高海拔地区蜱虫基因组分析。

IF 4.2 2区 生物学 Q2 MICROBIOLOGY
Yu Bao, Ye Mu, Jinghuan Hu, Mengchao Chen, Jing Xing
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引用次数: 0

摘要

例如,低温、强紫外线辐射和缺氧),对生物适应提出了独特的挑战。然而,大型真菌适应高海拔环境的遗传机制尚不清楚。在这项研究中,我们重新测序和组装了从QTP收集的三个拉螨物种的基因组,旨在揭示它们适应高海拔的基因组基础。基因组数据表明,高海拔物种的基因组略大于低海拔物种,特别是由于LTR反转录转座子的存在,这也与海拔呈负相关。在高海拔物种中,扩展和正向选择的基因家族在DNA损伤修复、维持细胞膜稳定性、信号转导、酶活性、应激反应和繁殖等相关途径中富集。相比之下,在高海拔物种中,收缩的基因家族主要与疾病和免疫反应有关,这可能是由于极端高海拔环境中病原体压力降低所致。此外,高原拉虫的种特异性基因在酶活性、膜稳定性和信号转导等方面的功能丰富,进一步支持了它们的适应性作用。碳水化合物活性酶(CAZymes)的分析显示,高海拔和低海拔物种之间的基因家族分布明显不同,有几个家族在低海拔物种中缺失,表明它们可能参与环境适应。总之,我们的研究结果表明,LTR逆转录转座子驱动的基因组大小扩张、基因家族的协调进化、正选择和CAZymes的分化可能共同促成了拉虫对极端高海拔环境的适应。本研究为真菌适应高原恶劣环境的遗传机制提供了基础数据,为进一步研究嗜极真菌奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Genomic Analysis of <i>Laccaria</i> Genomes at High Altitude.

Genomic Analysis of <i>Laccaria</i> Genomes at High Altitude.

Genomic Analysis of <i>Laccaria</i> Genomes at High Altitude.

Genomic Analysis of Laccaria Genomes at High Altitude.

The Qinghai-Tibet Plateau (QTP) harbors extreme environmental conditions (e.g., low temperature, intense UV radiation, and hypoxia), presenting unique challenges for biological adaptation. However, the genetic mechanisms underlying the adaptation of macrofungi to high-altitude environments on the QTP remain poorly understood. In this study, we de novo sequenced and assembled the genomes of three Laccaria species collected from the QTP, aiming to unravel the genomic basis of their adaptation to high altitudes. The genomic data indicates that the genome of high-altitude species is slightly larger than that of their low-altitude relatives, particularly due to LTR retrotransposons, which also show a negative correlation with altitude. The expanded and positively selected gene families in high-altitude species were enriched in pathways related to DNA damage repair, maintenance of cell membrane stability, signal transduction, enzyme activity, stress response, and reproduction. In contrast, contracted gene families in high-altitude species were primarily associated with disease and immune responses, likely due to the reduced pathogen pressure in extreme high-altitude environments. Additionally, species-specific genes of high-altitude Laccaria were enriched in functions related to enzyme activity, membrane stability, and signal transduction, further supporting their adaptive roles. Analysis of carbohydrate-active enzymes (CAZymes) showed distinct gene family distributions between high- and low-altitude species, with several families absent in the low-altitude species, suggesting their potential involvement in environmental adaptation. Overall, our findings indicate that genome size expansion driven by LTR retrotransposons, coordinated evolution of gene families, positive selection, and divergence in CAZymes collectively may contribute to the adaptation of Laccaria to extreme high-altitude environments. This study provides basic data into the genetic mechanisms of fungal adaptation to harsh plateau environments and lays a foundation for further research on extremophilic fungi.

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来源期刊
Journal of Fungi
Journal of Fungi Medicine-Microbiology (medical)
CiteScore
6.70
自引率
14.90%
发文量
1151
审稿时长
11 weeks
期刊介绍: Journal of Fungi (ISSN 2309-608X) is an international, peer-reviewed scientific open access journal that provides an advanced forum for studies related to pathogenic fungi, fungal biology, and all other aspects of fungal research. The journal publishes reviews, regular research papers, and communications in quarterly issues. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on paper length. Full experimental details must be provided so that the results can be reproduced.
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