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Binding of the transcription activator-like effector augments transcriptional regulation by another transcription factor
Author(s) -
Katja Leben,
Žiga Strmšek,
Tina Lebar,
Anže Verbič,
Matej Dragovan,
Neža Omersa,
Gregor Anderluh,
Roman Jerala
Publication year - 2022
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkac454
Subject(s) - biology , general transcription factor , transcription factor , transcription (linguistics) , dna binding protein , e box , effector , rna polymerase ii , sp3 transcription factor , dna binding domain , transcription factor ii e , promoter , dna , transcription coregulator , taf2 , response element , microbiology and biotechnology , eukaryotic transcription , genetics , transcriptional regulation , enhancer , gene expression , gene , linguistics , philosophy
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.

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