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Tuning Plant Promoters Using a Simple Split Luciferase Method to Assess Transcription Factor-DNA Interactions

[Image: see text] Sequence features, including the affinity of binding motifs for their cognate transcription factors, are important contributors to promoter behavior. The ability to predictably recode affinity enables the development of synthetic promoters with varying levels of response to known c...

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Autores principales: Cai, Y.-M., Witham, S., Patron, N. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661027/
https://www.ncbi.nlm.nih.gov/pubmed/37856867
http://dx.doi.org/10.1021/acssynbio.3c00094
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author Cai, Y.-M.
Witham, S.
Patron, N. J.
author_facet Cai, Y.-M.
Witham, S.
Patron, N. J.
author_sort Cai, Y.-M.
collection PubMed
description [Image: see text] Sequence features, including the affinity of binding motifs for their cognate transcription factors, are important contributors to promoter behavior. The ability to predictably recode affinity enables the development of synthetic promoters with varying levels of response to known cellular signals. Here we describe a luminescence-based microplate assay for comparing the interactions of transcription factors with short DNA probes. We then demonstrate how these data can be used to design synthetic plant promoters of varying strengths that respond to the same transcription factor.
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spelling pubmed-106610272023-11-21 Tuning Plant Promoters Using a Simple Split Luciferase Method to Assess Transcription Factor-DNA Interactions Cai, Y.-M. Witham, S. Patron, N. J. ACS Synth Biol [Image: see text] Sequence features, including the affinity of binding motifs for their cognate transcription factors, are important contributors to promoter behavior. The ability to predictably recode affinity enables the development of synthetic promoters with varying levels of response to known cellular signals. Here we describe a luminescence-based microplate assay for comparing the interactions of transcription factors with short DNA probes. We then demonstrate how these data can be used to design synthetic plant promoters of varying strengths that respond to the same transcription factor. American Chemical Society 2023-10-19 /pmc/articles/PMC10661027/ /pubmed/37856867 http://dx.doi.org/10.1021/acssynbio.3c00094 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Cai, Y.-M.
Witham, S.
Patron, N. J.
Tuning Plant Promoters Using a Simple Split Luciferase Method to Assess Transcription Factor-DNA Interactions
title Tuning Plant Promoters Using a Simple Split Luciferase Method to Assess Transcription Factor-DNA Interactions
title_full Tuning Plant Promoters Using a Simple Split Luciferase Method to Assess Transcription Factor-DNA Interactions
title_fullStr Tuning Plant Promoters Using a Simple Split Luciferase Method to Assess Transcription Factor-DNA Interactions
title_full_unstemmed Tuning Plant Promoters Using a Simple Split Luciferase Method to Assess Transcription Factor-DNA Interactions
title_short Tuning Plant Promoters Using a Simple Split Luciferase Method to Assess Transcription Factor-DNA Interactions
title_sort tuning plant promoters using a simple split luciferase method to assess transcription factor-dna interactions
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10661027/
https://www.ncbi.nlm.nih.gov/pubmed/37856867
http://dx.doi.org/10.1021/acssynbio.3c00094
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