Skip to main content
. 2012 Sep 14;7(9):e45011. doi: 10.1371/journal.pone.0045011

Table 1. Polymorphism of the exons encoding the pathogen-recognition extracellular domains of Toll-like receptor genes among Stewart Island robin Petroica australis rakiura founders of Ulva Island.

Gene (target exon) N 1 Fragment length (bp) Observed haplotypes SNPs Amino acids syn∶nsyn π (±SE)2 Genbank accession
TLR1LA (ex 2) 10 founders (+2 & 5) 1,166 2 172: C/T Arg/Trp 1∶1 8.89 (6.84) JX502625: JX502627
291: G/A Ser
TLR1LB (ex 1) 10 founders (+2 & 5) 971 2 154: C/T Leu 2∶1 16.01 (11.04) JX502628: JX502630
185: C/T Ala/Val
369: G/A Val
TLR2A (ex 2) 10 founders (+6 & 5) 1,034 2 891: C/T Gly 1∶0 5.01 (4.86) JX502631: JX502633
TLR2B (ex 2) 10 founders (+7 & 6) 1,021 3 108: G/A Glu 4∶1 21.40 (13.68) JX502634: JX502637
324: C/T Asn
632: C/T Thr/Met
645: C/T Asn
846: G/A Arg
TLR3 (ex 4) 9 founders (+53 & 5) 1,087 1 (none) - - - JX502638
TLR4 (ex 3) 10 founders (+5 & 6) 649 5 94: A/C/T Ile/Leu/Phe 0∶4 27.13 (18.17) JX502639: JX502644
142: C/T Leu/Phe
220: A/T Thr/Ser
520: G/A Asp/Asn
TLR5 (ex 1) 10 founders (+2 & 5) 1,229 3 371: G/A Arg/Gln 0∶2 4.66 (4.36) JX502645: JX502648
817: G/T Asp/Tyr
TLR7 (ex 2)4 10 founders (+6 & 7) 1,0105 ≥2 162: G/A Asn/Asp 0∶3 N/A4 JX502657: JX502665
672: C/T Pro/Ser
723: G/A Ser/Gly
TLR15 (ex 1) 10 founders (+6 & 6) 1,279 2 997: G/A Asp/Asn 0∶1 0.65 (1.40) JX502649: JX502651
TLR21 (ex 1) 10 founders (+7 & 7) 618 4 118: G/A Asn/Asp 1∶2 14.42 (11.62) JX502652: JX502656
169: C/T Arg/Trp
300: G/A Pro
Mean 1,006 ≥2.6 2.4 9∶15
1

Numbers in brackets are the number of offspring used to infer the genotypes of the missing 11th (female) and 12th (male) founders. See Methods.

2

Nucleotide diversity (×104).

3

These five birds are also the offspring of the 10th founder that could not be genotyped for this locus.

4

TLR7 primers co-amplified two loci, excludes SNPs that clearly do not follow Mendelian inheritance (likely to be fixed differences). Genotypes could not be inferred.

5

Length of cloned product (see Results); initial, population-level sequence analyses were based on directly sequenced PCR products (sequence length = 947 bp).