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A structural interpretation of the effect of GC-content on efficiency of RNA interference
BACKGROUND: RNA interference (RNAi) mediated by small interfering RNAs (siRNAs) or short hairpin RNAs (shRNAs) has become a powerful technique for eukaryotic gene knockdown. siRNA GC-content negatively correlates with RNAi efficiency, and it is of interest to have a convincing mechanistic interpreta...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648742/ https://www.ncbi.nlm.nih.gov/pubmed/19208134 http://dx.doi.org/10.1186/1471-2105-10-S1-S33 |
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author | Chan, Chi Yu Carmack, C Steven Long, Dang D Maliyekkel, Anil Shao, Yu Roninson, Igor B Ding, Ye |
author_facet | Chan, Chi Yu Carmack, C Steven Long, Dang D Maliyekkel, Anil Shao, Yu Roninson, Igor B Ding, Ye |
author_sort | Chan, Chi Yu |
collection | PubMed |
description | BACKGROUND: RNA interference (RNAi) mediated by small interfering RNAs (siRNAs) or short hairpin RNAs (shRNAs) has become a powerful technique for eukaryotic gene knockdown. siRNA GC-content negatively correlates with RNAi efficiency, and it is of interest to have a convincing mechanistic interpretation of this observation. We here examine this issue by considering the secondary structures for both the target messenger RNA (mRNA) and the siRNA guide strand. RESULTS: By analyzing a unique homogeneous data set of 101 shRNAs targeted to 100 endogenous human genes, we find that: 1) target site accessibility is more important than GC-content for efficient RNAi; 2) there is an appreciable negative correlation between GC-content and RNAi activity; 3) for the predicted structure of the siRNA guide strand, there is a lack of correlation between RNAi activity and either the stability or the number of free dangling nucleotides at an end of the structure; 4) there is a high correlation between target site accessibility and GC-content. For a set of representative structural RNAs, the GC content of 62.6% for paired bases is significantly higher than the GC content of 38.7% for unpaired bases. Thus, for a structured RNA, a region with higher GC content is likely to have more stable secondary structure. Furthermore, by partial correlation analysis, the correlation for GC-content is almost completely diminished, when the effect of target accessibility is controlled. CONCLUSION: These findings provide a target-structure-based interpretation and mechanistic insight for the effect of GC-content on RNAi efficiency. |
format | Text |
id | pubmed-2648742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26487422009-02-28 A structural interpretation of the effect of GC-content on efficiency of RNA interference Chan, Chi Yu Carmack, C Steven Long, Dang D Maliyekkel, Anil Shao, Yu Roninson, Igor B Ding, Ye BMC Bioinformatics Research BACKGROUND: RNA interference (RNAi) mediated by small interfering RNAs (siRNAs) or short hairpin RNAs (shRNAs) has become a powerful technique for eukaryotic gene knockdown. siRNA GC-content negatively correlates with RNAi efficiency, and it is of interest to have a convincing mechanistic interpretation of this observation. We here examine this issue by considering the secondary structures for both the target messenger RNA (mRNA) and the siRNA guide strand. RESULTS: By analyzing a unique homogeneous data set of 101 shRNAs targeted to 100 endogenous human genes, we find that: 1) target site accessibility is more important than GC-content for efficient RNAi; 2) there is an appreciable negative correlation between GC-content and RNAi activity; 3) for the predicted structure of the siRNA guide strand, there is a lack of correlation between RNAi activity and either the stability or the number of free dangling nucleotides at an end of the structure; 4) there is a high correlation between target site accessibility and GC-content. For a set of representative structural RNAs, the GC content of 62.6% for paired bases is significantly higher than the GC content of 38.7% for unpaired bases. Thus, for a structured RNA, a region with higher GC content is likely to have more stable secondary structure. Furthermore, by partial correlation analysis, the correlation for GC-content is almost completely diminished, when the effect of target accessibility is controlled. CONCLUSION: These findings provide a target-structure-based interpretation and mechanistic insight for the effect of GC-content on RNAi efficiency. BioMed Central 2009-01-30 /pmc/articles/PMC2648742/ /pubmed/19208134 http://dx.doi.org/10.1186/1471-2105-10-S1-S33 Text en Copyright © 2009 Chan 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 Chan, Chi Yu Carmack, C Steven Long, Dang D Maliyekkel, Anil Shao, Yu Roninson, Igor B Ding, Ye A structural interpretation of the effect of GC-content on efficiency of RNA interference |
title | A structural interpretation of the effect of GC-content on efficiency of RNA interference |
title_full | A structural interpretation of the effect of GC-content on efficiency of RNA interference |
title_fullStr | A structural interpretation of the effect of GC-content on efficiency of RNA interference |
title_full_unstemmed | A structural interpretation of the effect of GC-content on efficiency of RNA interference |
title_short | A structural interpretation of the effect of GC-content on efficiency of RNA interference |
title_sort | structural interpretation of the effect of gc-content on efficiency of rna interference |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648742/ https://www.ncbi.nlm.nih.gov/pubmed/19208134 http://dx.doi.org/10.1186/1471-2105-10-S1-S33 |
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