Shifts in morphology, gene expression, and selection underlie web loss in Hawaiian Tetragnatha spiders

Abstract Background A striking aspect of evolution is that it often converges on similar trajectories. Evolutionary convergence can occur in deep time or over short time scales, and is associated with the imposition of similar selective pressures. Repeated convergent events provide a framework to in...

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Main Authors: Cory A. Berger, Michael S. Brewer, Nobuaki Kono, Hiroyuki Nakamura, Kazuharu Arakawa, Susan R. Kennedy, Hannah M. Wood, Seira A. Adams, Rosemary G. Gillespie
Format: Article
Language:English
Published: BMC 2021-03-01
Series:BMC Ecology and Evolution
Subjects:
Online Access:https://doi.org/10.1186/s12862-021-01779-9
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spelling doaj-1a678f6b60b441539f41b8d2f4135e4e2021-08-29T11:06:39ZengBMCBMC Ecology and Evolution2730-71822021-03-0121111710.1186/s12862-021-01779-9Shifts in morphology, gene expression, and selection underlie web loss in Hawaiian Tetragnatha spidersCory A. Berger0Michael S. Brewer1Nobuaki Kono2Hiroyuki Nakamura3Kazuharu Arakawa4Susan R. Kennedy5Hannah M. Wood6Seira A. Adams7Rosemary G. Gillespie8Department of Environmental Science, Policy and Management, University of California, BerkeleyDepartment of Biology, N1088 Howell Science Complex, East Carolina UniversityInstitute for Advanced Biosciences, Keio UniversityEnzyme Research Team, RIKEN Center for Sustainable Resource ScienceInstitute for Advanced Biosciences, Keio UniversityBiodiversity and Biocomplexity Unit, Okinawa Institute of Science and Technology Graduate UniversitySmithsonian Institution, Entomology, MRC105Department of Environmental Science, Policy and Management, University of California, BerkeleyDepartment of Environmental Science, Policy and Management, University of California, BerkeleyAbstract Background A striking aspect of evolution is that it often converges on similar trajectories. Evolutionary convergence can occur in deep time or over short time scales, and is associated with the imposition of similar selective pressures. Repeated convergent events provide a framework to infer the genetic basis of adaptive traits. The current study examines the genetic basis of secondary web loss within web-building spiders (Araneoidea). Specifically, we use a lineage of spiders in the genus Tetragnatha (Tetragnathidae) that has diverged into two clades associated with the relatively recent (5 mya) colonization of, and subsequent adaptive radiation within, the Hawaiian Islands. One clade has adopted a cursorial lifestyle, and the other has retained the ancestral behavior of capturing prey with sticky orb webs. We explore how these behavioral phenotypes are reflected in the morphology of the spinning apparatus and internal silk glands, and the expression of silk genes. Several sister families to the Tetragnathidae have undergone similar web loss, so we also ask whether convergent patterns of selection can be detected in these lineages. Results The cursorial clade has lost spigots associated with the sticky spiral of the orb web. This appears to have been accompanied by loss of silk glands themselves. We generated phylogenies of silk proteins (spidroins), which showed that the transcriptomes of cursorial Tetragnatha contain all major spidroins except for flagelliform. We also found an uncharacterized spidroin that has higher expression in cursorial species. We found evidence for convergent selection acting on this spidroin, as well as genes involved in protein metabolism, in the cursorial Tetragnatha and divergent cursorial lineages in the families Malkaridae and Mimetidae. Conclusions Our results provide strong evidence that independent web loss events and the associated adoption of a cursorial lifestyle are based on similar genetic mechanisms. Many genes we identified as having evolved convergently are associated with protein synthesis, degradation, and processing, which are processes that play important roles in silk production. This study demonstrates, in the case of independent evolution of web loss, that similar selective pressures act on many of the same genes to produce the same phenotypes and behaviors.https://doi.org/10.1186/s12862-021-01779-9ConvergenceTetragnathaSpidroinsWeb lossTranscriptomicsSelection
