Coordination of two enhancers drives expression of olfactory trace amine-associated receptors
Olfactory sensory neurons (OSNs) are functionally defined by their expression of a unique odorant receptor (OR). Mechanisms underlying singular OR expression are well studied, and involve a massive cross-chromosomal enhancer interaction network. Trace amine-associated receptors (TAARs) form a distin...
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Veröffentlicht in: | Nature communications 2021-06, Vol.12 (1), p.3798-3798, Article 3798 |
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Sprache: | eng |
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Zusammenfassung: | Olfactory sensory neurons (OSNs) are functionally defined by their expression of a unique odorant receptor (OR). Mechanisms underlying singular OR expression are well studied, and involve a massive cross-chromosomal enhancer interaction network. Trace amine-associated receptors (TAARs) form a distinct family of olfactory receptors, and here we find that mechanisms regulating
Taar
gene choice display many unique features. The epigenetic signature of
Taar
genes in TAAR OSNs is different from that in OR OSNs. We further identify that two TAAR enhancers conserved across placental mammals are absolutely required for expression of the entire
Taar
gene repertoire. Deletion of either enhancer dramatically decreases the expression probabilities of different
Taar
genes, while deletion of both enhancers completely eliminates the TAAR OSN populations. In addition, both of the enhancers are sufficient to drive transgene expression in the partially overlapped TAAR OSNs. We also show that the TAAR enhancers operate in
cis
to regulate
Taar
gene expression. Our findings reveal a coordinated control of
Taar
gene choice in OSNs by two remote enhancers, and provide an excellent model to study molecular mechanisms underlying formation of an olfactory subsystem.
In our nose, some neuron subpopulations express a family of trace amine associated receptors (TAARs, smelling e.g., rotten fish). Fei et al. identify two conserved enhancers across placental mammals named TAAR enhancer 1 and 2 that coordinately regulate expression of the entire Taar gene repertoire. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-021-23823-4 |