比较基因组学揭示了 11 种沙蝇解毒和杀虫剂靶基因的进化动态。

IF 3.2 2区 生物学 Q2 EVOLUTIONARY BIOLOGY
Jason Charamis, Sofia Balaska, Panagiotis Ioannidis, Vít Dvořák, Konstantinos Mavridis, Mary Ann McDowell, Pavlos Pavlidis, René Feyereisen, Petr Volf, John Vontas
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引用次数: 0

摘要

每年有超过一百万人感染利什曼病寄生虫及其他细菌和病毒病原体。由于基因组资源有限,阻碍了人们了解沙蝇对异种生物适应性的进展。为了填补这一空白,我们对 11 个沙蝇物种的转录组进行了测序、组装和注释。随后,我们利用这些基因组资源,就它们对异种生物(包括导致杀虫剂抗性的生物)的适应性提出了新的进化见解。具体来说,我们注释了 2,700 多个沙蝇解毒基因,并进行了大规模的系统发育比较,以揭示五大解毒基因家族的进化动态:这些基因包括细胞色素 P450s(CYPs)、谷胱甘肽-S-转移酶(GSTs)、UDP-糖基转移酶(UGTs)、羧基/胆碱酯酶(CCEs)和 ATP 结合盒(ABC)转运体。通过这种比较方法,我们发现沙蝇进化出了多种多样的 CYP 和 GST 基因,其中与已知的异生物代谢物进化相关的基因组有明显的品系特异性扩增。此外,我们还发现沙蝇在以下方面具有保守的直向同源基因:a)参与角质烃生物合成的 CYP4G 基因;b)参与异生物毒性的 ABCB 基因;c)两个主要的杀虫剂靶标:乙酰胆碱酯酶-1(Ace1)和电压门控钠通道(VGSC)。这项研究中产生的生物学见解和基因组资源为产生和检验沙蝇适应异种生物的分子机制假设奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative Genomics Uncovers the Evolutionary Dynamics of Detoxification and Insecticide Target Genes Across 11 Phlebotomine Sand Flies.

Sand flies infect more than 1 million people annually with Leishmania parasites and other bacterial and viral pathogens. Progress in understanding sand fly adaptations to xenobiotics has been hampered by the limited availability of genomic resources. To address this gap, we sequenced, assembled, and annotated the transcriptomes of 11 phlebotomine sand fly species. Subsequently, we leveraged these genomic resources to generate novel evolutionary insights pertaining to their adaptations to xenobiotics, including those contributing to insecticide resistance. Specifically, we annotated over 2,700 sand fly detoxification genes and conducted large-scale phylogenetic comparisons to uncover the evolutionary dynamics of the five major detoxification gene families: cytochrome P450s (CYPs), glutathione-S-transferases (GSTs), UDP-glycosyltransferases (UGTs), carboxyl/cholinesterases (CCEs), and ATP-binding cassette (ABC) transporters. Using this comparative approach, we show that sand flies have evolved diverse CYP and GST gene repertoires, with notable lineage-specific expansions in gene groups evolutionarily related to known xenobiotic metabolizers. Furthermore, we show that sand flies have conserved orthologs of (i) CYP4G genes involved in cuticular hydrocarbon biosynthesis, (ii) ABCB genes involved in xenobiotic toxicity, and (iii) two primary insecticide targets, acetylcholinesterase-1 (Ace1) and voltage gated sodium channel (VGSC). The biological insights and genomic resources produced in this study provide a foundation for generating and testing hypotheses regarding the molecular mechanisms underlying sand fly adaptations to xenobiotics.

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来源期刊
Genome Biology and Evolution
Genome Biology and Evolution EVOLUTIONARY BIOLOGY-GENETICS & HEREDITY
CiteScore
5.80
自引率
6.10%
发文量
169
审稿时长
1 months
期刊介绍: About the journal Genome Biology and Evolution (GBE) publishes leading original research at the interface between evolutionary biology and genomics. Papers considered for publication report novel evolutionary findings that concern natural genome diversity, population genomics, the structure, function, organisation and expression of genomes, comparative genomics, proteomics, and environmental genomic interactions. Major evolutionary insights from the fields of computational biology, structural biology, developmental biology, and cell biology are also considered, as are theoretical advances in the field of genome evolution. GBE’s scope embraces genome-wide evolutionary investigations at all taxonomic levels and for all forms of life — within populations or across domains. Its aims are to further the understanding of genomes in their evolutionary context and further the understanding of evolution from a genome-wide perspective.
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