Single-Soma Deep RNA sequencing of Human DRG Neurons Reveals Novel Molecular and Cellular Mechanisms Underlying Somatosensation.
Single-Soma Deep RNA sequencing of Human DRG Neurons Reveals Novel Molecular and Cellular Mechanisms Underlying Somatosensation.
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人类 DRG 神经元的单体深度 RNA 测序揭示了体感的新分子和细胞机制。
DOI:
10.1101/2023.03.17.533207
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发表时间:
2023
期刊:
影响因子:
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通讯作者:
Wu
中科院分区:
文献类型:
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作者:
Yu,Huasheng;Usoskin,Dmitry;Nagi,SaadS;Hu,Yizhou;Kupari,Jussi;Bouchatta,Otmane;Cranfill,SunaLi;Gautam,Mayank;Su,Yijing;Lu,You;Wymer,James;Glanz,Max;Albrecht,Phillip;Song,Hongjun;Ming,Guo-Li;Prouty,Stephen;Seykora,John;Wu
The versatility of somatosensation arises from heterogenous human dorsal root ganglion (DRG) neurons. The critical information to decipher their functions, ie, the soma transcriptome, is lacking due to technical difficulties. Here we developed a novel approach to isolate individual human DRG neuron somas for deep RNA sequencing (RNA-seq). On average,> 9000 unique genes per neuron were detected, and 16 neuronal types were identified. Cross-species analyses revealed that touch-, cold-, and itch-sensing neuronal types were relatively conserved, while the pain-sensing neurons displayed marked divergence. Soma transcriptomes of human DRG neurons predicted novel functional features, which were confirmed using single-cell in vivo electrophysiological recordings. These results support a close relationship the between physiological properties of human sensory afferents and molecular profiles uncovered by the single-soma RNA-seq dataset. In summary, by conducting single-soma RNA-seq of human DRG neurons, we generated an unprecedented neural atlas for human somatosensation.(which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. The copyright holder for this preprint this version posted March 18, 2023.; https://doi. org/10.1101/2023.03. 17.533207 doi: bioRxiv preprint