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Journal ArticleDOI

Dosage compensation of the active X chromosome in mammals.

Di Kim Nguyen, +1 more
- 01 Jan 2006 - 
- Vol. 38, Iss: 1, pp 47-53
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TLDR
It is shown that doubling of the global expression level of the X chromosome leads to dosage compensation in somatic tissues from several mammalian species.
Abstract
Monosomy of the X chromosome owing to divergence between the sex chromosomes leads to dosage compensation mechanisms to restore balanced expression between the X and the autosomes In Drosophila melanogaster, upregulation of the male X leads to dosage compensation It has been hypothesized that mammals likewise upregulate their active X chromosome Together with X inactivation, this mechanism would maintain balanced expression between the X chromosome and autosomes and between the sexes Here, we show that doubling of the global expression level of the X chromosome leads to dosage compensation in somatic tissues from several mammalian species X-linked genes are highly expressed in brain tissues, consistent with a role in cognitive functions Furthermore, the X chromosome is expressed but not upregulated in spermatids and secondary oocytes, preserving balanced expression of the genome in these haploid cells Upon fertilization, upregulation of the active X must occur to achieve the observed dosage compensation in early embryos

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Citations
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Journal ArticleDOI

Gene body-specific methylation on the active X chromosome

TL;DR: A bipartite methylation-demethylation program results in Xa-specific hypomethylation at gene promoters and hypermethylation at genes bodies, suggesting a relationship between global methylation and expression potentiality.
Journal ArticleDOI

The X chromosome in immune functions: when a chromosome makes the difference

TL;DR: This work reviews the main mechanisms responsible for increased immune activity in females, which provides a survival advantage in the face of pathogenic insult but can also enhance the susceptibility of females to autoimmunity.
Journal ArticleDOI

X chromosome dosage compensation: how mammals keep the balance

TL;DR: Various facets of the ever-expanding field of mammalian dosage compensation are reviewed and its evolutionary, developmental, and mechanistic components are discussed.
Journal ArticleDOI

Dosage compensation in mammals: fine-tuning the expression of the X chromosome

TL;DR: The discovery and possible implications of a second form of dosage compensation in mammals that deals with the unique, potentially haploinsufficient, status of the X chromosome with respect to autosomal gene expression are reviewed.
References
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Journal ArticleDOI

Gene Action in the X -chromosome of the Mouse ( Mus musculus L.)

TL;DR: Ohno and Hauschka1 showed that in female mice one chromosome of mammary carcinoma cells and of normal diploid cells of the ovary, mammary gland and liver was heteropyKnotic and suggested that the so-called sex chromatin was composed of one heteropyknotic X-chromosome.
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A gene atlas of the mouse and human protein-encoding transcriptomes

TL;DR: In this paper, high-density oligonucleotide arrays offer the opportunity to examine patterns of gene expression on a genome scale, and the authors have designed custom arrays that interrogate the expression of the vast majority of proteinencoding human and mouse genes and have used them to profile a panel of 79 human and 61 mouse tissues.
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X-inactivation profile reveals extensive variability in X-linked gene expression in females

TL;DR: A comprehensive X-inactivation profile of the human X chromosome is presented, representing an estimated 95% of assayable genes in fibroblast-based test systems, and suggests a remarkable and previously unsuspected degree of expression heterogeneity among females.
Journal ArticleDOI

Large-scale analysis of the human and mouse transcriptomes

TL;DR: This work generated and analyzed gene expression from 91 human and mouse samples across a diverse array of tissues, organs, and cell lines to reveal insights into molecular and physiological gene function, mechanisms of transcriptional regulation, disease etiology, and comparative genomics.
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