Department of Biomedical Engineering, Yale University, New Haven, CT 06520, USA.
Department of Genetics, Yale University School of Medicine, New Haven, CT 06520, USA; Program in Computational Biology and Bioinformatics, Yale University, New Haven, CT 06520, USA.
Cell. 2024 Nov 14;187(23):6760-6779.e24. doi: 10.1016/j.cell.2024.09.001. Epub 2024 Sep 30.
The capability to spatially explore RNA biology in formalin-fixed paraffin-embedded (FFPE) tissues holds transformative potential for histopathology research. Here, we present pathology-compatible deterministic barcoding in tissue (Patho-DBiT) by combining in situ polyadenylation and computational innovation for spatial whole transcriptome sequencing, tailored to probe the diverse RNA species in clinically archived FFPE samples. It permits spatial co-profiling of gene expression and RNA processing, unveiling region-specific splicing isoforms, and high-sensitivity transcriptomic mapping of clinical tumor FFPE tissues stored for 5 years. Furthermore, genome-wide single-nucleotide RNA variants can be captured to distinguish malignant subclones from non-malignant cells in human lymphomas. Patho-DBiT also maps microRNA regulatory networks and RNA splicing dynamics, decoding their roles in spatial tumorigenesis. Single-cell level Patho-DBiT dissects the spatiotemporal cellular dynamics driving tumor clonal architecture and progression. Patho-DBiT stands poised as a valuable platform to unravel rich RNA biology in FFPE tissues to aid in clinical pathology evaluation.
空间探索福尔马林固定石蜡包埋(FFPE)组织中 RNA 生物学的能力为组织病理学研究带来了变革性的潜力。在这里,我们通过结合原位多聚腺苷酸化和计算创新,提出了适用于临床存档 FFPE 样本中多样化 RNA 物种探测的组织兼容确定性条形码(Patho-DBiT)。它允许对基因表达和 RNA 加工进行空间共分析,揭示特定区域的剪接异构体,并对存储了 5 年的临床肿瘤 FFPE 组织进行高灵敏度转录组图谱绘制。此外,还可以捕获全基因组单核苷酸 RNA 变体,以区分人类淋巴瘤中的恶性亚克隆和非恶性细胞。Patho-DBiT 还绘制了 microRNA 调控网络和 RNA 剪接动态,解析它们在空间肿瘤发生中的作用。单细胞水平的 Patho-DBiT 剖析了驱动肿瘤克隆结构和进展的时空细胞动力学。Patho-DBiT 有望成为一个有价值的平台,用于揭示 FFPE 组织中的丰富 RNA 生物学,以辅助临床病理学评估。