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Gene interaction studies in cellular reprogramming of adult stem cells to embyronic like stem cells

The sophisticated process of reprogramming of adult stem cells to embryonic-like stem cells, known as cellular reprogramming, involves the risk of generation of tumorigenic cells due to the complexity involved. Oct4 protein is the inevitable element for inducing pluripotency along with Sox2 and Nano...

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Detalles Bibliográficos
Autores principales: Gangadaran, Nishanthi, James, Jannet Vennila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Biomedical Informatics 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488832/
https://www.ncbi.nlm.nih.gov/pubmed/23144550
http://dx.doi.org/10.6026/97320630008912
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author Gangadaran, Nishanthi
James, Jannet Vennila
author_facet Gangadaran, Nishanthi
James, Jannet Vennila
author_sort Gangadaran, Nishanthi
collection PubMed
description The sophisticated process of reprogramming of adult stem cells to embryonic-like stem cells, known as cellular reprogramming, involves the risk of generation of tumorigenic cells due to the complexity involved. Oct4 protein is the inevitable element for inducing pluripotency along with Sox2 and Nanog proteins. In this study, the set of genes interacting with Oct4, Sox2 and Nanog were analyzed and categorized based on their molecular function. Later, the domains of translated products of 46 transcription factors interacting with Oct4, Sox2 and Nanog were identified, clustered them based on the nature of the domain and multiple sequence alignment was performed to find any functionally important consensus regions in the sequence. The key finding of this study is the 13 member cluster of homeo domain transcription factors exhibited some consensus in their sequence.
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spelling pubmed-34888322012-11-09 Gene interaction studies in cellular reprogramming of adult stem cells to embyronic like stem cells Gangadaran, Nishanthi James, Jannet Vennila Bioinformation Hypothesis The sophisticated process of reprogramming of adult stem cells to embryonic-like stem cells, known as cellular reprogramming, involves the risk of generation of tumorigenic cells due to the complexity involved. Oct4 protein is the inevitable element for inducing pluripotency along with Sox2 and Nanog proteins. In this study, the set of genes interacting with Oct4, Sox2 and Nanog were analyzed and categorized based on their molecular function. Later, the domains of translated products of 46 transcription factors interacting with Oct4, Sox2 and Nanog were identified, clustered them based on the nature of the domain and multiple sequence alignment was performed to find any functionally important consensus regions in the sequence. The key finding of this study is the 13 member cluster of homeo domain transcription factors exhibited some consensus in their sequence. Biomedical Informatics 2012-10-01 /pmc/articles/PMC3488832/ /pubmed/23144550 http://dx.doi.org/10.6026/97320630008912 Text en © 2012 Biomedical Informatics This is an open-access article, which permits unrestricted use, distribution, and reproduction in any medium, for non-commercial purposes, provided the original author and source are credited.
spellingShingle Hypothesis
Gangadaran, Nishanthi
James, Jannet Vennila
Gene interaction studies in cellular reprogramming of adult stem cells to embyronic like stem cells
title Gene interaction studies in cellular reprogramming of adult stem cells to embyronic like stem cells
title_full Gene interaction studies in cellular reprogramming of adult stem cells to embyronic like stem cells
title_fullStr Gene interaction studies in cellular reprogramming of adult stem cells to embyronic like stem cells
title_full_unstemmed Gene interaction studies in cellular reprogramming of adult stem cells to embyronic like stem cells
title_short Gene interaction studies in cellular reprogramming of adult stem cells to embyronic like stem cells
title_sort gene interaction studies in cellular reprogramming of adult stem cells to embyronic like stem cells
topic Hypothesis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488832/
https://www.ncbi.nlm.nih.gov/pubmed/23144550
http://dx.doi.org/10.6026/97320630008912
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