Potential functional pathways of plant RNA virus-derived small RNAs in a vector insect

阿尔戈瑙特 免疫沉淀 反式siRNA 生物 小干扰RNA 核糖核酸 基因沉默 RNA沉默 RNA干扰 基因 小RNA 细胞生物学 小RNA 病毒学 分子生物学 遗传学
作者
Wan Zhao,Qiong Li,Feng Cui
出处
期刊:Methods [Elsevier BV]
卷期号:183: 38-42 被引量:9
标识
DOI:10.1016/j.ymeth.2019.10.006
摘要

During infection, RNA viruses can produce two types of virus-derived small RNAs (vsRNAs), small interfering RNA (siRNA) and microRNA (miRNA), that play a key role in RNA silencing-mediated antiviral mechanisms in various hosts by associating with different Argonaute (Ago) proteins. Ago1 has been widely identified as an essential part of the miRNA pathway, while Ago2 is required for the siRNA pathway. Thus, analysis of the interaction between vsRNAs and Ago proteins can provide a clue about which pathway the vsRNA may be involved in. In this study, using rice stripe virus (RSV)-small brown planthoppers (Laodelphax striatellus, Fallen) as an infection model, the interactions of eight vsRNAs derived from four viral genomic RNA fragments and Ago1 or Ago2 were detected via the RNA immunoprecipitation (RIP) method. vsRNA4-1 and vsRNA4-2 derived from RSV RNA4 were significantly enriched in Ago1-immunoprecipitated complexes, whereas vsRNA2-1 and vsRNA3-2 seemed enriched in Ago2-immunoprecipitated complexes. vsRNA1-2 and vsRNA2-2 were detected in both of the two Ago-immunoprecipitated complexes. In contrast, vsRNA1-1 and vsRNA3-1 did not accumulate in either Ago1- or Ago2-immunoprecipitated complexes, indicating that regulatory pathways other than miRNA or siRNA pathways might be employed. In addition, two conserved L. striatellus miRNAs were analysed via the RIP method. Both miRNAs accumulated in Ago1-immunoprecipitated complexes, which was consistent with previous studies, suggesting that our experimental system can be widely used. In conclusion, our study provides an accurate and convenient detection system to determine the potential pathway of vsRNAs, and this method may also be suitable for studying other sRNAs.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
chuzihang完成签到 ,获得积分10
1秒前
小匣子完成签到 ,获得积分10
2秒前
2秒前
8D完成签到,获得积分10
3秒前
现代完成签到,获得积分10
8秒前
hdc12138完成签到,获得积分10
12秒前
clanoi完成签到 ,获得积分10
14秒前
S179完成签到,获得积分10
15秒前
xiong xiong完成签到,获得积分10
18秒前
XXXX完成签到 ,获得积分10
21秒前
小小脑CTS完成签到 ,获得积分10
21秒前
YanYan完成签到 ,获得积分10
22秒前
boymin2015完成签到 ,获得积分10
23秒前
Cradoc完成签到,获得积分10
26秒前
程志强完成签到 ,获得积分10
29秒前
31秒前
许鸽完成签到,获得积分10
31秒前
麻辣烫完成签到 ,获得积分10
31秒前
枫叶人生完成签到,获得积分10
35秒前
37秒前
Fanfan完成签到 ,获得积分10
37秒前
JYM完成签到,获得积分10
37秒前
i2stay完成签到,获得积分0
37秒前
share发布了新的文献求助10
40秒前
cjg完成签到,获得积分10
41秒前
邵小庆发布了新的文献求助10
42秒前
学术牛马完成签到,获得积分10
46秒前
活雷锋应助开冲采纳,获得10
47秒前
看文献完成签到,获得积分0
48秒前
maomao完成签到 ,获得积分10
52秒前
啊啊啊完成签到 ,获得积分10
55秒前
ding应助开冲采纳,获得10
58秒前
活力的千柳完成签到 ,获得积分10
1分钟前
1分钟前
1分钟前
QuanruiYao完成签到,获得积分20
1分钟前
苹果姐完成签到 ,获得积分10
1分钟前
文文武完成签到 ,获得积分10
1分钟前
飞飞wolf完成签到,获得积分10
1分钟前
skysleeper发布了新的文献求助10
1分钟前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Autoparametric Resonance in Mechanical Systems 1000
Effects of Two Weeks of Red Light Therapy on Choroidal Thickness and Axial Length in Young Adults 700
Cosmos as Art Object: Studies in Plato's Timaeus and Other Dialogues 600
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
the fractional Laplacian 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7668050
求助须知:如何正确求助?哪些是违规求助? 9236700
关于积分的说明 19881028
捐赠科研通 7237217
什么是DOI,文献DOI怎么找? 3284036
关于科研通互助平台的介绍 2442942
邀请新用户注册赠送积分活动 2285554