A model for genetic and epigenetic regulatory networks identifies rare for transcription factor induced pluripotency

With relatively low efficiency, differentiated cells can be reprogrammed to a pluripotent state by ectopic expression of a few transcription factors. An understanding of the mechanisms that underlie data emerging from such experiments can help design optimal strategies for creating pluripotent cells...

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Main Authors: Artyomov, Maxim N., Meissner, Alexander, Chakraborty, Arup K.
Other Authors: Massachusetts Institute of Technology. Department of Biological Engineering
Format: Article
Language:en_US
Published: Public Library of Science 2010
Online Access:http://hdl.handle.net/1721.1/57580
https://orcid.org/0000-0003-1268-9602
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author Artyomov, Maxim N.
Meissner, Alexander
Chakraborty, Arup K.
author2 Massachusetts Institute of Technology. Department of Biological Engineering
author_facet Massachusetts Institute of Technology. Department of Biological Engineering
Artyomov, Maxim N.
Meissner, Alexander
Chakraborty, Arup K.
author_sort Artyomov, Maxim N.
collection MIT
description With relatively low efficiency, differentiated cells can be reprogrammed to a pluripotent state by ectopic expression of a few transcription factors. An understanding of the mechanisms that underlie data emerging from such experiments can help design optimal strategies for creating pluripotent cells for patient-specific regenerative medicine. We have developed a computational model for the architecture of the epigenetic and genetic regulatory networks which describes transformations resulting from expression of reprogramming factors. Importantly, our studies identify the rare temporal pathways that result in induced pluripotent cells. Further experimental tests of predictions emerging from our model should lead to fundamental advances in our understanding of how cellular identity is maintained and transformed.
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spelling mit-1721.1/575802022-10-01T00:12:42Z A model for genetic and epigenetic regulatory networks identifies rare for transcription factor induced pluripotency Artyomov, Maxim N. Meissner, Alexander Chakraborty, Arup K. Massachusetts Institute of Technology. Department of Biological Engineering Massachusetts Institute of Technology. Department of Chemical Engineering Massachusetts Institute of Technology. Department of Chemistry Chakraborty, Arup K. Chakraborty, Arup K. Artyomov, Maxim N. With relatively low efficiency, differentiated cells can be reprogrammed to a pluripotent state by ectopic expression of a few transcription factors. An understanding of the mechanisms that underlie data emerging from such experiments can help design optimal strategies for creating pluripotent cells for patient-specific regenerative medicine. We have developed a computational model for the architecture of the epigenetic and genetic regulatory networks which describes transformations resulting from expression of reprogramming factors. Importantly, our studies identify the rare temporal pathways that result in induced pluripotent cells. Further experimental tests of predictions emerging from our model should lead to fundamental advances in our understanding of how cellular identity is maintained and transformed. 2010-08-27T14:16:35Z 2010-08-27T14:16:35Z 2010-05 2009-06 Article http://purl.org/eprint/type/JournalArticle 1553-7358 1553-734X http://hdl.handle.net/1721.1/57580 Artyomov, Maxim N., Alexander Meissner, and Arup K. Chakraborty. “A Model for Genetic and Epigenetic Regulatory Networks Identifies Rare Pathways for Transcription Factor Induced Pluripotency.” PLoS Comput Biol 6.5 (2010): e1000785. https://orcid.org/0000-0003-1268-9602 en_US http://dx.doi.org/10.1371/journal.pcbi.1000785 PLoS Computational Biology Creative Commons Attribution http://creativecommons.org/licenses/by/2.5/ application/pdf Public Library of Science PLoS
spellingShingle Artyomov, Maxim N.
Meissner, Alexander
Chakraborty, Arup K.
A model for genetic and epigenetic regulatory networks identifies rare for transcription factor induced pluripotency
title A model for genetic and epigenetic regulatory networks identifies rare for transcription factor induced pluripotency
title_full A model for genetic and epigenetic regulatory networks identifies rare for transcription factor induced pluripotency
title_fullStr A model for genetic and epigenetic regulatory networks identifies rare for transcription factor induced pluripotency
title_full_unstemmed A model for genetic and epigenetic regulatory networks identifies rare for transcription factor induced pluripotency
title_short A model for genetic and epigenetic regulatory networks identifies rare for transcription factor induced pluripotency
title_sort model for genetic and epigenetic regulatory networks identifies rare for transcription factor induced pluripotency
url http://hdl.handle.net/1721.1/57580
https://orcid.org/0000-0003-1268-9602
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