Distinct cis-acting regions control six6 expression during eye field and optic cup stages of eye formation

Dev Biol. 2017 Jun 15;426(2):418-428. doi: 10.1016/j.ydbio.2017.04.003. Epub 2017 Apr 21.

Abstract

The eye field transcription factor, Six6, is essential for both the early (specification and proliferative growth) phase of eye formation, as well as for normal retinal progenitor cell differentiation. While genomic regions driving six6 optic cup expression have been described, the sequences controlling eye field and optic vesicle expression are unknown. Two evolutionary conserved regions 5' and a third 3' to the six6 coding region were identified, and together they faithfully replicate the endogenous X. laevis six6 expression pattern. Transgenic lines were generated and used to determine the onset and expression patterns controlled by the regulatory regions. The conserved 3' region was necessary and sufficient for eye field and optic vesicle expression. In contrast, the two conserved enhancer regions located 5' of the coding sequence were required together for normal optic cup and mature retinal expression. Gain-of-function experiments indicate endogenous six6 and GFP expression in F1 transgenic embryos are similarly regulated in response to candidate trans-acting factors. Importantly, CRISPR/CAS9-mediated deletion of the 3' eye field/optic vesicle enhancer in X. laevis, resulted in a reduction in optic vesicle size. These results identify the cis-acting regions, demonstrate the modular nature of the elements controlling early versus late retinal expression, and identify potential regulators of six6 expression during the early stages of eye formation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Base Sequence
  • Binding Sites
  • CRISPR-Cas Systems
  • Conserved Sequence
  • Eye / growth & development*
  • Female
  • Gene Expression Regulation, Developmental / genetics*
  • Genes, Reporter
  • Larva
  • Male
  • RNA, Guide, CRISPR-Cas Systems / genetics
  • Regulatory Sequences, Nucleic Acid*
  • Sequence Alignment
  • Sequence Homology, Nucleic Acid
  • Species Specificity
  • Transgenes
  • Xenopus Proteins / genetics
  • Xenopus Proteins / physiology
  • Xenopus laevis / genetics*
  • Xenopus laevis / growth & development

Substances

  • RNA, Guide, CRISPR-Cas Systems
  • Xenopus Proteins