RT Journal Article
SR Electronic
T1 Patch-seq of mouse DRG neurons reveals candidate genes for specific mechanosensory functions
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 2021.07.07.451447
DO 10.1101/2021.07.07.451447
A1 Thibaud Parpaite
A1 Lucie Brosse
A1 Nina Séjourné
A1 Amandine Laur
A1 Yasmine Mechioukhi
A1 Patrick Delmas
A1 Bertrand Coste
YR 2021
UL http://biorxiv.org/content/early/2021/07/08/2021.07.07.451447.abstract
AB A variety of mechanosensory neurons are involved in touch, proprioception and pain. Many molecular components of the mechanotransduction machinery subserving these sensory modalities remain to be discovered. Here, we combined recordings of mechanosensitive (MS) currents in mechanosensory neurons with single cell RNA sequencing. In silico combined analysis with a large-scale dataset enables assigning each transcriptome to DRG genetic clusters. Correlation of current signatures with single-cell transcriptomes provides a one-to-one correspondence between mechanoelectric properties and transcriptomically-defined neuronal populations. Moreover, gene expression differential comparison provides a set of candidate genes for mechanotransduction complexes. Piezo2 was expectedly found to be enriched in rapidly adapting MS current-expressing neurons, whereas Tmem120a and Tmem150c, thought to mediate slow-type MS currents, were uniformly expressed in all neuron subtypes, irrespective of their mechano-phenotype. Further knock-down experiments disqualified them as mediating DRG MS currents. This dataset constitutes an open-resource to explore further the cell-type-specific determinants of mechanosensory properties.Competing Interest StatementThe authors have declared no competing interest.