How Can Termites Achieve Their Unparalleled Postembryonic Developmental Plasticity? A Test for the Role of Intermolt-Specific High Juvenile Hormone Titers

Author:

Korb Judith,Greiner Carolin,Foget Marion,Geiler Adrian

Abstract

Termites are “social cockroaches” and amongst the most phenotypically plastic insects. The different castes (i.e., two types of reproductives, workers, and soldiers) within termite societies are all encoded by a single genome and present the result of differential postembryonic development. Besides the default progressive development into winged sexuals of solitary hemimetabolous insects, termites have two postembryonic, non-terminal molts (stationary and regressive; i.e., molts associated, respectively, with no change or reduction of size/morphological differentiation) which allow them to retain workers, and two terminal developmental types to become soldiers and replacement reproductives. Despite this unique plasticity, especially the mechanisms underlying the non-terminal development are poorly understood. In 1982, Nijhout and Wheeler proposed a model how this diversity might have evolved. They proposed that varying juvenile hormone (JH) titers at the start, mid-phase, and end of each intermolt period account for the developmental diversity. We tested this rarely addressed model in the lower termite Cryptotermes secundus using phase-specific pharmacological manipulations of JH titers. Our results partially support the Nijhout and Wheeler model. These data are supplemented with gene expression studies of JH-related genes that characterize different postembryonic developmental trajectories. Our study provides new insights into the evolution of the unique postembryonic developmental plasticity of termites that constitutes the foundation of their social life.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Frontiers Media SA

Subject

Ecology,Ecology, Evolution, Behavior and Systematics

Reference58 articles.

1. Evolution of life types in termites;Abe;Evolution and Coadaptation in Biotic Communities,1987

2. The mevalonate pathway and the synthesis of juvenile hormone in insects.;Bellés;Annu. Rev. Entomol.,2005

3. The MEKRE93 (Methoprene tolerant-Krüppel homolog 1-E93) pathway in the regulation of insect metamorphosis, and the homology of the pupal stage.;Bellés;Insect Biochem. Mol. Biol.,2014

4. Endocrine changes in maturing primary queens of Zootermopsis angusticollis.;Brent;J. Insect Physiol.,2005

Cited by 6 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