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. 2003 Sep;165(1):343–352. doi: 10.1093/genetics/165.1.343

A gene block causing cross-incompatibility hidden in wild and cultivated rice.

Kazuki Matsubara 1, Khin-Thidar 1, Yoshio Sano 1
PMCID: PMC1462754  PMID: 14504241

Abstract

Unidirectional cross-incompatibility was detected in advanced generations of backcrossing between wild (Oryza rufipogon) and cultivated (O. sativa) rice strains. The near-isogenic line (NIL) of T65wx (Japonica type) carrying an alien segment of chromosome 6 from a wild strain gave a reduced seed setting only when crossed with T65wx as the male. Cytological observations showed that abortion of hybrid seeds occurred as a consequence of a failure of early endosperm development followed by abnormalities in embryo development. The genetic basis of cross-incompatibility reactions in the female and male was investigated by testcrosses using recombinant inbred lines (RILs) that were established through dissecting the introgressed segments of wild and cultivated (Indica type) strains. The results revealed that the cross-incompatibility reaction was controlled by Cif in the female and by cim in the male. When the female plant with Cif was crossed with the male plant with cim, a failure of early endosperm development was observed in the hybrid zygotes. Among cultivars of O. sativa, cim was distributed predominantly in the Japonica type but not in the Indica type. In addition, a dominant suppressor, Su-Cif, which changes the reaction in the female from incompatible to compatible was proposed to present near the centromere of chromosome 6 of the Indica type. Further, the death of young F(1) zygotes was controlled by the parental genotypes rather than by the genotype of the hybrid zygote itself since all three genes acted sporophytically, which strongly suggests an involvement of parent-of-origin effects. We discuss the results in relation to the origin of a crossing barrier as well as their maintenance within the primary gene pool.

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Selected References

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  1. Berger F. Endosperm development. Curr Opin Plant Biol. 1999 Feb;2(1):28–32. doi: 10.1016/s1369-5266(99)80006-5. [DOI] [PubMed] [Google Scholar]
  2. Berger Frédéric. Endosperm: the crossroad of seed development. Curr Opin Plant Biol. 2003 Feb;6(1):42–50. doi: 10.1016/s1369526602000043. [DOI] [PubMed] [Google Scholar]
  3. Browning H., Strome S. A sperm-supplied factor required for embryogenesis in C. elegans. Development. 1996 Jan;122(1):391–404. doi: 10.1242/dev.122.1.391. [DOI] [PubMed] [Google Scholar]
  4. Evans M. M., Kermicle J. L. Interaction between maternal effect and zygotic effect mutations during maize seed development. Genetics. 2001 Sep;159(1):303–315. doi: 10.1093/genetics/159.1.303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Goldberg R. B., de Paiva G., Yadegari R. Plant embryogenesis: zygote to seed. Science. 1994 Oct 28;266(5185):605–614. doi: 10.1126/science.266.5185.605. [DOI] [PubMed] [Google Scholar]
  6. Grossniklaus U., Vielle-Calzada J. P., Hoeppner M. A., Gagliano W. B. Maternal control of embryogenesis by MEDEA, a polycomb group gene in Arabidopsis. Science. 1998 Apr 17;280(5362):446–450. doi: 10.1126/science.280.5362.446. [DOI] [PubMed] [Google Scholar]
  7. Harushima Yoshiaki, Nakagahra Masahiro, Yano Masahiro, Sasaki Takuji, Kurata Nori. Diverse variation of reproductive barriers in three intraspecific rice crosses. Genetics. 2002 Jan;160(1):313–322. doi: 10.1093/genetics/160.1.313. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hill D. P., Shakes D. C., Ward S., Strome S. A sperm-supplied product essential for initiation of normal embryogenesis in Caenorhabditis elegans is encoded by the paternal-effect embryonic-lethal gene, spe-11. Dev Biol. 1989 Nov;136(1):154–166. doi: 10.1016/0012-1606(89)90138-3. [DOI] [PubMed] [Google Scholar]
  9. Kinoshita T., Yadegari R., Harada J. J., Goldberg R. B., Fischer R. L. Imprinting of the MEDEA polycomb gene in the Arabidopsis endosperm. Plant Cell. 1999 Oct;11(10):1945–1952. doi: 10.1105/tpc.11.10.1945. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Li Z., Pinson S. R., Paterson A. H., Park W. D., Stansel J. W. Genetics of hybrid sterility and hybrid breakdown in an intersubspecific rice (Oryza sativa L.) population. Genetics. 1997 Apr;145(4):1139–1148. doi: 10.1093/genetics/145.4.1139. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Lin B. Y. Ploidy barrier to endosperm development in maize. Genetics. 1984 May;107(1):103–115. doi: 10.1093/genetics/107.1.103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Murray M. G., Thompson W. F. Rapid isolation of high molecular weight plant DNA. Nucleic Acids Res. 1980 Oct 10;8(19):4321–4325. doi: 10.1093/nar/8.19.4321. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Oka H. Analysis of genes controlling f(1) sterility in rice by the use of isogenic lines. Genetics. 1974 Jul;77(3):521–534. doi: 10.1093/genetics/77.3.521. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Orr H. A. Dobzhansky, Bateson, and the genetics of speciation. Genetics. 1996 Dec;144(4):1331–1335. doi: 10.1093/genetics/144.4.1331. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. STEBBINS G. L. The inviability, weakness, and sterility of interspecific hybrids. Adv Genet. 1958;9:147–215. doi: 10.1016/s0065-2660(08)60162-5. [DOI] [PubMed] [Google Scholar]
  16. Scott R. J., Spielman M., Bailey J., Dickinson H. G. Parent-of-origin effects on seed development in Arabidopsis thaliana. Development. 1998 Sep;125(17):3329–3341. doi: 10.1242/dev.125.17.3329. [DOI] [PubMed] [Google Scholar]
  17. Takayama S., Shiba H., Iwano M., Shimosato H., Che F. S., Kai N., Watanabe M., Suzuki G., Hinata K., Isogai A. The pollen determinant of self-incompatibility in Brassica campestris. Proc Natl Acad Sci U S A. 2000 Feb 15;97(4):1920–1925. doi: 10.1073/pnas.040556397. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Yano M., Katayose Y., Ashikari M., Yamanouchi U., Monna L., Fuse T., Baba T., Yamamoto K., Umehara Y., Nagamura Y. Hd1, a major photoperiod sensitivity quantitative trait locus in rice, is closely related to the Arabidopsis flowering time gene CONSTANS. Plant Cell. 2000 Dec;12(12):2473–2484. doi: 10.1105/tpc.12.12.2473. [DOI] [PMC free article] [PubMed] [Google Scholar]

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