Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
Department of Systems Biology, Harvard Medical School, Boston, MA, USA.
Nat Methods. 2019 Jun;16(6):533-544. doi: 10.1038/s41592-019-0404-0. Epub 2019 May 20.
Fluorescence in situ hybridization (FISH) reveals the abundance and positioning of nucleic acid sequences in fixed samples. Despite recent advances in multiplexed amplification of FISH signals, it remains challenging to achieve high levels of simultaneous amplification and sequential detection with high sampling efficiency and simple workflows. Here we introduce signal amplification by exchange reaction (SABER), which endows oligonucleotide-based FISH probes with long, single-stranded DNA concatemers that aggregate a multitude of short complementary fluorescent imager strands. We show that SABER amplified RNA and DNA FISH signals (5- to 450-fold) in fixed cells and tissues. We also applied 17 orthogonal amplifiers against chromosomal targets simultaneously and detected mRNAs with high efficiency. We then used 10-plex SABER-FISH to identify in vivo introduced enhancers with cell-type-specific activity in the mouse retina. SABER represents a simple and versatile molecular toolkit for rapid and cost-effective multiplexed imaging of nucleic acid targets.
荧光原位杂交(FISH)揭示了固定样本中核酸序列的丰度和定位。尽管 FISH 信号的多重扩增最近取得了进展,但仍然难以实现高水平的同时扩增和顺序检测,同时具有高采样效率和简单的工作流程。在这里,我们引入了交换反应信号放大(SABER),它为基于寡核苷酸的 FISH 探针赋予了长的单链 DNA 连接体,这些连接体聚集了大量短的互补荧光成像链。我们表明,SABER 可放大固定细胞和组织中的 RNA 和 DNA FISH 信号(5 到 450 倍)。我们还针对染色体靶标同时应用了 17 个正交放大器,并高效检测了 mRNAs。然后,我们使用 10 重 SABER-FISH 在体内鉴定具有特定细胞类型活性的增强子在小鼠视网膜中的作用。SABER 代表了一种简单而通用的分子工具包,用于快速且具有成本效益的核酸靶标的多重成像。