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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE-Hindawi Access to Research
2011
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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. |
format | Online Article Text |
id | pubmed-3137993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | SAGE-Hindawi Access to Research |
record_format | MEDLINE/PubMed |
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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