Field‐work reveals a novel function for MAX2 in a native tobacco's high‐light adaptions

Author:

Li Suhua12ORCID,Baldwin Gundega2,Yang Caiqiong2,Lu Ruirui1,Meng Shuaishuai1,Huang Jianbei3ORCID,Wang Ming24,Baldwin Ian T.2ORCID

Affiliation:

1. Shenzhen Branch, Guangdong Laboratory of Lingnan Modern Agriculture, Key Laboratory of Synthetic Biology, Ministry of Agriculture and Rural Affairs, Agricultural Genomics Institute at Shenzhen Chinese Academy of Agricultural Sciences Shenzhen China

2. Department of Molecular Ecology Max Planck Institute for Chemical Ecology Jena Germany

3. Department of Biogeochemical Processes Max Planck Institute for Biogeochemistry Jena Germany

4. Department of Plant Pathology Nanjing Agricultural University Nanjing China

Abstract

AbstractLaboratory studies have revealed that strigolatone (SL) and karrikin (KAR) signalling mediate responses to abiotic and biotic stresses, and reshape branching architecture that could increase reproductive performance and crop yields. To understand the ecological function of SL and KAR signalling, transgenic lines of wild tobacco Nicotiana attenuata, silenced in SL/KAR biosynthesis/signalling were grown in the glasshouse and in two field plots in the Great Basin Desert in Utah over four field seasons. Of the lines silenced in SL and KAR signalling components (irMAX2, irD14, irKAI2 and irD14 × irKAI2 plants), which exhibited the expected increases in shoot branching, only irMAX2 plants showed a strong leaf‐bleaching phenotype when grown in the field. In the field, irMAX2 plants had lower sugar and higher leaf amino acid contents, lower lifetime fitness and were more susceptible to herbivore attack compared to wild‐type plants. These irMAX2 phenotypes were not observed in glasshouse‐grown plants. Transcriptomic analysis revealed dramatic responses to high‐light intensity in irMAX2 leaves in the field: lutein contents decreased, and transcriptional responses to high‐intensity light, singlet oxygen and hydrogen peroxide increased. PAR and UV‐B manipulations in the field revealed that the irMAX2 bleaching phenotype is reversed by decreasing PAR, but not UV‐B fluence. We propose that NaMAX2 functions in high‐light adaptation and fitness optimisation by regulating high‐light responses independently of its roles in the SL and KAR signalling pathways. The work provides another example of the value of studying the function of genes in the complex environments in which plants evolved, namely nature.

Publisher

Wiley

Subject

Plant Science,Physiology

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