Literature DB >> 15110720

Involvement of Pax6 and Otx2 in the forebrain-specific regulation of the vertebrate homeobox gene ANF/Hesx1.

Derek Spieler1, Nicole Bäumer, Jürg Stebler, Marion Köprunner, Michal Reichman-Fried, Ulrike Teichmann, Erez Raz, Michael Kessel, Lars Wittler.   

Abstract

During early vertebrate development, ANF homeobox genes are expressed in the prospective forebrain. Their regulation is essential for correct morphogenesis and function of the prosencephalon. We identified a 1-kb fragment upstream of the chicken GANF gene sufficient to drive lacZ expression in the endogenous expression domain. Concordant with the high conservation of this sequence in five investigated species, this element is also active in the corresponding expression domain of the zebrafish orthologue. In vivo analysis of two in vitro-identified Otx2 binding sites in this conserved sequence revealed their necessity for activation of the chicken ANF promoter. In addition, we identified a Pax6-binding site close to the transcriptional start site that is occupied in vivo by Pax6 protein. Pax6 and GANF exhibit mutually exclusive expression domains in the anterior embryonic region. Overexpression of Pax6 in chick embryos inhibited the endogenous GANF expression, and in Pax6(-/-) mice the expression domain of the murine ANF orthologue Hesx1 was expanded and sustained, indicating inhibitory effects of Pax6 on GANF. However, a mutation of the Pax6 site did not abolish reporter activity from an electroporated vector. We conclude that Otx2 and Pax6 are key molecules involved in conserved mechanisms of ANF gene regulation.

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Year:  2004        PMID: 15110720     DOI: 10.1016/j.ydbio.2004.01.044

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  15 in total

1.  HESX1- and TCF3-mediated repression of Wnt/β-catenin targets is required for normal development of the anterior forebrain.

Authors:  Cynthia L Andoniadou; Massimo Signore; Rodrigo M Young; Carles Gaston-Massuet; Stephen W Wilson; Elaine Fuchs; Juan Pedro Martinez-Barbera
Journal:  Development       Date:  2011-10-17       Impact factor: 6.868

2.  Congenital pituitary hypoplasia model demonstrates hypothalamic OTX2 regulation of pituitary progenitor cells.

Authors:  Ryusaku Matsumoto; Hidetaka Suga; Takashi Aoi; Hironori Bando; Hidenori Fukuoka; Genzo Iguchi; Satoshi Narumi; Tomonobu Hasegawa; Keiko Muguruma; Wataru Ogawa; Yutaka Takahashi
Journal:  J Clin Invest       Date:  2020-02-03       Impact factor: 14.808

3.  Molecular links among the causative genes for ocular malformation: Otx2 and Sox2 coregulate Rax expression.

Authors:  Hiroki Danno; Tatsuo Michiue; Keisuke Hitachi; Akira Yukita; Shoichi Ishiura; Makoto Asashima
Journal:  Proc Natl Acad Sci U S A       Date:  2008-04-02       Impact factor: 11.205

Review 4.  Human pituitary development and application of iPSCs for pituitary disease.

Authors:  Ryusaku Matsumoto; Yutaka Takahashi
Journal:  Cell Mol Life Sci       Date:  2020-11-18       Impact factor: 9.261

5.  Characterization of Three-Dimensional Retinal Tissue Derived from Human Embryonic Stem Cells in Adherent Monolayer Cultures.

Authors:  Ratnesh K Singh; Ramya K Mallela; Pamela K Cornuet; Aaron N Reifler; Andrew P Chervenak; Michael D West; Kwoon Y Wong; Igor O Nasonkin
Journal:  Stem Cells Dev       Date:  2015-09-10       Impact factor: 3.272

6.  B1 SOX coordinate cell specification with patterning and morphogenesis in the early zebrafish embryo.

Authors:  Yuichi Okuda; Eri Ogura; Hisato Kondoh; Yusuke Kamachi
Journal:  PLoS Genet       Date:  2010-05-06       Impact factor: 5.917

7.  Confirmation of RAX gene involvement in human anophthalmia.

Authors:  L Lequeux; M Rio; A Vigouroux; M Titeux; H Etchevers; F Malecaze; N Chassaing; P Calvas
Journal:  Clin Genet       Date:  2008-09-09       Impact factor: 4.438

Review 8.  Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.

Authors:  Qing Fang; Akima S George; Michelle L Brinkmeier; Amanda H Mortensen; Peter Gergics; Leonard Y M Cheung; Alexandre Z Daly; Adnan Ajmal; María Ines Pérez Millán; A Bilge Ozel; Jacob O Kitzman; Ryan E Mills; Jun Z Li; Sally A Camper
Journal:  Endocr Rev       Date:  2016-11-09       Impact factor: 19.871

9.  A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency.

Authors:  Daniel Diaczok; Christopher Romero; Janice Zunich; Ian Marshall; Sally Radovick
Journal:  J Clin Endocrinol Metab       Date:  2008-08-26       Impact factor: 5.958

10.  A rare de novo nonsense mutation in OTX2 causes early onset retinal dystrophy and pituitary dysfunction.

Authors:  Robert H Henderson; Kathleen A Williamson; Joanna S Kennedy; Andrew R Webster; Graham E Holder; Anthony G Robson; David R FitzPatrick; Veronica van Heyningen; Anthony T Moore
Journal:  Mol Vis       Date:  2009-11-21       Impact factor: 2.367

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