Center for Computational Biology, Johns Hopkins University, Baltimore, MD, USA; Department of Biomedical Engineering, Johns Hopkins School of Medicine and Whiting School of Engineering, Baltimore, MD, USA.
Center for Computational Biology, Johns Hopkins University, Baltimore, MD, USA; Department of Biomedical Engineering, Johns Hopkins School of Medicine and Whiting School of Engineering, Baltimore, MD, USA; Department of Computer Science, Johns Hopkins University, Baltimore, MD, USA.
Cell Rep Methods. 2024 Mar 25;4(3):100736. doi: 10.1016/j.crmeth.2024.100736. Epub 2024 Mar 19.
Differential transcript usage (DTU) plays a crucial role in determining how gene expression differs among cells, tissues, and developmental stages, contributing to the complexity and diversity of biological systems. In abnormal cells, it can also lead to deficiencies in protein function and underpin disease pathogenesis. Analyzing DTU via RNA sequencing (RNA-seq) data is vital, but the genetic heterogeneity in populations with complex diseases presents an intricate challenge due to diverse causal events and undetermined subtypes. Although the majority of common diseases in humans are categorized as complex, state-of-the-art DTU analysis methods often overlook this heterogeneity in their models. We therefore developed SPIT, a statistical tool that identifies predominant subgroups in transcript usage within a population along with their distinctive sets of DTU events. This study provides comprehensive assessments of SPIT's methodology and applies it to analyze brain samples from individuals with schizophrenia, revealing previously unreported DTU events in six candidate genes.
差异转录本使用(DTU)在决定基因表达在细胞、组织和发育阶段之间的差异方面起着至关重要的作用,有助于生物系统的复杂性和多样性。在异常细胞中,它还可能导致蛋白质功能缺陷,并为疾病发病机制提供基础。通过 RNA 测序(RNA-seq)数据分析 DTU 至关重要,但由于复杂疾病人群中的遗传异质性存在多种因果事件和不确定的亚型,这是一个复杂的挑战。尽管人类的大多数常见疾病都被归类为复杂疾病,但最先进的 DTU 分析方法在其模型中往往忽略了这种异质性。因此,我们开发了 SPIT,这是一种统计工具,可识别群体中转录本使用中的主要亚群及其独特的 DTU 事件集。本研究全面评估了 SPIT 方法,并将其应用于分析精神分裂症个体的大脑样本,揭示了六个候选基因中以前未报道过的 DTU 事件。