The hAT family hopper transposon exists as highly similar yet discontinuous elements in the Bactrocera tephritid fly genus

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Alfred M. Handler, Richard B. Furlong
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引用次数: 0

Abstract

The hAT family transposable element, hopper, was originally discovered as a defective 3120-bp full-length element in a wild-type strain of the oriental fruit fly, Bactrocera dorsalis (Hendel) (Diptera: Tephritidae), and subsequently a functional 3131-bp element, hopperBdwe, was isolated from a white eye mutant strain. The latter study showed that closely related elements exist in melonfly, Zeugodacus cucurbitae (Coquillett) (Diptera: Tephritidae), a closely related subgenus, suggesting that hopper could have a widespread presence in the Bactrocera genus. To further understand the distribution of hopper within and beyond the B. dorsalis species complex, primer pairs from hopperBdwe and its adjacent genomic insertion site were used to survey the presence and relatedness of hopper in five species within the complex and four species beyond the complex. Based on sequence identity of a 1.94 kb internal nucleotide sequence, the closest relationships were with mutated elements from B. dorsalis s.s. and species synonymized with B. dorsalis including B. papayae, B. philippinensis and B. invadens, ranging in identity between 88.4% and 99.5%. Notably, Bactrocera carambolae (Drew & Hancock) (Diptera: Tephritidae), which is most closely related to B. dorsalis beyond the synonymized species, shared hopper identities of 97.3%–99.5%. Beyond the B. dorsalis complex, Z. cucurbitae, Bactrocera tryoni (Froggatt) (Diptera: Tephritidae) and Bactrocera zonata (Saunders) (Diptera: Tephritidae) shared identities of 83.1%–97.1%, while hopper was absent from the Bactrocera oleae (Gmelin) (Diptera: Tephritidae) strain tested. While the functional autonomous hopperBdwe element was not detected in these species, another closely related hopper element isolated from a B. dorsalis genetic sexing strain has an uninterrupted transposase open reading frame. The discontinuous presence of hopper in the Bactrocera genus has implications for its use for genomic manipulation and understanding the phylogenetic relationship of these species.

Abstract Image

Abstract Image

hAT 家族跳虫转座子作为高度相似但不连续的元素存在于 Bactrocera tephritid 苍蝇属中。
hAT 家族转座元件 hopper 最初是在东方果蝇 Bactrocera dorsalis (Hendel) (双翅目:Tephritidae)的一个野生型品系中发现的,是一个有缺陷的 3120-bp 全长元件。后一项研究表明,在瓜蝇(Zeugodacus cucurbitae (Coquillett) (Diptera: Tephritidae))这一密切相关的亚属中也存在密切相关的元件,这表明跳虫可能广泛存在于 Bactrocera 属中。为了进一步了解跳虫在 B. dorsalis 种群内外的分布情况,研究人员使用来自 hopperBdwe 及其邻近基因组插入位点的引物对调查了跳虫在该种群内 5 个物种和该种群外 4 个物种中的存在情况和亲缘关系。根据 1.94 kb 内部核苷酸序列的序列同一性,与 B. dorsalis s.s.和与 B. dorsalis 同名的物种(包括 B.papayae、B.philippinensis 和 B.invadens)的变异元件关系最密切,同一性在 88.4% 到 99.5% 之间。值得注意的是,Bactrocera carambolae(Drew & Hancock)(双翅目:Tephritidae)与 B. dorsalis 的亲缘关系最为密切,除同名物种外,其与 B. dorsalis 的同源性为 97.3%-99.5%。在 B. dorsalis 复合体之外,Z. cucurbitae、Bactrocera tryoni (Froggatt) (双翅目:栉孔蝇科)和 Bactrocera zonata (Saunders) (双翅目:栉孔蝇科)的同源性为 83.1%-97.1%,而在所测试的 Bactrocera oleae (Gmelin) (双翅目:栉孔蝇科)菌株中则没有跳虫。虽然在这些物种中没有检测到功能自主的 hopperBdwe 元件,但从 B. dorsalis 基因性别鉴定菌株中分离出的另一个密切相关的 hopper 元件具有不间断的转座酶开放阅读框。跳虫在Bactrocera属中的不连续存在对其在基因组操作中的应用以及了解这些物种的系统发育关系都有影响。
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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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