病原体感染改变了黑腹果蝇转座元件的基因表达谱。

IF 2.1 3区 生物学 Q3 GENETICS & HEREDITY
Sabrina L Mostoufi, Nadia D Singh
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引用次数: 0

摘要

可转座元件在真核生物基因组中占很大比例,其中许多被认为是古代病毒感染的残留物。目前的研究已开始强调转座元件在免疫系统对感染的反应中所起的作用。然而,我们对感染过程中转座元件表达的了解大多受限于每项研究中特定的宿主和病原体因素,因此很难对各项研究进行比较,也很难就转座元件在感染过程中的作用形成更广泛的模式。在这里,我们利用黑腹果蝇模型的工具和资源,分析了受细菌、真菌和病毒感染的果蝇的多个基因表达数据集。我们分析了病原体种类、宿主基因型、宿主组织和性别的差异,以了解这些因素如何影响感染过程中转座元件的表达。我们的研究结果突显了病原体之间共享和独特的转座元件表达模式,并表明病原体因素对转座元件表达的影响大于宿主因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pathogen infection alters the gene expression landscape of transposable elements in Drosophila melanogaster.

Transposable elements make up substantial proportions of eukaryotic genomes and many are thought to be remnants of ancient viral infections. Current research has begun to highlight the role transposable elements can play in the immune system response to infections. However, most of our knowledge about transposable element expression during infection is limited by the specific host and pathogen factors from each study, making it difficult to compare studies and develop broader patterns regarding the role of transposable elements during infection. Here, we use the tools and resources available in the model, Drosophila melanogaster, to analyze multiple gene expression datasets of flies subject to bacterial, fungal, and viral infections. We analyzed differences in pathogen species, host genotype, host tissue, and sex to understand how these factors impact transposable element expression during infection. Our results highlight both shared and unique transposable element expression patterns between pathogens and suggest a larger effect of pathogen factors over host factors for influencing transposable element expression.

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来源期刊
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics GENETICS & HEREDITY-
CiteScore
5.10
自引率
3.80%
发文量
305
审稿时长
3-8 weeks
期刊介绍: G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights. G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.
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