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Systematic dissection of genomic features determining the vast diversity of conotoxins

BACKGROUND: Conus, a highly diverse species of venomous predators, has attracted significant attention in neuroscience and new drug development due to their rich collection of neuroactive peptides called conotoxins. Recent advancements in transcriptome, proteome, and genome analyses have facilitated...

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Autores principales: Zheng, Jian-Wei, Lu, Yang, Yang, Yu-Feng, Huang, Dan, Li, Da-Wei, Wang, Xiang, Gao, Yang, Yang, Wei-Dong, Guan, Yuanfang, Li, Hong-Ye
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10561478/
https://www.ncbi.nlm.nih.gov/pubmed/37814244
http://dx.doi.org/10.1186/s12864-023-09689-4
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author Zheng, Jian-Wei
Lu, Yang
Yang, Yu-Feng
Huang, Dan
Li, Da-Wei
Wang, Xiang
Gao, Yang
Yang, Wei-Dong
Guan, Yuanfang
Li, Hong-Ye
author_facet Zheng, Jian-Wei
Lu, Yang
Yang, Yu-Feng
Huang, Dan
Li, Da-Wei
Wang, Xiang
Gao, Yang
Yang, Wei-Dong
Guan, Yuanfang
Li, Hong-Ye
author_sort Zheng, Jian-Wei
collection PubMed
description BACKGROUND: Conus, a highly diverse species of venomous predators, has attracted significant attention in neuroscience and new drug development due to their rich collection of neuroactive peptides called conotoxins. Recent advancements in transcriptome, proteome, and genome analyses have facilitated the identification of conotoxins within Conus’ venom glands, providing insights into the genetic features and evolutionary patterns of conotoxin genes. However, the underlying mechanism behind the extraordinary hypervariability of conotoxins remains largely unknown. RESULTS: We analyzed the transcriptomes of 34 Conus species, examining various tissues such as the venom duct, venom bulb, and salivary gland, leading to the identification of conotoxin genes. Genetic variation analysis revealed that a subset of these genes (15.78% of the total) in Conus species underwent positive selection (Ka/Ks > 1, p < 0.01). Additionally, we reassembled and annotated the genome of C. betulinus, uncovering 221 conotoxin-encoding genes. These genes primarily consisted of three exons, with a significant portion showing high transcriptional activity in the venom ducts. Importantly, the flanking regions and adjacent introns of conotoxin genes exhibited a higher prevalence of transposon elements, suggesting their potential contribution to the extensive variability observed in conotoxins. Furthermore, we detected genome duplication in C. betulinus, which likely contributed to the expansion of conotoxin gene numbers. Interestingly, our study also provided evidence of introgression among Conus species, indicating that interspecies hybridization may have played a role in shaping the evolution of diverse conotoxin genes. CONCLUSIONS: This study highlights the impact of adaptive evolution and introgressive hybridization on the genetic diversity of conotoxin genes and the evolution of Conus. We also propose a hypothesis suggesting that transposable elements might significantly contribute to the remarkable diversity observed in conotoxins. These findings not only enhance our understanding of peptide genetic diversity but also present a novel approach for peptide bioengineering. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09689-4.
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spelling pubmed-105614782023-10-10 Systematic dissection of genomic features determining the vast diversity of conotoxins Zheng, Jian-Wei Lu, Yang Yang, Yu-Feng Huang, Dan Li, Da-Wei Wang, Xiang Gao, Yang Yang, Wei-Dong Guan, Yuanfang Li, Hong-Ye BMC Genomics Research BACKGROUND: Conus, a highly diverse species of venomous predators, has attracted significant attention in neuroscience and new drug development due to their rich collection of neuroactive peptides called conotoxins. Recent advancements in transcriptome, proteome, and genome analyses have facilitated the identification of conotoxins within Conus’ venom glands, providing insights into the genetic features and evolutionary patterns of conotoxin genes. However, the underlying mechanism behind the extraordinary hypervariability of conotoxins remains largely unknown. RESULTS: We analyzed the transcriptomes of 34 Conus species, examining various tissues such as the venom duct, venom bulb, and salivary gland, leading to the identification of conotoxin genes. Genetic variation analysis revealed that a subset of these genes (15.78% of the total) in Conus species underwent positive selection (Ka/Ks > 1, p < 0.01). Additionally, we reassembled and annotated the genome of C. betulinus, uncovering 221 conotoxin-encoding genes. These genes primarily consisted of three exons, with a significant portion showing high transcriptional activity in the venom ducts. Importantly, the flanking regions and adjacent introns of conotoxin genes exhibited a higher prevalence of transposon elements, suggesting their potential contribution to the extensive variability observed in conotoxins. Furthermore, we detected genome duplication in C. betulinus, which likely contributed to the expansion of conotoxin gene numbers. Interestingly, our study also provided evidence of introgression among Conus species, indicating that interspecies hybridization may have played a role in shaping the evolution of diverse conotoxin genes. CONCLUSIONS: This study highlights the impact of adaptive evolution and introgressive hybridization on the genetic diversity of conotoxin genes and the evolution of Conus. We also propose a hypothesis suggesting that transposable elements might significantly contribute to the remarkable diversity observed in conotoxins. These findings not only enhance our understanding of peptide genetic diversity but also present a novel approach for peptide bioengineering. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-023-09689-4. BioMed Central 2023-10-09 /pmc/articles/PMC10561478/ /pubmed/37814244 http://dx.doi.org/10.1186/s12864-023-09689-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Zheng, Jian-Wei
Lu, Yang
Yang, Yu-Feng
Huang, Dan
Li, Da-Wei
Wang, Xiang
Gao, Yang
Yang, Wei-Dong
Guan, Yuanfang
Li, Hong-Ye
Systematic dissection of genomic features determining the vast diversity of conotoxins
title Systematic dissection of genomic features determining the vast diversity of conotoxins
title_full Systematic dissection of genomic features determining the vast diversity of conotoxins
title_fullStr Systematic dissection of genomic features determining the vast diversity of conotoxins
title_full_unstemmed Systematic dissection of genomic features determining the vast diversity of conotoxins
title_short Systematic dissection of genomic features determining the vast diversity of conotoxins
title_sort systematic dissection of genomic features determining the vast diversity of conotoxins
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10561478/
https://www.ncbi.nlm.nih.gov/pubmed/37814244
http://dx.doi.org/10.1186/s12864-023-09689-4
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