Lineage-specific gene acquisition or loss is involved in interspecific hybrid sterility in rice
Understanding the genetic basis of reproductive barriers between species has been a central issue in evolutionary biology. The S₁ locus in rice causes hybrid sterility and is a major reproductive barrier between two rice species, Oryza sativa and Oryza glaberrima. The O. glaberrima-derived allele (d...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2018-02, Vol.115 (9), p.E1955-E1962 |
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Sprache: | eng |
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Zusammenfassung: | Understanding the genetic basis of reproductive barriers between species has been a central issue in evolutionary biology. The S₁ locus in rice causes hybrid sterility and is a major reproductive barrier between two rice species, Oryza sativa and Oryza glaberrima. The O. glaberrima-derived allele (denoted S₁
g) on the S₁ locus causes preferential abortion of gametes with its allelic alternative (denoted S₁
s) in S₁
g/S₁
s heterozygotes. Here, we used mutagenesis and screening of fertile hybrid plants to isolate a mutant with an allele, S₁
mut, which does not confer sterility in the S₁
mut/S₁
g and S₁
mut/S₁
s hybrids. We found that the causal mutation of the S₁
mut allele was a deletion in the peptidase-coding gene (denoted “SSP”) in the S₁ locus of O. glaberrima. No orthologous genes of SSP were found in the O. sativa genome. Transformation experiments indicated that the introduction of SSP in carriers of the S₁
s allele did not induce sterility. In S₁
mut/S₁
s heterozygotes, the insertion of SSP led to sterility, suggesting that SSP complemented the loss of the functional phenotype of the mutant and that multiple factors are involved in the phenomenon. The polymorphisms caused by the lineage-specific acquisition or loss of the SSP gene were implicated in the generation of hybrid sterility. Our results demonstrated that artificial disruption of a single gene for the reproductive barrier creates a “neutral” allele, which facilitates interspecific hybridization for breeding programs. |
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ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.1711656115 |