Identification and functional verification of the target protein of pedunsaponin A in the gills of Pomacea canaliculata

福寿螺 RNA干扰 生物 小干扰RNA 核糖核酸 细胞生物学 分子生物学 解剖 基因 生物化学 生态学 蜗牛 渔业
作者
Chunping Yang,Yuqing Ma,Bin Wang,Yanmei Wang,Jingxiang Liu,Chunxian Jiang,Min Zhang,Xiaoyan Qiu,Liya Luo,Huabao Chen
出处
期刊:Pest Management Science [Wiley]
卷期号:78 (3): 947-954 被引量:5
标识
DOI:10.1002/ps.6704
摘要

Based on previous research indicating that pedunsaponin A (PA) can destroy the gills of Pomacea canaliculata, we chose the gill as the main research object, and identified the target protein of PA in the gills of P. canaliculata through proteomics and RNA interference (RNAi).Proteomics showed that 180 proteins were downregulated after PA treatment in P. canaliculata. Among them, we chose advillin (PcAdv), receptor type tyrosine protein phosphatase (PcRT) and unconventional myosin heavy chain 6 (PcUM) as candidate target proteins through bioinformatics analysis. The small interfering RNA (siRNA) with the best interference effect was identified through further screening. Gene interference rates were 97%, 98% and 82% for PcAdv, PcRT and PcUM, respectively. The results showed that after RNAi treatment, the mortality of P. canaliculata treated with PcAdv (60.0%) was significantly lower than that for the control (93.3%); histological analysis showed that the structure of the gill was intact, cilia shedding was reduced, and the survival rate of hemocytes had increased.These findings indicate that, when the protein was absent or suppressed, the channel for entry of PA into the hemocytes of P. canaliculata was blocked, which reduced PA binding to hemocytes, and that there is a close relationship between shedding of gill cilia and PA entry into hemocytes. PcAdv is thus the key protein in PA destruction of gill cilia. Locating the proteins in gills that interact with drugs and investigating their mode of action is of great importance in the development of new molluscicides to control P. canaliculata populations.
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
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

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
Owen应助上杉绘梨衣采纳,获得10
刚刚
缓慢沁完成签到,获得积分10
1秒前
悦耳虔纹发布了新的文献求助10
1秒前
量子星尘发布了新的文献求助10
3秒前
tian发布了新的文献求助10
4秒前
4秒前
云小澈完成签到,获得积分10
5秒前
柏忆南完成签到 ,获得积分10
5秒前
丘比特应助无聊水煮鱼采纳,获得10
7秒前
nono发布了新的文献求助10
7秒前
打打应助kk采纳,获得10
8秒前
科目三应助flysky120采纳,获得10
9秒前
浮游应助zyjsunye采纳,获得10
11秒前
12秒前
针地很不戳完成签到,获得积分10
13秒前
14秒前
2758543477完成签到,获得积分10
15秒前
拉克丝发布了新的文献求助10
16秒前
浮游应助怡然凌兰采纳,获得10
16秒前
Una发布了新的文献求助10
16秒前
华子的五A替身完成签到,获得积分10
16秒前
17秒前
19秒前
19秒前
QQ糖完成签到,获得积分20
20秒前
郭嘉仪发布了新的文献求助10
20秒前
22秒前
tian完成签到,获得积分10
23秒前
23秒前
吴小利发布了新的文献求助20
23秒前
23秒前
SciGPT应助有一套采纳,获得10
24秒前
lihaih完成签到,获得积分10
26秒前
27秒前
鲤鱼山人完成签到 ,获得积分10
27秒前
不见高山完成签到,获得积分10
27秒前
浮浮世世发布了新的文献求助10
27秒前
郭郭完成签到 ,获得积分10
27秒前
艾七七完成签到,获得积分10
29秒前
树池完成签到,获得积分10
29秒前
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
《微型计算机》杂志2006年增刊 1600
Symbiosis: A Very Short Introduction 1500
Einführung in die Rechtsphilosophie und Rechtstheorie der Gegenwart 1500
Binary Alloy Phase Diagrams, 2nd Edition 1000
Air Transportation A Global Management Perspective 9th Edition 700
Letters from Rewi Alley to Ida Pruitt, 1954-1964, vol. 1 600
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 内科学 生物化学 物理 计算机科学 纳米技术 遗传学 基因 复合材料 化学工程 物理化学 病理 催化作用 免疫学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 4967242
求助须知:如何正确求助?哪些是违规求助? 4225288
关于积分的说明 13158632
捐赠科研通 4011895
什么是DOI,文献DOI怎么找? 2195351
邀请新用户注册赠送积分活动 1208788
关于科研通互助平台的介绍 1122525