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园艺学报 ›› 2023, Vol. 50 ›› Issue (8): 1637-1648.doi: 10.16420/j.issn.0513-353x.2022-0590

• 遗传育种·种质资源·分子生物学 • 上一篇    下一篇

番木瓜CpWRI3参与调控果实成熟过程中脂肪酸合成

莫雨杏*, 周艳*, 林润婷, 多泳星, 张涛, 刘锴栋**()   

  1. 岭南师范学院生命科学与技术学院,广东湛江 524048
  • 收稿日期:2022-08-26 修回日期:2023-01-18 出版日期:2023-08-25 发布日期:2023-08-23
  • 通讯作者:
    **(E-mail:
  • 作者简介:

    * 共同第一作者

  • 基金资助:
    广东省自然科学基金项目(2019A1515012180); 广东省自然科学基金项目(2022A1515010719); 广东省普通高校重点领域专项(2021ZDZX4035); 广东省科技专项资金项目(2021A05192); 广东省科技专项资金项目(2021A05222); 岭南师范学院雷阳学者岗位计划项目(2022); 岭南师范学院高层次人才项目(ZL2021003); 广东省大学生攀登计划项目(pdjh2021b0310); 国家大学生创新创业训练计划项目(202101)

Papaya CpWRI3 is Involved in the Regulation of Fatty Acid Accumulation During Fruit Postharvest

MO Yuxing, ZHOU Yan, LIN Runting, DUO Yongxing, ZHANG Tao, LIU Kaidong**()   

  1. Life Science and Technology School of Lingnan Normal University,Zhanjiang,Guangdong 524048,China
  • Received:2022-08-26 Revised:2023-01-18 Published:2023-08-25 Online:2023-08-23

摘要:

以番木瓜(Carica papaya L.)果实为研究材料,通过前期构建的果实成熟数字基因表达谱,克隆得到1个编码WRI家族调控因子的基因,命名为CpWRI3。氨基酸序列比对和进化分析发现CpWRI3与拟南芥AtWRI3/4同源性较高。转录因子活性分析表明,CpWRI3具有一定的转录激活活性。实时荧光定量PCR分析表明,CpWRI3的表达水平随着果实成熟不断升高,采后8 d达到峰值,表明其在果实成熟的后期发挥重要作用。在果实中瞬时过量表达CpWRI3促进了月桂酸、棕榈油酸和亚油酸含量的提升。体外凝胶阻滞试验(EMSA)证实CpWRI3能与下游靶基因CpKAS1CpACC1启动子上AW-box元件的序列特异结合。利用荧光素酶系统进一步证明CpWRI3可以在植物体内诱导CpKAS1CpACC1启动子的表达。上述结果表明CpWRI3能参与调控月桂酸、棕榈油酸和亚油酸等脂肪酸合成。

关键词: 番木瓜, 果实, 成熟, 脂肪酸, 转录调控, WRI家族

Abstract:

A WRI family regulator gene named CpWRI3 was cloned from papaya fruit. Amino acid sequence alignment and evolutionary analyses showed that CpWRI3 has high homology with AtWRI3/4. Transcriptional factor activity analysis showed that CpWRI3 has transcriptional activate function. The expression level of CpWRI3 increased during the fruit ripening process,peaked at eight days after harvested,indicating that CpWRI3 plays an important role in the late stage of fruit ripening. In order to explore the role of CpWRI3 in regulating fatty acid biosynthesis,transient overexpression of CpWRI3 was performed. The data showed that overexpression of CpWRI3 significantly induced the contents of lauric acid,palmitoleic acid and linoleic acid in papaya fruit. In vitro Electrophoretic Mobility Shift Assay(EMSA)confirmed that CpWRI3 could specifically bind to AW-box elements on promoters of downstream target genes CpKAS1 and CpACC1. Using luciferase system,CpWRI3 can induce the promoter activities of CpKAS1 and CpACC1 genes in plants. These results revealed that CpWRI3 may induce the biosynthesis of lauric acid,palmitoleic acid and linoleic acid.

Key words: papaya, fruit, ripening, fatty acid, transcription regulation, WRI family