highlight the critical role that Hedgehog pathway activity plays in mediating patterning of the proximal/distal axis of the optic vesicle during the early phases of eye development and they provide genetic confirmation for the integral role that patched l-mediated negative regulation of Hedgehog signaling plays during vertebrate eye development. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:10 / 22
页数:13
相关论文
共 74 条
[1]   Molecular mechanisms of optic vesicle development: Complexities, ambiguities and controversies [J].
Adler, Ruben ;
Canto-Soler, M. Valeria .
DEVELOPMENTAL BIOLOGY, 2007, 305 (01) :1-13
[2]   Patched1 functions as a gatekeeper by promoting cell cycle progression [J].
Adolphe, C ;
Hetherington, R ;
Ellis, T ;
Wainwright, B .
CANCER RESEARCH, 2006, 66 (04) :2081-2088
[3]   A general role of hedgehog in the regulation of proliferation [J].
Agathocleous, Michalis ;
Locker, Morgane ;
Harris, William A. ;
Perron, Muriel .
CELL CYCLE, 2007, 6 (02) :156-159
[4]   Hedgehog signaling in vertebrate eye development: a growing puzzle [J].
Amato, MA ;
Boy, S ;
Perron, M .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2004, 61 (7-8) :899-910
[5]   Identification of 315 genes essential for early zebrafish development [J].
Amsterdam, A ;
Nissen, RM ;
Sun, ZX ;
Swindell, EC ;
Farrington, S ;
Hopkins, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (35) :12792-12797
[6]  
Barbieri AM, 2002, DEVELOPMENT, V129, P805
[7]   A homeobox gene, vax2, controls the patterning of the eye dorsoventral axis [J].
Barbieri, AM ;
Lupo, G ;
Bulfone, A ;
Andreazzoli, M ;
Mariani, M ;
Fougerousse, F ;
Consalez, GG ;
Borsani, G ;
Beckmann, JS ;
Barsacchi, G ;
Ballabio, A ;
Banfi, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (19) :10729-10734
[8]  
Barresi MJF, 2000, DEVELOPMENT, V127, P2189
[9]  
BARTH KA, 1995, DEVELOPMENT, V121, P1755
[10]   IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy [J].
Beales, Philip L. ;
Bland, Elizabeth ;
Tobin, Jonathan L. ;
Bacchelli, Chiara ;
Tuysuz, Beyhan ;
Hill, Josephine ;
Rix, Suzanne ;
Pearson, Chad G. ;
Kai, Masatake ;
Hartley, Jane ;
Johnson, Colin ;
Irving, Melita ;
Elcioglu, Nursel ;
Winey, Mark ;
Tada, Masazumi ;
Scambler, Peter J. .
NATURE GENETICS, 2007, 39 (06) :727-729