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Analysis of Genes for Stigma Coloration in Rice - IRRI books

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Table 3. Segregation analysis <strong>of</strong> fragments homologous to B1 and B2 <strong>in</strong> F 2<br />

population.<br />

Fragment<br />

Size (kb)<br />

P1 a<br />

P2 b<br />

F 2 population<br />

Present<br />

Absent<br />

c 2 (3:1) c<br />

B2<br />

B1<br />

15 Present Absent 103 40<br />

7.1 Absent Present 129 154<br />

2.5 Present Absent 108 35<br />

0.0<br />

16.3**<br />

0.0<br />

a b c Maternal parent Kasalath (<strong>in</strong>dica). Paternal parent F1134 (japonica). **= significant at the 1%<br />

level.<br />

The presence-to-absence ratios <strong>of</strong> the three fragments were estimated <strong>in</strong> the F 2<br />

population (Table 3). The observed ratios <strong>of</strong> 2 fragments, the B2-homologous 15-kb<br />

fragment and the B1-homologous 2.5-kb fragment, were consistent with a 3:1 ratio and<br />

thus showed normal Mendelian <strong>in</strong>heritance. However, the segregation <strong>of</strong> the B1-<br />

homologous 7.1-kb fragment deviated from 3:1. The deviation might be expla<strong>in</strong>ed by<br />

the fact that a gametophyte gene (Nakagahra 1972), which affected pollen fertility, was<br />

l<strong>in</strong>ked to the B1-homologous 7.1-kb fragment, because RFLP probes l<strong>in</strong>ked to it also<br />

showed deviated segregation (unpubl. data).<br />

All three fragments were null alleles, i.e., present only <strong>in</strong> either the <strong>in</strong>dica or japonica<br />

parent. Two B1-homologous sequences were revealed to be <strong>in</strong>dependent alleles by<br />

segregation analysis, and probably occupy different map positions <strong>in</strong> <strong>in</strong>dicas and<br />

japonicas.<br />

The orig<strong>in</strong> <strong>of</strong> the sequences <strong>of</strong> these plasmid-like DNAs is unknown. If nuclear<br />

sequences homologous to the plasmids were derived from mitochondrial plasmids, our<br />

results might be expla<strong>in</strong>ed by the fact that transmission event <strong>of</strong> the plasmids <strong>in</strong>to the<br />

nuclear genome had occurred <strong>in</strong>dependently <strong>in</strong> <strong>in</strong>dicas and japonicas. Alternatively,<br />

sequence transposition could have occurred dur<strong>in</strong>g the course <strong>of</strong> rice differentiation<br />

<strong>in</strong>to subspecies. Further mapp<strong>in</strong>g <strong>of</strong> these sequences is currently be<strong>in</strong>g done.<br />

References cited<br />

Kadowaki K, Ishige T, Suzuki S, Harada K, Sh<strong>in</strong>jyo C (1986) Differences <strong>in</strong> the characteristics<br />

<strong>of</strong> mitochondrial DNA between normal and male sterile cytoplasms <strong>of</strong> Japonica rice. Jpn. J.<br />

Breed. 36:333–339.<br />

Kadowaki K, Yazaki K, Osumi T, Harada K, Katsuta M, Nakagahra M (1988) Distribution <strong>of</strong><br />

mitochondrial plasmid-like DNA <strong>in</strong> cultivated rice ( Oryza sativa L.) and its relationship with<br />

varietal groups. Theor. Appl. Genet. 76:809–814.<br />

Maniatis T, Fritsh E F, Sambrook J (1982) Molecular clon<strong>in</strong>g. A laboratory manual. Cold Spr<strong>in</strong>g<br />

Harbor Laboratory, Cold Spr<strong>in</strong>g Harbor, New York.<br />

Mignouna H, Virmani S S, Briquet M (1987) Mitochondrial DNA modifications associated with<br />

cytoplasmic male sterility <strong>in</strong> rice. Theor. Appl. Genet. 74:666–669.<br />

Murray M G, Thompson W F (1980) Rapid isolation <strong>of</strong> high molecular weight plant DNA.<br />

Nucleic Acids Res. 8:4321–4325.<br />

Nuclear DNAs homologous to mitochondrial plasmid-like DNAs <strong>in</strong> rice 371

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