TY  - JOUR
A1  - Dong, Xue
A1  - Hu, Mengzhu
A1  - Cui, Xiaonan
A1  - Zhou, Wenjian
A1  - Cai, Jingtao
A1  - Mao, Guangyao
A1  - Shi, Weiyang
T1  - High-resolution spatial transcriptomics in fixed tissue using a cost-effective PCL-seq workflow
Y1  - 2025/09/01 
JF  - Genome Research 
JO  - Genome Research 
SP  - 2052 
EP  - 2063 
DO  - 10.1101/gr.279906.124 
VL  - 35 
IS  - 9 
UR  - http://genome.cshlp.org/content/35/9/2052.abstract 
N2  - The spatial heterogeneity of gene expression has driven the development of diverse spatial transcriptomics technologies. Here, we present photocleavage and ligation sequencing (PCL-seq), a spatial indexing method utilizing a light-controlled DNA labeling strategy applied to tissue sections. PCL-seq employs photocleavable oligonucleotides and ligation adapters to construct transcriptional profiles of specific regions of interest (ROIs) designated via microscopically controlled photo-illumination. In frozen mouse embryos, PCL-seq generates spatially aligned gene expression matrices and produces high-quality data, detecting approximately 170,000 unique molecular identifiers (UMIs) and 8600 genes (illumination diameter = 100 µm). Moreover, PCL-seq is compatible with formalin-fixed paraffin-embedded (FFPE) tissues, successfully identifying thousands of differentially enriched transcripts in the digits and vertebrae of mouse embryo FFPE sections. Additionally, PCL-seq achieves subcellular resolution, as demonstrated by differential expression profiling between nuclear and cytoplasmic compartments. These characteristics establish PCL-seq as an accessible and versatile workflow for spatial transcriptomic analyses in both frozen and FFPE tissues with subcellular resolution. 
ER  -