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From RNAi Screens to Molecular Function in Embryonic Stem Cells

The ability of embryonic stem (ES) cells to generate any of the around 220 cell types of the adult body has fascinated scientists ever since their discovery. The capacity to re-program fully differentiated cells into induced pluripotent stem (iPS) cells has further stimulated the interest in ES cell...

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Detalles Bibliográficos
Autores principales: Ding, Li, Poser, Ina, Paszkowski-Rogacz, Maciej, Buchholz, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Humana Press Inc 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3285751/
https://www.ncbi.nlm.nih.gov/pubmed/21526416
http://dx.doi.org/10.1007/s12015-011-9269-z
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author Ding, Li
Poser, Ina
Paszkowski-Rogacz, Maciej
Buchholz, Frank
author_facet Ding, Li
Poser, Ina
Paszkowski-Rogacz, Maciej
Buchholz, Frank
author_sort Ding, Li
collection PubMed
description The ability of embryonic stem (ES) cells to generate any of the around 220 cell types of the adult body has fascinated scientists ever since their discovery. The capacity to re-program fully differentiated cells into induced pluripotent stem (iPS) cells has further stimulated the interest in ES cell research. Fueled by this interest, intense research has provided new insights into the biology of ES cells in the recent past. The development of large-scale and high throughput RNAi technologies has made it possible to sample the role of every gene in maintaining ES cell identity. Here, we review the RNAi screens performed in ES cells to date and discuss the challenges associated with these large-scale experiments. Furthermore, we provide a perspective on how to streamline the molecular characterization following the initial phenotypic description utilizing bacterial artificial chromosome (BAC) transgenesis.
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spelling pubmed-32857512012-03-08 From RNAi Screens to Molecular Function in Embryonic Stem Cells Ding, Li Poser, Ina Paszkowski-Rogacz, Maciej Buchholz, Frank Stem Cell Rev Article The ability of embryonic stem (ES) cells to generate any of the around 220 cell types of the adult body has fascinated scientists ever since their discovery. The capacity to re-program fully differentiated cells into induced pluripotent stem (iPS) cells has further stimulated the interest in ES cell research. Fueled by this interest, intense research has provided new insights into the biology of ES cells in the recent past. The development of large-scale and high throughput RNAi technologies has made it possible to sample the role of every gene in maintaining ES cell identity. Here, we review the RNAi screens performed in ES cells to date and discuss the challenges associated with these large-scale experiments. Furthermore, we provide a perspective on how to streamline the molecular characterization following the initial phenotypic description utilizing bacterial artificial chromosome (BAC) transgenesis. Humana Press Inc 2011-04-28 2012 /pmc/articles/PMC3285751/ /pubmed/21526416 http://dx.doi.org/10.1007/s12015-011-9269-z Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Article
Ding, Li
Poser, Ina
Paszkowski-Rogacz, Maciej
Buchholz, Frank
From RNAi Screens to Molecular Function in Embryonic Stem Cells
title From RNAi Screens to Molecular Function in Embryonic Stem Cells
title_full From RNAi Screens to Molecular Function in Embryonic Stem Cells
title_fullStr From RNAi Screens to Molecular Function in Embryonic Stem Cells
title_full_unstemmed From RNAi Screens to Molecular Function in Embryonic Stem Cells
title_short From RNAi Screens to Molecular Function in Embryonic Stem Cells
title_sort from rnai screens to molecular function in embryonic stem cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3285751/
https://www.ncbi.nlm.nih.gov/pubmed/21526416
http://dx.doi.org/10.1007/s12015-011-9269-z
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