Sex-specific embryonic origin of postnatal phenotypic variability

Preimplantation developmental plasticity has evolved in order to offer the best chances of survival under changing environments. Conversely, environmental conditions experienced in early life can dramatically influence neonatal and adult biology, which may result in detrimental long-term effects. Several studies have shown that small size at birth, which is associated with a greater risk of metabolic syndrome, is largely determined before the formation of the blastocysts because 70%-80% of variation in bodyweight at birth has neither a genetic nor environmental component. In addition, it has been reported that adult bodyweight is programmed by energy-dependent process during the pronuclear stage in the mouse. Although the early embryo has a high developmental plasticity and adapts and survives to adverse environmental conditions, this adaptation may have adverse consequences and there is strong evidence that in vitro culture can be a risk factor for abnormal fetal outcomes in animals systems, with growing data suggesting that a similar link may be apparent for humans. In this context, male and female preimplantation embryos display sex-specific transcriptional and epigenetic regulation, which, in the case of bovine blastocysts, expands to one-third of the transcripts detected through microarray analysis. This sex-specific bias may convert the otherwise buffered stochastic variability in developmental networks in a sex-determined response to the environmental hazard. It has been widely reported that environment can affect preimplantation development in a sex-specific manner, resulting in either a short-term sex ratio adjustment or in long-term sex-specific effects on adult health. The present article reviews current knowledge about the natural phenotypic variation caused by epigenetic mechanisms and the mechanisms modulating sex-specific changes in phenotype during early embryo development resulting in sex ratio adjustments or detrimental sex-specific consequences for adult health. Understanding the natural embryo sexual dimorphism for programming trajectories will help understand the early mechanisms of response to environmental insults. © 2013 IETS.

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Main Authors: Laguna-Barraza, R., Bermejo-Álvarez, P., Ramos-Ibeas, P., De Frutos, C., López-Cardona, A. P., Calle, A., Fernandez-Gonzalez, R., Pericuesta, E., Ramírez, M. A., Gutierrez-Adan, A.
Format: journal article biblioteca
Language:eng
Published: 2013
Online Access:http://hdl.handle.net/20.500.12792/2283
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spelling dig-inia-es-20.500.12792-22832020-12-15T09:46:45Z Sex-specific embryonic origin of postnatal phenotypic variability Laguna-Barraza, R. Bermejo-Álvarez, P. Ramos-Ibeas, P. De Frutos, C. López-Cardona, A. P. Calle, A. Fernandez-Gonzalez, R. Pericuesta, E. Ramírez, M. A. Gutierrez-Adan, A. Preimplantation developmental plasticity has evolved in order to offer the best chances of survival under changing environments. Conversely, environmental conditions experienced in early life can dramatically influence neonatal and adult biology, which may result in detrimental long-term effects. Several studies have shown that small size at birth, which is associated with a greater risk of metabolic syndrome, is largely determined before the formation of the blastocysts because 70%-80% of variation in bodyweight at birth has neither a genetic nor environmental component. In addition, it has been reported that adult bodyweight is programmed by energy-dependent process during the pronuclear stage in the mouse. Although the early embryo has a high developmental plasticity and adapts and survives to adverse environmental conditions, this adaptation may have adverse consequences and there is strong evidence that in vitro culture can be a risk factor for abnormal fetal outcomes in animals systems, with growing data suggesting that a similar link may be apparent for humans. In this context, male and female preimplantation embryos display sex-specific transcriptional and epigenetic regulation, which, in the case of bovine blastocysts, expands to one-third of the transcripts detected through microarray analysis. This sex-specific bias may convert the otherwise buffered stochastic variability in developmental networks in a sex-determined response to the environmental