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Characterizing short germline-specific promoters with a range of expression levels in C. elegans

A core tenet of synthetic biology is that well-characterized regulatory elements are essential for engineering biological systems. Here, we characterize the specificity and expression levels of 18 short (254 to 880 bp) candidate germline promoters using a single-copy gfp reporter assay in C. elegans...

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Detalles Bibliográficos
Autores principales: Aljohani, Mohammed D., El Mouridi, Sonia, Frøkjær-Jensen, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Caltech Library 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366684/
https://www.ncbi.nlm.nih.gov/pubmed/37497182
http://dx.doi.org/10.17912/micropub.biology.000843
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author Aljohani, Mohammed D.
El Mouridi, Sonia
Frøkjær-Jensen, Christian
author_facet Aljohani, Mohammed D.
El Mouridi, Sonia
Frøkjær-Jensen, Christian
author_sort Aljohani, Mohammed D.
collection PubMed
description A core tenet of synthetic biology is that well-characterized regulatory elements are essential for engineering biological systems. Here, we characterize the specificity and expression levels of 18 short (254 to 880 bp) candidate germline promoters using a single-copy gfp reporter assay in C. elegans . Six promoters resulted in ubiquitous expression, three did not drive detectable expression, and nine were germline-specific. Several promoters drove stronger germline expression than the commonly-used mex-5 promoter. The promoters range across expression levels and facilitate, for example, low expression of toxic transgenes or high expression of gene editing enzymes, and their compactness facilitates gene synthesis.
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spelling pubmed-103666842023-07-26 Characterizing short germline-specific promoters with a range of expression levels in C. elegans Aljohani, Mohammed D. El Mouridi, Sonia Frøkjær-Jensen, Christian MicroPubl Biol Materials and Reagents A core tenet of synthetic biology is that well-characterized regulatory elements are essential for engineering biological systems. Here, we characterize the specificity and expression levels of 18 short (254 to 880 bp) candidate germline promoters using a single-copy gfp reporter assay in C. elegans . Six promoters resulted in ubiquitous expression, three did not drive detectable expression, and nine were germline-specific. Several promoters drove stronger germline expression than the commonly-used mex-5 promoter. The promoters range across expression levels and facilitate, for example, low expression of toxic transgenes or high expression of gene editing enzymes, and their compactness facilitates gene synthesis. Caltech Library 2023-07-10 /pmc/articles/PMC10366684/ /pubmed/37497182 http://dx.doi.org/10.17912/micropub.biology.000843 Text en Copyright: © 2023 by the authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Materials and Reagents
Aljohani, Mohammed D.
El Mouridi, Sonia
Frøkjær-Jensen, Christian
Characterizing short germline-specific promoters with a range of expression levels in C. elegans
title Characterizing short germline-specific promoters with a range of expression levels in C. elegans
title_full Characterizing short germline-specific promoters with a range of expression levels in C. elegans
title_fullStr Characterizing short germline-specific promoters with a range of expression levels in C. elegans
title_full_unstemmed Characterizing short germline-specific promoters with a range of expression levels in C. elegans
title_short Characterizing short germline-specific promoters with a range of expression levels in C. elegans
title_sort characterizing short germline-specific promoters with a range of expression levels in c. elegans
topic Materials and Reagents
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366684/
https://www.ncbi.nlm.nih.gov/pubmed/37497182
http://dx.doi.org/10.17912/micropub.biology.000843
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