| Literature DB >> 30218368 |
Marissa Cloutier1, Clair Harris1, Srimonta Gayen1, Emily Maclary1,2, Sundeep Kalantry3.
Abstract
X-chromosome inactivation is a dosage compensation mechanism that equalizes X-linked gene expression between male and female mammals through the transcriptional silencing of most genes on one of the two X-chromosomes in females. With a few key exceptions, once the X-chromosome is inactivated replicated copies of that X-chromosome are maintained as inactive in all descendant cells. X-inactivation is therefore a paradigm of epigenetic inheritance. Imprinted X-inactivation is a specialized form of X-inactivation that results in the silencing of the paternally derived X-chromosome. Due to its parent-of-origin-specific pattern of inactivation, imprinted X-inactivation is a model of mitotic as well as meiotic, i.e., transgenerational, epigenetic inheritance. All cells of the early mouse embryo undergo imprinted X-inactivation, a pattern that is subsequently maintained in extraembryonic cell types in vivo and in vitro. Here, we describe both high- and low-throughput approaches to interrogate imprinted X-inactivation in the mouse embryo as well in cultured extraembryonic stem cells.Entities:
Keywords: Allele-specific gene expression analyses; Extraembryonic endoderm (XEN) stem cells; Preimplantation mouse embryogenesis; Trophoblast stem cells (TSCs); X-chromosome inactivation
Mesh:
Year: 2018 PMID: 30218368 PMCID: PMC6209079 DOI: 10.1007/978-1-4939-8766-5_14
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745