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Isoform specific knockdown of the ETS transcription factor Pointed in Drosophila S2 cells

Alternate splicing of the pointed ( pnt ) gene locus produces two major isoforms, PntP1 and PntP2. Understanding their individual contributions to key developmental processes and identification of their genome-wide transcriptional targets has been hampered by a number of factors including their esse...

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Autor principal: Vivekanand, Pavithra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Caltech Library 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245148/
https://www.ncbi.nlm.nih.gov/pubmed/37292519
http://dx.doi.org/10.17912/micropub.biology.000731
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author Vivekanand, Pavithra
author_facet Vivekanand, Pavithra
author_sort Vivekanand, Pavithra
collection PubMed
description Alternate splicing of the pointed ( pnt ) gene locus produces two major isoforms, PntP1 and PntP2. Understanding their individual contributions to key developmental processes and identification of their genome-wide transcriptional targets has been hampered by a number of factors including their essential roles during embryonic development, and co-expression in several tissues. siRNAs were designed to target isoform-specific exons that code for the unique N-terminal region of either PntP1 or PntP2. The efficacy and specificity of the siRNAs were examined by co-transfection of isoform specific siRNAs with plasmids encoding epitope tagged PntP1 or PntP2 in Drosophila S2 cells. All P1-specific siRNAs were demonstrated to knockdown PntP1 protein level to greater than 95%, while having nominal impact on PntP2 level. Similarly, PntP2 siRNAs while ineffective at eliminating PntP1, were shown to reduce PntP2 protein level by 87-99%.
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spelling pubmed-102451482023-06-08 Isoform specific knockdown of the ETS transcription factor Pointed in Drosophila S2 cells Vivekanand, Pavithra MicroPubl Biol New Finding Alternate splicing of the pointed ( pnt ) gene locus produces two major isoforms, PntP1 and PntP2. Understanding their individual contributions to key developmental processes and identification of their genome-wide transcriptional targets has been hampered by a number of factors including their essential roles during embryonic development, and co-expression in several tissues. siRNAs were designed to target isoform-specific exons that code for the unique N-terminal region of either PntP1 or PntP2. The efficacy and specificity of the siRNAs were examined by co-transfection of isoform specific siRNAs with plasmids encoding epitope tagged PntP1 or PntP2 in Drosophila S2 cells. All P1-specific siRNAs were demonstrated to knockdown PntP1 protein level to greater than 95%, while having nominal impact on PntP2 level. Similarly, PntP2 siRNAs while ineffective at eliminating PntP1, were shown to reduce PntP2 protein level by 87-99%. Caltech Library 2023-05-23 /pmc/articles/PMC10245148/ /pubmed/37292519 http://dx.doi.org/10.17912/micropub.biology.000731 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 New Finding
Vivekanand, Pavithra
Isoform specific knockdown of the ETS transcription factor Pointed in Drosophila S2 cells
title Isoform specific knockdown of the ETS transcription factor Pointed in Drosophila S2 cells
title_full Isoform specific knockdown of the ETS transcription factor Pointed in Drosophila S2 cells
title_fullStr Isoform specific knockdown of the ETS transcription factor Pointed in Drosophila S2 cells
title_full_unstemmed Isoform specific knockdown of the ETS transcription factor Pointed in Drosophila S2 cells
title_short Isoform specific knockdown of the ETS transcription factor Pointed in Drosophila S2 cells
title_sort isoform specific knockdown of the ets transcription factor pointed in drosophila s2 cells
topic New Finding
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245148/
https://www.ncbi.nlm.nih.gov/pubmed/37292519
http://dx.doi.org/10.17912/micropub.biology.000731
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