一种新的半足动物模式系统Murgantia histrionica中类似oncopelus的基因表达模式提示了古代调控网络的分化。

IF 4.1 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY Evodevo Pub Date : 2020-04-22 eCollection Date: 2020-01-01 DOI:10.1186/s13227-020-00154-x
Jessica Hernandez, Leslie Pick, Katie Reding
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引用次数: 6

摘要

背景:从昆虫模型系统的研究中,我们了解了很多基础生物学的知识。杰出的昆虫模型系统,黑腹果蝇,是一种具有衍生的节形成模式的全变形昆虫。虽然近年来已经开创了其他昆虫模型,但其中大多数属于全变形谱系。相比之下,半代谢昆虫获得的关注较少,尽管它们包括农业害虫,人类疾病的媒介,并在形式和功能上呈现出许多进化的新颖性。乳草虫(Oncopeltus fasciatus,半翅目)是一种新兴的模式系统,与全变性昆虫相近。然而,这一目的比较研究是有限的,因为许多食植物半纲动物依赖新鲜植物,卵沉积在植物材料中,从胚胎到成虫的发育时间长,因此难以在实验室中稳定维持。结果:本文提出了一种新的半足纲模式种——小丑蝽(murgtia histrionica)。murgantia是五蝽科臭虫家族的一员,与Oncopeltus有共同的祖先,大约200万年前,它很容易在实验室中饲养,产生大量的卵,并且适合分子遗传技术。我们使用Murgantia来询问配对规则基因(PRGs)是否以类似于全变形昆虫或Oncopeltus的方式部署。具体来说,PRGs偶跳、奇跳、配对和马虎配对最初在果蝇和许多全变性昆虫的pr条纹中表达,但在Oncopeltus中表达为节段条纹。我们发现这些基因同样在Murgantia的节段条纹中表达,而runt在两个物种中都表现出部分pr特征。与Oncopeltus一样,E75A在Murgantia胚胚期和胚胚期以清晰的pr模式表达,尽管它在果蝇的分节中没有作用。因此,在Murgantia发育过程中,诊断全变形昆虫和Oncopeltus之间分裂的基因以一种类似Oncopeltus的方式表达。结论:Murgantia和Oncopeltus之间基因表达的相似性表明Oncopeltus并不是唯一一个没有利用果蝇PRGs同源物进行pr模式的例外物种。相反,pr模式的策略,包括在prg网络中使用E75A,可能在半翅目昆虫中是保守的,在半代谢昆虫中可能更广泛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Oncopeltus-like gene expression patterns in Murgantia histrionica, a new hemipteran model system, suggest ancient regulatory network divergence.

Background: Much has been learned about basic biology from studies of insect model systems. The pre-eminent insect model system, Drosophila melanogaster, is a holometabolous insect with a derived mode of segment formation. While additional insect models have been pioneered in recent years, most of these fall within holometabolous lineages. In contrast, hemimetabolous insects have garnered less attention, although they include agricultural pests, vectors of human disease, and present numerous evolutionary novelties in form and function. The milkweed bug, Oncopeltus fasciatus (order: Hemiptera)-close outgroup to holometabolous insects-is an emerging model system. However, comparative studies within this order are limited as many phytophagous hemipterans are difficult to stably maintain in the lab due to their reliance on fresh plants, deposition of eggs within plant material, and long development time from embryo to adult.

Results: Here we present the harlequin bug, Murgantia histrionica, as a new hemipteran model species. Murgantia-a member of the stink bug family Pentatomidae which shares a common ancestor with Oncopeltus ~ 200 mya-is easy to rear in the lab, produces a large number of eggs, and is amenable to molecular genetic techniques. We use Murgantia to ask whether Pair-Rule Genes (PRGs) are deployed in ways similar to holometabolous insects or to Oncopeltus. Specifically, PRGs even-skipped, odd-skipped, paired and sloppy-paired are initially expressed in PR-stripes in Drosophila and a number of holometabolous insects but in segmental-stripes in Oncopeltus. We found that these genes are likewise expressed in segmental-stripes in Murgantia, while runt displays partial PR-character in both species. Also like Oncopeltus, E75A is expressed in a clear PR-pattern in blastoderm- and germband-stage Murgantia embryos, although it plays no role in segmentation in Drosophila. Thus, genes diagnostic of the split between holometabolous insects and Oncopeltus are expressed in an Oncopeltus-like fashion during Murgantia development.

Conclusions: The similarity in gene expression between Murgantia and Oncopeltus suggests that Oncopeltus is not a sole outlier species in failing to utilize orthologs of Drosophila PRGs for PR-patterning. Rather, strategies deployed for PR-patterning, including the use of E75A in the PRG-network, are likely conserved within Hemiptera, and possibly more broadly among hemimetabolous insects.

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来源期刊
Evodevo
Evodevo EVOLUTIONARY BIOLOGY-DEVELOPMENTAL BIOLOGY
CiteScore
7.50
自引率
0.00%
发文量
18
审稿时长
>12 weeks
期刊介绍: EvoDevo publishes articles on a broad range of topics associated with the translation of genotype to phenotype in a phylogenetic context. Understanding the history of life, the evolution of novelty and the generation of form, whether through embryogenesis, budding, or regeneration are amongst the greatest challenges in biology. We support the understanding of these processes through the many complementary approaches that characterize the field of evo-devo. The focus of the journal is on research that promotes understanding of the pattern and process of morphological evolution. All articles that fulfill this aim will be welcome, in particular: evolution of pattern; formation comparative gene function/expression; life history evolution; homology and character evolution; comparative genomics; phylogenetics and palaeontology
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