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The human Y and inactive X chromosomes similarly modulate autosomal gene expression.
San Roman, Adrianna K; Skaletsky, Helen; Godfrey, Alexander K; Bokil, Neha V; Teitz, Levi; Singh, Isani; Blanton, Laura V; Bellott, Daniel W; Pyntikova, Tatyana; Lange, Julian; Koutseva, Natalia; Hughes, Jennifer F; Brown, Laura; Phou, Sidaly; Buscetta, Ashley; Kruszka, Paul; Banks, Nicole; Dutra, Amalia; Pak, Evgenia; Lasutschinkow, Patricia C; Keen, Colleen; Davis, Shanlee M; Lin, Angela E; Tartaglia, Nicole R; Samango-Sprouse, Carole; Muenke, Maximilian; Page, David C.
Afiliação
  • San Roman AK; Whitehead Institute; Cambridge, MA 02142, USA.
  • Skaletsky H; Whitehead Institute; Cambridge, MA 02142, USA.
  • Godfrey AK; Howard Hughes Medical Institute, Whitehead Institute; Cambridge, MA 02142, USA.
  • Bokil NV; Whitehead Institute; Cambridge, MA 02142, USA.
  • Teitz L; Department of Biology, Massachusetts Institute of Technology; Cambridge, MA 02139, USA.
  • Singh I; Whitehead Institute; Cambridge, MA 02142, USA.
  • Blanton LV; Department of Biology, Massachusetts Institute of Technology; Cambridge, MA 02139, USA.
  • Bellott DW; Whitehead Institute; Cambridge, MA 02142, USA.
  • Pyntikova T; Department of Biology, Massachusetts Institute of Technology; Cambridge, MA 02139, USA.
  • Lange J; Whitehead Institute; Cambridge, MA 02142, USA.
  • Koutseva N; Harvard Medical School, Boston, MA 02115, USA.
  • Hughes JF; Whitehead Institute; Cambridge, MA 02142, USA.
  • Brown L; Whitehead Institute; Cambridge, MA 02142, USA.
  • Phou S; Whitehead Institute; Cambridge, MA 02142, USA.
  • Buscetta A; Whitehead Institute; Cambridge, MA 02142, USA.
  • Kruszka P; Department of Biology, Massachusetts Institute of Technology; Cambridge, MA 02139, USA.
  • Banks N; Whitehead Institute; Cambridge, MA 02142, USA.
  • Dutra A; Whitehead Institute; Cambridge, MA 02142, USA.
  • Pak E; Whitehead Institute; Cambridge, MA 02142, USA.
  • Lasutschinkow PC; Howard Hughes Medical Institute, Whitehead Institute; Cambridge, MA 02142, USA.
  • Keen C; Whitehead Institute; Cambridge, MA 02142, USA.
  • Davis SM; Howard Hughes Medical Institute, Whitehead Institute; Cambridge, MA 02142, USA.
  • Lin AE; Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda; MD 20892, USA.
  • Tartaglia NR; Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda; MD 20892, USA.
  • Samango-Sprouse C; Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda; MD 20892, USA.
  • Muenke M; Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health; Bethesda, MD 20892 USA.
  • Page DC; Cytogenetics and Microscopy Core, National Human Genome Research Institute, National Institutes of Health; Bethesda, MD 20892 USA.
bioRxiv ; 2023 Jun 07.
Article em En | MEDLINE | ID: mdl-37333288
ABSTRACT
Somatic cells of human males and females have 45 chromosomes in common, including the "active" X chromosome. In males the 46th 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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: BioRxiv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: BioRxiv Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos