Medium-Throughput RNA In Situ Hybridization of Serial Sections from Paraffin-Embedded Tissue Microarrays.
Arabidopsis
Data integration
Digoxigenin-labeled riboprobes
Medium-throughput RNA in situ hybridization
Plants
Seed development
Slide scanner
Tissue microarray paraffin serial sections
Tissue-specific transcriptomics
Journal
Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969
Informations de publication
Date de publication:
2019
2019
Historique:
entrez:
5
4
2019
pubmed:
5
4
2019
medline:
3
8
2019
Statut:
ppublish
Résumé
(m)RNA spatiotemporal pattern of distribution is of key importance to decipher gene function. In this post-genomic era, numerous transcriptomic studies are made publicly available, sometimes reaching a tissular resolution and even more rarely the cellular level. This "one tissue-numerous genes" information can be completed by the reverse "one gene-numerous tissues" picture through traditional RNA in situ hybridization (ISH). Here, we present a method including (1) principles of transcriptomic data mining to be performed prior and following ISH and (2) a detailed step-by-step medium-throughput ISH protocol performed on serial sections from tissue microarrays. In a recent work, we implemented this method for 39 selected genes studied by medium-throughput ISH complementing an existing tissue-specific transcriptomic dataset focused on the model plant Arabidopsis seed development kinetics (Francoz et al., Scientific Reports 6:24644, 2016). This full integration of ISH and transcriptomics demonstrated the complementarity of both techniques in terms of tissue/cell specificity, signal sensitivity, gene specificity, and spatiotemporal resolution.
Identifiants
pubmed: 30945181
doi: 10.1007/978-1-4939-9045-0_6
doi:
Substances chimiques
Arabidopsis Proteins
0
RNA Probes
0
RNA, Plant
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng