Department of Bioinformatics, University of British Columbia, Vancouver, BC, Canada; BC Children's Hospital Research Institute, Centre for Molecular Medicine and Therapeutics, University of British Columbia, Vancouver, BC, Canada.
BC Children's Hospital Research Institute, Centre for Molecular Medicine and Therapeutics, University of British Columbia, Vancouver, BC, Canada; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
Brain Res. 2019 Oct 15;1721:146345. doi: 10.1016/j.brainres.2019.146345. Epub 2019 Jul 23.
In the blood, mosaic somatic aneuploidy (mSA) of all chromosomes has been found to be associated with adverse health outcomes, including hematological cancer. Sex chromosome mSA in the blood has been found to occur at a higher rate than autosomal mSA. Mosaic loss of the Y chromosome is the most common copy number alteration in males, and has been found to be associated with Alzheimer's disease (AD) in blood lymphocytes. mSA of the sex chromosomes has also been identified in the brain; however, little is known about its frequency across individuals. Using WGS data from 362 males and 719 females from the ROSMAP cohort, we quantified the relative rate of sex chromosome mSA in the dorsolateral prefrontal cortex (DLPFC), cerebellum and whole blood. To ascertain the functionality of observed sex chromosome mosaicism in the DLPFC, we examined its correlation with chromosome X and Y gene expression as well as neuropathological and clinical characteristics of AD and cognitive ageing. In males, we found that mSA of the Y chromosome occurs more frequently in blood than in the DLPFC or cerebellum. In the DLPFC, the presence of at least one APOE4 allele was associated with a reduction in read depth of the Y chromosome (p = 1.9e-02). In the female DLPFC, a reduction in chromosome X read depth was associated with reduced cognition at the last clinical visit and faster rate of cognitive decline (p = 7.8e-03; p = 1.9e-02). mSA of all sex chromosomes in the DLPFC were associated with aggregate measures of gene expression, implying functional impact. Our results provide insight into the relative rate of mSA between tissues and suggest that Y and female X chromosome read depth in the DLPFC is modestly associated with late AD risk factors and cognitive pathologies.
在血液中,已发现所有染色体的镶嵌性体细胞非整倍体(mSA)与不良健康结果相关,包括血液癌。在血液中已发现性染色体 mSA 的发生率高于常染色体 mSA。Y 染色体的镶嵌性缺失是男性中最常见的拷贝数改变,并且已发现与血液淋巴细胞中的阿尔茨海默病(AD)相关。在大脑中也已经鉴定出性染色体的 mSA;然而,个体之间的其频率知之甚少。使用来自 ROSMAP 队列的 362 名男性和 719 名女性的 WGS 数据,我们定量了性染色体 mSA 在背外侧前额叶皮层(DLPFC)、小脑和全血中的相对速率。为了确定 DLPFC 中观察到的性染色体镶嵌性的功能,我们检查了其与染色体 X 和 Y 基因表达以及 AD 和认知老化的神经病理学和临床特征的相关性。在男性中,我们发现 Y 染色体的 mSA 在血液中比在 DLPFC 或小脑更频繁发生。在 DLPFC 中,至少存在一个 APOE4 等位基因与 Y 染色体的读取深度降低相关(p=1.9e-02)。在女性 DLPFC 中,染色体 X 读取深度降低与最后一次临床就诊时的认知能力下降以及认知能力下降速度加快相关(p=7.8e-03;p=1.9e-02)。DLPFC 中所有性染色体的 mSA 与基因表达的综合指标相关,表明存在功能影响。我们的结果提供了组织之间 mSA 相对速率的见解,并表明 DLPFC 中的 Y 染色体和女性 X 染色体的读取深度与 AD 的晚期风险因素和认知病理适度相关。