collection DOAJ
language English
format Article
sources DOAJ
author Cory A. Berger
Michael S. Brewer
Nobuaki Kono
Hiroyuki Nakamura
Kazuharu Arakawa
Susan R. Kennedy
Hannah M. Wood
Seira A. Adams
Rosemary G. Gillespie
spellingShingle Cory A. Berger
Michael S. Brewer
Nobuaki Kono
Hiroyuki Nakamura
Kazuharu Arakawa
Susan R. Kennedy
Hannah M. Wood
Seira A. Adams
Rosemary G. Gillespie
Shifts in morphology, gene expression, and selection underlie web loss in Hawaiian Tetragnatha spiders
BMC Ecology and Evolution
Convergence
Tetragnatha
Spidroins
Web loss
Transcriptomics
Selection
author_facet Cory A. Berger
Michael S. Brewer
Nobuaki Kono
Hiroyuki Nakamura
Kazuharu Arakawa
Susan R. Kennedy
Hannah M. Wood
Seira A. Adams
Rosemary G. Gillespie
author_sort Cory A. Berger
title Shifts in morphology, gene expression, and selection underlie web loss in Hawaiian Tetragnatha spiders
title_short Shifts in morphology, gene expression, and selection underlie web loss in Hawaiian Tetragnatha spiders
title_full Shifts in morphology, gene expression, and selection underlie web loss in Hawaiian Tetragnatha spiders
title_fullStr Shifts in morphology, gene expression, and selection underlie web loss in Hawaiian Tetragnatha spiders
title_full_unstemmed Shifts in morphology, gene expression, and selection underlie web loss in Hawaiian Tetragnatha spiders
title_sort shifts in morphology, gene expression, and selection underlie web loss in hawaiian tetragnatha spiders
publisher BMC
series BMC Ecology and Evolution
issn 2730-7182
publishDate 2021-03-01
description Abstract Background A striking aspect of evolution is that it often converges on similar trajectories. Evolutionary convergence can occur in deep time or over short time scales, and is associated with the imposition of similar selective pressures. Repeated convergent events provide a framework to infer the genetic basis of adaptive traits. The current study examines the genetic basis of secondary web loss within web-building spiders (Araneoidea). Specifically, we use a lineage of spiders in the genus Tetragnatha (Tetragnathidae) that has diverged into two clades associated with the relatively recent (5 mya) colonization of, and subsequent adaptive radiation within, the Hawaiian Islands. One clade has adopted a cursorial lifestyle, and the other has retained the ancestral behavior of capturing prey with sticky orb webs. We explore how these behavioral phenotypes are reflected in the morphology of the spinning apparatus and internal silk glands, and the expression of silk genes. Several sister families to the Tetragnathidae have undergone similar web loss, so we also ask whether convergent patterns of selection can be detected in these lineages. Results The cursorial clade has lost spigots associated with the sticky spiral of the orb web. This appears to have been accompanied by loss of silk glands themselves. We generated phylogenies of silk proteins (spidroins), which showed that the transcriptomes of cursorial Tetragnatha contain all major spidroins except for flagelliform. We also found an uncharacterized spidroin that has higher expression in cursorial species. We found evidence for convergent selection acting on this spidroin, as well as genes involved in protein metabolism, in the cursorial Tetragnatha and divergent cursorial lineages in the families Malkaridae and Mimetidae. Conclusions Our results provide strong evidence that independent web loss events and the associated adoption of a cursorial lifestyle are based on similar genetic mechanisms. Many genes we identified as having evolved convergently are associated with protein synthesis, degradation, and processing, which are processes that play important roles in silk production. This study demonstrates, in the case of independent evolution of web loss, that similar selective pressures act on many of the same genes to produce the same phenotypes and behaviors.
topic Convergence
Tetragnatha
Spidroins
Web loss
Transcriptomics
Selection
url https://doi.org/10.1186/s12862-021-01779-9
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