Mechanisms of Olfaction in Insects - ResearchSpace@Auckland ...
Mechanisms of Olfaction in Insects - ResearchSpace@Auckland ...
Mechanisms of Olfaction in Insects - ResearchSpace@Auckland ...
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General Introduction 31<br />
BmOr2<br />
HvOr2<br />
MsepOR2<br />
DiOR2<br />
PxOR2<br />
EpOR2<br />
0.1<br />
100<br />
*<br />
80<br />
HvOr15<br />
HvOr14<br />
MsepOR1<br />
HvOr6<br />
HvOr16<br />
HvOr11<br />
BmOr3<br />
PxOR1<br />
BmOr7<br />
BmOr5<br />
BmOr9<br />
BmOr4<br />
MsepOR3<br />
HvOr13<br />
DiOR3<br />
BmOr1<br />
DiOR1<br />
EpOR1<br />
PxOR3<br />
PxOR4<br />
Male-biased<br />
sex pheromone<br />
receptor clade<br />
31<br />
77<br />
99<br />
BmOr6<br />
100 BmOr22<br />
BmOr21<br />
HvOr19<br />
41 62<br />
99<br />
100<br />
98 HvOr21<br />
BmOr19<br />
BmOr17<br />
BmOr8<br />
BmOr20<br />
100<br />
43<br />
BmOr38<br />
BmOr35<br />
BmOr37<br />
96 HvOr12<br />
45<br />
41<br />
BmOr24<br />
69<br />
BmOr25<br />
99<br />
100<br />
88 89 HvOr7<br />
BmOr11<br />
HvOr9<br />
BmOr23<br />
BmOr42<br />
54<br />
100 HvOr18<br />
40<br />
100<br />
100<br />
HvOr20<br />
BmOr28<br />
57<br />
95<br />
BmOr14<br />
100 BmOr34<br />
100<br />
BmOr33<br />
BmOr30<br />
BmOr36<br />
34<br />
HvOr3<br />
100 BmOR22J<br />
100<br />
BmOr15<br />
99<br />
BmOr12<br />
30 73<br />
100<br />
100<br />
HvOr8<br />
BmOr13<br />
EpOR3 *<br />
EpOR3<br />
BmOR49 BmOR49J<br />
100<br />
100 BmOr48<br />
BmOr46 Female-biased<br />
100 BmOr47<br />
BmOr45 receptor clade<br />
100 BmOR19J<br />
94<br />
97<br />
HvOr10<br />
BmOr10<br />
40<br />
100<br />
BmOr16<br />
89 BmOR23J<br />
BmOr26<br />
HvOr17<br />
98<br />
BmOr29<br />
BmOr27<br />
Or83b clade<br />
98<br />
99<br />
48<br />
100<br />
60<br />
25 100<br />
Figure 1.8: Phylogenetic tree constructed from lepidopteran odorant receptors with<br />
the three E. postvittana ORs <strong>in</strong>dicated by *. Adapted from Jordan et al. (2009) where<br />
the tree was orig<strong>in</strong>ally constructed us<strong>in</strong>g the FITCH method from Jones-Thorton<br />
distances and the given bootstrap values calculated us<strong>in</strong>g 1000 replicates.<br />
50<br />
62<br />
96<br />
33<br />
100<br />
25<br />
34<br />
91<br />
100<br />
94<br />
100<br />
100<br />
100<br />
*