Tbx12 regulates eye development in Xenopus embryos

Biochemical and Biophysical Research Communications

Volumn 318, Issue 2, 2004, Pages 485-489

  Carson, Christian T ^a   Pagratis, Maria ^a   Parr, Brian A ^a,b  

^a UNIVERSITY OF COLORADO   (United States)

^b UNIVERSITY OF COLORADO   (United States)

Author keywords

Retina; T box; Xenopus

Indexed keywords

PROTEIN; PROTEIN TBX12; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; EMBRYO; EMBRYO DEVELOPMENT; EYE DEVELOPMENT; GENE ACTIVITY; GENE EXPRESSION; GENETIC TRANSCRIPTION; NONHUMAN; PRIORITY JOURNAL; RETINA; RETINA CELL; RETINA DEVELOPMENT; VERTEBRATE; XENOPUS;

ANIMALS; EYE; GENE EXPRESSION; IN SITU HYBRIDIZATION; INJECTIONS; MICE; MUTATION; PHENOTYPE; PIGMENT EPITHELIUM OF EYE; RETINA; RNA, MESSENGER; T-BOX DOMAIN PROTEINS; XENOPUS LAEVIS;

VERTEBRATA;

EID: 2142761522     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbrc.2004.04.079     Document Type: Article

References (31)

