Cargando…

Co-expression networks in generation of induced pluripotent stem cells

We developed an adenoviral vector, in which Yamanaka's four reprogramming factors (RFs) were controlled by individual CMV promoters in a single cassette (Ad-SOcMK). This permitted coordinated expression of RFs (SOX2, OCT3/4, c-MYC and KLF4) in a cell for a transient period of time, synchronizin...

Descripción completa

Detalles Bibliográficos
Autores principales: Paul, Sharan, Pflieger, Lance, Dansithong, Warunee, Figueroa, Karla P., Gao, Fuying, Coppola, Giovanni, Pulst, Stefan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810748/
https://www.ncbi.nlm.nih.gov/pubmed/26892236
http://dx.doi.org/10.1242/bio.016402
_version_ 1782423842339160064
author Paul, Sharan
Pflieger, Lance
Dansithong, Warunee
Figueroa, Karla P.
Gao, Fuying
Coppola, Giovanni
Pulst, Stefan M.
author_facet Paul, Sharan
Pflieger, Lance
Dansithong, Warunee
Figueroa, Karla P.
Gao, Fuying
Coppola, Giovanni
Pulst, Stefan M.
author_sort Paul, Sharan
collection PubMed
description We developed an adenoviral vector, in which Yamanaka's four reprogramming factors (RFs) were controlled by individual CMV promoters in a single cassette (Ad-SOcMK). This permitted coordinated expression of RFs (SOX2, OCT3/4, c-MYC and KLF4) in a cell for a transient period of time, synchronizing the reprogramming process with the majority of transduced cells assuming induced pluripotent stem cell (iPSC)-like characteristics as early as three days post-transduction. These reprogrammed cells resembled human embryonic stem cells (ESCs) with regard to morphology, biomarker expression, and could be differentiated into cells of the germ layers in vitro and in vivo. These iPSC-like cells, however, failed to expand into larger iPSC colonies. The short and synchronized reprogramming process allowed us to study global transcription changes within short time intervals. Weighted gene co-expression network analysis (WGCNA) identified sixteen large gene co-expression modules, each including members of gene ontology categories involved in cell differentiation and development. In particular, the brown module contained a significant number of ESC marker genes, whereas the turquoise module contained cell-cycle-related genes that were downregulated in contrast to upregulation in human ESCs. Strong coordinated expression of all four RFs via adenoviral transduction may constrain stochastic processes and lead to silencing of genes important for cellular proliferation.
format Online
Article
Text
id pubmed-4810748
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher The Company of Biologists Ltd
record_format MEDLINE/PubMed
spelling pubmed-48107482016-04-04 Co-expression networks in generation of induced pluripotent stem cells Paul, Sharan Pflieger, Lance Dansithong, Warunee Figueroa, Karla P. Gao, Fuying Coppola, Giovanni Pulst, Stefan M. Biol Open Research Article We developed an adenoviral vector, in which Yamanaka's four reprogramming factors (RFs) were controlled by individual CMV promoters in a single cassette (Ad-SOcMK). This permitted coordinated expression of RFs (SOX2, OCT3/4, c-MYC and KLF4) in a cell for a transient period of time, synchronizing the reprogramming process with the majority of transduced cells assuming induced pluripotent stem cell (iPSC)-like characteristics as early as three days post-transduction. These reprogrammed cells resembled human embryonic stem cells (ESCs) with regard to morphology, biomarker expression, and could be differentiated into cells of the germ layers in vitro and in vivo. These iPSC-like cells, however, failed to expand into larger iPSC colonies. The short and synchronized reprogramming process allowed us to study global transcription changes within short time intervals. Weighted gene co-expression network analysis (WGCNA) identified sixteen large gene co-expression modules, each including members of gene ontology categories involved in cell differentiation and development. In particular, the brown module contained a significant number of ESC marker genes, whereas the turquoise module contained cell-cycle-related genes that were downregulated in contrast to upregulation in human ESCs. Strong coordinated expression of all four RFs via adenoviral transduction may constrain stochastic processes and lead to silencing of genes important for cellular proliferation. The Company of Biologists Ltd 2016-02-18 /pmc/articles/PMC4810748/ /pubmed/26892236 http://dx.doi.org/10.1242/bio.016402 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Paul, Sharan
Pflieger, Lance
Dansithong, Warunee
Figueroa, Karla P.
Gao, Fuying
Coppola, Giovanni
Pulst, Stefan M.
Co-expression networks in generation of induced pluripotent stem cells
title Co-expression networks in generation of induced pluripotent stem cells
title_full Co-expression networks in generation of induced pluripotent stem cells
title_fullStr Co-expression networks in generation of induced pluripotent stem cells
title_full_unstemmed Co-expression networks in generation of induced pluripotent stem cells
title_short Co-expression networks in generation of induced pluripotent stem cells
title_sort co-expression networks in generation of induced pluripotent stem cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810748/
https://www.ncbi.nlm.nih.gov/pubmed/26892236
http://dx.doi.org/10.1242/bio.016402
work_keys_str_mv AT paulsharan coexpressionnetworksingenerationofinducedpluripotentstemcells
AT pfliegerlance coexpressionnetworksingenerationofinducedpluripotentstemcells
AT dansithongwarunee coexpressionnetworksingenerationofinducedpluripotentstemcells
AT figueroakarlap coexpressionnetworksingenerationofinducedpluripotentstemcells
AT gaofuying coexpressionnetworksingenerationofinducedpluripotentstemcells
AT coppolagiovanni coexpressionnetworksingenerationofinducedpluripotentstemcells
AT pulststefanm coexpressionnetworksingenerationofinducedpluripotentstemcells