The human inactive X chromosome modulates expression of the active X chromosome

Adrianna K. San Roman(Whitehead Institute for Biomedical Research), Alexander K. Godfrey(Whitehead Institute for Biomedical Research), Helen Skaletsky(Howard Hughes Medical Institute), Daniel W. Bellott(Whitehead Institute for Biomedical Research), Abigail F. Groff(Whitehead Institute for Biomedical Research), Hannah L. Harris(Whitehead Institute for Biomedical Research), Laura V. Blanton(Whitehead Institute for Biomedical Research), Jennifer F. Hughes(Whitehead Institute for Biomedical Research), Laura G. Brown(Howard Hughes Medical Institute), Sidaly Phou(Howard Hughes Medical Institute), Ashley Buscetta(National Institutes of Health), Paul Kruszka(National Institutes of Health), Nicole Banks(National Institutes of Health), Amalia Dutra(National Institutes of Health), Evgenia Pak(National Institutes of Health), Patricia C. Lasutschinkow, Colleen Keen, Shanlee Davis(University of Colorado Denver), Nicole Tartaglia(Children's Hospital Colorado), Carole Samango‐Sprouse(George Washington University), Maximilian Muenke(National Institutes of Health), David C. Page(Howard Hughes Medical Institute)
Cell Genomics
February 1, 2023
Cited by 85Open Access
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Abstract

The “inactive” X chromosome (Xi) has been assumed to have little impact, in trans, on the “active” X (Xa). To test this, we quantified Xi and Xa gene expression in individuals with one Xa and zero to three Xis. Our linear modeling revealed modular Xi and Xa transcriptomes and significant Xi-driven expression changes for 38% (162/423) of expressed X chromosome genes. By integrating allele-specific analyses, we found that modulation of Xa transcript levels by Xi contributes to many of these Xi-driven changes (≥121 genes). By incorporating metrics of evolutionary constraint, we identified 10 X chromosome genes most likely to drive sex differences in common disease and sex chromosome aneuploidy syndromes. We conclude that human X chromosomes are regulated both in cis, through Xi-wide transcriptional attenuation, and in trans, through positive or negative modulation of individual Xa genes by Xi. The sum of these cis and trans effects differs widely among genes.


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