A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance

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A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance. / Livigni, Alessandra; Peradziryi, Hanna; Sharov, Alexei A; Chia, Gloryn; Hammachi, Fella; Migueles, Rosa Portero; Sukparangsi, Woranop; Pernagallo, Salvatore; Bradley, Mark; Nichols, Jennifer; Ko, Minoru S H; Brickman, Joshua M.

In: Current biology : CB, Vol. 23, No. 22, 18.11.2013, p. 2233-44.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Livigni, A, Peradziryi, H, Sharov, AA, Chia, G, Hammachi, F, Migueles, RP, Sukparangsi, W, Pernagallo, S, Bradley, M, Nichols, J, Ko, MSH & Brickman, JM 2013, 'A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance', Current biology : CB, vol. 23, no. 22, pp. 2233-44. https://doi.org/10.1016/j.cub.2013.09.048

APA

Livigni, A., Peradziryi, H., Sharov, A. A., Chia, G., Hammachi, F., Migueles, R. P., Sukparangsi, W., Pernagallo, S., Bradley, M., Nichols, J., Ko, M. S. H., & Brickman, J. M. (2013). A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance. Current biology : CB, 23(22), 2233-44. https://doi.org/10.1016/j.cub.2013.09.048

Vancouver

Livigni A, Peradziryi H, Sharov AA, Chia G, Hammachi F, Migueles RP et al. A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance. Current biology : CB. 2013 Nov 18;23(22):2233-44. https://doi.org/10.1016/j.cub.2013.09.048

Author

Livigni, Alessandra ; Peradziryi, Hanna ; Sharov, Alexei A ; Chia, Gloryn ; Hammachi, Fella ; Migueles, Rosa Portero ; Sukparangsi, Woranop ; Pernagallo, Salvatore ; Bradley, Mark ; Nichols, Jennifer ; Ko, Minoru S H ; Brickman, Joshua M. / A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance. In: Current biology : CB. 2013 ; Vol. 23, No. 22. pp. 2233-44.

Bibtex

@article{336061a1ab6347118bf8b32ecda34c60,
title = "A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance",
abstract = "BACKGROUND: The class V POU domain transcription factor Oct4 (Pou5f1) is a pivotal regulator of embryonic stem cell (ESC) self-renewal and reprogramming of somatic cells to induced pluripotent stem (iPS) cells. Oct4 is also an important evolutionarily conserved regulator of progenitor cell differentiation during embryonic development.RESULTS: Here we examine the function of Oct4 homologs in Xenopus embryos and compare this to the role of Oct4 in maintaining mammalian embryo-derived stem cells. Based on a combination of expression profiling of Oct4/POUV-depleted Xenopus embryos and in silico analysis of existing mammalian Oct4 target data sets, we defined a set of evolutionary-conserved Oct4/POUV targets. Most of these targets were regulators of cell adhesion. This is consistent with Oct4/POUV phenotypes observed in the adherens junctions in Xenopus ectoderm, mouse embryonic, and epiblast stem cells. A number of these targets could rescue both Oct4/POUV phenotypes in cellular adhesion and multipotent progenitor cell maintenance, whereas expression of cadherins on their own could only transiently support adhesion and block differentiation in both ESC and Xenopus embryos.CONCLUSIONS: Currently, the list of Oct4 transcriptional targets contains thousands of genes. Using evolutionary conservation, we identified a core set of functionally relevant factors that linked the maintenance of adhesion to Oct4/POUV. We found that the regulation of adhesion by the Oct4/POUV network occurred at both transcriptional and posttranslational levels and was required for pluripotency.",
keywords = "Adherens Junctions, Animals, Cadherins, Cell Adhesion, Cell Differentiation, Cell Movement, Cells, Cultured, Ectoderm, Embryo, Nonmammalian, Embryonic Stem Cells, Gastrula, Gene Expression Regulation, Developmental, Gene Regulatory Networks, Octamer Transcription Factor-3, Xenopus Proteins, Xenopus laevis",
author = "Alessandra Livigni and Hanna Peradziryi and Sharov, {Alexei A} and Gloryn Chia and Fella Hammachi and Migueles, {Rosa Portero} and Woranop Sukparangsi and Salvatore Pernagallo and Mark Bradley and Jennifer Nichols and Ko, {Minoru S H} and Brickman, {Joshua M}",
note = "Copyright {\textcopyright} 2013 Elsevier Ltd. All rights reserved.",
year = "2013",
month = nov,
day = "18",
doi = "10.1016/j.cub.2013.09.048",
language = "English",
volume = "23",
pages = "2233--44",
journal = "Current Biology",
issn = "0960-9822",
publisher = "Cell Press",
number = "22",

