Stomatal evolution and plant adaptation to future climate

Author:

Chen Guang1,Qin Yuan2ORCID,Wang Jian1,Li Sujuan1,Zeng Fanrong2,Deng Fenglin2ORCID,Chater Caspar34ORCID,Xu Shengchun15,Chen Zhong‐Hua67ORCID

Affiliation:

1. Central Laboratory, Zhejiang Academy of Agricultural Sciences Hangzhou China

2. College of Agriculture, Collaborative Innovation Centre for Grain Industry Yangtze University Jingzhou China

3. Royal Botanic Gardens Kew, Richmond UK

4. Plants, Photosynthesis, and Soil, School of Biosciences University of Sheffield Sheffield UK

5. Xianghu Laboratory Hangzhou China

6. School of Science Western Sydney University Penrith Australia

7. Hawkesbury Institute for the Environment Western Sydney University Penrith Australia

Abstract

AbstractGlobal climate change is affecting plant photosynthesis and transpiration processes, as well as increasing weather extremes impacting socio‐political and environmental events and decisions for decades to come. One major research challenge in plant biology and ecology is the interaction of photosynthesis with the environment. Stomata control plant gas exchange and their evolution was a crucial innovation that facilitated the earliest land plants to colonize terrestrial environments. Stomata couple homoiohydry, together with cuticles, intercellular gas space, with the endohydric water‐conducting system, enabling plants to adapt and diversify across the planet. Plants control stomatal movement in response to environmental change through regulating guard cell turgor mediated by membrane transporters and signaling transduction. However, the origin, evolution, and active control of stomata remain controversial topics. We first review stomatal evolution and diversity, providing fossil and phylogenetic evidence of their origins. We summarize functional evolution of guard cell membrane transporters in the context of climate changes and environmental stresses. Our analyses show that the core signaling elements of stomatal movement are more ancient than stomata, while genes involved in stomatal development co‐evolved de novo with the earliest stomata. These results suggest that novel stomatal development‐specific genes were acquired during plant evolution, whereas genes regulating stomatal movement, especially cell signaling pathways, were inherited ancestrally and co‐opted by dynamic functional differentiation. These two processes reflect the different adaptation strategies during land plant evolution.

Funder

Agriculture Research System of China

Australian Research Council

National Natural Science Foundation of China

Publisher

Wiley

Cited by 2 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