帽捕捉机制介导的两种不同贝戈莫病毒转录起始位点的揭示

IF 2.1 4区 农林科学 Q2 AGRICULTURE, MULTIDISCIPLINARY
Muhammad Arif
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引用次数: 0

摘要

植物病毒造成了巨大的经济损失,给可持续农业带来了风险。新型病毒性疾病的扩散主要归因于气候变化、国际贸易和病毒的快速进化能力等因素。无花果树病毒(Begomoviruses)是一类主要的植物感染病毒,在许多作物物种中引起毁灭性的病毒性疾病,对全球农业构成了迫在眉睫的威胁。许多植物病毒的转录起始位点(TSS)通常位于基因间区(IR),即病毒基因之间的非编码区(NC)。启动子在启动转录过程中起着至关重要的作用,它能帮助细胞转录机制的招募。TSS是RNA聚合酶启动转录过程的精确核苷酸序列。本研究的主要目的是确定两种破坏性乞猴病毒(Geminiviridae、棉花叶枯病病毒科)的 TSSs 总数:棉花卷叶木尔坦病毒(CLCuMuV)和阿格拉通黄脉花叶病毒(AYVMV)的 TSSs 总数。将这两种乞猴病毒及其感染克隆与所选的异源植物病毒一起有意识地感染 N. benthamiana 植物。通过采用高通量测序评估封端 RNA 领导(CRLs),确定了异源病毒 mRNA 的 5′末端。通过将收集到的异源病毒 CRLs 与每种贝可病毒的基因组进行比对,仅考虑与贝可病毒基因组完全匹配的 CRLs,从而确定疑似贝可病毒 mRNA 的 5′末端。在这项研究中,通过互补方法确定了两种贝戈莫病毒的 TSSs。利用高通量测序技术对两种贝戈莫病毒进行测序,有助于获得数百万个序列。了解无花果树病毒的 TSSs 和启动子成分对于了解它们的致病能力、与宿主生物的相互作用以及开发有效的方法来管理和控制它们对具有重要经济价值的作物植物造成的病害至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cap-snatching mechanism-mediated unveiling of the transcriptional initiation sites of two distinct begomoviruses

Cap-snatching mechanism-mediated unveiling of the transcriptional initiation sites of two distinct begomoviruses

Significant economic losses are inflicted by plant viruses, which pose a risk to sustainable agriculture. The proliferation of novel viral diseases is predominantly attributable to factors such as climate change, international trade, and the rapid evolutionary capabilities of viruses. Begomoviruses are a major group of plant-infecting viruses that pose an imminent threat to global agriculture by causing devastating viral diseases in many crop species. The transcriptional start sites (TSSs) of many plant viruses are typically found in the intergenic region (IR), which is the non-coding (NC) area between the viral genes. The promoters play a crucial role in initiating the transcription process by aiding in the recruitment of cellular transcription machinery. The TSSs are precise nucleotide sequences where RNA polymerase initiates the transcription process. The primary objective of this study was to determine the total number of TSSs for two devastating begomoviruses, family: Geminiviridae, Cotton leaf curl Multan virus (CLCuMuV) and Ageratum yellow vein mosaic virus (AYVMV), using the cap-snatching method in conjunction with one heterologous plant virus. These two begomoviruses, along with their infectious clones, were intentionally infected with selected heterologous plant virus in N. benthamiana plants. The identification of the 5′ ends of heterologous viral mRNA was accomplished by employing high-throughput sequencing to assess the capped RNA leaders (CRLs). The determination of the 5′ termini of suspected begomoviral mRNAs was achieved by aligning the collected CRLs of heterologous virus with the genome of each begomovirus, taking into account only those that were a perfect match with the begomoviral genome. In this study, the TSSs of both begomoviruses were identified via complementary approach. The utilization of high-throughput sequencing for both begomoviruses has facilitated the acquisition of millions of sequences. Comprehending the TSSs and promoter components of begomoviruses is crucial for understanding their ability to cause disease, their interactions with host organisms, and for developing effective methods to manage and control the diseases, they inflict on economically significant crop plants.

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来源期刊
Journal of Plant Diseases and Protection
Journal of Plant Diseases and Protection 农林科学-农业综合
CiteScore
4.30
自引率
5.00%
发文量
124
审稿时长
3 months
期刊介绍: The Journal of Plant Diseases and Protection (JPDP) is an international scientific journal that publishes original research articles, reviews, short communications, position and opinion papers dealing with applied scientific aspects of plant pathology, plant health, plant protection and findings on newly occurring diseases and pests. "Special Issues" on coherent themes often arising from International Conferences are offered.
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