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Alternative Splicing in Self-Renewal of Embryonic Stem Cells

Much of embryonic stem cell biology has focused on transcriptional expression and regulation of genes that could mediate its unique potential in self-renewal or pluripotency. In alignment with our present understanding on the genetic, protein, and epigenetic factors that may direct cell fate, we pre...

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Detalles Bibliográficos
Autores principales: Cheong, Clara Y., Lufkin, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3137993/
https://www.ncbi.nlm.nih.gov/pubmed/21776282
http://dx.doi.org/10.4061/2011/560261
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author Cheong, Clara Y.
Lufkin, Thomas
author_facet Cheong, Clara Y.
Lufkin, Thomas
author_sort Cheong, Clara Y.
collection PubMed
description Much of embryonic stem cell biology has focused on transcriptional expression and regulation of genes that could mediate its unique potential in self-renewal or pluripotency. In alignment with our present understanding on the genetic, protein, and epigenetic factors that may direct cell fate, we present a short overview of the often overlooked contribution of alternative splice variants to regulatory diversity. Progressing beyond the limitations of a fixed genomic sequence, alternative splicing offers an additional layer of complexity to produce protein variants that may differ in function and localization that can direct embryonic stem cells to specific differentiation pathways. In light of the number of variants that can be produced at key ES cell genes alone, it is challenging to consider how much more multifaceted transcriptional regulation truly is, and if this can be captured more fully in future works.
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spelling pubmed-31379932011-07-20 Alternative Splicing in Self-Renewal of Embryonic Stem Cells Cheong, Clara Y. Lufkin, Thomas Stem Cells Int Review Article Much of embryonic stem cell biology has focused on transcriptional expression and regulation of genes that could mediate its unique potential in self-renewal or pluripotency. In alignment with our present understanding on the genetic, protein, and epigenetic factors that may direct cell fate, we present a short overview of the often overlooked contribution of alternative splice variants to regulatory diversity. Progressing beyond the limitations of a fixed genomic sequence, alternative splicing offers an additional layer of complexity to produce protein variants that may differ in function and localization that can direct embryonic stem cells to specific differentiation pathways. In light of the number of variants that can be produced at key ES cell genes alone, it is challenging to consider how much more multifaceted transcriptional regulation truly is, and if this can be captured more fully in future works. SAGE-Hindawi Access to Research 2011-06-09 /pmc/articles/PMC3137993/ /pubmed/21776282 http://dx.doi.org/10.4061/2011/560261 Text en Copyright © 2011 C. Y. Cheong and T. Lufkin. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Cheong, Clara Y.
Lufkin, Thomas
Alternative Splicing in Self-Renewal of Embryonic Stem Cells
title Alternative Splicing in Self-Renewal of Embryonic Stem Cells
title_full Alternative Splicing in Self-Renewal of Embryonic Stem Cells
title_fullStr Alternative Splicing in Self-Renewal of Embryonic Stem Cells
title_full_unstemmed Alternative Splicing in Self-Renewal of Embryonic Stem Cells
title_short Alternative Splicing in Self-Renewal of Embryonic Stem Cells
title_sort alternative splicing in self-renewal of embryonic stem cells
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3137993/
https://www.ncbi.nlm.nih.gov/pubmed/21776282
http://dx.doi.org/10.4061/2011/560261
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