4.8 Article

Resource allocation strategies among vegetative growth, sexual reproduction, asexual reproduction and defense during growing season of Aconitum kusnezoffii Reichb.

Journal

PLANT JOURNAL
Volume 105, Issue 4, Pages 957-977

Publisher

WILEY
DOI: 10.1111/tpj.15080

Keywords

resource allocation; vegetative growth; sexual– asexual reproduction; secondary metabolite (SM); Aconitum kusnezoffii Reichb; lateral root (daughter root fuzi); transcriptome

Categories

Funding

  1. Natural Science Foundation of Jilin Province [20190201298JC]

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The study on Aconitum kusnezoffii Reichb. found that vegetative growth precedes sexual development, with asexual reproduction starting earlier. The principal root serves as a buffer for resources post-flower formation, and defense compounds can be reused for other processes.
Natural plants must actively allocate their limited resources for survival and reproduction. Although vegetative growth, sexual reproduction, asexual reproduction and defense are all basic processes in the life cycle of plants, the strategies used to allocate resources between these processes are poorly understood. These processes are conspicuous in naturally grown Aconitum kusnezoffii Reichb., which makes it a suitable study subject. Here, the morphology, dry matter, total organic carbon, total nitrogen and aconitum alkaloid levels of shoot, principal root (PR) and lateral roots were measured throughout the growing season. Then, transcriptome and metabolite content analyses were performed. We found that vegetative growth began first. After vegetative growth ceased, sexual development began. Flower organ development was accompanied by increased photosynthesis and the PR consumed temporarily stored resources after flower formation. Asexual propagule development initiated earlier than sexual reproduction and kept accumulating resources after that. Development was slow before flower formation, mainly manifesting as increasing length; then, after flower formation it accelerated via enhanced material transport and accumulation. Defense compounds were maintained at low levels before flowering. In particular, the turnover of defense compounds was enhanced before and after flower bud emergence, providing resources for other processes. After flower formation, defense compounds were accumulated. The pattern found herein provides a vivid example for further studies on resource allocation strategies. The exciting finding that the PR, as a more direct storage site for photosynthate, is a buffer unit for resources, and that defense compounds can be reused for other processes, suggests a need to explore potential mechanisms.

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