Molecular profiling of activated olfactory neurons identifies odorant receptors for odors in vivo

被引:92
作者
Jiang, Yue [1 ,2 ,3 ]
Gong, Naihtta Natalie [1 ]
Hu, Xiaoyang Serene [1 ]
Ni, Mengjue Jessica [1 ]
Pasi, Radhika [1 ]
Matsunami, Hiroaki [1 ,4 ]
机构
[1] Duke Univ Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
[2] Duke Univ Med Ctr, Univ Program Genet & Genom, Durham, NC USA
[3] Duke Univ, Dept Stat Sci, Durham, NC USA
[4] Duke Univ Med Ctr, Duke Inst Brain Sci, Dept Neurobiol, Durham, NC USA
基金
美国国家卫生研究院;
关键词
DIFFERENTIAL EXPRESSION ANALYSIS; FUNCTIONAL EXPRESSION; REGULARIZATION; SPECIFICITY; FAMILY; STATE; SMELL; MAP;
D O I
10.1038/nn.4104
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The mammalian olfactory system uses a large family of odorant receptors (ORs) to detect and discriminate amongst a myriad of volatile odor molecules. Understanding odor coding requires comprehensive mapping between ORs and corresponding odors. We developed a means of high-throughput in vivo identification of OR repertoires responding to odorants using phosphorylated ribosome immunoprecipitation of mRNA from olfactory epithelium of odor-stimulated mice followed by RNA-Seq. This approach screened the endogenously expressed ORs against an odor in one set of experiments using awake and freely behaving mice. In combination with validations in a heterologous system, we identified sets of ORs for two odorants, acetophenone and 2,5-dihydro-2,4,5-trimethylthiazoline (TMT), encompassing 69 OR-odorant pairs. We also identified shared amino acid residues specific to the acetophenone or TMT receptors and developed models to predict receptor activation by acetophenone. Our results provide a method for understanding the combinatorial coding of odors in vivo.
引用
收藏
页码:1446 / +
页数:11
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