Refining the annotation of Rhodnius prolixus aspartic proteases A1 family genes through proteogenomics

IF 1.7 Q3 PARASITOLOGY
Radouane Ouali, Sabrina Bousbata
{"title":"Refining the annotation of Rhodnius prolixus aspartic proteases A1 family genes through proteogenomics","authors":"Radouane Ouali,&nbsp;Sabrina Bousbata","doi":"10.1016/j.crpvbd.2025.100253","DOIUrl":null,"url":null,"abstract":"<div><div><em>Rhodnius prolixus</em> 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 <em>R. prolixus</em>. These findings pave the way for future studies on insect digestive biology and their potential applications in vector control strategies.</div></div>","PeriodicalId":94311,"journal":{"name":"Current research in parasitology & vector-borne diseases","volume":"7 ","pages":"Article 100253"},"PeriodicalIF":1.7000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current research in parasitology & vector-borne diseases","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667114X25000135","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PARASITOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Rhodnius prolixus 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 R. prolixus. These findings pave the way for future studies on insect digestive biology and their potential applications in vector control strategies.

Abstract Image

利用蛋白质基因组学技术对长叶红蛋白酶A1家族基因的注释进行完善
长鼻红蝇(半翅目:红蝇科:Triatominae)是一种噬血模式生物和恰加斯病的媒介,依靠一系列复杂的消化酶来处理其血餐。其中,来自A1肽酶家族的天冬氨酸蛋白酶在营养分解中起重要作用。本研究旨在通过蛋白质基因组学技术完善该生物A1肽酶家族的基因注释。通过蛋白质组学对天冬氨酸蛋白酶基因序列和蛋白质异构体的综合分析,揭示了现有基因注释的差异,包括鉴定新的开放阅读框和先前分离的基因序列的巩固。我们的努力纠正了7个基因注释,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上得到了证实,而两个基因在转录组学数据上得到了支持。此外,我们的研究结果强调了选择性剪接的实例,如在RPRC015076中所见,其中蛋白质形式T1IFK7和R4G5J6通过内含子保留表达。本研究不仅为长尾草A1肽酶家族提供了更准确、更全面的基因组框架,而且对长尾草消化酶的功能复杂性和调控提供了新的认识。这些发现为进一步研究昆虫消化生物学及其在病媒控制策略中的潜在应用铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
3.60
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信