1. Jean D., Ewan K., Gruss P. Molecular regulators involved in vertebrate eye development. Mech. Dev. 76:1998;3-18
2. Herrmann B.G., Labeit S., Poustka A., King T.R., Lehrach H. Cloning of the T gene required in mesoderm formation in the mouse (see comments). Nature. 343:1990;617-622
3. Muller C.W., Herrmann B.G. Crystallographic structure of the T domain-DNA complex of the Brachyury transcription factor. Nature. 389:1997;884-888
4. Kispert A., Herrmann B.G. The Brachyury gene encodes a novel DNA binding protein (published erratum appears in EMBO J. 12 (12) (1993) 4898-4899). EMBO J. 12:1993;3211-3220
5. Kispert A., Koschorz B., Herrmann B.G. The T protein encoded by Brachyury is a tissue-specific transcription factor. EMBO J. 14:1995;4763-4772
6. Zhang J., Houston D.W., King M.L., Payne C., Wylie C., Heasman J. The role of maternal VegT in establishing the primary germ layers in Xenopus embryos (see comments). Cell. 94:1998;515-524
7. Chapman D.L., Papaioannou V.E. Three neural tubes in mouse embryos with mutations in the T-box gene Tbx6. Nature. 391:1998;695-697
8. Ohuchi H., Takeuchi J., Yoshioka H., Ishimaru Y., Ogura K., Takahashi N., Ogura T., Noji S. Correlation of wing-leg identity in ectopic FGF-induced chimeric limbs with the differential expression of chick Tbx5 and Tbx4. Development. 125:1998;51-60
9. Isaac A., Rodriguez-Esteban C., Ryan A., Altabef M., Tsukui T., Patel K., Tickle C., Izpisua-Belmonte J.C. Tbx genes and limb identity in chick embryo development. Development. 125:1998;1867-1875
10. Gibson-Brown J.J., Agulnik S.I., Silver L.M., Niswander L., Papaioannou V.E. Involvement of T-box genes Tbx2-Tbx5 in vertebrate limb specification and development. Development. 125:1998;2499-2509
11. Bamshad M., Lin R.C., Law D.J., Watkins W.C., Krakowiak P.A., Moore M.E., Franceschini P., Lala R., Holmes L.B., Gebuhr T.C., Bruneau B.G., Schinzel A., Seidman J.G., Seidman C.E., Jorde L.B. Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome (published erratum appears in Nat. Genet. 19 (1) (1998) 102). Nat. Genet. 16:1997;311-315
12. Merscher S., Funke B., Epstein J.A., Heyer J., Puech A., Lu M.M., Xavier R.J., Demay M.B., Russell R.G., Factor S., Tokooya K., Jore B.S., Lopez M., Pandita R.K., Lia M., Carrion D., Xu H., Schorle H., Kobler J.B., Scambler P., Wynshaw-Boris A., Skoultchi A.I., Morrow B.E., Kucherlapati R. TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome. Cell. 104:2001;619-629
13. Basson C.T., Bachinsky D.R., Lin R.C., Levi T., Elkins J.A., Soults J., Grayzel D., Kroumpouzou E., Traill T.A., Leblanc-Straceski J., Renault B., Kucherlapati R., Seidman J.G., Seidman C.E. Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome (published erratum appears in Nat. Genet. 15 (4) (1997) 411). Nat. Genet. 15:1997;30-35
14. Li Q.Y., Newbury-Ecob R.A., Terrett J.A., Wilson D.I., Curtis A.R., Yi C.H., Gebuhr T., Bullen P.J., Robson S.C., Strachan T., Bonnet D., Lyonnet S., Young I.D., Raeburn J.A., Buckler A.J., Law D.J., Brook J.D. Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family. Nat. Genet. 15:1997;21-29
15. Chapman D.L., Garvey N., Hancock S., Alexiou M., Agulnik S.I., Gibson-Brown J.J., Cebra-Thomas J., Bollag R.J., Silver L.M., Papaioannou V.E. Expression of the T-box family genes, Tbx1-Tbx5, during early mouse development. Dev. Dyn. 206:1996;379-390
16. Koshiba-Takeuchi K., Takeuchi J.K., Matsumoto K., Momose T., Uno K., Hoepker V., Ogura K., Takahashi N., Nakamura H., Yasuda K., Ogura T. Tbx5 and the retinotectum projection. Science. 287:2000;134-137
17. Carson C.T., Kinzler E.R., Parr B.A. Tbx12, a novel T-box gene, is expressed during early stages of heart and retinal development. Mech. Dev. 96:2000;137-140
18. Turner D.L., Weintraub H. Expression of achaete-scute homolog 3 in Xenopus embryos converts ectodermal cells to a neural fate. Genes Dev. 8:1994;1434-1447
19. Hemmati-Brivanlou A., Frank D., Bolce M.E., Brown B.D., Sive H.L., Harland R.M. Localization of specific mRNAs in Xenopus embryos by whole-mount in situ hybridization. Development. 110:1990;325-330
20. Parr B.A., Shea M.J., Vassileva G., McMahon A.P. Mouse Wnt genes exhibit discrete domains of expression in the early embryonic CNS and limb buds. Development. 119:1993;247-261
21. Brown D.D., Binder O., Pagratis M., Parr B.A., Conlon F.L. Developmental expression of the Xenopus laevis Tbx20 orthologue. Dev. Genes Evol. 212:2003;604-607
22. Conlon F.L., Sedgwick S.G., Weston K.M., Smith J.C. Inhibition of Xbra transcription activation causes defects in mesodermal patterning and reveals autoregulation of Xbra in dorsal mesoderm. Development. 122:1996;2427-2435
23. Horb M.E., Thomsen G.H. Tbx5 is essential for heart development. Development. 126:1999;1739-1751
24. Carreira S., Dexter T.J., Yavuzer U., Easty D.J., Goding C.R. Brachyury-related transcription factor Tbx2 and repression of the melanocyte-specific TRP-1 promoter. Mol. Cell. Biol. 18:1998;5099-5108
25. Kanekar S., Perron M., Dorsky R., Harris W.A., Jan L.Y., Jan Y.N., Vetter M.L. Xath5 participates in a network of bHLH genes in the developing Xenopus retina. Neuron. 19:1997;981-994
26. Dorsky R.I., Chang W.S., Rapaport D.H., Harris W.A. Regulation of neuronal diversity in the Xenopus retina by Delta signalling. Nature. 385:1997;67-70
27. Macdonald R., Barth K.A., Xu Q., Holder N., Mikkola I., Wilson S.W. Midline signalling is required for Pax gene regulation and patterning of the eyes. Development. 121:1995;3267-3278
28. Schulte D., Furukawa T., Peters M.A., Kozak C.A., Cepko C.L. Misexpression of the Emx-related homeobox genes cVax and mVax2 ventralizes the retina and perturbs the retinotectal map. Neuron. 24:1999;541-553
29. Barbieri A.M., Lupo G., Bulfone A., Andreazzoli M., Mariani M., Fougerousse F., Consalez G.G., Borsani G., Beckmann J.S., Barsacchi G., Ballabio A., Banfi S. A homeobox gene, vax2, controls the patterning of the eye dorsoventral axis. Proc. Natl. Acad. Sci. USA. 96:1999;10729-10734
30. Ekker S.C., Ungar A.R., Greenstein P., von Kessler D.P., Porter J.A., Moon R.T., Beachy P.A. Patterning activities of vertebrate hedgehog proteins in the developing eye and brain. Curr. Biol. 5:1995;944-955
31. Huh S., Hatini V., Marcus R.C., Li S.C., Lai E. Dorsal-ventral patterning defects in the eye of BF-1-deficient mice associated with a restricted loss of shh expression. Dev. Biol. 211:1999;53-63