Laura V Blanton, Adrianna K San Roman, Geryl Wood, Ashley Buscetta, Nicole Banks, Helen Skaletsky, Alexander K Godfrey, Thao T Pham, Jennifer F Hughes, Laura G Brown, Paul Kruszka, Angela E Lin, Daniel L Kastner, Maximilian Muenke, David C Page
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引用次数: 0
Abstract
Recent in vitro studies of human sex chromosome aneuploidy showed that the Xi ("inactive" X) and Y chromosomes broadly modulate autosomal and Xa ("active" X) gene expression. We tested these findings in vivo. Linear modeling of CD4+ T cells and monocytes from individuals with one to three X chromosomes and zero to two Y chromosomes revealed 82 sex-chromosomal and 344 autosomal genes whose expression changed significantly with Xi and/or Y dosage in vivo. Changes in sex-chromosomal expression were remarkably constant in vivo and in vitro; autosomal responses to Xi and/or Y dosage were largely cell-type specific (∼2.6-fold more variation than sex-chromosomal responses). Targets of the sex-chromosomal transcription factors ZFX and ZFY accounted for a significant fraction of these autosomal responses both in vivo and in vitro. We conclude that the human Xi and Y transcriptomes are surprisingly robust and stable, yet they modulate autosomal and Xa genes in a cell-type-specific fashion.
最近对人类性染色体非整倍体的体外研究表明,Xi("非活性 "X)和 Y 染色体可广泛调节常染色体和 Xa("活性 "X)基因的表达。我们在体内检验了这些发现。对具有一至三条 X 染色体和零至两条 Y 染色体的个体的 CD4+ T 细胞和单核细胞进行线性建模,发现有 82 个性染色体基因和 344 个常染色体基因的表达在体内随 Xi 和/或 Y 的剂量发生显著变化。性染色体表达的变化在体内和体外都非常稳定;常染色体对Xi和/或Y剂量的反应在很大程度上具有细胞类型特异性(比性染色体反应的变化大2.6倍)。性染色体转录因子 ZFX 和 ZFY 的靶标在体内和体外均占这些常染色体反应的很大一部分。我们的结论是,人类的 Xi 和 Y 转录组具有惊人的稳健性和稳定性,但它们以细胞类型特异性的方式调节常染色体基因和 Xa 基因。