Decoder-seq enhances mRNA capture efficiency in spatial RNA sequencing.
Jiao CaoZhong ZhengDi SunXin ChenRui ChengTianpeng LvYu AnJunhua ZhengJia SongLingling WuChaoyong James YangPublished in: Nature biotechnology (2024)
Spatial transcriptomics technologies with high resolution often lack high sensitivity in mRNA detection. Here we report a dendrimeric DNA coordinate barcoding design for spatial RNA sequencing (Decoder-seq), which offers both high sensitivity and high resolution. Decoder-seq combines dendrimeric nanosubstrates with microfluidic coordinate barcoding to generate spatial arrays with a DNA density approximately ten times higher than previously reported methods while maintaining flexibility in resolution. We show that the high RNA capture efficiency of Decoder-seq improved the detection of lowly expressed olfactory receptor (Olfr) genes in mouse olfactory bulbs and contributed to the discovery of a unique layer enrichment pattern for two Olfr genes. The near-cellular resolution provided by Decoder-seq has enabled the construction of a spatial single-cell atlas of the mouse hippocampus, revealing dendrite-enriched mRNAs in neurons. When applying Decoder-seq to human renal cell carcinomas, we dissected the heterogeneous tumor microenvironment across different cancer subtypes and identified spatial gradient-expressed genes related to epithelial-mesenchymal transition with the potential to predict tumor prognosis and progression.
Keyphrases
- single cell
- rna seq
- high throughput
- high resolution
- genome wide
- epithelial mesenchymal transition
- single molecule
- endothelial cells
- dna methylation
- mass spectrometry
- spinal cord
- circulating tumor
- brain injury
- mesenchymal stem cells
- young adults
- quantum dots
- risk assessment
- cell free
- real time pcr
- lymph node metastasis
- sensitive detection