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Plateau Grass and Greenhouse Flower? Distinct Genetic Basis of Closely Related Toad Tadpoles Respectively Adapted to High Altitude and Karst Caves
Genetic adaptation to extremes is a fascinating topic. Nevertheless, few studies have explored the genetic adaptation of closely related species respectively inhabiting distinct extremes. With deep transcriptome sequencing, we attempt to detect the genetic architectures of tadpoles of five closely r...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073644/ https://www.ncbi.nlm.nih.gov/pubmed/31979140 http://dx.doi.org/10.3390/genes11020123 |
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author | Chang, Liming Zhu, Wei Shi, Shengchao Zhang, Meihua Jiang, Jianping Li, Cheng Xie, Feng Wang, Bin |
author_facet | Chang, Liming Zhu, Wei Shi, Shengchao Zhang, Meihua Jiang, Jianping Li, Cheng Xie, Feng Wang, Bin |
author_sort | Chang, Liming |
collection | PubMed |
description | Genetic adaptation to extremes is a fascinating topic. Nevertheless, few studies have explored the genetic adaptation of closely related species respectively inhabiting distinct extremes. With deep transcriptome sequencing, we attempt to detect the genetic architectures of tadpoles of five closely related toad species adapted to the Tibetan Plateau, middle-altitude mountains and karst caves. Molecular evolution analyses indicated that not only the number of fast evolving genes (FEGs), but also the functioning coverage of FEGs, increased with elevation. Enrichment analyses correspondingly revealed that the highland species had most of the FEGs involved in high-elevation adaptation, for example, amino acid substitutions of XRCC6 in its binding domains might improve the capacity of DNA repair of the toad. Yet, few FEGs and positively selected genes (PSGs) involved in high-elevation adaptation were identified in the cave species, and none of which potentially contributed to cave adaptation. Accordingly, it is speculated that in the closely related toad tadpoles, genetic selection pressures increased with elevation, and cave adaptation was most likely derived from other factors (e.g., gene loss, pseudogenization or deletion), which could not be detected by our analyses. The findings supply a foundation for understanding the genetic adaptations of amphibians inhabiting extremes. |
format | Online Article Text |
id | pubmed-7073644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70736442020-03-19 Plateau Grass and Greenhouse Flower? Distinct Genetic Basis of Closely Related Toad Tadpoles Respectively Adapted to High Altitude and Karst Caves Chang, Liming Zhu, Wei Shi, Shengchao Zhang, Meihua Jiang, Jianping Li, Cheng Xie, Feng Wang, Bin Genes (Basel) Article Genetic adaptation to extremes is a fascinating topic. Nevertheless, few studies have explored the genetic adaptation of closely related species respectively inhabiting distinct extremes. With deep transcriptome sequencing, we attempt to detect the genetic architectures of tadpoles of five closely related toad species adapted to the Tibetan Plateau, middle-altitude mountains and karst caves. Molecular evolution analyses indicated that not only the number of fast evolving genes (FEGs), but also the functioning coverage of FEGs, increased with elevation. Enrichment analyses correspondingly revealed that the highland species had most of the FEGs involved in high-elevation adaptation, for example, amino acid substitutions of XRCC6 in its binding domains might improve the capacity of DNA repair of the toad. Yet, few FEGs and positively selected genes (PSGs) involved in high-elevation adaptation were identified in the cave species, and none of which potentially contributed to cave adaptation. Accordingly, it is speculated that in the closely related toad tadpoles, genetic selection pressures increased with elevation, and cave adaptation was most likely derived from other factors (e.g., gene loss, pseudogenization or deletion), which could not be detected by our analyses. The findings supply a foundation for understanding the genetic adaptations of amphibians inhabiting extremes. MDPI 2020-01-22 /pmc/articles/PMC7073644/ /pubmed/31979140 http://dx.doi.org/10.3390/genes11020123 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Chang, Liming Zhu, Wei Shi, Shengchao Zhang, Meihua Jiang, Jianping Li, Cheng Xie, Feng Wang, Bin Plateau Grass and Greenhouse Flower? Distinct Genetic Basis of Closely Related Toad Tadpoles Respectively Adapted to High Altitude and Karst Caves |
title | Plateau Grass and Greenhouse Flower? Distinct Genetic Basis of Closely Related Toad Tadpoles Respectively Adapted to High Altitude and Karst Caves |
title_full | Plateau Grass and Greenhouse Flower? Distinct Genetic Basis of Closely Related Toad Tadpoles Respectively Adapted to High Altitude and Karst Caves |
title_fullStr | Plateau Grass and Greenhouse Flower? Distinct Genetic Basis of Closely Related Toad Tadpoles Respectively Adapted to High Altitude and Karst Caves |
title_full_unstemmed | Plateau Grass and Greenhouse Flower? Distinct Genetic Basis of Closely Related Toad Tadpoles Respectively Adapted to High Altitude and Karst Caves |
title_short | Plateau Grass and Greenhouse Flower? Distinct Genetic Basis of Closely Related Toad Tadpoles Respectively Adapted to High Altitude and Karst Caves |
title_sort | plateau grass and greenhouse flower? distinct genetic basis of closely related toad tadpoles respectively adapted to high altitude and karst caves |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073644/ https://www.ncbi.nlm.nih.gov/pubmed/31979140 http://dx.doi.org/10.3390/genes11020123 |
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