Cargando…

New Strains for Tissue-Specific RNAi Studies in Caenorhabditis elegans

RNA interference is a powerful tool for dissecting gene function. In Caenorhabditis elegans, ingestion of double stranded RNA causes strong, systemic knockdown of target genes. Further insight into gene function can be revealed by tissue-specific RNAi techniques. Currently available tissue-specific...

Descripción completa

Detalles Bibliográficos
Autores principales: Watts, Jason S., Harrison, Henry F., Omi, Shizue, Guenthers, Quentin, Dalelio, James, Pujol, Nathalie, Watts, Jennifer L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642939/
https://www.ncbi.nlm.nih.gov/pubmed/32943454
http://dx.doi.org/10.1534/g3.120.401749
_version_ 1783606178468593664
author Watts, Jason S.
Harrison, Henry F.
Omi, Shizue
Guenthers, Quentin
Dalelio, James
Pujol, Nathalie
Watts, Jennifer L.
author_facet Watts, Jason S.
Harrison, Henry F.
Omi, Shizue
Guenthers, Quentin
Dalelio, James
Pujol, Nathalie
Watts, Jennifer L.
author_sort Watts, Jason S.
collection PubMed
description RNA interference is a powerful tool for dissecting gene function. In Caenorhabditis elegans, ingestion of double stranded RNA causes strong, systemic knockdown of target genes. Further insight into gene function can be revealed by tissue-specific RNAi techniques. Currently available tissue-specific C. elegans strains rely on rescue of RNAi function in a desired tissue or cell in an otherwise RNAi deficient genetic background. We attempted to assess the contribution of specific tissues to polyunsaturated fatty acid (PUFA) synthesis using currently available tissue-specific RNAi strains. We discovered that rde-1 (ne219), a commonly used RNAi-resistant mutant strain, retains considerable RNAi capacity against RNAi directed at PUFA synthesis genes. By measuring changes in the fatty acid products of the desaturase enzymes that synthesize PUFAs, we found that the before mentioned strain, rde-1 (ne219) and the reported germline only RNAi strain, rrf-1 (pk1417) are not appropriate genetic backgrounds for tissue-specific RNAi experiments. However, the knockout mutant rde-1 (ne300) was strongly resistant to dsRNA induced RNAi, and thus is more appropriate for construction of a robust tissue-specific RNAi strains. Using newly constructed strains in the rde-1(null) background, we found considerable desaturase activity in intestinal, epidermal, and germline tissues, but not in muscle. The RNAi-specific strains reported in this study will be useful tools for C. elegans researchers studying a variety of biological processes.
format Online
Article
Text
id pubmed-7642939
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Genetics Society of America
record_format MEDLINE/PubMed
spelling pubmed-76429392020-11-13 New Strains for Tissue-Specific RNAi Studies in Caenorhabditis elegans Watts, Jason S. Harrison, Henry F. Omi, Shizue Guenthers, Quentin Dalelio, James Pujol, Nathalie Watts, Jennifer L. G3 (Bethesda) Investigations RNA interference is a powerful tool for dissecting gene function. In Caenorhabditis elegans, ingestion of double stranded RNA causes strong, systemic knockdown of target genes. Further insight into gene function can be revealed by tissue-specific RNAi techniques. Currently available tissue-specific C. elegans strains rely on rescue of RNAi function in a desired tissue or cell in an otherwise RNAi deficient genetic background. We attempted to assess the contribution of specific tissues to polyunsaturated fatty acid (PUFA) synthesis using currently available tissue-specific RNAi strains. We discovered that rde-1 (ne219), a commonly used RNAi-resistant mutant strain, retains considerable RNAi capacity against RNAi directed at PUFA synthesis genes. By measuring changes in the fatty acid products of the desaturase enzymes that synthesize PUFAs, we found that the before mentioned strain, rde-1 (ne219) and the reported germline only RNAi strain, rrf-1 (pk1417) are not appropriate genetic backgrounds for tissue-specific RNAi experiments. However, the knockout mutant rde-1 (ne300) was strongly resistant to dsRNA induced RNAi, and thus is more appropriate for construction of a robust tissue-specific RNAi strains. Using newly constructed strains in the rde-1(null) background, we found considerable desaturase activity in intestinal, epidermal, and germline tissues, but not in muscle. The RNAi-specific strains reported in this study will be useful tools for C. elegans researchers studying a variety of biological processes. Genetics Society of America 2020-09-17 /pmc/articles/PMC7642939/ /pubmed/32943454 http://dx.doi.org/10.1534/g3.120.401749 Text en Copyright © 2020 Watts et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Watts, Jason S.
Harrison, Henry F.
Omi, Shizue
Guenthers, Quentin
Dalelio, James
Pujol, Nathalie
Watts, Jennifer L.
New Strains for Tissue-Specific RNAi Studies in Caenorhabditis elegans
title New Strains for Tissue-Specific RNAi Studies in Caenorhabditis elegans
title_full New Strains for Tissue-Specific RNAi Studies in Caenorhabditis elegans
title_fullStr New Strains for Tissue-Specific RNAi Studies in Caenorhabditis elegans
title_full_unstemmed New Strains for Tissue-Specific RNAi Studies in Caenorhabditis elegans
title_short New Strains for Tissue-Specific RNAi Studies in Caenorhabditis elegans
title_sort new strains for tissue-specific rnai studies in caenorhabditis elegans
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642939/
https://www.ncbi.nlm.nih.gov/pubmed/32943454
http://dx.doi.org/10.1534/g3.120.401749
work_keys_str_mv AT wattsjasons newstrainsfortissuespecificrnaistudiesincaenorhabditiselegans
AT harrisonhenryf newstrainsfortissuespecificrnaistudiesincaenorhabditiselegans
AT omishizue newstrainsfortissuespecificrnaistudiesincaenorhabditiselegans
AT guenthersquentin newstrainsfortissuespecificrnaistudiesincaenorhabditiselegans
AT daleliojames newstrainsfortissuespecificrnaistudiesincaenorhabditiselegans
AT pujolnathalie newstrainsfortissuespecificrnaistudiesincaenorhabditiselegans
AT wattsjenniferl newstrainsfortissuespecificrnaistudiesincaenorhabditiselegans