Dynamic m6A mRNA methylation reveals the involvement of AcALKBH10 in ripening‐related quality regulation in kiwifruit

Author:

Su Dan1ORCID,Shu Peng12ORCID,Hu Nan3,Chen Yuan1,Wu Yi1,Deng Heng1ORCID,Du Xiaofei1,Zhang Xumeng1,Wang Ruochen1,Li Huajia4,Zeng Yunliu5ORCID,Li Dawei6ORCID,Xie Yue7,Li Mingzhang7,Hong Yiguo89,Liu Kaidong10ORCID,Liu Mingchun1ORCID

Affiliation:

1. Key Laboratory of Bio‐resource and Eco‐environment of Ministry of Education, College of Life Sciences Sichuan University Chengdu 610065 Sichuan China

2. Clinical Medical Research Center Xinqiao Hospital, Army Medical University Chongqing 400037 China

3. College of Biology and Food Engineering Anyang Institute of Technology Anyang 455000 Henan China

4. Institute of Agro‐Products Processing Science and Technology Sichuan Academy of Agricultural Sciences Chengdu 610066 China

5. National Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops, College of Horticulture and Forestry Science Huazhong Agricultural University Wuhan 430070 China

6. Wuhan Botanical Garden Chinese Academy of Sciences Jiufeng 1 Road Wuhan 430074 Hubei China

7. China‐New Zealand the Belt and Road Joint Laboratory on Kiwifruit, Kiwifruit Breeding and Utilization Key Laboratory of Sichuan Province Sichuan Academy of Natural Resource Sciences Chengdu 610041 China

8. School of Science and the Environment University of Worcester Worcester WR2 6AJ UK

9. State Key Laboratory of North China Crop Improvement and Regulation, College of Horticulture Hebei Agricultural University Baoding 071000 China

10. Life Science and Technology School Lingnan Normal University Zhanjiang 524048 China

Abstract

Summary Kiwifruit ripening is a complex and highly coordinated process that occurs in conjunction with the formation of fruit edible quality. The significance of epigenetic changes, particularly the impact of N6‐methyladenosine (m6A) RNA modification on fruit ripening and quality formation, has been largely overlooked. We monitored m6A levels and gene expression changes in kiwifruit at four different stages using LC‐MS/MS, MeRIP, RNA‐seq, and validated the function of AcALKBH10 through heterologous transgenic expression in tomato. Notable m6A modifications occurred predominantly at the stop codons and the 3′ UTRs and exhibited a gradual reduction in m6A levels during the fruit ripening process. Moreover, these m6A modifications in the aforementioned sites demonstrated a discernible inverse relationship with the levels of mRNA abundance throughout the ripening process, suggesting a repression effect of m6A modification in the modulation of kiwifruit ripening. We further demonstrated that AcALKBH10 rather than AcECT9 predominantly regulates m6A levels in ripening‐related genes, thereby exerting the regulatory control over the ripening process and the accumulation of soluble sugars and organic acids, ultimately influencing fruit ripening and quality formation. In conclusion, our findings illuminate the epi‐regulatory mechanism involving m6A in kiwifruit ripening, offering a fresh perspective for cultivating high‐quality kiwifruit with enhanced nutritional attributes.

Funder

Fundamental Research Funds for the Central Universities

Natural Science Foundation of Sichuan Province

Publisher

Wiley

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