Cargando…
Genomic and transcriptomic analyses support a silk gland origin of spider venom glands
BACKGROUND: Spiders comprise a hyperdiverse lineage of predators with venom systems, yet the origin of functionally novel spider venom glands remains unclear. Previous studies have hypothesized that spider venom glands originated from salivary glands or evolved from silk-producing glands present in...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10099834/ https://www.ncbi.nlm.nih.gov/pubmed/37055766 http://dx.doi.org/10.1186/s12915-023-01581-7 |
_version_ | 1785025142728949760 |
---|---|
author | Zhu, Bingyue Jin, Pengyu Zhang, Yiming Shen, Yunxiao Wang, Wei Li, Shuqiang |
author_facet | Zhu, Bingyue Jin, Pengyu Zhang, Yiming Shen, Yunxiao Wang, Wei Li, Shuqiang |
author_sort | Zhu, Bingyue |
collection | PubMed |
description | BACKGROUND: Spiders comprise a hyperdiverse lineage of predators with venom systems, yet the origin of functionally novel spider venom glands remains unclear. Previous studies have hypothesized that spider venom glands originated from salivary glands or evolved from silk-producing glands present in early chelicerates. However, there is insufficient molecular evidence to indicate similarity among them. Here, we provide comparative analyses of genome and transcriptome data from various lineages of spiders and other arthropods to advance our understanding of spider venom gland evolution. RESULTS: We generated a chromosome-level genome assembly of a model spider species, the common house spider (Parasteatoda tepidariorum). Module preservation, GO semantic similarity, and differentially upregulated gene similarity analyses demonstrated a lower similarity in gene expressions between the venom glands and salivary glands compared to the silk glands, which questions the validity of the salivary gland origin hypothesis but unexpectedly prefers to support the ancestral silk gland origin hypothesis. The conserved core network in the venom and silk glands was mainly correlated with transcription regulation, protein modification, transport, and signal transduction pathways. At the genetic level, we found that many genes in the venom gland-specific transcription modules show positive selection and upregulated expressions, suggesting that genetic variation plays an important role in the evolution of venom glands. CONCLUSIONS: This research implies the unique origin and evolutionary path of spider venom glands and provides a basis for understanding the diverse molecular characteristics of venom systems. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01581-7. |
format | Online Article Text |
id | pubmed-10099834 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100998342023-04-14 Genomic and transcriptomic analyses support a silk gland origin of spider venom glands Zhu, Bingyue Jin, Pengyu Zhang, Yiming Shen, Yunxiao Wang, Wei Li, Shuqiang BMC Biol Research Article BACKGROUND: Spiders comprise a hyperdiverse lineage of predators with venom systems, yet the origin of functionally novel spider venom glands remains unclear. Previous studies have hypothesized that spider venom glands originated from salivary glands or evolved from silk-producing glands present in early chelicerates. However, there is insufficient molecular evidence to indicate similarity among them. Here, we provide comparative analyses of genome and transcriptome data from various lineages of spiders and other arthropods to advance our understanding of spider venom gland evolution. RESULTS: We generated a chromosome-level genome assembly of a model spider species, the common house spider (Parasteatoda tepidariorum). Module preservation, GO semantic similarity, and differentially upregulated gene similarity analyses demonstrated a lower similarity in gene expressions between the venom glands and salivary glands compared to the silk glands, which questions the validity of the salivary gland origin hypothesis but unexpectedly prefers to support the ancestral silk gland origin hypothesis. The conserved core network in the venom and silk glands was mainly correlated with transcription regulation, protein modification, transport, and signal transduction pathways. At the genetic level, we found that many genes in the venom gland-specific transcription modules show positive selection and upregulated expressions, suggesting that genetic variation plays an important role in the evolution of venom glands. CONCLUSIONS: This research implies the unique origin and evolutionary path of spider venom glands and provides a basis for understanding the diverse molecular characteristics of venom systems. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01581-7. BioMed Central 2023-04-13 /pmc/articles/PMC10099834/ /pubmed/37055766 http://dx.doi.org/10.1186/s12915-023-01581-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Zhu, Bingyue Jin, Pengyu Zhang, Yiming Shen, Yunxiao Wang, Wei Li, Shuqiang Genomic and transcriptomic analyses support a silk gland origin of spider venom glands |
title | Genomic and transcriptomic analyses support a silk gland origin of spider venom glands |
title_full | Genomic and transcriptomic analyses support a silk gland origin of spider venom glands |
title_fullStr | Genomic and transcriptomic analyses support a silk gland origin of spider venom glands |
title_full_unstemmed | Genomic and transcriptomic analyses support a silk gland origin of spider venom glands |
title_short | Genomic and transcriptomic analyses support a silk gland origin of spider venom glands |
title_sort | genomic and transcriptomic analyses support a silk gland origin of spider venom glands |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10099834/ https://www.ncbi.nlm.nih.gov/pubmed/37055766 http://dx.doi.org/10.1186/s12915-023-01581-7 |
work_keys_str_mv | AT zhubingyue genomicandtranscriptomicanalysessupportasilkglandoriginofspidervenomglands AT jinpengyu genomicandtranscriptomicanalysessupportasilkglandoriginofspidervenomglands AT zhangyiming genomicandtranscriptomicanalysessupportasilkglandoriginofspidervenomglands AT shenyunxiao genomicandtranscriptomicanalysessupportasilkglandoriginofspidervenomglands AT wangwei genomicandtranscriptomicanalysessupportasilkglandoriginofspidervenomglands AT lishuqiang genomicandtranscriptomicanalysessupportasilkglandoriginofspidervenomglands |