红阳猕猴桃核酮糖-1,5-双磷酸羧化酶/加氧酶小亚基基因的克隆与表达分析OA
Cloning and expression analysis of a Ribulose-1,5-bisphosphate carboxylase/oxygenase small subunit gene(AcRbcS)in Actinidia chinensis'Hongyang'
核酮糖-1,5-二磷酸羧化酶/加氧酶(Rubisco)在植物光合作用中具有重要作用,其高表达与光合效率密切相关.克隆红阳猕猴桃(Actinidia chinensis'Hongyang')中编码Rubisco小亚基的基因,分析其表达模式及生物学功能,可为提高红阳猕猴桃光合生产力的定向育种提供理论依据.通过基因克隆技术,从红阳猕猴桃叶片样品中获得Rubisco小亚基基因AcRbcS(Actinidia chinensis ribulose 1,5-bisphosphate carboxylase/oxygenase small subunit),并利用 RNA-seq 和实时荧光定量 PCR技术分析其在叶片不同发育时期的表达模式.结果表明,AcRbcS的CDS全长序列为369 bp,编码122个氨基酸残基,蛋白分子量为13.75 kDa;红阳猕猴桃叶片中AcRbcS的表达随叶片发育而上升,在淡绿期达到峰值.研究结果为后续通过分子育种手段提高红阳猕猴桃光合作用效率和果实品质提供了重要参考.
Ribulose-1,5-bisphosphate carboxylase/oxygenase(Rubisco)plays a crucial role in plant photosynthesis,and its high expression is closely related to photosynthetic efficiency.Cloning the gene encoding the small subunit of ribulose-1,5-bi-sphosphate carboxylase/oxygenase(RuBisCo)in Hongyang kiwifruit(Actinidia chinensis'Hongyang'),and analyzing its expression pattern and biological function can provide a theoretical basis for targeted breeding strategies aimed at enhancing the photosynthetic productivity of Hongyang kiwifruit.The AcRbcS gene,a small subunit gene,was cloned from Hongyang kiwifruit leaf.Its expression profile in different leaf development stages was investigated using RNA-seq and real-time quantitative PCR(qPCR).The results showed that the full-length coding sequence(CDS)of AcRbcS was 369 bp,encoding a protein of 122 amino acids with a molecular weight of 13.75 kDa.The expression level of AcRbcS increased progressively during leaf development,reaching a peak at the light-green stage.This study provided valuable insights for future molecular breeding efforts to improve the photosynthetic efficiency and fruit quality of Hongyang kiwifruit.
何斌;刘仕丽;叶佳成;唐大海;刘林娅;黄亚成
六盘水师范学院生物科学与技术学院,贵州六盘水,553004六盘水师范学院生物科学与技术学院,贵州六盘水,553004六盘水师范学院生物科学与技术学院,贵州六盘水,553004六盘水师范学院生物科学与技术学院,贵州六盘水,553004六盘水师范学院生物科学与技术学院,贵州六盘水,553004六盘水师范学院生物科学与技术学院,贵州六盘水,553004
红阳猕猴桃Rubisco小亚基基因克隆实时荧光定量PCR
Actinidia chinensis'Hongyang'RbcSgene cloningQPCR
《中国南方果树》 2026 (1)
179-183,5
贵州省科技厅项目(黔科合基础MS[2025]099)六盘水师范学院高层次人才科研启动基金项目(LPSSYKYJJ202205)六盘水师范学院科研培育项目(LPSSY2023KJZDPY07)贵州省教育厅自然科学研究项目(黔教技[2022]054号)大学生创新创业训练计划项目资助(S202310977072)六盘水师范学院大学生科研训练计划项目(2024DK228)资助.
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