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Chromosome Imbalance as a Driver of Sex Disparity in Disease

机译:染色体失衡是疾病中性别差异的驱动因素

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It has long been recognized that men and women exhibit different risks for diverse disorders ranging from metabolic to autoimmune diseases. However, the underlying causes of these dis- parities remain obscure. Analysis of patients with chromosomal abnormalities, including Turner syndrome (45X) and Klinefelter syndrome (47XXY), has highlighted the importance of X-linked gene dosage as a contributing factor for disease susceptibility. Escape from X-inactivation and X-linked imprinting can result in transcriptional differences between normal men and women as well as in patients with sex chromosome abnormalities. Animal models support a role for X-linked gene dosage in disease with O-linked N-acetylglucosamine transferase (OGT) emerging as a prime candidate for a pleiotropic effector. OGT encodes a highly regulated nutrient-sensing epigenetic modifier with established links to immunity, metabolism and development
机译:长期以来,人们认识到男人和女人表现出从代谢性疾病到自身免疫性疾病的各种疾病的不同风险。但是,造成这些差异的根本原因仍然不清楚。对包括Turner综合征(45X)和Klinefelter综合征(47XXY)在内的染色体异常患者的分析强调了X连锁基因剂量作为疾病易感性因素的重要性。逃脱X灭活和X连锁印记可导致正常男女之间以及性染色体异常患者中的转录差异。动物模型支持X连锁基因剂量在疾病中的作用,而O连锁N-乙酰氨基葡萄糖转移酶(OGT)成为多效效应物的主要候选者。 OGT编码高度调节的营养敏感表观遗传修饰剂,与免疫,代谢和发育建立了联系

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