Cargando…
Evolutionary Impacts of Pattern Recognition Receptor Genes on Carnivora Complex Habitat Stress Adaptation
SIMPLE SUMMARY: Carnivora is a complex and diverse group, and its members are considered the most proficient carnivores in nature. However, the evolutionary impacts of pattern recognition receptor (PRR) genes on Carnivora’s stress adaptation to complex habitats are poorly understood. In this study,...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9739989/ https://www.ncbi.nlm.nih.gov/pubmed/36496853 http://dx.doi.org/10.3390/ani12233331 |
_version_ | 1784847946609590272 |
---|---|
author | Wu, Xiaoyang Chen, Jun Wang, Xibao Shang, Yongquan Wei, Qinguo Zhang, Honghai |
author_facet | Wu, Xiaoyang Chen, Jun Wang, Xibao Shang, Yongquan Wei, Qinguo Zhang, Honghai |
author_sort | Wu, Xiaoyang |
collection | PubMed |
description | SIMPLE SUMMARY: Carnivora is a complex and diverse group, and its members are considered the most proficient carnivores in nature. However, the evolutionary impacts of pattern recognition receptor (PRR) genes on Carnivora’s stress adaptation to complex habitats are poorly understood. In this study, we explored the evolution of 946 PRR gene sequences in 43 Carnivora species to elucidate the molecular mechanisms of carnivore adaptation to complex habitats. We found that the PRRs were relatively conserved, and different gene families showed different evolutionary patterns. PRRs were highly purified based on their overall roles in Carnivora species but interspersed with positive-selection patterns during evolution. In addition, the selection pressure of toll-like receptor 10 was relaxed in seven species with pseudogenes, which may have emerged during recent evolutionary events. Our findings offer valuable insights into the molecular and functional evolution of PRR genes, which are important for immune adaptations in Carnivora. ABSTRACT: Many mammals develop specific immune responses owing to the changes in their ecological niche and diet that are essential for animal survival. However, pattern recognition receptors (PRRs) serve as the first line of defense in innate immunity and generate immune responses in the host. However, the evolutionary impacts on PRR genes in Carnivora are not well studied. Herein, we explored the evolution of 946 PRR gene sequences in 43 Carnivora species to elucidate the molecular mechanisms of carnivore adaptation to complex habitats. We found that the PRRs were relatively conserved, and different gene families showed different evolutionary patterns. PRRs were highly purified based on their overall roles in Carnivora species but interspersed with positive-selection patterns during evolution. Different niche types may have jointly driven the evolution of PRR genes. In particular, the selection pressure of toll-like receptor (TLR) 10 was relaxed in seven species with pseudogenes, which may have emerged during recent evolutionary events. We speculated that a “functional compensation” mechanism may exist for genes with overlapping functions in the TLR gene family. Additionally, TLR2, TLR4, NLRC5, and DECTIN1 were subject to positive selection in semi-aquatic species, and the adaptive evolution of these genes may have been related to the adaptation to semi-aquatic environments. In summary, our findings offer valuable insights into the molecular and functional evolution of PRR genes, which are important for immune adaptations in Carnivora. |
format | Online Article Text |
id | pubmed-9739989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97399892022-12-11 Evolutionary Impacts of Pattern Recognition Receptor Genes on Carnivora Complex Habitat Stress Adaptation Wu, Xiaoyang Chen, Jun Wang, Xibao Shang, Yongquan Wei, Qinguo Zhang, Honghai Animals (Basel) Article SIMPLE SUMMARY: Carnivora is a complex and diverse group, and its members are considered the most proficient carnivores in nature. However, the evolutionary impacts of pattern recognition receptor (PRR) genes on Carnivora’s stress adaptation to complex habitats are poorly understood. In this study, we explored the evolution of 946 PRR gene sequences