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家蚕中肠的全面转录组测序:揭示 BmNPV 敏感和 BmNPV 抗性品系中的广泛异构体多样性和可变剪接。

Comprehensive transcriptome sequencing of silkworm Midguts: Uncovering extensive isoform diversity and alternative splicing in BmNPV-Sensitive and BmNPV-resistant strains.

机构信息

School of Life Sciences, Jiangsu University, Zhenjiang 212013, Jiangsu Province, China.

School of Life Sciences, Jiangsu University, Zhenjiang 212013, Jiangsu Province, China.

出版信息

J Invertebr Pathol. 2024 Jun;204:108104. doi: 10.1016/j.jip.2024.108104. Epub 2024 Apr 10.

Abstract

The silkworm, Bombyx mori, stands out as one of the few economically valuable insects within the realm of model organisms. However, Bombyx mori nucleopolyhedrovirus (BmNPV) poses a significant threat, decreasing the quality and quantity of silkworm cocoons. Over the past few decades, a multitude of researchers has delved into the mechanisms that underlie silkworm resistance to BmNPV, employing diverse methodologies and approaching the problem from various angles. Despite this extensive research, the role of alternative splicing (AS) in the silkworm's response to BmNPV infection has been largely unexplored. This study leveraged both third-generation (Oxford Nanopore Technologies) and second-generation (Illumina) high-throughput sequencing technologies to meticulously identify and analyze AS patterns in the context of BmNPV response, utilizing two distinct silkworm strains-the susceptible strain 306 and the resistant strain NB. Consequently, we identified five crucial genes (Dsclp, LOC692903, LOC101743583, LOC101742498, LOC101743809) that are linked to the response to BmNPV infection through AS and differential expression. Additionally, a thorough comparative analysis was conducted on their diverse transcriptomic expression profiles, including alternative polyadenylation, simple sequence repeats, and transcription factors.

摘要

家蚕作为模式生物中少数几种具有经济价值的昆虫之一,其地位举足轻重。然而,家蚕核型多角体病毒(BmNPV)却构成了严重威胁,降低了蚕茧的质量和数量。在过去的几十年中,众多研究人员深入研究了家蚕对 BmNPV 抗性的机制,采用了多种方法,并从不同角度探讨了这一问题。尽管进行了广泛的研究,但替代剪接(AS)在蚕对 BmNPV 感染反应中的作用在很大程度上仍未得到探索。本研究利用第三代(Oxford Nanopore Technologies)和第二代(Illumina)高通量测序技术,细致地鉴定和分析了 BmNPV 反应背景下的 AS 模式,使用了两个不同的家蚕品系——敏感品系 306 和抗性品系 NB。因此,我们确定了五个关键基因(Dsclp、LOC692903、LOC101743583、LOC101742498、LOC101743809),它们通过 AS 和差异表达与 BmNPV 感染的反应有关。此外,还对它们在不同转录组表达谱中的多样化的可变多聚腺苷酸化、简单重复序列和转录因子进行了全面的比较分析。

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