A novel function for Egr4 in posterior hindbrain development

Research output: Contribution to journalArticle

Abstract

Segmentation of the vertebrate hindbrain is an evolutionarily conserved process. Here, we identify the transcription factor early growth response 4 (egr4) as a novel regulator of posterior hindbrain development in Xenopus. egr4 is specifically and transiently expressed in rhombomeres 5 and 6 (r5/r6), and Egr4 knockdown causes a loss of mafb/kreisler and krox20/egr2 expression in r5/r6 and r5, respectively. This phenotype can be fully rescued by injection of frog or mouse Egr4 mRNA. Moreover Egr4-depleted embryos exhibit a specific loss of the neural crest stream adjacent to r5, and have inner ear defects. While the homeodomain protein vHnf1/Hnf1b directly activates Mafb and Krox20 expression in the mouse hindbrain to specify r5, we show that in Xenopus this process is indirect through the activation of Egr4. We provide evidence that rearrangements in the regulatory sequences around egr4 and mafb genes may account for this difference.

Original languageEnglish (US)
Article number7750
JournalScientific Reports
Volume5
DOIs
StatePublished - 2015

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Rhombencephalon
Xenopus
Early Growth Response Transcription Factors
Homeodomain Proteins
Neural Crest
Inner Ear
Growth
Anura
Vertebrates
Embryonic Structures
Phenotype
Messenger RNA
Injections
Genes

ASJC Scopus subject areas

  • General

Cite this

A novel function for Egr4 in posterior hindbrain development. / Bae, Chang Joon; Jeong, Juhee; Saint-Jeannet, Jean-Pierre.

In: Scientific Reports, Vol. 5, 7750, 2015.

Research output: Contribution to journalArticle

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