通过综合功能基因组分析脑年龄的调控基因组电路。

IF 7.9
Xingzhong Zhao, Anyi Yang, Jing Ding, Yucheng T Yang, Xing-Ming Zhao
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引用次数: 0

摘要

脑年龄差距(BAG)是评估大脑健康状况和检测年龄相关认知退化的有价值的生物标志物。然而,人们对BAG的遗传结构和潜在机制知之甚少。在这里,我们使用我们提出的对抗卷积网络(ACN)从磁共振成像中估计大脑年龄,并提高了准确性,然后将ACN模型应用于来自UK Biobank的老年队列。BAG的遗传力在调控区显著富集,并与神经胶质细胞有关。我们对一组bag相关基因进行了优先排序,并进一步表征了它们在脑细胞类型和区域中的表达模式。发现两个bag相关基因RUNX2和KLF3与表观遗传时钟和多种衰老相关生物学途径相关。最后,两个bag相关的枢纽转录因子KLF3和SOX10被确定为多种脑部疾病多效性风险基因的调节因子。总之,我们改进了对BAG的估计,并确定了与脑疾病有关的BAG相关基因和调控网络。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulatory Genomic Circuitry of Brain Age by Integrative Functional Genomic Analyses.

Brain age gap (BAG) is a valuable biomarker for evaluating brain healthy status and detecting age-associated cognitive degeneration. However, the genetic architecture of BAG and the underlying mechanisms are poorly understood. Here, we estimated brain age from magnetic resonance imaging with improved accuracy using our proposed adversarial convolution network (ACN), followed by applying the ACN model to an elder cohort from UK Biobank. The genetic heritability of BAG was significantly enriched in the regulatory regions and implicated in glial cells. We prioritized a set of BAG-associated genes, and further characterized their expression patterns across brain cell types and regions. Two BAG-associated genes, RUNX2 and KLF3, were found as associated with epigenetic clock and diverse aging-related biological pathways. Finally, two BAG-associated hub transcription factors, KLF3 and SOX10, were identified as regulators of pleiotropic risk genes from diverse brain disorders. Altogether, we improve the estimation of BAG, and identify BAG-associated genes and regulatory networks that are implicated in brain disorders.

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