NAC transcription factor SlNOR-like1 plays a dual regulatory role in tomato fruit cuticle formation

Author:

Liu Gang-Shuai1,Huang Hua2,Grierson Donald34ORCID,Gao Ying35,Ji Xiang1,Peng Zhen-Zhen1,Li Hong-Li1,Niu Xiao-Lin1,Jia Wen1,He Jian-Lin1,Xiang Lan-Ting1,Gao Hai-Yan6,Qu Gui-Qin1ORCID,Zhu Hong-Liang1ORCID,Zhu Ben-Zhong1,Luo Yun-Bo1,Fu Da-Qi1ORCID

Affiliation:

1. Laboratory of Fruit Biology, College of Food Science & Nutritional Engineering, China Agricultural University , Beijing 100083 , China

2. Institute of Fruit Tree Research, Guangdong Academy of Agricultural Sciences; Key Laboratory of South Subtropical Fruit Biology and Genetic Resource Utilization, Ministry of Agriculture and Rural Affairs, Guangdong Provincial Key Laboratory of Tropical and Subtropical Fruit Tree Research , Guangzhou 510640 , China

3. Laboratory of Fruit Quality Biology/Zhejiang Provincial Key Laboratory of Horticultural Plant Integrative Biology, Zhejiang University , Zijingang Campus, Hangzhou 310058 , China

4. Plant Sciences Division, School of Biosciences, University of Nottingham, Sutton Bonington Campus , Loughborough LE12 5RD , UK

5. Key Laboratory of Plant Hormones and Development Regulation of Chongqing, School of Life Sciences, Chongqing University , Chongqing 401331 , China

6. Key Laboratory of Post-Harvest Handing of Fruits, Ministry of Agriculture and Rural Affairs, Key Laboratory of Fruits and Vegetables Postharvest and Processing Technology Research of Zhejiang Province, Key Laboratory of Postharvest Preservation and Processing of Fruits and Vegetables, China National Light Industry, Food Science Institute, Zhejiang Academy of Agricultural Sciences , Hangzhou 310021 , China

Abstract

Abstract The plant cuticle is an important protective barrier on the plant surface, constructed mainly by polymerized cutin matrix and a complex wax mixture. Although the pathway of plant cuticle biosynthesis has been clarified, knowledge of the transcriptional regulation network underlying fruit cuticle formation remains limited. In the present work, we discovered that tomato fruits of the NAC transcription factor SlNOR-like1 knockout mutants (nor-like1) produced by CRISPR/Cas9 [clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein 9] displayed reduced cutin deposition and cuticle thickness, with a microcracking phenotype, while wax accumulation was promoted. Further research revealed that SlNOR-like1 promotes cutin deposition by binding to the promoters of glycerol-3-phosphate acyltransferase6 (SlGPAT6; a key gene for cutin monomer formation) and CUTIN DEFICIENT2 (SlCD2; a positive regulator of cutin production) to activate their expression. Meanwhile, SlNOR-like1 inhibits wax accumulation, acting as a transcriptional repressor by targeting wax biosynthesis, and transport-related genes 3-ketoacyl-CoA synthase1 (SlKCS1), ECERIFERUM 1-2 (SlCER1-2), SlWAX2, and glycosylphosphatidylinositol-anchored lipid transfer protein 1-like (SlLTPG1-like). In conclusion, SlNOR-like1 executes a dual regulatory effect on tomato fruit cuticle development. Our results provide a new model for the transcriptional regulation of fruit cuticle formation.

Funder

National Natural Science Foundation of China

Scientific Innovation Strategy-Construction of High Level Academy of Agriculture Sciences

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Physiology

Reference55 articles.

1. Molecular characterization of the CER1 gene of Arabidopsis involved in epicuticular wax biosynthesis and pollen fertility;Aarts;The Plant Cell,1995

2. Fruit-surface flavonoid accumulation in tomato is controlled by a SIMYB12-regulated transcriptional network;Adato;PLoS Genetics,2009

3. Transient increase in locular pressure and occlusion of endocarpic apertures in ripening tomato fruit;Almeida;Journal of Plant Physiology,2001

4. Differential expression analysis for sequence count data;Anders;Genome Biology,2010

5. The plant cuticle: an ancient guardian barrier set against long-standing rivals;Arya;Frontiers in Plant Science,2021

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3