hazard. It has been widely reported that environment can affect preimplantation development in a sex-specific manner, resulting in either a short-term sex ratio adjustment or in long-term sex-specific effects on adult health. The present article reviews current knowledge about the natural phenotypic variation caused by epigenetic mechanisms and the mechanisms modulating sex-specific changes in phenotype during early embryo development resulting in sex ratio adjustments or detrimental sex-specific consequences for adult health. Understanding the natural embryo sexual dimorphism for programming trajectories will help understand the early mechanisms of response to environmental insults. © 2013 IETS. 2020-10-22T12:46:38Z 2020-10-22T12:46:38Z 2013 journal article http://hdl.handle.net/20.500.12792/2283 10.1071/RD12262 eng Attribution-NonCommercial-ShareAlike 4.0 International http://creativecommons.org/licenses/by-nc-sa/4.0/ open access
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description Preimplantation developmental plasticity has evolved in order to offer the best chances of survival under changing environments. Conversely, environmental conditions experienced in early life can dramatically influence neonatal and adult biology, which may result in detrimental long-term effects. Several studies have shown that small size at birth, which is associated with a greater risk of metabolic syndrome, is largely determined before the formation of the blastocysts because 70%-80% of variation in bodyweight at birth has neither a genetic nor environmental component. In addition, it has been reported that adult bodyweight is programmed by energy-dependent process during the pronuclear stage in the mouse. Although the early embryo has a high developmental plasticity and adapts and survives to adverse environmental conditions, this adaptation may have adverse consequences and there is strong evidence that in vitro culture can be a risk factor for abnormal fetal outcomes in animals systems, with growing data suggesting that a similar link may be apparent for humans. In this context, male and female preimplantation embryos display sex-specific transcriptional and epigenetic regulation, which, in the case of bovine blastocysts, expands to one-third of the transcripts detected through microarray analysis. This sex-specific bias may convert the otherwise buffered stochastic variability in developmental networks in a sex-determined response to the environmental hazard. It has been widely reported that environment can affect preimplantation development in a sex-specific manner, resulting in either a short-term sex ratio adjustment or in long-term sex-specific effects on adult health. The present article reviews current knowledge about the natural phenotypic variation caused by epigenetic mechanisms and the mechanisms modulating sex-specific changes in phenotype during early embryo development resulting in sex ratio adjustments or detrimental sex-specific consequences for adult health. Understanding the natural embryo sexual dimorphism for programming trajectories will help understand the early mechanisms of response to environmental insults. © 2013 IETS.
format journal article
author Laguna-Barraza, R.
Bermejo-Álvarez, P.
Ramos-Ibeas, P.
De Frutos, C.
López-Cardona, A. P.
Calle, A.
Fernandez-Gonzalez, R.
Pericuesta, E.
Ramírez, M. A.
Gutierrez-Adan, A.
spellingShingle Laguna-Barraza, R.
Bermejo-Álvarez, P.
Ramos-Ibeas, P.
De Frutos, C.
López-Cardona, A. P.
Calle, A.
Fernandez-Gonzalez, R.
Pericuesta, E.
Ramírez, M. A.
Gutierrez-Adan, A.
Sex-specific embryonic origin of postnatal phenotypic variability
author_facet Laguna-Barraza, R.
Bermejo-Álvarez, P.
Ramos-Ibeas, P.
De Frutos, C.
López-Cardona, A. P.
Calle, A.
Fernandez-Gonzalez, R.
Pericuesta, E.
Ramírez, M. A.
Gutierrez-Adan, A.
author_sort Laguna-Barraza, R.
title Sex-specific embryonic origin of postnatal phenotypic variability
title_short Sex-specific embryonic origin of postnatal phenotypic variability
title_full Sex-specific embryonic origin of postnatal phenotypic variability
title_fullStr Sex-specific embryonic origin of postnatal phenotypic variability
title_full_unstemmed Sex-specific embryonic origin of postnatal phenotypic variability
title_sort sex-specific embryonic origin of postnatal phenotypic variability
publishDate 2013
url http://hdl.handle.net/20.500.12792/2283
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