ZFIN ID: ZDB-PUB-151204-2
Analyses of fugu hoxa2 genes provide evidence for subfunctionalization of neural crest cell and rhombomere cis-regulatory modules during vertebrate evolution
McEllin, J.A., Alexander, T.B., Tümpel, S., Wiedemann, L.M., Krumlauf, R.
Date: 2016
Source: Developmental Biology 409(2): 530-42 (Journal)
Registered Authors: Krumlauf, Robb
Keywords: Enhancers, Evolution of cis-elements, Gene regulation, Hindbrain, Hox genes, Neural crest
MeSH Terms:
  • Animals
  • Base Sequence
  • Biological Evolution*
  • Conserved Sequence/genetics
  • Embryo, Nonmammalian/metabolism
  • Enhancer Elements, Genetic*
  • Homeodomain Proteins/genetics*
  • Homeodomain Proteins/metabolism
  • Mice, Transgenic
  • Molecular Sequence Data
  • Neural Crest/cytology*
  • Rhombencephalon/cytology
  • Rhombencephalon/embryology*
  • Sequence Alignment
  • Takifugu/embryology
  • Takifugu/genetics*
  • Zebrafish/genetics
PubMed: 26632170 Full text @ Dev. Biol.
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ABSTRACT
Hoxa2 gene is a primary player in regulation of craniofacial programs of head development in vertebrates. Here we investigate the evolution of a Hoxa2 neural crest enhancer identified originally in mouse by comparing and contrasting the fugu hoxa2a and hoxa2b genes with their orthologous teleost and mammalian sequences. Using sequence analyses in combination with transgenic regulatory assays in zebrafish and mouse embryos we demonstrate subfunctionalization of regulatory activity for expression in hindbrain segments and neural crest cells between these two fugu co-orthologs. hoxa2a regulatory sequences have retained the ability to mediate expression in neural crest cells while those of hoxa2b include cis-elements that direct expression in rhombomeres. Functional dissection of the neural crest regulatory potential of the fugu hoxa2a and hoxa2b genes identify the previously unknown cis-element NC5, which is implicated in generating the differential activity of the enhancers from these genes. The NC5 region plays a similar role in the ability of this enhancer to mediate reporter expression in mice, suggesting it is a conserved component involved in control of neural crest expression of Hoxa2 in vertebrate craniofacial development.
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