Single-Molecule Fluorescence In Situ Hybridization for Spatial Detection of mRNAs in Sections of Mammalian Testes

Methods Mol Biol. 2023:2656:21-35. doi: 10.1007/978-1-0716-3139-3_3.

Abstract

Single-molecule fluorescence in situ hybridization (smFISH) enables the detection and localization of individual mRNAs in tissue sections with single-molecule resolution while preserving spatial context, and thus, is a useful tool for examining gene expression in biological systems. In particular, the growing reliance on single-cell RNA sequencing (scRNA-seq) to explore cellular heterogeneity has reinvigorated this approach as a validation tool to spatially re-map mRNA expression patterns described in isolated cells to their parent tissue. While use of antibody-based methods, such as indirect immunofluorescence (IIF), remain popular as validation strategies, smFISH often affords superior specificity and maintains congruency with scRNA-seq. Here, we present a detailed protocol that combines multiplexed smFISH using the RNAscope approach with IIF to co-visualize mRNAs and proteins within sections of mouse testes. We provide step-by-step guidelines from testis preparation through visualization that enables mapping of combinations of up to four mRNA/protein targets in frozen sections on the RNAscope platform.

Keywords: Immunohistochemistry; RNAscope; Spermatogenesis; scRNA-seq; smFISH.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • In Situ Hybridization, Fluorescence / methods
  • Male
  • Mammals* / genetics
  • Mice
  • Nanotechnology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Testis* / metabolism

Substances

  • RNA, Messenger