Wyss Institute, Harvard Medical School, Boston, MA 02115, USA.
Science. 2014 Mar 21;343(6177):1360-3. doi: 10.1126/science.1250212. Epub 2014 Feb 27.
Understanding the spatial organization of gene expression with single-nucleotide resolution requires localizing the sequences of expressed RNA transcripts within a cell in situ. Here, we describe fluorescent in situ RNA sequencing (FISSEQ), in which stably cross-linked complementary DNA (cDNA) amplicons are sequenced within a biological sample. Using 30-base reads from 8102 genes in situ, we examined RNA expression and localization in human primary fibroblasts with a simulated wound-healing assay. FISSEQ is compatible with tissue sections and whole-mount embryos and reduces the limitations of optical resolution and noisy signals on single-molecule detection. Our platform enables massively parallel detection of genetic elements, including gene transcripts and molecular barcodes, and can be used to investigate cellular phenotype, gene regulation, and environment in situ.
要了解基因表达的空间组织,需要以单核苷酸分辨率定位细胞内表达的 RNA 转录本序列。在这里,我们描述了荧光原位 RNA 测序(FISSEQ),其中在生物样本内对稳定交联的互补 DNA(cDNA)扩增子进行测序。使用来自原位 8102 个基因的 30 个碱基读长,我们使用模拟伤口愈合测定法检查了人原代成纤维细胞中的 RNA 表达和定位。FISSEQ 与组织切片和整个胚胎兼容,并减少了单个分子检测中光学分辨率和嘈杂信号的限制。我们的平台可以实现遗传元件(包括基因转录本和分子条形码)的大规模并行检测,并可用于原位研究细胞表型、基因调控和环境。