Binding of the transcription activator-like effector augments transcriptional regulation by another transcription factor

Author:

Leben Katja12ORCID,Strmšek Žiga1ORCID,Lebar Tina1ORCID,Verbič Anže12ORCID,Dragovan Matej1,Omersa Neža3ORCID,Anderluh Gregor3ORCID,Jerala Roman1ORCID

Affiliation:

1. Department of Synthetic Biology and Immunology, National Institute of Chemistry , Hajdrihova 19, SI-1000 Ljubljana , Slovenia

2. Interdisciplinary Doctoral Programme in Biomedicine, University of Ljubljana , Kongresni trg 12, SI-1000 Ljubljana , Slovenia

3. Department of Molecular Biology and Nanobiotechnology, National Institute of Chemistry , Hajdrihova 19, SI-1000 Ljubljana , Slovenia

Abstract

Abstract DNA transcription is regulated by a range of diverse mechanisms and primarily by transcription factors that recruit the RNA polymerase complex to the promoter region on the DNA. Protein binding to DNA at nearby or distant sites can synergistically affect this process in a variety of ways, but mainly through direct interactions between DNA-binding proteins. Here we show that a Transcription Activator-Like Effector (TALE), which lacks an activation domain, can enhance transcription in mammalian cells when it binds in the vicinity of and without direct interaction with several different dimeric or monomeric transcription factors. This effect was observed for several TALEs regardless of the recognition sequences and their DNA-bound orientation. TALEs can exert an effect over the distance of tens of nucleotides and it also potentiated KRAB-mediated repression. The augmentation of transcriptional regulation of another transcription factor is characteristic of TALEs, as it was not observed for dCas9/gRNA, zinc finger, or Gal4 DNA-binding domains. We propose that this mechanism involves an allosteric effect exerted on DNA structure or dynamics. This mechanism could be used to modulate transcription but may also play a role in the natural context of TALEs.

Funder

Slovenian Research Agency

Publisher

Oxford University Press (OUP)

Subject

Genetics

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