Advanced search
Start date
Betweenand
Related content
(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Epigenetic remodeling in preimplantation embryos: cows are not big mice

Full text
Author(s):
Ross, Pablo J. [1] ; Sampaio, Rafael V. [2, 1]
Total Authors: 2
Affiliation:
[1] Univ Calif Davis, Dept Anim Sci, Davis, CA 95616 - USA
[2] Univ Sao Paulo, Fac Anim Sci & Food Engn, Dept Vet Med, Sao Paulo - Brazil
Total Affiliations: 2
Document type: Journal article
Source: ANIMAL REPRODUCTION; v. 15, n. 3, p. 204-214, JUL-SEP 2018.
Web of Science Citations: 1
Abstract

Epigenetic mechanisms allow the establishment and maintenance of multiple cellular phenotypes from a single genomic code. At the initiation of development, the oocyte and spermatozoa provide their fully differentiated chromatin that soon after fertilization undergo extensive remodeling, resulting in a totipotent state that can then drive cellular differentiation towards all cell types. These remodeling involves different epigenetic modifications, including DNA methylation, post-translational modifications of histones, non-coding RNAs, and large-scale chromatin conformation changes. Moreover, epigenetic remodeling is responsible for reprogramming somatic cells to totipotency upon somatic cell nuclear transfer/cloning, which is often incomplete and inefficient. Given that environmental factors, such as assisted reproductive techniques (ARTs), can affect epigenetic remodeling, there is interest in understanding the mechanisms driving these changes. We describe and discuss our current understanding of mechanisms responsible for the epigenetic remodeling that ensues during preimplantation development of mammals, presenting findings from studies of mouse embryos and when available comparing them to what is known for human and cattle embryos. (AU)

FAPESP's process: 15/08807-6 - H3K9 methylation as regulator of epigenetic memory on bovine nuclear reprograming.
Grantee:Rafael Vilar Sampaio
Support type: Scholarships in Brazil - Post-Doctorate
FAPESP's process: 13/08135-2 - CTC - Center for Cell-Based Therapy
Grantee:Dimas Tadeu Covas
Support type: Research Grants - Research, Innovation and Dissemination Centers - RIDC