TABLE 2.
Polymorphism data summary
Locus | Species | na | Sb | Sync | Repc | θtd | θsd | De | L (bp)f |
---|---|---|---|---|---|---|---|---|---|
A. Regions of reduced frequency of crossing over | |||||||||
ND5–ND4 | D. yakuba | 11 | 8 | 6 | 2 | 0.0016 | 0.0046 | −1.27 | 1657 |
D. santomea | 10 | 4 | 4 | 0 | 0.00085 | 0.0032 | −0.52 | ||
Dhc-Yh3 | D. yakuba | 11 | 0 | 0 | 0 | 0 | 0 | — | 1219 |
D. santomea | 10 | 0 | 0 | 0 | 0 | 0 | — | ||
CG17629 | D. yakuba | 11 | 1 | 1 | 0 | 0.0004 | 0.0016 | 0.67 | 936 |
D. santomea | 10 | 3 | 1 | 2 | 0.0011 | 0.001 | −1.03 | ||
Pp1Y1 | D. yakuba | 11 | 1 | 0 | 1 | 0.0007 | 0 | −1.13 | 490 |
D. santomea | 10 | 0 | 0 | 0 | 0 | 0 | — | ||
y | D. yakuba | 16 | 6 | 6 | 0 | 0.0019 | 0.0078 | −1.17 | 965 |
D. santomea | 16 | 0 | 0 | 0 | 0 | 0 | — | ||
su(f) | D. yakuba | 16 | 1 | 0 | 0 | 0.0005 | 0.0008 | 0.15 | 607 |
D. santomea | 16 | 0 | 0 | 0 | 0 | 0 | — | ||
l(2)gl | D. yakuba | 16 | 1 | 1 | 0 | 0.0005 | 0.0021 | 1.03 | 608 |
D. santomea | 16 | 3 | 2 | 1 | 0.0015 | 0.0042 | 0.17 | ||
His3 | D. yakuba | 16 | 3 | 0 | 0 | 0.0018 | 0.0022 | −0.65 | 496 |
D. santomea | 16 | 0 | 0 | 0 | 0 | 0 | — | ||
Kr | D. yakuba | 16 | 3 | 3 | 0 | 0.002 | 0.0086 | 0.01 | 456 |
D. santomea | 16 | 0 | 0 | 0 | 0 | 0 | — | ||
Lsp1-γ | D. yakuba | 16 | 3 | 2 | 0 | 0.0018 | 0.006 | −0.41 | 508 |
D. santomea | 16 | 4 | 0 | 3 | 0.0024 | 0.002 | −1.55* | ||
Ssl1 | D. yakuba | 16 | 2 | 2 | 0 | 0.0012 | 0.0051 | −0.58 | 501 |
D. santomea | 16 | 1 | 1 | 0 | 0.0006 | 0.0025 | 0.15 | ||
krzg | D. yakuba | 16 | 0 | — | — | 0 | 0 | — | 165 |
D. santomea | 16 | 2 | — | — | 0.0036 | 0.0036 | −1.50* | ||
B. Regions of nonreduced frequency of crossing over | |||||||||
rux | D. yakuba | 16 | 28 | 20 | 7 | 0.0090 | 0.023 | −1.62* | 940 |
D. santomea | 16 | 21 | 17 | 3 | 0.0067 | 0.02 | −1.42 | ||
per | D. yakuba | 16 | 3 | 0 | 0 | 0.001 | 0.0013 | −1.35 | 905 |
D. santomea | 14 | 5 | 0 | 1 | 0.0017 | 0.0019 | −1.36 | ||
sog | D. yakuba | 16 | 25 | 23 | 2 | 0.007 | 0.024 | −0.63 | 1100 |
D. santomea | 16 | 18 | 17 | 1 | 0.0049 | 0.018 | −0.59 | ||
bnb | D. yakuba | 14 | 33 | 24 | 9 | 0.012 | 0.037 | −0.86 | 837 |
D. santomea | 16 | 25 | 18 | 7 | 0.009 | 0.026 | −0.97 | ||
Hex-A | D. yakuba | 16 | 3 | 3 | 0 | 0.0014 | 0.058 | −0.63 | 639 |
D. santomea | 16 | 9 | 8 | 1 | 0.0042 | 0.016 | −0.67 | ||
Rad1 | D. yakuba | 16 | 16 | 14 | 1 | 0.011 | 0.04 | −1.45 | 428 |
D. santomea | 16 | 10 | 8 | 1 | 0.007 | 0.024 | −1.48* | ||
RpL27A | D. yakuba | 14 | 20 | 2 | 1 | 0.0076 | 0.01 | 0.13 | 822 |
D. santomea | 14 | 19 | 2 | 1 | 0.0073 | 0.0099 | −1.17 | ||
salr | D. yakuba | 16 | 28 | 25 | 2 | 0.0086 | 0.038 | −0.72 | 869 |
D. santomea | 16 | 26 | 22 | 3 | 0.0090 | 0.033 | −0.58 | ||
Rep4 | D. yakuba | 16 | 25 | 19 | 6 | 0.0093 | 0.032 | −0.76 | 808 |
D. santomea | 16 | 14 | 11 | 3 | 0.0052 | 0.019 | −1.61* | ||
Sara | D. yakuba | 16 | 21 | 13 | 7 | 0.0068 | 0.02 | −0.26 | 887 |
D. santomea | 16 | 12 | 8 | 4 | 0.0040 | 0.012 | 0.52 | ||
Hex-C | D. yakuba | 16 | 21 | 19 | 2 | 0.011 | 0.04 | 0.65 | 552 |
D. santomea | 16 | 13 | 12 | 1 | 0.0071 | 0.021 | −0.73 | ||
Ngp | D. yakuba | 16 | 3 | 3 | 0 | 0.0012 | 0.005 | 0.47 | 767 |
D. santomea | 16 | 5 | 4 | 1 | 0.0020 | 0.0067 | −0.32 | ||
sfl | D. yakuba | 16 | 40 | 40 | 0 | 0.014 | 0.058 | −0.86 | 867 |
D. santomea | 16 | 37 | 37 | 0 | 0.013 | 0.053 | −0.59 | ||
Est6 | D. yakuba | 16 | 37 | 22 | 8 | 0.016 | 0.043 | 0.17 | 687 |
D. santomea | 16 | 27 | 15 | 9 | 0.012 | 0.027 | 0.12 | ||
Xdh | D. yakuba | 16 | 32 | 23 | 9 | 0.012 | 0.036 | −0.14 | 782 |
D. santomea | 16 | 24 | 18 | 6 | 0.0092 | 0.028 | −1.95** | ||
AP-50 | D. yakuba | 16 | 35 | 25 | 2 | 0.01 | 0.035 | −0.63 | 1025 |
D. santomea | 16 | 29 | 22 | 1 | 0.0085 | 0.029 | −1.84* | ||
Mlc1 | D. yakuba | 16 | 7 | 0 | 0 | 0.0059 | 0.0071 | −1.52 | 359 |
D. santomea | 16 | 10 | 0 | 0 | 0.0084 | 0.01 | −1.54* |
P < 0.05,
P < 0.01. —, values could not be estimated because of lack of informative sites.
Sample size.
Number of polymorphic sites.
Number of synonymous (syn) and nonsynonymous (rep) polymorphic sites estimated using Nei and Gojobori (1986).
Watterson's (1975) estimate of total and silent (synonymous and noncoding) heterozygosity.
Tajima's (1989b) D-statistic. Significance was calculated with coalescent simulations without recombination.
Size of the sequenced region.
This locus does not include the coding region sequence.