Development to term of cloned cattle derived from donor cells treated with valproic acid.

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Abstrakt

Tytuł:: Development to term of cloned cattle derived from donor cells treated with valproic acid.
Autorzy:: Sangalli JR; Departamento de Medicina Veterinária, Faculdade de Zootecnia e Engenharia de Alimentos, Universidade de São Paulo, Pirassununga, São Paulo, Brazil; Departamento de Cirurgia, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, São Paulo, São Paulo, Brazil; Department of Biomedical Science, Ontario Veterinary College, University of Guelph, Ontario, Canada.
Chiaratti MR; Departamento de Cirurgia, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, São Paulo, São Paulo, Brazil; Departamento de Genética e Evolução, Centro de Ciências Biológicas e da Saúde, Universidade Federal de São Carlos, São Carlos, Brazil.
De Bem TH; Departamento de Medicina Veterinária, Faculdade de Zootecnia e Engenharia de Alimentos, Universidade de São Paulo, Pirassununga, São Paulo, Brazil; Departamento de Genética, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, São Paulo, Brazil.
de Araújo RR; Departamento de Medicina Veterinária, Faculdade de Zootecnia e Engenharia de Alimentos, Universidade de São Paulo, Pirassununga, São Paulo, Brazil; Departamento de Cirurgia, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, São Paulo, São Paulo, Brazil.
Bressan FF; Departamento de Medicina Veterinária, Faculdade de Zootecnia e Engenharia de Alimentos, Universidade de São Paulo, Pirassununga, São Paulo, Brazil.
Sampaio RV; Departamento de Medicina Veterinária, Faculdade de Zootecnia e Engenharia de Alimentos, Universidade de São Paulo, Pirassununga, São Paulo, Brazil; Departamento de Cirurgia, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, São Paulo, São Paulo, Brazil; Department of Biomedical Science, Ontario Veterinary College, University of Guelph, Ontario, Canada.
Perecin F; Departamento de Medicina Veterinária, Faculdade de Zootecnia e Engenharia de Alimentos, Universidade de São Paulo, Pirassununga, São Paulo, Brazil.
Smith LC; Centre de recherche em reproduction animale, Faculté de médecine vétérinaire, Université de Montréal, St. Hyacinthe, Québec, Canada.
King WA; Department of Biomedical Science, Ontario Veterinary College, University of Guelph, Ontario, Canada.
Meirelles FV; Departamento de Medicina Veterinária, Faculdade de Zootecnia e Engenharia de Alimentos, Universidade de São Paulo, Pirassununga, São Paulo, Brazil.
Źródło:: PloS one [PLoS One] 2014 Jun 24; Vol. 9 (6), pp. e101022. Date of Electronic Publication: 2014 Jun 24 (Print Publication: 2014).
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
Język:: English
Imprint Name(s):: Original Publication: San Francisco, CA : Public Library of Science
MeSH Terms:: Nuclear Transfer Techniques*
Cell Differentiation/*drug effects
Cloning, Organism/*methods
Histone Deacetylase Inhibitors/*pharmacology
Valproic Acid/*pharmacology
Acetylation/drug effects ; Animals ; Cattle ; Cell Proliferation/drug effects ; DNA Methylation/drug effects ; Embryonic Development/drug effects ; Histones/metabolism ; Octamer Transcription Factor-3/genetics ; Octamer Transcription Factor-3/metabolism ; Receptor, IGF Type 2/genetics ; Receptor, IGF Type 2/metabolism
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Substance Nomenclature:: 0 (Histone Deacetylase Inhibitors)
0 (Histones)
0 (Octamer Transcription Factor-3)
0 (Receptor, IGF Type 2)
614OI1Z5WI (Valproic Acid)
Entry Date(s):: Date Created: 20140625 Date Completed: 20151123 Latest Revision: 20211021
Update Code:: 20240104
PubMed Central ID:: PMC4069182
DOI:: 10.1371/journal.pone.0101022
PMID:: 24959750
: Czasopismo naukowe

Pełny tekst

Cloning of mammals by somatic cell nuclear transfer (SCNT) is still plagued by low efficiency. The epigenetic modifications established during cellular differentiation are a major factor determining this low efficiency as they act as epigenetic barriers restricting reprogramming of somatic nuclei. In this regard, most factors that promote chromatin decondensation, including histone deacetylase inhibitors (HDACis), have been found to increase nuclear reprogramming efficiency, making their use common to improve SCNT rates. Herein we used valproic acid (VPA) in SCNT to test whether the treatment of nuclear donor cells with this HDACi improves pre- and post-implantation development of cloned cattle. We found that the treatment of fibroblasts with VPA increased histone acetylation without affecting DNA methylation. Moreover, the treatment with VPA resulted in increased expression of IGF2R and PPARGC1A, but not of POU5F1. However, when treated cells were used as nuclear donors no difference of histone acetylation was found after oocyte reconstruction compared to the use of untreated cells. Moreover, shortly after artificial activation the histone acetylation levels were decreased in the embryos produced with VPA-treated cells. With respect to developmental rates, the use of treated cells as donors resulted in no difference during pre- and post-implantation development. In total, five clones developed to term; three produced with untreated cells and two with VPA-treated cells. Among the calves from treated group, one stillborn calf was delivered at day 270 of gestation whereas the other one was delivered at term but died shortly after birth. Among the calves from the control group, one died seven days after birth whereas the other two are still alive and healthy. Altogether, these results show that in spite of the alterations in fibroblasts resulting from the treatment with VPA, their use as donor cells in SCNT did not improve pre- and post-implantation development of cloned cattle.

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