Home News About Us Contact Contributors Disclaimer Privacy Policy Help FAQ

Quick Search
My eDoc
Support Wiki
Direct access to
document ID:

          Document History for Document ID 648367

Back to latest document version
Document Version Version Comment Date Status
648367.0 [No comment] 23.03.2016 15:37 Released

ID: 648367.0, MPI für molekulare Biomedizin / Yearbook 2013
Reprogramming to pluripotency is an ancient trait of vertebrate Oct4 and Pou2 proteins
Authors:Tapia, N.; Reinhardt, P.; Duemmler, A.; Wu, G.; Arauzo-Bravo, M. J.; Esch, D.; Greber, B.; Cojocaru, V.; Rascon, C. A.; Tazaki, A.; Kump, K.; Voss, R.; Tanaka, E. M.; Schöler, H. R.
Date of Publication (YYYY-MM-DD):2012
Title of Journal:Nat Commun
Start Page:1279
Review Status:Internal review
Audience:Not Specified
Abstract / Description:The evolutionary origins of the gene network underlying cellular pluripotency, a central theme in developmental biology, have yet to be elucidated. In mammals, Oct4 is a factor crucial in the reprogramming of differentiated cells into induced pluripotent stem cells. The Oct4 and Pou2 genes evolved from a POU class V gene ancestor, but it is unknown whether pluripotency induced by Oct4 gene activity is a feature specific to mammals or was already present in ancestral vertebrates. Here we report that different vertebrate Pou2 and Oct4 homologues can induce pluripotency in mouse and human fibroblasts and that the inability of zebrafish Pou2 to establish pluripotency is not representative of all Pou2 genes, as medaka Pou2 and axolotl Pou2 are able to reprogram somatic cells into pluripotent cells. Therefore, our results indicate that induction of pluripotency is not a feature specific to mammals, but existed in the Oct4/Pou2 common ancestral vertebrate.
External Publication Status:published
Document Type:Article
Communicated by:keuker
Affiliations:MPI für molekulare Biomedizin
External Affiliations:%G eng
Identifiers:ISSN:2041-1723 (Electronic) 2041-1723 (Linking) %R 10.1... [ID No:1]
URL:http://www.ncbi.nlm.nih.gov/pubmed/23232409 [ID No:2]