33. A new locus affecting high F1 pollen sterility found in backcross progenies of Japonica rice and African rice

K. DOI, K. TAGUCHI and A. YOSHIMURA
Plant Breeding Laboratory, Faculty of Agriculture, Kyushu University, Fukuoka, 812-8581 Japan

     Some QTLs affecting pollen sterility were detected in advanced backcross QTL analysis using BC2F1 population which was obtained from the cross between Japonica rice (Oryza sativa L. cv. Taichung 65) as a recurrent parent and African rice (O. glaberrima Steud., Acc. IRGC104038) as a donor parent (Doi et al. 1997). We report here the identification of one of the QTLs detected on chromosome 10 (referred to as S(t) hereafter).
     Further backcrossing with Taichung 65 was continued after QTL analysis. The BC5F1 plants heterozygous for putative S(t) region of chromosome 10 were selected using RFLP markers and they were backcrossed with Taichung 65. Resulting BC6F1 population consisting of 57 plants was used as the mapping population. Flowering spikelets were collected from each plant and stored in 70% ethanol. Pollen fertility was estimated as the percentage of pollen grains that could be stained with I2-KI solution.
     The mapping population was classified into three groups with discrete pollen fertility classes; high-sterile (pollen fertility was 0-20%), semi-sterile (40-60%) and fertile (80- 100%) (Fig. 1). The number of plants in each group were 28, 23 and 6, respectively. When divided into two groups; high sterile group and semi-sterile plus fertile group, the observed segregation of 28 : 29 fit the expected monogenic ratio of 1: 1. Linkage analysis using RFLP markers revealed that S(t) was located between G1084 and R1629 on chromosome 10. The gene S(t) was linked to G1084 and R1629 with map distances of 3.5 cM and 1.8 cM, respectively (Fig. 2). Since no locus affecting such high F1 pollen sterility has been reported in this region, S(t) is a new locus for F1 pollen sterility. Therefore, this gene contolling high F1 pollen sterility was designated as S18.
    Sano (1990) reported that the F1 sterility locus S1 found in the progenies from the cross between O. sativa and O. glaberrima caused semi-sterility and it was tightly linked to wx locus. All semi-sterile plants observed in the present population were heterozygous for wx-linked RFLP markers (C1496 and C1084). However, this S1-region did not affect the high pollen sterility. Therefore, the high-sterility and the semi-sterility are separately governed by S18 and S1, respectively.
    This study was supported in part by the Program for Promotion of Basic Research Activities for Innovative Biosciences.


References

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