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通过蛋白质基因组学优化天冬氨酸蛋白酶A1家族基因的注释。

Refining the annotation of aspartic proteases A1 family genes through proteogenomics.

作者信息

Ouali Radouane, Bousbata Sabrina

机构信息

Laboratory of Vector-Pathogen Biology, Proteomic Platform, Department of Molecular Biology, Université Libre de Bruxelles, Gosselies, 6041, Belgium.

出版信息

Curr Res Parasitol Vector Borne Dis. 2025 Mar 12;7:100253. doi: 10.1016/j.crpvbd.2025.100253. eCollection 2025.

Abstract

Stål (Hemiptera: Reduviidae: Triatominae) a hematophagous model organism and vector of Chagas disease, relies on a complex repertoire of digestive enzymes to process its blood meals. Among these, aspartic proteases from the A1 peptidase family play a crucial role in nutrient breakdown. This study aims to refine the gene annotation of the A1 peptidase family in this organism through proteogenomics. A comprehensive analysis of aspartic protease gene sequences and protein isoforms, identified by proteomics, revealed discrepancies in existing gene annotations, including the identification of novel open reading frames and the consolidation of previously separated gene sequences. Our efforts led to the correction of seven gene annotations, reducing the total count of A1 peptidase genes from 19 to 15. Notably, 11 of these genes were confirmed at the protein level, while two were supported by transcriptomic data. Furthermore, our findings highlight instances of alternative splicing, as seen in RPRC015076, where proteoforms T1IFK7 and R4G5J6 are expressed through intron retention. This study not only provides a more accurate and comprehensive genomic framework for the A1 peptidase family but also offers new insights into the functional complexity and regulation of digestive enzymes in . These findings pave the way for future studies on insect digestive biology and their potential applications in vector control strategies.

摘要

锥蝽(半翅目:猎蝽科:锥蝽亚科)是一种吸血的模式生物,也是恰加斯病的传播媒介,它依靠一套复杂的消化酶来处理其血餐。其中,A1肽酶家族的天冬氨酸蛋白酶在营养物质分解中起关键作用。本研究旨在通过蛋白质基因组学完善该生物中A1肽酶家族的基因注释。对通过蛋白质组学鉴定出的天冬氨酸蛋白酶基因序列和蛋白质异构体进行的全面分析,揭示了现有基因注释中的差异,包括新开放阅读框的鉴定以及先前分离的基因序列的整合。我们的工作导致七个基因注释得到修正,使A1肽酶基因总数从19个减少到15个。值得注意的是,其中11个基因在蛋白质水平得到确认,两个得到转录组数据支持。此外,我们的发现突出了可变剪接的实例,如在RPRC015076中所见,其中蛋白质变体T1IFK7和R4G5J6通过内含子保留表达。本研究不仅为A1肽酶家族提供了更准确和全面的基因组框架,还为该生物中消化酶的功能复杂性和调控提供了新见解。这些发现为未来昆虫消化生物学研究及其在病媒控制策略中的潜在应用铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba18/11978366/58f40dc3e40e/ga1.jpg

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