2022
DOI: 10.1101/2022.04.11.487922
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An intrinsically disordered transcription activation domain alters the DNA binding affinity and specificity of NFκB p50/RelA

Abstract: Many transcription factors contain intrinsically disordered transcription activation domains (TADs), which mediate interactions with co-activators to activate transcription. Historically, DNA-binding domains and TADs have been considered as modular units, but recent studies have shown that TADs can influence DNA binding. We biophysically characterized the NFκB p50/RelA heterodimer including the RelA TAD and investigated the influence of the TAD on NFκB-DNA interactions. In solution the RelA TAD is disordered b… Show more

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Cited by 2 publications
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“…I use the term IDR to refer to regions described as the 'non-DBD' by Brodsky et al 2020. Classically, it was argued that DNA binding domains and activation domains were independent, modular components, but this idea is approaching the end of its usefulness. In the few cases that have been carefully examined, activation domains can modulate DNA affinity, increase specificity for cognate motifs, or increase affinity for random DNA (Liu et al 2008;Krois et al 2018;Baughman et al 2022). For the remainder of this piece, I assume that true modularity is rare.…”
mentioning
confidence: 99%
“…I use the term IDR to refer to regions described as the 'non-DBD' by Brodsky et al 2020. Classically, it was argued that DNA binding domains and activation domains were independent, modular components, but this idea is approaching the end of its usefulness. In the few cases that have been carefully examined, activation domains can modulate DNA affinity, increase specificity for cognate motifs, or increase affinity for random DNA (Liu et al 2008;Krois et al 2018;Baughman et al 2022). For the remainder of this piece, I assume that true modularity is rare.…”
mentioning
confidence: 99%