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Comparison of chicken 7SK and U6 RNA polymerase III promoters for short hairpin RNA expression

BACKGROUND: RNA polymerase III (pol III) type 3 promoters such as U6 or 7SK are commonly used to express short-hairpin RNA (shRNA) effectors for RNA interference (RNAi). To extend the use of RNAi for studies of development using the chicken as a model system, we have developed a system for expressin...

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Autores principales: Bannister, Stephanie C, Wise, Terry G, Cahill, David M, Doran, Timothy J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2235858/
https://www.ncbi.nlm.nih.gov/pubmed/18021456
http://dx.doi.org/10.1186/1472-6750-7-79
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author Bannister, Stephanie C
Wise, Terry G
Cahill, David M
Doran, Timothy J
author_facet Bannister, Stephanie C
Wise, Terry G
Cahill, David M
Doran, Timothy J
author_sort Bannister, Stephanie C
collection PubMed
description BACKGROUND: RNA polymerase III (pol III) type 3 promoters such as U6 or 7SK are commonly used to express short-hairpin RNA (shRNA) effectors for RNA interference (RNAi). To extend the use of RNAi for studies of development using the chicken as a model system, we have developed a system for expressing shRNAs using the chicken 7SK (ch7SK) promoter. RESULTS: We identified and characterised the ch7SK promoter sequence upstream of the full-length 7SK small nuclear RNA (snRNA) sequence in the chicken genome and used this to construct vectors to express shRNAs targeting enhanced green fluorescent protein (EGFP). We transfected chicken DF-1 cells with these constructs and found that anti-EGFP-shRNAs (shEGFP) expressed from the ch7SK promoter could induce efficient knockdown of EGFP expression. We further compared the efficiency of ch7SK-directed knockdown to that of chicken U6 (cU6) promoters and found that the efficiency of the ch7SK promoter was not greater than, but comparable to the efficiency of cU6 promoters. CONCLUSION: In this study we have demonstrated that the ch7SK promoter can express shRNAs capable of mediating efficient RNAi in a chicken cell line. However, our finding that RNAi driven by the ch7SK promoter is not more efficient than cU6 promoters contrasts previous comparisons of mammalian U6 and 7SK promoters. Since the ch7SK promoter is the first non-mammalian vertebrate 7SK promoter to be characterised, this finding may be helpful in understanding the divergence of pol III promoter activities between mammalian and non-mammalian vertebrates. This aside, our results clearly indicate that the ch7SK promoter is an efficient alternative to U6-based shRNA expression systems for inducing efficient RNAi activity in chicken cells.
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spelling pubmed-22358582008-02-09 Comparison of chicken 7SK and U6 RNA polymerase III promoters for short hairpin RNA expression Bannister, Stephanie C Wise, Terry G Cahill, David M Doran, Timothy J BMC Biotechnol Research Article BACKGROUND: RNA polymerase III (pol III) type 3 promoters such as U6 or 7SK are commonly used to express short-hairpin RNA (shRNA) effectors for RNA interference (RNAi). To extend the use of RNAi for studies of development using the chicken as a model system, we have developed a system for expressing shRNAs using the chicken 7SK (ch7SK) promoter. RESULTS: We identified and characterised the ch7SK promoter sequence upstream of the full-length 7SK small nuclear RNA (snRNA) sequence in the chicken genome and used this to construct vectors to express shRNAs targeting enhanced green fluorescent protein (EGFP). We transfected chicken DF-1 cells with these constructs and found that anti-EGFP-shRNAs (shEGFP) expressed from the ch7SK promoter could induce efficient knockdown of EGFP expression. We further compared the efficiency of ch7SK-directed knockdown to that of chicken U6 (cU6) promoters and found that the efficiency of the ch7SK promoter was not greater than, but comparable to the efficiency of cU6 promoters. CONCLUSION: In this study we have demonstrated that the ch7SK promoter can express shRNAs capable of mediating efficient RNAi in a chicken cell line. However, our finding that RNAi driven by the ch7SK promoter is not more efficient than cU6 promoters contrasts previous comparisons of mammalian U6 and 7SK promoters. Since the ch7SK promoter is the first non-mammalian vertebrate 7SK promoter to be characterised, this finding may be helpful in understanding the divergence of pol III promoter activities between mammalian and non-mammalian vertebrates. This aside, our results clearly indicate that the ch7SK promoter is an efficient alternative to U6-based shRNA expression systems for inducing efficient RNAi activity in chicken cells. BioMed Central 2007-11-19 /pmc/articles/PMC2235858/ /pubmed/18021456 http://dx.doi.org/10.1186/1472-6750-7-79 Text en Copyright © 2007 Bannister et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bannister, Stephanie C
Wise, Terry G
Cahill, David M
Doran, Timothy J
Comparison of chicken 7SK and U6 RNA polymerase III promoters for short hairpin RNA expression
title Comparison of chicken 7SK and U6 RNA polymerase III promoters for short hairpin RNA expression
title_full Comparison of chicken 7SK and U6 RNA polymerase III promoters for short hairpin RNA expression
title_fullStr Comparison of chicken 7SK and U6 RNA polymerase III promoters for short hairpin RNA expression
title_full_unstemmed Comparison of chicken 7SK and U6 RNA polymerase III promoters for short hairpin RNA expression
title_short Comparison of chicken 7SK and U6 RNA polymerase III promoters for short hairpin RNA expression
title_sort comparison of chicken 7sk and u6 rna polymerase iii promoters for short hairpin rna expression
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2235858/
https://www.ncbi.nlm.nih.gov/pubmed/18021456
http://dx.doi.org/10.1186/1472-6750-7-79
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