A triallelic system of S5 is a major regulator of the reproductive barrier and compatibility of indica–japonica hybrids in rice

Hybrid sterility is a major form of postzygotic reproductive isolation. Although reproductive isolation has been a key issue in evolutionary biology for many decades in a wide range of organisms, only very recently a few genes for reproductive isolation were identified. The Asian cultivated rice (Oryza sativa L.) is divided into two subspecies, indica and japonica. Hybrids between indica and japonica varieties are usually highly sterile. A special group of rice germplasm, referred to as wide-compatibility varieties, is able to produce highly fertile hybrids when crossed to both indica and japonica. In this study, we cloned S5, a major locus for indica–japonica hybrid sterility and wide compatibility, using a map-based cloning approach. We show that S5 encodes an aspartic protease conditioning embryo-sac fertility. The indica (S5-i) and japonica (S5-j) alleles differ by two nucleotides. The wide compatibility gene (S5-n) has a large deletion in the N terminus of the predicted S5 protein, causing subcellular mislocalization of the protein, and thus is presumably nonfunctional. This triallelic system has a profound implication in the evolution and artificial breeding of cultivated rice. Genetic differentiation between indica and japonica would have been enforced because of the reproductive barrier caused by S5-i and S5-j, and species coherence would have been maintained by gene flow enabled by the wide compatibility gene.

[1]  Alfredo G. Tomasselli,et al.  Membrane-anchored aspartyl protease with Alzheimer's disease β-secretase activity , 1999, Nature.

[2]  Qifa Zhang,et al.  Genetic diversity and differentiation of indica and japonica rice detected by RFLP analysis , 1992, Theoretical and Applied Genetics.

[3]  Qifa Zhang,et al.  Identification and confirmation of three neutral alleles conferring wide compatibility in inter-subspecific hybrids of rice (Oryza sativa L.) using near-isogenic lines , 2005, Theoretical and Applied Genetics.

[4]  L. Zhu,et al.  Mapping QTLs for defective female gametophyte development in an inter-subspecific cross in Oryza sativa L. , 2001, Theoretical and Applied Genetics.

[5]  N. Warthmann,et al.  Autoimmune Response as a Mechanism for a Dobzhansky-Muller-Type Incompatibility Syndrome in Plants , 2007, PLoS biology.

[6]  Yuan Qin,et al.  Localization of arabinogalactan proteins in egg cells, zygotes, and two-celled proembryos and effects of beta-D-glucosyl Yariv reagent on egg cell fertilization and zygote division in Nicotiana tabacum L. , 2006, Journal of experimental botany.

[7]  L. Bayraktaroglu,et al.  Truncated RanGAP encoded by the Segregation Distorter locus of Drosophila. , 1999, Science.

[8]  Chung-I Wu,et al.  A rapidly evolving homeobox at the site of a hybrid sterility gene. , 1998, Science.

[9]  Yan Fu,et al.  Molecular mapping of S-c, an F1 pollen sterility gene in cultivated rice , 2002, Euphytica.

[10]  Takuji Sasaki,et al.  The map-based sequence of the rice genome , 2005, Nature.

[11]  C. Zhuang,et al.  [Molecular mapping of the S-a locus for F1 pollen sterility in cultivated rice (Oryza sativa L.)]. , 1999, Yi chuan xue bao = Acta genetica Sinica.

[12]  Mingliang Xu,et al.  Delimiting a rice wide-compatibility gene S5n to a 50 kb region , 2005, Theoretical and Applied Genetics.

[13]  S. Mccouch,et al.  Molecular analysis of the inheritance of the S-5 locus, conferring wide compatibility in Indica/Japonica hybrids of rice (O. sativa L.) , 1995, Theoretical and Applied Genetics.

[14]  Qifa Zhang,et al.  Genetic dissection of embryo sac fertility, pollen fertility, and their contributions to spikelet fertility of intersubspecific hybrids in rice , 2004, Theoretical and Applied Genetics.

[15]  D. Davies,et al.  The structure and function of the aspartic proteinases. , 1990 .

