Skip to main content
. 2008 Jul;179(3):1527–1538. doi: 10.1534/genetics.108.089805

TABLE 3.

Polymorphism and neutral test of different groups of the Pi-ta gene

Total sites S π θ Tajima's D Fu and Li's D (with outgroup) Fay and Wu's H
All O. rufipogon
Entire gene 4306 72 0.00196 0.00410 1.86739* 2.60794* −0.83721
    Coding 2787 24 0.00089 0.00207 1.89395* −2.08664 2.17759
        N-terminal 705 13 0.00229 0.00429 −1.43175 −0.00616 1.37209
        NBS 357 3 0.00050 0.00193 −1.57449 −1.72555 0.17336
        LRR 1032 6 0.00060 0.00156 −1.66947 2.71653* 0.54334
    Intron 1519 44 0.00345 0.00760 1.90876* 2.47935* −3.01480
H1
Entire gene 4306 2 0.00012 0.00018 −1.31009 −1.26208 0.42857
    Codinga 2787 1 0.00009 0.00014 −1.05482 −2.08993 0.21429
        LRR 1032 1 0.00024 0.00037 −1.05482 −1.26208 0.21429
    Intron 1519 1 0.00017 0.00026 −1.05482 −1.26208 0.21429
H2
Entire gene 4306 60 0.00147 0.00357 2.19527** 2.39754* −1.36508
    Coding 2787 22 0.00068 0.00191 2.18652* −1.98819 1.79365
        N-terminal 705 12 0.00178 0.00416 −1.80016 −0.05768 1.15873
        NBS 357 3 0.00061 0.00203 −1.56135 −1.64357 0.20952
        LRR 1032 5 0.00032 0.00117 1.89379* 2.66924* 0.31746
    Intron 1519 42 0.00321 0.00759 2.07182* −2.22887 −3.15873

Significance levels were determined by 10,000 random coalescent simulations on the basis of the number of alleles and the observed number of segregating sites. S, number of segregating sites; π, nucleotide diversity; θ, Watterson's estimator, 4Neμ. Italics indicate the significant statistics. *P < 0.05; **P < 0.01.

a

The N-terminal and NBS of H1 have no variation, so these two parts were not included.