Tao Wang, Xin-Rui Ren, Zhi-Kun Guo, Yu-Xuan Zhao, Jin Geng, Guan-Hong Wang, Da-Wei Huang, Jin-Hua Xiao
{"title":"宿主的 mtDNA 变异和核反应长期并存","authors":"Tao Wang, Xin-Rui Ren, Zhi-Kun Guo, Yu-Xuan Zhao, Jin Geng, Guan-Hong Wang, Da-Wei Huang, Jin-Hua Xiao","doi":"10.1127/entomologia/2024/2530","DOIUrl":null,"url":null,"abstract":"Numerous studies have accumulatively discovered mitochondrial genome (mtDNA) diversity in the natural populations of the same species, and some of the mtDNA variations may be selected by the host’s environment. However, it remains unclear about the molecular mechanisms by which this long-term coexistence of mtDNA variations in the same species affects the metabolism and evolution of the host. By comparing two mitochondrial genomes of cultured population of Hermetia illucens, our study reveals that the mtDNAs of both strains (Ref-strain and Sub-strain) have great structural divergences, and mitochondria of the Sub-strain may be functionally defective, which is consistent with the observed lower body weights and higher oxidative stress levels in the midgut of Sub-strain. Moreover, the differentially expressed genes and differential metabolites between the midguts of both strains were related to the mitochondrial functions including oxidative stress, antioxidant and electron transport chain. Interesting, the midgut microbial compositions differed significantly in both strains. Additionally, 25 of 310 the potentially positively selected genes were related to mitochondrial function. Combination of these multidimensional investigations of both strains helped to reveal how the host insects adapt to mtDNA variations through cyto-nuclear interactions. This study can provide new evidence for understanding the nuclear response to the mitochondria dysfunction in insects, and its role in differentiation of the natural populations and even in the process of speciation.","PeriodicalId":11728,"journal":{"name":"Entomologia Generalis","volume":null,"pages":null},"PeriodicalIF":5.6000,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Long-term coexistence of mtDNA variations and nuclear responses of host\",\"authors\":\"Tao Wang, Xin-Rui Ren, Zhi-Kun Guo, Yu-Xuan Zhao, Jin Geng, Guan-Hong Wang, Da-Wei Huang, Jin-Hua Xiao\",\"doi\":\"10.1127/entomologia/2024/2530\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Numerous studies have accumulatively discovered mitochondrial genome (mtDNA) diversity in the natural populations of the same species, and some of the mtDNA variations may be selected by the host’s environment. However, it remains unclear about the molecular mechanisms by which this long-term coexistence of mtDNA variations in the same species affects the metabolism and evolution of the host. By comparing two mitochondrial genomes of cultured population of Hermetia illucens, our study reveals that the mtDNAs of both strains (Ref-strain and Sub-strain) have great structural divergences, and mitochondria of the Sub-strain may be functionally defective, which is consistent with the observed lower body weights and higher oxidative stress levels in the midgut of Sub-strain. Moreover, the differentially expressed genes and differential metabolites between the midguts of both strains were related to the mitochondrial functions including oxidative stress, antioxidant and electron transport chain. Interesting, the midgut microbial compositions differed significantly in both strains. Additionally, 25 of 310 the potentially positively selected genes were related to mitochondrial function. Combination of these multidimensional investigations of both strains helped to reveal how the host insects adapt to mtDNA variations through cyto-nuclear interactions. This study can provide new evidence for understanding the nuclear response to the mitochondria dysfunction in insects, and its role in differentiation of the natural populations and even in the process of speciation.\",\"PeriodicalId\":11728,\"journal\":{\"name\":\"Entomologia Generalis\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":5.6000,\"publicationDate\":\"2024-09-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Entomologia Generalis\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1127/entomologia/2024/2530\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENTOMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Entomologia Generalis","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1127/entomologia/2024/2530","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
Long-term coexistence of mtDNA variations and nuclear responses of host
Numerous studies have accumulatively discovered mitochondrial genome (mtDNA) diversity in the natural populations of the same species, and some of the mtDNA variations may be selected by the host’s environment. However, it remains unclear about the molecular mechanisms by which this long-term coexistence of mtDNA variations in the same species affects the metabolism and evolution of the host. By comparing two mitochondrial genomes of cultured population of Hermetia illucens, our study reveals that the mtDNAs of both strains (Ref-strain and Sub-strain) have great structural divergences, and mitochondria of the Sub-strain may be functionally defective, which is consistent with the observed lower body weights and higher oxidative stress levels in the midgut of Sub-strain. Moreover, the differentially expressed genes and differential metabolites between the midguts of both strains were related to the mitochondrial functions including oxidative stress, antioxidant and electron transport chain. Interesting, the midgut microbial compositions differed significantly in both strains. Additionally, 25 of 310 the potentially positively selected genes were related to mitochondrial function. Combination of these multidimensional investigations of both strains helped to reveal how the host insects adapt to mtDNA variations through cyto-nuclear interactions. This study can provide new evidence for understanding the nuclear response to the mitochondria dysfunction in insects, and its role in differentiation of the natural populations and even in the process of speciation.
期刊介绍:
Its scope covers all aspects of basic and applied research dealing with insects and more broadly with arthropods inhabiting wild, agricultural and/or urban habitats. The journal also considers research integrating various disciplines and issues within the broad field of entomology and ecology.
Entomologia Generalis publishes high quality research articles on advances in knowledge on the ecology and biology of arthropods, as well as on their importance for key ecosystems services, e.g. as biological control and pollination. The journal devotes special attention to contributions providing significant advances (i) on the fundamental knowledge and on sustainable control strategies of arthropod pests (including of stored products) and vectors of diseases, (ii) on the biology and ecology of beneficial arthropods, (iii) on the spread and impact of invasive pests, and (iv) on potential side effects of pest management methods.
Entomologia Generalis welcomes review articles on significant developments in the field of entomology. These are usually invited by the editorial board, but proposals may be sent to the Editor-in-Chief for preliminary assessment by the editorial board before formal submission to the journal. The journal also considers comments on papers published in Entomologia Generalis, as well as short notes on topics that are of broader interest.