}

RIS

TY - JOUR

T1 - A conserved Oct4/POUV-dependent network links adhesion and migration to progenitor maintenance

AU - Livigni, Alessandra

AU - Peradziryi, Hanna

AU - Sharov, Alexei A

AU - Chia, Gloryn

AU - Hammachi, Fella

AU - Migueles, Rosa Portero

AU - Sukparangsi, Woranop

AU - Pernagallo, Salvatore

AU - Bradley, Mark

AU - Nichols, Jennifer

AU - Ko, Minoru S H

AU - Brickman, Joshua M

N1 - Copyright © 2013 Elsevier Ltd. All rights reserved.

PY - 2013/11/18

Y1 - 2013/11/18

N2 - BACKGROUND: The class V POU domain transcription factor Oct4 (Pou5f1) is a pivotal regulator of embryonic stem cell (ESC) self-renewal and reprogramming of somatic cells to induced pluripotent stem (iPS) cells. Oct4 is also an important evolutionarily conserved regulator of progenitor cell differentiation during embryonic development.RESULTS: Here we examine the function of Oct4 homologs in Xenopus embryos and compare this to the role of Oct4 in maintaining mammalian embryo-derived stem cells. Based on a combination of expression profiling of Oct4/POUV-depleted Xenopus embryos and in silico analysis of existing mammalian Oct4 target data sets, we defined a set of evolutionary-conserved Oct4/POUV targets. Most of these targets were regulators of cell adhesion. This is consistent with Oct4/POUV phenotypes observed in the adherens junctions in Xenopus ectoderm, mouse embryonic, and epiblast stem cells. A number of these targets could rescue both Oct4/POUV phenotypes in cellular adhesion and multipotent progenitor cell maintenance, whereas expression of cadherins on their own could only transiently support adhesion and block differentiation in both ESC and Xenopus embryos.CONCLUSIONS: Currently, the list of Oct4 transcriptional targets contains thousands of genes. Using evolutionary conservation, we identified a core set of functionally relevant factors that linked the maintenance of adhesion to Oct4/POUV. We found that the regulation of adhesion by the Oct4/POUV network occurred at both transcriptional and posttranslational levels and was required for pluripotency.

AB - BACKGROUND: The class V POU domain transcription factor Oct4 (Pou5f1) is a pivotal regulator of embryonic stem cell (ESC) self-renewal and reprogramming of somatic cells to induced pluripotent stem (iPS) cells. Oct4 is also an important evolutionarily conserved regulator of progenitor cell differentiation during embryonic development.RESULTS: Here we examine the function of Oct4 homologs in Xenopus embryos and compare this to the role of Oct4 in maintaining mammalian embryo-derived stem cells. Based on a combination of expression profiling of Oct4/POUV-depleted Xenopus embryos and in silico analysis of existing mammalian Oct4 target data sets, we defined a set of evolutionary-conserved Oct4/POUV targets. Most of these targets were regulators of cell adhesion. This is consistent with Oct4/POUV phenotypes observed in the adherens junctions in Xenopus ectoderm, mouse embryonic, and epiblast stem cells. A number of these targets could rescue both Oct4/POUV phenotypes in cellular adhesion and multipotent progenitor cell maintenance, whereas expression of cadherins on their own could only transiently support adhesion and block differentiation in both ESC and Xenopus embryos.CONCLUSIONS: Currently, the list of Oct4 transcriptional targets contains thousands of genes. Using evolutionary conservation, we identified a core set of functionally relevant factors that linked the maintenance of adhesion to Oct4/POUV. We found that the regulation of adhesion by the Oct4/POUV network occurred at both transcriptional and posttranslational levels and was required for pluripotency.

KW - Adherens Junctions

KW - Animals

KW - Cadherins

KW - Cell Adhesion

KW - Cell Differentiation

KW - Cell Movement

KW - Cells, Cultured

KW - Ectoderm

KW - Embryo, Nonmammalian

KW - Embryonic Stem Cells

KW - Gastrula

KW - Gene Expression Regulation, Developmental

KW - Gene Regulatory Networks

KW - Octamer Transcription Factor-3

KW - Xenopus Proteins

KW - Xenopus laevis

U2 - 10.1016/j.cub.2013.09.048

DO - 10.1016/j.cub.2013.09.048

M3 - Journal article

C2 - 24210613

VL - 23

SP - 2233

EP - 2244

JO - Current Biology

JF - Current Biology

SN - 0960-9822

IS - 22

ER -

ID: 127290663