| Literature DB >> 32773035 |
Kun Tan1, Samantha H Jones1, Blue B Lake2, Jennifer N Chousal1, Eleen Y Shum1, Lingjuan Zhang3, Song Chen2, Abhishek Sohni1, Shivam Pandya1, Richard L Gallo3, Kun Zhang2, Heidi Cook-Andersen1,4, Miles F Wilkinson1,5.
Abstract
The UPF3B-dependent branch of the nonsense-mediated RNA decay (NMD) pathway is critical for human cognition. Here, we examined the role of UPF3B in the olfactory system. Single-cell RNA-sequencing (scRNA-seq) analysis demonstrated considerable heterogeneity of olfactory sensory neuron (OSN) cell populations in wild-type (WT) mice, and revealed that UPF3B loss influences specific subsets of these cell populations. UPF3B also regulates the expression of a large cadre of antimicrobial genes in OSNs, and promotes the selection of specific olfactory receptor (Olfr) genes for expression in mature OSNs (mOSNs). RNA-seq and Ribotag analyses identified classes of mRNAs expressed and translated at different levels in WT and Upf3b-null mOSNs. Integrating multiple computational approaches, UPF3B-dependent NMD target transcripts that are candidates to mediate the functions of NMD in mOSNs were identified in vivo. Together, our data provides a valuable resource for the olfactory field and insights into the roles of NMD in vivo.Entities:
Keywords: NMD; Upf3b; anti-microbial genes; developmental biology; mouse; neuroscience; olfactory receptor; olfactory sensory neuron; scRNA-seq
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Year: 2020 PMID: 32773035 PMCID: PMC7452722 DOI: 10.7554/eLife.57525
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.713