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Comparative Mapping of Seed Dormancy Loci Between Tropical and Temperate Ecotypes of Weedy Rice (Oryza sativa L.)

Genotypic variation at multiple loci for seed dormancy (SD) contributes to plant adaptation to diverse ecosystems. Weedy rice (Oryza sativa) was used as a model to address the similarity of SD genes between distinct ecotypes. A total of 12 quantitative trait loci (QTL) for SD were identified in one primary and two advanced backcross (BC) populations derived from a temperate ecotype of weedy rice (34.3°N Lat.). Nine (75%) of the 12 loci were mapped to the same positions as those identified from a tropical ecotype of weedy rice (7.1°N Lat.).

Lihua Zhang, Jieqiong Lou, Michael E. Foley and Xing-You Gu

G3: Genes, Genomes, Genetics August 1, 2017 vol. 7 no. 8 2605-2614; https://doi.org/10.1534/g3.117.040451

Abstract

Genotypic variation at multiple loci for seed dormancy (SD) contributes to plant adaptation to diverse ecosystems. Weedy rice (Oryza sativa) was used as a model to address the similarity of SD genes between distinct ecotypes. A total of 12 quantitative trait loci (QTL) for SD were identified in one primary and two advanced backcross (BC) populations derived from a temperate ecotype of weedy rice (34.3°N Lat.). Nine (75%) of the 12 loci were mapped to the same positions as those identified from a tropical ecotype of weedy rice (7.1°N Lat.). The high similarity suggested that the majority of SD genes were conserved during the ecotype differentiation. These common loci are largely those collocated/linked with the awn, hull color, pericarp color, or plant height loci. Phenotypic correlations observed in the populations support the notion that indirect selections for the wild-type morphological characteristics, together with direct selections for germination time, were major factors influencing allelic distributions of SD genes across ecotypes. Indirect selections for crop-mimic traits (e.g., plant height and flowering time) could also alter allelic frequencies for some SD genes in agroecosystems. In addition, 3 of the 12 loci were collocated with segregation distortion loci, indicating that some gametophyte development genes could also influence the genetic equilibria of SD loci in hybrid populations. The SD genes with a major effect on germination across ecotypes could be used as silencing targets to develop transgene mitigation (TM) strategies to reduce the risk of gene flow from genetically modified crops into weed/wild relatives.

 

See: http://www.g3journal.org/content/7/8/2605?etoc=

 

Figure 1 A framework linkage map and positions of seed dormancy QTL identified in this and previous research. The map was marked with RM loci segregating in the BC1F1 EM93-1//EM93-1/LD population. Asterisks indicate segregation distortion loci in favor of the allele from EM93-1 (*) or LD (**). Black bars indicate C.I. (equivalent to one-LOD support lengths) of qSD, qAn, or qHC detected in this BC1F1 population (Figure 2B). Five-point stars indicate qSDs detected in the BC2F1 (9) (Figure 3) and/or BC2F1 (139) (Figure 4), but not in this BC1F1 population. Ovals indicate approximate positions of qSDs previously detected in the BC1F1 EM93-1//EM93-1/SS18-2 population or its advanced generations (Gu et al. 2004; Ye et al. 2010). LD and SS18-2 are temperate and tropical ecotypes of weedy rice, respectively. Ch, chromosome; LD, pure line LüDao; LOD, logarithm of the odds; qAn, QTL for awn; qHC, QTL for hull color; qSD, QTL for seed dormancy; QTL, quantitative trait loci; RM, rice microsatellite.

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