X chromosome inactivation in human development

Author:

Patrat Catherine12ORCID,Ouimette Jean-François3ORCID,Rougeulle Claire3ORCID

Affiliation:

1. Université de Paris, UMR 1016, Institut Cochin, 75014 Paris, France

2. Service de Biologie de la Reproduction – CECOS, Paris Centre Hospital, APHP.centre, 75014 Paris, France

3. Université de Paris, Epigenetics and Cell Fate, CNRS, F-75013 Paris, France

Abstract

ABSTRACT X chromosome inactivation (XCI) is a key developmental process taking place in female mammals to compensate for the imbalance in the dosage of X-chromosomal genes between sexes. It is a formidable example of concerted gene regulation and a paradigm for epigenetic processes. Although XCI has been substantially deciphered in the mouse model, how this process is initiated in humans has long remained unexplored. However, recent advances in the experimental capacity to access human embryonic-derived material and in the laws governing ethical considerations of human embryonic research have allowed us to enlighten this black box. Here, we will summarize the current knowledge of human XCI, mainly based on the analyses of embryos derived from in vitro fertilization and of pluripotent stem cells, and highlight any unanswered questions.

Funder

Université de Recherche Paris Sciences et Lettres

Institut National de la Santé et de la Recherche Médicale

FP7 Health

Agence Nationale de la Recherche

Ligue Contre le Cancer

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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