TABLE 3.
Branch | MY | RH1 | Significance | SWS1 | Significance | LWS |
---|---|---|---|---|---|---|
a–b | 300 | ds = 0.60 ± 0.077 | ≪ | 1.53 ± 0.256 | ≫ | 0.80 ± 0.103 |
dn = 0.10 ± 0.013 | ≪ | 0.30 ± 0.026 | ≫ | 0.06 ± 0.010 | ||
b–human | 100 | ds = 2.00 ± 0.035 | ≫ | 0.50 ± 0.066 | 3.10 ± 1.948 | |
dn = 0.10 ± 0.013 | ≪ | 0.30 ± 0.026 | ≫ | 0.20 ± 0.020 | ||
b–elephant | 100 | ds = 2.10 ± 0.531 | 2.20 ± 0.597 | > | 1.00 ± 0.134 | |
dn = 0.10 ± 0.013 | ≪ | 0.40 ± 0.032 | ≫ | 0.30 ± 0.026 |
Standard errors were computed from [9p(1 − p)/{(3 − 4p)2n}]1/2, where p is the proportion of sites that differ and n is the number of nucleotide sites involved (Kimura and Ohta 1972). The ds and dn values indicate the rates of nucleotide substitution at ∼200 synonymous and ∼616 nonsynonymous sites, respectively. Single and double inequality signs indicate that the differences are significant at 5 and 1% levels, respectively.