(
A) The 7 bp deletion in the
trpa1b coding sequence generated a premature stop codon at 1412 bp. (
B) Amino acid sequences of the WT and mutant Trpa1b proteins. (
C)
In situ hybridization probing for
trpa1b mRNA in WT 3dpf larval zebrafish, demonstrating expression in RB neurons. (
D) Schematic of the Trpa1b protein structure, demonstrating that a truncated protein (in the unlikely event that it was translated) would lack a critical cysteine residue required for agonist binding (
Macpherson et al., 2007). (
E)
Trpa1b-/- nonsense mutants locomoted more in response to increasing temperatures at levels equivalent to their WT/heterozygous siblings. (
F) Normal AITC behavioral responses (increased locomotion) are abolished in
trpa1b-/- nonsense mutants. (
G) The 1 bp deletion in the
tlr7 coding sequence generated a premature stop codon at bp 665. (
H) Amino acid sequences of WT and mutant Tlr7 proteins. (
I) Schematic of the Tlr7 protein, demonstrating that a truncated protein (in the unlikely event of translation) would lack critical functional domains. (
J)
In situ hybridization probing for
tlr7 mRNA in WT 3dpf larval zebrafish. No
tlr7 expression was observed in RB somatosensory neurons. Premature stops are denoted with red highlighting. EC = extracellular, IC = intracellular, TM = transmembrane domain, LRR = leucine rich repeat, TIR = Toll Interleukin-1 Resistance domain. C and N denote c- and n-termini. (
E), Student’s
t-test.