A large-scale in situ screen provides molecular evidence for the induction of eye anterior segment structures by the developing lens

被引:104
作者
Thut, CJ
Rountree, RB
Hwa, M
Kingsley, DM
机构
[1] Stanford Univ, Sch Med, Dept Dev Biol, Beckman Ctr B300, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Howard Hughes Med Inst, Beckman Ctr B300, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
anterior segment; ciliary body; iris; lens induction; glaucoma; eye; in situ screen;
D O I
10.1006/dbio.2000.0140
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The anterior segment of the vertebrate eye includes the cornea, iris, ciliary body, trabecular meshwork, and lens. Although malformations of these structures have been implicated in many human eye diseases, little is known about the molecular mechanisms that control their development. To identify genes involved in anterior segment formation, we developed a large-scale in situ hybridization screen and examined the spatial and temporal expression of over 1000 genes during eye development. This screen identified 62 genes with distinct expression patterns in specific eye structures, including several expressed in novel patterns in the anterior segment. Using these genes as developmental markers, we tested for the presence of inductive signals that control the differentiation of anterior segment tissues. Organ culture recombination experiments showed that a chick lens is capable of inducing the expression of markers of the presumptive iris and ciliary body in the developing mouse neural retina. The inducing activity from the lens acts only over short ranges and is present at multiple stages of eye development. These studies provide molecular evidence that an evolutionarily conserved signal from the lens controls tissue specification in the developing optic cup. (C) 2001 Academic Press.
引用
收藏
页码:63 / 76
页数:14
相关论文
共 47 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene [J].
Alward, WLM ;
Semina, EV ;
Kalenak, JW ;
Héon, E ;
Sheth, BP ;
Stone, EM ;
Murray, JC .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1998, 125 (01) :98-100
[3]  
Bao ZZ, 1997, J NEUROSCI, V17, P1425
[4]   The lens organizes the anterior segment: Specification of neural crest cell differentiation in the avian eye [J].
Beebe, DC ;
Coats, JM .
DEVELOPMENTAL BIOLOGY, 2000, 220 (02) :424-431
[5]  
BEEBE DC, 1986, T OPHTHAL SOC UK, V105, P123
[6]  
BREITMAN ML, 1989, DEVELOPMENT, V106, P457
[7]   LENS DEVELOPMENT .I. ROLE OF LENS IN EYE GROWTH [J].
COULOMBRE, AJ ;
COULOMBRE, JL .
JOURNAL OF EXPERIMENTAL ZOOLOGY, 1964, 156 (01) :39-&
[8]  
Craig J E, 1999, Curr Opin Ophthalmol, V10, P126, DOI 10.1097/00055735-199904000-00009
[9]   The Drosophila bunched gene is a homologue of the growth factor stimulated mammalian TSC-22 sequence and is required during oogenesis [J].
Dobens, LL ;
Hsu, T ;
Twombly, V ;
Gelbart, WM ;
Raftery, LA ;
Kafatos, FC .
MECHANISMS OF DEVELOPMENT, 1997, 65 (1-2) :197-208
[10]  
Francis B A, 1997, Curr Opin Ophthalmol, V8, P19, DOI 10.1097/00055735-199704000-00005