Literature DB >> 26590638

Optogenetic Inhibitor of the Transcription Factor CREB.

Ahmed M Ali1, Jakeb M Reis2, Yan Xia3, Asim J Rashid4, Valentina Mercaldo4, Brandon J Walters4, Katherine E Brechun2, Vitali Borisenko2, Sheena A Josselyn4, John Karanicolas3, G Andrew Woolley5.   

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.
Copyright © 2015 Elsevier Ltd. All rights reserved.

Entities:  

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

Mesh:

Substances:

Year:  2015        PMID: 26590638      PMCID: PMC4656143          DOI: 10.1016/j.chembiol.2015.09.018

Source DB:  PubMed          Journal:  Chem Biol        ISSN: 1074-5521


  59 in total

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2.  A time-dependent role for the transcription factor CREB in neuronal allocation to an engram underlying a fear memory revealed using a novel in vivo optogenetic tool to modulate CREB function.

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8.  Selection of Protein-Protein Interactions of Desired Affinities with a Bandpass Circuit.

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