Literature DB >> 10940626

Murine hoxd4 expression in the CNS requires multiple elements including a retinoic acid response element.

F Zhang1, E Nagy Kovács, M S Featherstone.   

Abstract

We have identified a retinoic acid response element (RARE) within a neural enhancer located 3' to the Hoxd4 gene. This RARE is required for the initiation and maintenance of Hoxd4 transgene expression in neurectoderm, and for full anteriorized expression upon retinoic acid (RA) treatment. Mutations within the sequence TTTTCTG, located 2 bp downstream of the RARE, posteriorized transgene activity. However, the onset of transgene expression and its response to RA were indistinguishable from wild type. While the TTTTCTG motif resembles a CDX binding site, human CDX1 protein did not interact with this element in vitro. Three additional regions were also shown to control transgene expression in neurectoderm, establishing that multiple elements constitute the Hoxd4 neural enhancer.

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Year:  2000        PMID: 10940626     DOI: 10.1016/s0925-4773(00)00377-4

Source DB:  PubMed          Journal:  Mech Dev        ISSN: 0925-4773            Impact factor:   1.882


  15 in total

1.  Sequential histone modifications at Hoxd4 regulatory regions distinguish anterior from posterior embryonic compartments.

Authors:  Mojgan Rastegar; Laila Kobrossy; Erzsebet Nagy Kovacs; Isabel Rambaldi; Mark Featherstone
Journal:  Mol Cell Biol       Date:  2004-09       Impact factor: 4.272

Review 2.  Role of Hox genes in stem cell differentiation.

Authors:  Anne Seifert; David F Werheid; Silvana M Knapp; Edda Tobiasch
Journal:  World J Stem Cells       Date:  2015-04-26       Impact factor: 5.326

3.  The retinoid signaling pathway inhibits hematopoiesis and uncouples from the Hox genes during hematopoietic development.

Authors:  Istvan Szatmari; Michelina Iacovino; Michael Kyba
Journal:  Stem Cells       Date:  2010-09       Impact factor: 6.277

4.  The development and growth of tissues derived from cranial neural crest and primitive mesoderm is dependent on the ligation status of retinoic acid receptor γ: evidence that retinoic acid receptor γ functions to maintain stem/progenitor cells in the absence of retinoic acid.

Authors:  Htoo Aung Wai; Koichi Kawakami; Hironori Wada; Ferenc Müller; Ann Beatrice Vernallis; Geoffrey Brown; William Eustace Basil Johnson
Journal:  Stem Cells Dev       Date:  2014-11-10       Impact factor: 3.272

5.  Cell signaling switches HOX-PBX complexes from repressors to activators of transcription mediated by histone deacetylases and histone acetyltransferases.

Authors:  M Saleh; I Rambaldi; X J Yang; M S Featherstone
Journal:  Mol Cell Biol       Date:  2000-11       Impact factor: 4.272

6.  YAP regulates the expression of Hoxa1 and Hoxc13 in mouse and human oral and skin epithelial tissues.

Authors:  Ming Liu; Shuangyun Zhao; Qingjie Lin; Xiu-Ping Wang
Journal:  Mol Cell Biol       Date:  2015-02-17       Impact factor: 4.272

7.  Cyp26 enzymes generate the retinoic acid response pattern necessary for hindbrain development.

Authors:  Rafael E Hernandez; Aaron P Putzke; Jonathan P Myers; Lilyana Margaretha; Cecilia B Moens
Journal:  Development       Date:  2007-01       Impact factor: 6.868

Review 8.  Patterning of vertebrate cardiac progenitor fields by retinoic acid signaling.

Authors:  Tiffany B Duong; Joshua S Waxman
Journal:  Genesis       Date:  2021-10-19       Impact factor: 2.487

9.  Nuclear accumulation of an uncapped RNA produced by Drosha cleavage of a transcript encoding miR-10b and HOXD4.

Authors:  Sze Lynn Calista Phua; V Sivakamasundari; Yu Shao; Xiaohan Cai; Li-Feng Zhang; Thomas Lufkin; Mark Featherstone
Journal:  PLoS One       Date:  2011-10-03       Impact factor: 3.240

10.  Broken colinearity of the amphioxus Hox cluster.

Authors:  Juan Pascual-Anaya; Noritaka Adachi; Susana Alvarez; Shigeru Kuratani; Salvatore D'Aniello; Jordi Garcia-Fernàndez
Journal:  Evodevo       Date:  2012-12-03       Impact factor: 2.250

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