Profiling and quantification of pluripotency reprogramming reveal that WNT pathways and cell morphology have to be reprogramed extensively

Pluripotent state can be established via reprogramming of somatic nuclei by factors within an oocyte or by ectopic expression of a few transgenes. Considered as being extensive and intensive, the full complement of genes to be reprogrammed, however, has never been defined, nor has the degree of repr...

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Main Authors: Kejin Hu, Lara Ianov, David Crossman
Format: Article
Language:English
Published: Elsevier 2020-05-01
Series:Heliyon
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2405844020308793
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spelling doaj-31fd3eb9068149aa8d1255697bbc95c22020-11-25T03:49:17ZengElsevierHeliyon2405-84402020-05-0165e04035Profiling and quantification of pluripotency reprogramming reveal that WNT pathways and cell morphology have to be reprogramed extensivelyKejin Hu0Lara Ianov1David Crossman2Department of Biochemistry and Molecular Genetics, University of Alabama at Birmingham, Birmingham, AL, 35294, USA; Corresponding author.Civitan International Research Center, University of Alabama at Birmingham, Birmingham, AL, 35294, USAHeflin Center for Genomic Sciences, University of Alabama at Birmingham, Birmingham, AL, 35294, USAPluripotent state can be established via reprogramming of somatic nuclei by factors within an oocyte or by ectopic expression of a few transgenes. Considered as being extensive and intensive, the full complement of genes to be reprogrammed, however, has never been defined, nor has the degree of reprogramming been determined quantitatively. Here, we propose a new concept of reprogramome, which is defined as the full complement of genes to be reprogrammed to the expression levels found in pluripotent stem cells (PSCs). This concept in combination with RNA-seq enables us to precisely profile reprogramome and sub-reprogramomes, and study the reprogramming process with the help of other available tools such as GO analyses. With reprogramming of human fibroblasts into PSCs as an example, we have defined the full complement of the human fibroblast-to-PSC reprogramome. Furthermore, our analyses of the reprogramome revealed that WNT pathways and genes with roles in cellular morphogenesis should be extensively and intensely reprogrammed for the establishment of pluripotency. We further developed a new mathematical model to quantitate the overall reprogramming, as well as reprogramming in a specific cellular feature such as WNT signaling pathways and genes regulating cellular morphogenesis. We anticipate that our concept and mathematical model may be applied to study and quantitate other reprogramming (pluripotency reprogramming from other somatic cells, and lineage reprogramming), as well as transcriptional and epigenetic differences between any two types of cells including cancer cells and their normal counterparts.http://www.sciencedirect.com/science/article/pii/S2405844020308793Biological sciencesCell biologySystems biologyMathematical biosciencesBioinformaticsTranscriptomics
collection DOAJ
language English
format Article
sources DOAJ
author Kejin Hu
Lara Ianov
David Crossman
spellingShingle Kejin Hu
Lara Ianov
David Crossman
Profiling and quantification of pluripotency reprogramming reveal that WNT pathways and cell morphology have to be reprogramed extensively
Heliyon
Biological sciences
Cell biology
Systems biology
Mathematical biosciences
Bioinformatics
Transcriptomics
author_facet Kejin Hu
Lara Ianov
David Crossman
author_sort Kejin Hu
title Profiling and quantification of pluripotency reprogramming reveal that WNT pathways and cell morphology have to be reprogramed extensively
title_short Profiling and quantification of pluripotency reprogramming reveal that WNT pathways and cell morphology have to be reprogramed extensively
title_full Profiling and quantification of pluripotency reprogramming reveal that WNT pathways and cell morphology have to be reprogramed extensively
title_fullStr Profiling and quantification of pluripotency reprogramming reveal that WNT pathways and cell morphology have to be reprogramed extensively
title_full_unstemmed Profiling and quantification of pluripotency reprogramming reveal that WNT pathways and cell morphology have to be reprogramed extensively
title_sort profiling and quantification of pluripotency reprogramming reveal that wnt pathways and cell morphology have to be reprogramed extensively
publisher Elsevier
series Heliyon
issn 2405-8440
publishDate 2020-05-01
description Pluripotent state can be established via reprogramming of somatic nuclei by factors within an oocyte or by ectopic expression of a few transgenes. Considered as being extensive and intensive, the full complement of genes to be reprogrammed, however, has never been defined, nor has the degree of reprogramming been determined quantitatively. Here, we propose a new concept of reprogramome, which is defined as the full complement of genes to be reprogrammed to the expression levels found in pluripotent stem cells (PSCs). This concept in combination with RNA-seq enables us to precisely profile reprogramome and sub-reprogramomes, and study the reprogramming process with the help of other available tools such as GO analyses. With reprogramming of human fibroblasts into PSCs as an example, we have defined the full complement of the human fibroblast-to-PSC reprogramome. Furthermore, our analyses of the reprogramome revealed that WNT pathways and genes with roles in cellular morphogenesis should be extensively and intensely reprogrammed for the establishment of pluripotency. We further developed a new mathematical model to quantitate the overall reprogramming, as well as reprogramming in a specific cellular feature such as WNT signaling pathways and genes regulating cellular morphogenesis. We anticipate that our concept and mathematical model may be applied to study and quantitate other reprogramming (pluripotency reprogramming from other somatic cells, and lineage reprogramming), as well as transcriptional and epigenetic differences between any two types of cells including cancer cells and their normal counterparts.
topic Biological sciences
Cell biology
Systems biology
Mathematical biosciences
Bioinformatics
Transcriptomics
url http://www.sciencedirect.com/science/article/pii/S2405844020308793
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AT laraianov profilingandquantificationofpluripotencyreprogrammingrevealthatwntpathwaysandcellmorphologyhavetobereprogramedextensively
AT davidcrossman profilingandquantificationofpluripotencyreprogrammingrevealthatwntpathwaysandcellmorphologyhavetobereprogramedextensively
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