Optogenetic Inhibitor of the Transcription Factor CREB

Chem Biol. 2015 Nov 19;22(11):1531-1539. doi: 10.1016/j.chembiol.2015.09.018.

Abstract

Current approaches for optogenetic control of transcription do not mimic the activity of endogenous transcription factors, which act at numerous sites in the genome in a complex interplay with other factors. Optogenetic control of dominant negative versions of endogenous transcription factors provides a mechanism for mimicking the natural regulation of gene expression. Here we describe opto-DN-CREB, a blue-light-controlled inhibitor of the transcription factor CREB created by fusing the dominant negative inhibitor A-CREB to photoactive yellow protein (PYP). A light-driven conformational change in PYP prevents coiled-coil formation between A-CREB and CREB, thereby activating CREB. Optogenetic control of CREB function was characterized in vitro, in HEK293T cells, and in neurons where blue light enabled control of expression of the CREB targets NR4A2 and c-Fos. Dominant negative inhibitors exist for numerous transcription factors; linking these to optogenetic domains offers a general approach for spatiotemporal control of native transcriptional events.

Keywords: CREB; PYP; dominant negative; endogenous; genetically encoded; optogenetics; photo-control; photoactive yellow protein; photoisomerization; transcription factor.

Publication types

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

MeSH terms

  • Bacterial Proteins / chemistry
  • Bacterial Proteins / metabolism
  • CREB-Binding Protein / antagonists & inhibitors*
  • CREB-Binding Protein / metabolism
  • Coumaric Acids / chemistry
  • DNA / chemistry
  • DNA / metabolism
  • Electrophoretic Mobility Shift Assay
  • HEK293 Cells
  • Humans
  • Light
  • Nuclear Receptor Subfamily 4, Group A, Member 2 / metabolism
  • Optogenetics*
  • Photoreceptors, Microbial / chemistry
  • Photoreceptors, Microbial / metabolism
  • Propionates
  • Protein Binding
  • Proto-Oncogene Proteins c-fos / metabolism

Substances

  • Bacterial Proteins
  • Coumaric Acids
  • NR4A2 protein, human
  • Nuclear Receptor Subfamily 4, Group A, Member 2
  • Photoreceptors, Microbial
  • Propionates
  • Proto-Oncogene Proteins c-fos
  • photoactive yellow protein, Bacteria
  • DNA
  • CREB-Binding Protein
  • CREBBP protein, human
  • p-coumaric acid