Laboratory of Genetics, Wageningen University and Research, Droevendaalsesteeg 1, 6708 PB, Wageningen, The Netherlands.
Horticulture and Product Physiology Group, Wageningen University and Research, Droevendaalsesteeg 1, 6708 PB, Wageningen, The Netherlands.
Nat Commun. 2017 Nov 10;8(1):1421. doi: 10.1038/s41467-017-01576-3.
Exploiting genetic variation for more efficient photosynthesis is an underexplored route towards new crop varieties. This study demonstrates the genetic dissection of higher plant photosynthesis efficiency down to the genomic DNA level, by confirming that allelic sequence variation at the Arabidopsis thaliana YELLOW SEEDLING1 (YS1) gene explains natural diversity in photosynthesis acclimation to high irradiance. We use a genome-wide association study to identify quantitative trait loci (QTLs) involved in the Arabidopsis photosynthetic acclimation response. Candidate genes underlying the QTLs are prioritized according to functional clues regarding gene ontology, expression and function. Reverse genetics and quantitative complementation confirm the candidacy of YS1, which encodes a pentatrico-peptide-repeat (PPR) protein involved in RNA editing of plastid-encoded genes (anterograde signalling). Gene expression analysis and allele sequence comparisons reveal polymorphisms in a light-responsive element in the YS1 promoter that affect its expression, and that of its downstream targets, resulting in the variation in photosynthetic acclimation.
利用遗传变异来提高光合作用效率是开发新型作物品种的一条未被充分探索的途径。本研究通过证实拟南芥 YELLOW SEEDLING1 (YS1) 基因的等位基因序列变异可解释光合作用对高光强的适应的自然多样性,将高等植物光合作用效率的遗传解析细化到基因组 DNA 水平。我们利用全基因组关联研究来鉴定参与拟南芥光合作用适应反应的数量性状基因座 (QTL)。根据基因本体论、表达和功能方面的功能线索,对 QTL 下的候选基因进行优先级排序。反向遗传学和定量互补实验证实了 YS1 的候选性,该基因编码一种五肽重复 (PPR) 蛋白,参与质体编码基因的 RNA 编辑(顺式信号转导)。基因表达分析和等位基因序列比较揭示了 YS1 启动子中一个光响应元件的多态性,该元件影响其表达及其下游靶基因的表达,从而导致光合作用适应的变化。