10.01.2015 Views

Analysis of Genes for Stigma Coloration in Rice - IRRI books

Analysis of Genes for Stigma Coloration in Rice - IRRI books

Analysis of Genes for Stigma Coloration in Rice - IRRI books

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

Iwata, Kyushu University: F1 60, F1 85, F1 204, F1 214, F1 215, F1 217, F1 222, F1<br />

232, F1 233, F1 240, F1 244, F1 260, F1 283, F1 288, F1 293, F1 297, F1 304, F1 310,<br />

F1 312, and F5 814. Tongil-type Milyang 77ms was crossed with 10 Tongil-type<br />

marker l<strong>in</strong>es (Suh and Heu 1978): 1001, 1003, 1005, 1006, 1007, 1009, 1010, 2021,<br />

1023, and 1036, and with IR42667-36-mpl hav<strong>in</strong>g the mp-1 gene. L<strong>in</strong>kage relationships<br />

were <strong>in</strong>vestigated from the F 2 s. Recomb<strong>in</strong>ation values were calculated by the<br />

m<strong>in</strong>imum discrepancy method (Murty 1954).<br />

Male sterility <strong>of</strong> Milyang 67ms<br />

The l<strong>in</strong>kage relationships between the GMS gene <strong>of</strong> Milyang 67ms and the marker<br />

genes belong<strong>in</strong>g to l<strong>in</strong>kage group III are shown <strong>in</strong> Table 1. Of 22 marker genes (l<strong>in</strong>kage<br />

group given <strong>in</strong> parentheses)— C (I), 1g (II), nal-1 (II), eg (III), lax (III), d-10 (III), A (III),<br />

d-18 (III), fs-2 (III), spl-5 (IV), rfs (IV), spl-7 (VI+IX), nl-1 (VI+IX), la (VIII), d-k-4 (X),<br />

ch-1 (XI), ch-2 (XI), ch-3 (XI), fc-1 (XI), dl (XI), fl (fgl), and rk-2 (fgl)— eg, lax, d-10,<br />

and A belong<strong>in</strong>g to l<strong>in</strong>kage group III, from marker l<strong>in</strong>es F1 204 and F1 297, appeared<br />

to be l<strong>in</strong>ked with ms-m67(t). The other markers tested were <strong>in</strong>dependent <strong>of</strong> ms-m67(t).<br />

Complete l<strong>in</strong>kage was found between ms-m67(t) and the lax (lax panicle) gene <strong>in</strong> the<br />

repulsion phase. Relatively close l<strong>in</strong>kages were found between ms-m67(t) and eg (extra<br />

glume), d-10 (dwarf-10), and A (anthocyan<strong>in</strong> activator), with recomb<strong>in</strong>ation values <strong>of</strong><br />

13.7, 23.6, and 34.0%, respectively. Marker genes d-18 (dwarf-18) and fs-2 (f<strong>in</strong>e<br />

stripe-2) <strong>of</strong> l<strong>in</strong>kage group III were <strong>in</strong>dependent <strong>of</strong> ms-m67(t). Recomb<strong>in</strong>ation values<br />

between eg and d-10, d-10 and A, and eg and A were calculated as 31.2, 47.2, and<br />

50.5%, respectively. From these results, we can assume that ms-m67(t) is located on<br />

l<strong>in</strong>kage group III <strong>in</strong> the sequence eg-ms-m67(t) - d-10 - A, and is located distantly from<br />

d-18 and fs-2 (Fig. 1).<br />

Table 1. L<strong>in</strong>kage relationships between the male sterility gene ms-m67(t) <strong>of</strong> japonica male<br />

sterile rice Milyang 67ms and marker genes eg (extra glume), lax (lax panicle), d-10 (dwarf-<br />

10), A (anthocyan<strong>in</strong> activator), d-78 (dwarf-18), and fs-2 (f<strong>in</strong>e stripe-2) belong<strong>in</strong>g to l<strong>in</strong>kage<br />

group III.<br />

<strong>Genes</strong> comb<strong>in</strong>ed L<strong>in</strong>kage F 2 phenotype<br />

phase<br />

A B<br />

AB Ab aB ab<br />

Total<br />

c 2a<br />

Recomb<strong>in</strong>ation<br />

value (%)<br />

ms-m67(t)<br />

ms-m67(t)<br />

ms-m67(t)<br />

ms-m67(t)<br />

ms-m67(t)<br />

ms-m67(t)<br />

d-10<br />

d-10<br />

eg<br />

eg<br />

lax<br />

d-10<br />

A<br />

d-18<br />

fs-2<br />

eg<br />

A<br />

A<br />

Repulsion<br />

Repulsion<br />

Repulsion<br />

Coupl<strong>in</strong>g<br />

–<br />

–<br />

Coupl<strong>in</strong>g<br />

Coupl<strong>in</strong>g<br />

Coupl<strong>in</strong>g<br />

449<br />

389<br />

455<br />

402<br />

214<br />

214<br />

568<br />

347<br />

352<br />

211 216 4<br />

204 208 0<br />

205 208 12<br />

258 93 127<br />

66 68 19<br />

66 71 16<br />

115 117 100<br />

316 148 69<br />

313 143 72<br />

880<br />

801<br />

880<br />

880<br />

367<br />

367<br />

880<br />

880<br />

880<br />

80.15**<br />

100.00**<br />

57.75**<br />

23.29**<br />

1.07<br />

2.54<br />

76.70**<br />

16.62**<br />

12.14**<br />

13.7<br />

0.0<br />

23.6<br />

34.0<br />

Independent<br />

Independent<br />

31.2<br />

47.2<br />

50.5<br />

a ** = significant at the 1% level.<br />

122 Suh et al

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!