[16]  Chung-I Wu,et al.  The Normal Function of a Speciation Gene, Odysseus, and Its Hybrid Sterility Effect , 2004, Science.

[17]  Xiaochun Ge,et al.  An Arabidopsis aspartic protease functions as an anti‐cell‐death component in reproduction and embryogenesis , 2005, EMBO reports.

[18]  J. Wang,et al.  A genome-wide analysis of wide compatibility in rice and the precise location of the S5 locus in the molecular map , 1997, Theoretical and Applied Genetics.

[19]  M. James,et al.  Crystal structure of human pepsin and its complex with pepstatin , 1995, Protein science : a publication of the Protein Society.

[20]  G. Khush,et al.  The rice nucellin gene ortholog OsAsp1 encodes an active aspartic protease without a plant-specific insert and is strongly expressed in early embryo. , 2005, Plant & cell physiology.

[21]  S. Mccouch,et al.  New insights into the history of rice domestication. , 2007, Trends in genetics : TIG.

[22]  Peter Hajdukiewicz,et al.  The small, versatilepPZP family ofAgrobacterium binary vectors for plant transformation , 1994, Plant Molecular Biology.

[23]  N. Su,et al.  Fine mapping of S32(t), a new gene causing hybrid embryo sac sterility in a Chinese landrace rice (Oryza sativa L.) , 2007, Theoretical and Applied Genetics.

[24]  E. Harlow,et al.  Using Antibodies: A Laboratory Manual , 1999 .

[25]  Lei Wang,et al.  Natural variation in Ghd7 is an important regulator of heading date and yield potential in rice , 2008, Nature Genetics.

[26]  H. Araki,et al.  Varietal Screening of Compatibility Types Revealed in F1 Fertility of Distant Crosses in Rice , 1984 .

[27]  Qifa Zhang,et al.  Optimising the tissue culture conditions for high efficiency transformation of indica rice , 2004, Plant Cell Reports.

[28]  U. Grossniklaus,et al.  The FERONIA Receptor-like Kinase Mediates Male-Female Interactions During Pollen Tube Reception , 2007, Science.

[29]  李佩芳 International Rice Genome Sequencing Project. 2005. The map-based sequence of the rice genome. , 2005 .

[30]  Chau-Ti Ting,et al.  Genes and speciation , 2001, Nature Reviews Genetics.

[31]  H. A. Orr,et al.  Gene Transposition as a Cause of Hybrid Sterility in Drosophila , 2006, Science.

[32]  A. Wlodawer,et al.  Transport and Activation of the Vacuolar Aspartic Proteinase Phytepsin in Barley (Hordeum vulgare L.)* , 1998, The Journal of Biological Chemistry.

[33]  M. Maroof,et al.  Molecularmarker diversity and hybrid sterility in indica-japonica rice crosses , 1997, Theoretical and Applied Genetics.

[34]  H. Araki,et al.  Genetics of 1 Sterility in Remote Crosses of Rice , 2008 .

[35]  Kanu Patel,et al.  An extracellular aspartic protease functions in Arabidopsis disease resistance signaling , 2004, The EMBO journal.

[36]  N. Rawlings,et al.  Families of aspartic peptidases, and those of unknown catalytic mechanism. , 1995, Methods in enzymology.

[37]  D. Davies,et al.  Structure and Function of the Aspartic Proteinases , 1990, Advances in Experimental Medicine and Biology.

[38]  J. Glaszmann Isozymes and classification of Asian rice varieties , 1987, Theoretical and Applied Genetics.

[39]  Qifa Zhang,et al.  An analysis of hybrid sterility in rice using a diallel cross of 21 parents involving indica, japonica and wide compatibility varieties , 2004, Euphytica.

[40]  Qifa Zhang,et al.  Delimitation of the rice wide compatibility gene S5n to a 40-kb DNA fragment , 2005, Theoretical and Applied Genetics.

[41]  T. Dobzhansky Genetics and the Origin of Species , 1937 .

[42]  M. Bevan,et al.  GUS fusions: beta‐glucuronidase as a sensitive and versatile gene fusion marker in higher plants. , 1987, The EMBO journal.