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Neuron. 2015 Apr 8;86(1):247-63. doi: 10.1016/j.neuron.2015.02.038. Epub 2015 Mar 19.

MEF2D drives photoreceptor development through a genome-wide competition for tissue-specific enhancers.

Author information

1
Department of Neurobiology, Harvard Medical School, 220 Longwood Avenue, Boston MA 02115, USA.
2
Department of Ophthalmology, Boston Children's Hospital, 300 Longwood Avenue, Boston, MA 02115, USA.
3
Berman-Gund Laboratory For the Study of Retinal Degenerations, Department of Ophthalmology, Harvard Medical School, Massachusetts Eye and Ear Infirmary, Boston, MA 02114, USA.
4
Department of Neurobiology, Harvard Medical School, 220 Longwood Avenue, Boston MA 02115, USA. Electronic address: michael_greenberg@hms.harvard.edu.

Abstract

Organismal development requires the precise coordination of genetic programs to regulate cell fate and function. MEF2 transcription factors (TFs) play essential roles in this process but how these broadly expressed factors contribute to the generation of specific cell types during development is poorly understood. Here we show that despite being expressed in virtually all mammalian tissues, in the retina MEF2D binds to retina-specific enhancers and controls photoreceptor cell development. MEF2D achieves specificity by cooperating with a retina-specific factor CRX, which recruits MEF2D away from canonical MEF2 binding sites and redirects it to retina-specific enhancers that lack the consensus MEF2-binding sequence. Once bound to retina-specific enhancers, MEF2D and CRX co-activate the expression of photoreceptor-specific genes that are critical for retinal function. These findings demonstrate that broadly expressed TFs acquire specific functions through competitive recruitment to enhancers by tissue-specific TFs and through selective activation of these enhancers to regulate tissue-specific genes.

PMID:
25801704
PMCID:
PMC4393375
DOI:
10.1016/j.neuron.2015.02.038
[Indexed for MEDLINE]
Free PMC Article

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