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The hard clam genome reveals massive expansion and diversification of inhibitors of apoptosis in Bivalvia
BACKGROUND: Inhibitors of apoptosis (IAPs) are critical regulators of programmed cell death that are essential for development, oncogenesis, and immune and stress responses. However, available knowledge regarding IAP is largely biased toward humans and model species, while the distribution, function...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831173/ https://www.ncbi.nlm.nih.gov/pubmed/33487168 http://dx.doi.org/10.1186/s12915-020-00943-9 |
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author | Song, Hao Guo, Ximing Sun, Lina Wang, Qianghui Han, Fengming Wang, Haiyan Wray, Gregory A. Davidson, Phillip Wang, Qing Hu, Zhi Zhou, Cong Yu, Zhenglin Yang, Meijie Feng, Jie Shi, Pu Zhou, Yi Zhang, Libin Zhang, Tao |
author_facet | Song, Hao Guo, Ximing Sun, Lina Wang, Qianghui Han, Fengming Wang, Haiyan Wray, Gregory A. Davidson, Phillip Wang, Qing Hu, Zhi Zhou, Cong Yu, Zhenglin Yang, Meijie Feng, Jie Shi, Pu Zhou, Yi Zhang, Libin Zhang, Tao |
author_sort | Song, Hao |
collection | PubMed |
description | BACKGROUND: Inhibitors of apoptosis (IAPs) are critical regulators of programmed cell death that are essential for development, oncogenesis, and immune and stress responses. However, available knowledge regarding IAP is largely biased toward humans and model species, while the distribution, function, and evolutionary novelties of this gene family remain poorly understood in many taxa, including Mollusca, the second most speciose phylum of Metazoa. RESULTS: Here, we present a chromosome-level genome assembly of an economically significant bivalve, the hard clam Mercenaria mercenaria, which reveals an unexpected and dramatic expansion of the IAP gene family to 159 members, the largest IAP gene repertoire observed in any metazoan. Comparative genome analysis reveals that this massive expansion is characteristic of bivalves more generally. Reconstruction of the evolutionary history of molluscan IAP genes indicates that most originated in early metazoans and greatly expanded in Bivalvia through both lineage-specific tandem duplication and retroposition, with 37.1% of hard clam IAPs located on a single chromosome. The expanded IAPs have been subjected to frequent domain shuffling, which has in turn shaped their architectural diversity. Further, we observed that extant IAPs exhibit dynamic and orchestrated expression patterns among tissues and in response to different environmental stressors. CONCLUSIONS: Our results suggest that sophisticated regulation of apoptosis enabled by the massive expansion and diversification of IAPs has been crucial for the evolutionary success of hard clam and other molluscan lineages, allowing them to cope with local environmental stresses. This study broadens our understanding of IAP proteins and expression diversity and provides novel resources for studying molluscan biology and IAP function and evolution. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-020-00943-9. |
format | Online Article Text |
id | pubmed-7831173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78311732021-01-26 The hard clam genome reveals massive expansion and diversification of inhibitors of apoptosis in Bivalvia Song, Hao Guo, Ximing Sun, Lina Wang, Qianghui Han, Fengming Wang, Haiyan Wray, Gregory A. Davidson, Phillip Wang, Qing Hu, Zhi Zhou, Cong Yu, Zhenglin Yang, Meijie Feng, Jie Shi, Pu Zhou, Yi Zhang, Libin Zhang, Tao BMC Biol Research Article BACKGROUND: Inhibitors of apoptosis (IAPs) are critical regulators of programmed cell death that are essential for development, oncogenesis, and immune and stress responses. However, available knowledge regarding IAP is largely biased toward humans and model species, while the distribution, function, and evolutionary novelties of this gene family remain poorly understood in many taxa, including Mollusca, the second most speciose phylum of Metazoa. RESULTS: Here, we present a chromosome-level genome assembly of an economically significant bivalve, the hard clam Mercenaria mercenaria, which reveals an unexpected and dramatic expansion of the IAP gene family to 159 members, the largest IAP gene repertoire observed in any metazoan. Comparative genome analysis reveals that this massive expansion is characteristic of bivalves more generally. Reconstruction of the evolutionary history of molluscan IAP genes indicates that most originated in early metazoans and greatly expanded in Bivalvia through both lineage-specific tandem duplication and retroposition, with 37.1% of hard clam IAPs located on a single chromosome. The expanded IAPs have been subjected to frequent domain shuffling, which has in turn shaped their architectural diversity. Further, we observed that extant IAPs exhibit dynamic and orchestrated expression patterns among tissues and in response to different environmental stressors. CONCLUSIONS: Our results suggest that sophisticated regulation of apoptosis enabled by the massive expansion and diversification of IAPs has been crucial for the evolutionary success of hard clam and other molluscan lineages, allowing them to cope with local environmental stresses. This study broadens our understanding of IAP proteins and expression diversity and provides novel resources for studying molluscan biology and IAP function and evolution. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-020-00943-9. BioMed Central 2021-01-25 /pmc/articles/PMC7831173/ /pubmed/33487168 http://dx.doi.org/10.1186/s12915-020-00943-9 Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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 Song, Hao Guo, Ximing Sun, Lina Wang, Qianghui Han, Fengming Wang, Haiyan Wray, Gregory A. Davidson, Phillip Wang, Qing Hu, Zhi Zhou, Cong Yu, Zhenglin Yang, Meijie Feng, Jie Shi, Pu Zhou, Yi Zhang, Libin Zhang, Tao The hard clam genome reveals massive expansion and diversification of inhibitors of apoptosis in Bivalvia |
title | The hard clam genome reveals massive expansion and diversification of inhibitors of apoptosis in Bivalvia |
title_full | The hard clam genome reveals massive expansion and diversification of inhibitors of apoptosis in Bivalvia |
title_fullStr | The hard clam genome reveals massive expansion and diversification of inhibitors of apoptosis in Bivalvia |
title_full_unstemmed | The hard clam genome reveals massive expansion and diversification of inhibitors of apoptosis in Bivalvia |
title_short | The hard clam genome reveals massive expansion and diversification of inhibitors of apoptosis in Bivalvia |
title_sort | hard clam genome reveals massive expansion and diversification of inhibitors of apoptosis in bivalvia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831173/ https://www.ncbi.nlm.nih.gov/pubmed/33487168 http://dx.doi.org/10.1186/s12915-020-00943-9 |
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