对一种社会性半翅目昆虫的基因组和转录组分析为了解昆虫的社会性提供了新的视角

IF 5.5 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Ecology Resources Pub Date : 2024-09-12 DOI:10.1111/1755-0998.14019
Hui Zhang, Qian Liu, Jianjun Lu, Liying Wu, Zhentao Cheng, Gexia Qiao, Xiaolei Huang
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引用次数: 0

摘要

社会性的起源是最重要的进化转变之一。昆虫的社会性是在一些半翅目蚜虫中进化而来的,它们可以通过孤雌生殖产生具有不同形态和行为的兵士和正常若虫。基因组数据资源的缺乏阻碍了对其社会性进化的分子机制的研究。在本文中,我们首次生成了具有高度特化兵士的社会性半翅目昆虫(Pseudoregma bambucicola)的染色体级基因组,并进行了基因组和转录组比较分析,以阐明种姓分化的分子特征和调控机制。P. bambucicola的已知蚜虫基因组较大,为582.2 Mb,N50长度为11.24 Mb,约99.6%的组装固定在6条染色体上,支架N50为98.27 Mb。共预测了 14,027 个编码蛋白质的基因,其中 37.33% 的基因被鉴定为重复序列。社会进化伴随着基因组组织的各种变化,包括与转录因子、转座元件有关的基因家族的扩展,以及某些糖转运体和参与碳水化合物代谢的 UGPases 的物种特异性扩展。我们还描述了与种姓分化相关的大型候选基因集的特征,发现了表达调控和正选择作用于能量代谢和肌肉结构的证据,从而解释了士兵的特异性状,包括形态和行为特化、发育停滞和不育。总之,这项研究为社会性蚜虫的分子基础和昆虫社会性的进化提供了新的见解,也为进一步的比较和功能研究提供了宝贵的数据资源。
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Genomic and transcriptomic analyses of a social hemipteran provide new insights into insect sociality
The origin of sociality represents one of the most important evolutionary transitions. Insect sociality evolved in some hemipteran aphids, which can produce soldiers and normal nymphs with distinct morphology and behaviour through parthenogenesis. The lack of genomic data resources has hindered the investigations into molecular mechanisms underlying their social evolution. Herein, we generated the first chromosomal‐level genome of a social hemipteran (Pseudoregma bambucicola) with highly specialized soldiers and performed comparative genomic and transcriptomic analyses to elucidate the molecular signatures and regulatory mechanisms of caste differentiation. P. bambucicola has a larger known aphid genome of 582.2 Mb with an N50 length of 11.24 Mb, and about 99.6% of the assembly was anchored to six chromosomes with a scaffold N50 of 98.27 Mb. A total of 14,027 protein‐coding genes were predicted and 37.33% of the assembly were identified as repeat sequences. The social evolution is accompanied by a variety of changes in genome organization, including expansion of gene families related to transcription factors, transposable elements, as well as species‐specific expansions of certain sugar transporters and UGPases involved in carbohydrate metabolism. We also characterized large candidate gene sets linked to caste differentiation and found evidence of expression regulation and positive selection acting on energy metabolism and muscle structure, explaining the soldier‐specific traits including morphological and behavioural specialization, developmental arrest and infertility. Overall, this study offers new insights into the molecular basis of social aphids and the evolution of insect sociality and also provides valuable data resources for further comparative and functional studies.
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来源期刊
Molecular Ecology Resources
Molecular Ecology Resources 生物-进化生物学
CiteScore
15.60
自引率
5.20%
发文量
170
审稿时长
3 months
期刊介绍: Molecular Ecology Resources promotes the creation of comprehensive resources for the scientific community, encompassing computer programs, statistical and molecular advancements, and a diverse array of molecular tools. Serving as a conduit for disseminating these resources, the journal targets a broad audience of researchers in the fields of evolution, ecology, and conservation. Articles in Molecular Ecology Resources are crafted to support investigations tackling significant questions within these disciplines. In addition to original resource articles, Molecular Ecology Resources features Reviews, Opinions, and Comments relevant to the field. The journal also periodically releases Special Issues focusing on resource development within specific areas.
期刊最新文献
Genomic and transcriptomic analyses of a social hemipteran provide new insights into insect sociality Whole-genome resequencing improves the utility of otoliths as a critical source of DNA for fish stock research and monitoring. Issue Information Deep estimation of the intensity and timing of natural selection from ancient genomes. The accuracy of predicting maladaptation to new environments with genomic data.
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