The E1a Adenoviral Gene Upregulates the Yamanaka Factors to Induce Partial Cellular Reprogramming

Author:

Mendoza Gracia12ORCID,González-Pastor Rebeca13ORCID,Sánchez Juan Miguel4ORCID,Arce-Cerezo Altamira5,Quintanilla Miguel6ORCID,Moreno-Bueno Gema678ORCID,Pujol Anna5,Belmar-López Carolina19,de Martino Alba1,Riu Efrén5,Rodriguez Tristan A.4,Martin-Duque Pilar1281011ORCID

Affiliation:

1. Instituto Aragonés de Ciencias de la Salud (IACS), 50009 Zaragoza, Spain

2. Instituto de Investigación Sanitaria Aragón (IIS Aragón), 50009 Zaragoza, Spain

3. Centro de Investigación Biomédica (CENBIO), Facultad de Ciencias de la Salud Eugenio Espejo, Universidad UTE, Quito 170527, Ecuador

4. National Heart and Lung Institute, Imperial College London, London W12 ONN, UK

5. Centro de Biotecnología Animal y de Terapia Génica (CBATEG), Universidad Autónoma de Barcelona, 08193 Bellaterra, Spain

6. Departamento de Bioquímica, Instituto de Investigaciones Biomédicas ‘Alberto Sols’, Universidad Autónoma de Madrid (UAM), (UAM-CSIC), 28029 Madrid, Spain

7. Fundación MD Anderson Internacional, 28033 Madrid, Spain

8. Centro de Investigación Biomédica en Red, Instituto de Salud Carlos III, Red de Cáncer (CIBERONC) and Red de Nanomedicina y Nanomateriales (CIBER-BBN), 28029 Madrid, Spain

9. OncoGenomics Lab, Universidad Privada San Juan Bautista, Lima 15038, Peru

10. Fundación Araid, 50018 Zaragoza, Spain

11. Departamento de Cirugía, Facultad de Medicina, Universidad de Zaragoza, 50009 Zaragoza, Spain

Abstract

The induction of pluripotency by enforced expression of different sets of genes in somatic cells has been achieved with reprogramming technologies first described by Yamanaka’s group. Methodologies for generating induced pluripotent stem cells are as varied as the combinations of genes used. It has previously been reported that the adenoviral E1a gene can induce the expression of two of the Yamanaka factors (c-Myc and Oct-4) and epigenetic changes. Here, we demonstrate that the E1a-12S over-expression is sufficient to induce pluripotent-like characteristics closely to epiblast stem cells in mouse embryonic fibroblasts through the activation of the pluripotency gene regulatory network. These findings provide not only empirical evidence that the expression of one single factor is sufficient for partial reprogramming but also a potential mechanistic explanation for how viral infection could lead to neoplasia if they are surrounded by the appropriate environment or the right medium, as happens with the tumorogenic niche.

Funder

Instituto de Salud Carlos III

Fondo Europeo de Desarrollo Regional

CIBER-BBN

Aragon Government

Miguel Servet Program

Publisher

MDPI AG

Subject

General Medicine

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