孤雌繁殖和有性繁殖后代早期发育过程中基因表达模式的差异

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Riho Kamiyama, Michihiko Takahashi, Mamoru Takata, Kenji Matsuura
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引用次数: 0

摘要

群居昆虫表现出生殖分工,受影响种姓决定的外部和内部因素的支配。白蚁有一种独特的生殖系统,被称为无性蚁后继承(AQS),蚁后通过孤雌生殖产生年轻的蚁后,而工蚁和幼蚁则通过有性繁殖产生。这种固有的种姓分化偏见可能是由于基因表达的差异可能受到父母起源效应的影响,因为孤雌生殖的女儿只继承母亲的基因组,而有性生殖的女儿继承父亲和母亲的基因组。本研究表明,单性繁殖和有性繁殖的白蚁发育胚胎的基因表达模式存在显著差异。然而,SNP分析表明,这些差异不能归因于父母的起源效应。通过对katatresis后雌性胚胎的RNA-seq分析,我们发现了21个基因,包括jhbp、nlk和wge,这些基因已知与种姓分化和形态发生有关,在孤雌生殖和有性生殖的女儿中表达差异显著。尽管有12个基因表现出群体特异性表达模式,但对有性繁殖胚胎的SNP分析并未发现除线粒体基因外的任何亲本来源偏倚表达。这些发现表明,早期发育基因表达部分解释了种姓分化偏见。进一步的研究需要阐明这些跨代效应背后的分子机制,从基因表达的角度深入了解群居昆虫的AQS进化和复杂的种姓决定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differences in gene expression patterns between parthenogenetically and sexually produced offspring during early development of Reticulitermes speratus.

Social insects exhibit reproductive division of labour, governed by both external and internal factors influencing caste determination. In termites with a unique reproductive system known as asexual queen succession (AQS), queens produce neotenic queens via parthenogenesis, while workers and alates arise through sexual reproduction. This inherent caste differentiation bias may have resulted from differences in gene expression potentially influenced by the parent-of-origin effect, as parthenogenetic daughters inherit only maternal genomes, while sexually produced daughters inherit both paternal and maternal genomes. Here, we show that gene expression patterns in developing embryos of the termite Reticulitermes speratus differ significantly between parthenogenetic and sexually produced offspring. However, SNP analysis indicated that these differences were not attributable to the parent-of-origin effect. Through RNA-seq analysis of female embryos post-katatrepsis, we identified 21 genes, including jhbp, nlk, and wge, which are known to be involved in caste differentiation and morphogenesis, with significant expression differences between parthenogenetic and sexually produced daughters. SNP analysis of sexually produced embryos did not reveal any parent-of-origin biased expression except for mitochondrial genes, though 12 genes exhibited colony-specific expression patterns. These findings suggested that early developmental gene expression partly explained caste differentiation biases. Further research is essential to elucidate the molecular mechanisms behind these transgenerational effects, providing insight into the evolution of AQS and complex caste determination in social insects from a gene expression perspective.

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来源期刊
Insect Molecular Biology
Insect Molecular Biology 生物-昆虫学
CiteScore
4.80
自引率
3.80%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Insect Molecular Biology has been dedicated to providing researchers with the opportunity to publish high quality original research on topics broadly related to insect molecular biology since 1992. IMB is particularly interested in publishing research in insect genomics/genes and proteomics/proteins. This includes research related to: • insect gene structure • control of gene expression • localisation and function/activity of proteins • interactions of proteins and ligands/substrates • effect of mutations on gene/protein function • evolution of insect genes/genomes, especially where principles relevant to insects in general are established • molecular population genetics where data are used to identify genes (or regions of genomes) involved in specific adaptations • gene mapping using molecular tools • molecular interactions of insects with microorganisms including Wolbachia, symbionts and viruses or other pathogens transmitted by insects Papers can include large data sets e.g.from micro-array or proteomic experiments or analyses of genome sequences done in silico (subject to the data being placed in the context of hypothesis testing).
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