DNA methylation machinery is involved in development and reproduction in the viviparous pea aphid (Acyrthosiphon pisum)

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Insect Molecular Biology Pub Date : 2024-06-26 DOI:10.1111/imb.12936
Kane Yoon, Stephanie Williams, Elizabeth J. Duncan
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Abstract

Epigenetic mechanisms, such as DNA methylation, have been proposed to mediate plastic responses in insects. The pea aphid (Acyrthosiphon pisum), like the majority of extant aphids, displays cyclical parthenogenesis - the ability of mothers to switch the reproductive mode of their offspring from reproducing parthenogenetically to sexually in response to environmental cues. The pea aphid genome encodes two paralogs of the de novo DNA methyltransferase gene, dnmt3a and dnmt3x. Here we show, using phylogenetic analysis, that this gene duplication event occurred at least 150 million years ago, likely after the divergence of the lineage leading to the Aphidomorpha (phylloxerans, adelgids and true aphids) from that leading to the scale insects (Coccomorpha) and that the two paralogs are maintained in the genomes of all aphids examined. We also show that the mRNA of both dnmt3 paralogs is maternally expressed in the viviparous aphid ovary. During development both paralogs are expressed in the germ cells of embryos beginning at stage 5 and persisting throughout development. Treatment with 5-azactyidine, a chemical that generally inhibits the DNA methylation machinery, leads to defects of oocytes and early-stage embryos and causes a proportion of later stage embryos to be born dead or die soon after birth. These phenotypes suggest a role for DNA methyltransferases in reproduction, consistent with that seen in other insects. Taking the vast evolutionary history of the dnmt3 paralogs, and the localisation of their mRNAs in the ovary, we suggest there is a role for dnmt3a and/or dnmt3x in early development, and a role for DNA methylation machinery in reproduction and development of the viviparous pea aphid.

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DNA 甲基化机制参与胎生豌豆蚜(Acyrthosiphon pisum)的发育和繁殖。
DNA 甲基化等表观遗传机制被认为是昆虫可塑性反应的中介。豌豆蚜(Acyrthosiphon pisum)与现存的大多数蚜虫一样,表现出周期性孤雌生殖--母蚜能够根据环境线索将其后代的生殖模式从孤雌生殖转换为有性生殖。豌豆蚜基因组中编码了两个新DNA甲基转移酶基因的旁系亲属,即dnmt3a和dnmt3x。在这里,我们利用系统发生学分析表明,这一基因复制事件发生在至少 1.5 亿年前,很可能是在蚜虫科(phylloxerans、adelgids 和真蚜虫)与鳞翅目昆虫科(Coccomorpha)分化之后,而且这两个对等基因保留在所有被研究蚜虫的基因组中。我们还发现,两个 dnmt3 旁系亲属的 mRNA 在胎生蚜虫的子房中都有母性表达。在发育过程中,这两个旁系亲属都在胚胎的生殖细胞中表达,从第 5 阶段开始并持续整个发育过程。5-azactyidine 是一种通常能抑制 DNA 甲基化机制的化学物质,用它处理卵母细胞和早期胚胎会导致缺陷,并导致一部分后期胚胎先天死亡或出生后不久死亡。这些表型表明 DNA 甲基转移酶在繁殖过程中的作用,这与在其他昆虫中看到的情况一致。考虑到 dnmt3 旁系亲属的漫长进化史及其 mRNA 在卵巢中的定位,我们认为 dnmt3a 和/或 dnmt3x 在早期发育中发挥作用,DNA 甲基化机制在胎生豌豆蚜的繁殖和发育中发挥作用。
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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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