The human Y and inactive X chromosomes similarly modulate autosomal gene expression

Adrianna K. San Roman(Whitehead Institute for Biomedical Research), Helen Skaletsky(Howard Hughes Medical Institute), Alexander K. Godfrey(Whitehead Institute for Biomedical Research), Neha V. Bokil(Whitehead Institute for Biomedical Research), Levi S. Teitz(Whitehead Institute for Biomedical Research), Isani Singh(Harvard University), Laura V. Blanton(Whitehead Institute for Biomedical Research), Daniel W. Bellott(Whitehead Institute for Biomedical Research), Tatyana Pyntikova(Whitehead Institute for Biomedical Research), Julian Lange(Whitehead Institute for Biomedical Research), Natalia Koutseva(Whitehead Institute for Biomedical Research), Jennifer F. Hughes(Whitehead Institute for Biomedical Research), Laura 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), Angela E. Lin(Boston Children's Hospital), Nicole Tartaglia(Children's Hospital Colorado), Carole Samango‐Sprouse(Florida International University), Maximilian Muenke(National Institutes of Health), David C. Page(Whitehead Institute for Biomedical Research)
Cell Genomics
December 13, 2023
Cited by 51Open Access
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Abstract

chromosome is a Y; in females it is an "inactive" X (Xi). Through linear modeling of autosomal gene expression in cells from individuals with zero to three Xi and zero to four Y chromosomes, we found that Xi and Y impact autosomal expression broadly and with remarkably similar effects. Studying sex chromosome structural anomalies, promoters of Xi- and Y-responsive genes, and CRISPR inhibition, we traced part of this shared effect to homologous transcription factors-ZFX and ZFY-encoded by Chr X and Y. This demonstrates sex-shared mechanisms by which Xi and Y modulate autosomal expression. Combined with earlier analyses of sex-linked gene expression, our studies show that 21% of all genes expressed in lymphoblastoid cells or fibroblasts change expression significantly in response to Xi or Y chromosomes.


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