in 43 Carnivora species to elucidate the molecular mechanisms of carnivore adaptation to complex habitats. We found that the PRRs were relatively conserved, and different gene families showed different evolutionary patterns. PRRs were highly purified based on their overall roles in Carnivora species but interspersed with positive-selection patterns during evolution. In addition, the selection pressure of toll-like receptor 10 was relaxed in seven species with pseudogenes, which may have emerged during recent evolutionary events. Our findings offer valuable insights into the molecular and functional evolution of PRR genes, which are important for immune adaptations in Carnivora. ABSTRACT: Many mammals develop specific immune responses owing to the changes in their ecological niche and diet that are essential for animal survival. However, pattern recognition receptors (PRRs) serve as the first line of defense in innate immunity and generate immune responses in the host. However, the evolutionary impacts on PRR genes in Carnivora are not well studied. Herein, we explored the evolution of 946 PRR gene sequences in 43 Carnivora species to elucidate the molecular mechanisms of carnivore adaptation to complex habitats. We found that the PRRs were relatively conserved, and different gene families showed different evolutionary patterns. PRRs were highly purified based on their overall roles in Carnivora species but interspersed with positive-selection patterns during evolution. Different niche types may have jointly driven the evolution of PRR genes. In particular, the selection pressure of toll-like receptor (TLR) 10 was relaxed in seven species with pseudogenes, which may have emerged during recent evolutionary events. We speculated that a “functional compensation” mechanism may exist for genes with overlapping functions in the TLR gene family. Additionally, TLR2, TLR4, NLRC5, and DECTIN1 were subject to positive selection in semi-aquatic species, and the adaptive evolution of these genes may have been related to the adaptation to semi-aquatic environments. In summary, our findings offer valuable insights into the molecular and functional evolution of PRR genes, which are important for immune adaptations in Carnivora. MDPI 2022-11-28 /pmc/articles/PMC9739989/ /pubmed/36496853 http://dx.doi.org/10.3390/ani12233331 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wu, Xiaoyang Chen, Jun Wang, Xibao Shang, Yongquan Wei, Qinguo Zhang, Honghai Evolutionary Impacts of Pattern Recognition Receptor Genes on Carnivora Complex Habitat Stress Adaptation |
title | Evolutionary Impacts of Pattern Recognition Receptor Genes on Carnivora Complex Habitat Stress Adaptation |
title_full | Evolutionary Impacts of Pattern Recognition Receptor Genes on Carnivora Complex Habitat Stress Adaptation |
title_fullStr | Evolutionary Impacts of Pattern Recognition Receptor Genes on Carnivora Complex Habitat Stress Adaptation |
title_full_unstemmed | Evolutionary Impacts of Pattern Recognition Receptor Genes on Carnivora Complex Habitat Stress Adaptation |
title_short | Evolutionary Impacts of Pattern Recognition Receptor Genes on Carnivora Complex Habitat Stress Adaptation |
title_sort | evolutionary impacts of pattern recognition receptor genes on carnivora complex habitat stress adaptation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9739989/ https://www.ncbi.nlm.nih.gov/pubmed/36496853 http://dx.doi.org/10.3390/ani12233331 |
work_keys_str_mv | AT wuxiaoyang evolutionaryimpactsofpatternrecognitionreceptorgenesoncarnivoracomplexhabitatstressadaptation AT chenjun evolutionaryimpactsofpatternrecognitionreceptorgenesoncarnivoracomplexhabitatstressadaptation AT wangxibao evolutionaryimpactsofpatternrecognitionreceptorgenesoncarnivoracomplexhabitatstressadaptation AT shangyongquan evolutionaryimpactsofpatternrecognitionreceptorgenesoncarnivoracomplexhabitatstressadaptation AT weiqinguo evolutionaryimpactsofpatternrecognitionreceptorgenesoncarnivoracomplexhabitatstressadaptation AT zhanghonghai evolutionaryimpactsofpatternrecognitionreceptorgenesoncarnivoracomplexhabitatstressadaptation |