M2WISH: An easy and efficient protocol for whole‐mount mRNAin situ hybridization that allows 3D cell resolution of gene expression in Arabidopsis thaliana

Author:

Chelysheva Liudmila1,Morin Halima2,Biot Eric1,Nicolas Antoine13,Rech Philippe14,da Costa Marco15,Barel Lisa1,Laufs Patrick1ORCID,Palauqui Jean‐Christophe1ORCID

Affiliation:

1. Université Paris‐Saclay INRAE, AgroParisTech, Institut Jean‐Pierre Bourgin (IJPB) 78000 Versailles France

2. Institute of Plant Sciences Paris‐Saclay (IPS2), CNRS, Université Paris Diderot, INRA, Univ Paris Sud, Univ d'Evry Université Paris‐Saclay Rue de Noetzlin 91190 Gif‐sur‐Yvette France

3. Université Paris‐Saclay 91405 Orsay France

4. Institut de Systématique, Évolution, Biodiversité (ISYEB), Muséum National d'Histoire Naturelle, CNRS Sorbonne Université, EPHE, UA 57 rue Cuvier 75005 Paris France

5. Sorbonne Université, CNRS, Laboratoire de Biologie du Développement ‐Institut de Biologie Paris Seine (LBD‐IBPS), Team “Epigenetic Control of Developmental Homeostasis and Plasticity” Paris France

Abstract

SUMMARYGene expression analysis is essential for understanding the mechanisms involved in plant development. Here, we developed M2WISH, a protocol based on MicroWave treatment for Wholemount mRNA In Situ Hybridization in Arabidopsis. By permeabilizing tissues without damaging cellular organization this protocol results in high and homogeneous hybridization yields that enable systematic analysis of gene expression dynamics. Moreover, when combined with cellular histochemical staining, M2WISH successfully provides a cellular resolution of gene expression. Thus, we demonstrate the robustness of M2WISH with 10 genes on roots, aerial meristems, leaves, and embryos in the seed. We applied M2WISH to study the spatial dynamics of WUSCHEL (WUS) and CLAVATA3 (CLV3) expression during in vitro meristematic conversion of roots into shoot apical meristems. Thus, we showed that shoot apical meristems could arise from two different types of root structures that differed by their CLV3 gene expression patterns. We constructed 3D cellular representations of WUS and CLV3 gene co‐expression pattern and stressed the variability inherent to meristem conversion. Thus, this protocol generates a large amount of data on the localization of gene expression, which can be used to model complex systems.

Publisher

Wiley

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