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肠道病毒71型2A蛋白的研究进展
2014年
肠道病毒71(enterovirus 71,EV71)是手足口病(hand,foot and mouth disease,HFMD)主要致病原之一。手足口病临床上常表现为发热,手掌、脚掌及口腔黏膜皮疹或疱疹。然而,EV71感染导致的手足口病易伴随神经系统并发症,甚至死亡。EV71非结构蛋白2A作为蛋白酶和转录激活因子,在EV71生命周期中发挥重要作用。本文对2A的结构与功能研究进展进行综述,揭示2A的双重功能如何促进病毒复制和调控靶细胞,为进一步研究靶向2A的抗病毒疫苗和药物提供理论基础。
刘永娟张凤凤涂会林何小华刘万红
关键词:肠道病毒71蛋白酶转录激活因子
Advance in immunology of human enterovirus 71
Human enterovirus 71(EV71) is a common causative agent of hand,foot and mouth disease in young children.It can...
Liu WanhongZhou BingfeiHe Xiaohua
关键词:EV71RECEPTORCYTOKINEVACCINE
一种潜在的新肿瘤分子标志物RASSF4的研究进展
2014年
RAS相关结构域家族(RASSFs)由10个成员组成,这些家族成员已被确认为抑癌基因,可以通过多种途径调控细胞增殖、促进细胞凋亡和衰老,维持微管的稳定性、调节细胞的黏附和运动性。研究发现RASSF4在正常组织中广泛表达,而在人类肿瘤细胞中由于启动子甲基化表达下调,RASSF4还可诱导细胞凋亡,其关于信号转导途径的研究也有了一定发展。本文就其研究进展进行综述。
张凤凤刘永娟朱果果程青青王志浩刘万红何小华
关键词:甲基化细胞凋亡
一种新的柯萨奇病毒A组16型中国湖北分离株(CV-A16WH16)全基因组序列测定及分析
2015年
目的对分离自2010年中国湖北手足口患者的柯萨奇病毒A组16型(coxsackievirus A16,CVA16)病毒WH16株进行全基因组克隆、序列测定及进化分析。方法利用RT-PCR扩增覆盖基因组全长的cDNA片段,利用Over-lap PCR进行分步连接,得到CV-A16 WH16的全基因组cDNA克隆。对cDNA克隆进行测序,并利用BioEdit 4.8.8、EditSeq 5.01和MEGA 6.06软件进行序列分析和进化树构建。结果CV-A16 WH16基因组(未包含多聚腺苷酸尾)长度为7 406nt;WH16与CV-A16TS10/07、CV-A16原型株G-10以及EV71原型株BrCr的核苷酸一致性分别为97.7%、79.1%和79.5%,而氨基酸一致性分别为98.9%、94.7%和88.7%。全基因组进化树分析表明,CV-A16 WH16与CV-A16TS10/07亲缘关系最近,与G-10株存在显著差异;开放阅读框核苷酸序列进化树分析表明,CV-A16 WH16与EV71BrCr的亲缘关系较近。结论进化树分析表明,与G-10相比,CV-A16 WH16部分区域的核苷酸序列和BrCr的亲缘关系更近。
刘希佳何小华刘万红
关键词:柯萨奇病毒A16进化树
Characterization and molecular phylogeny of coxsackievirus A16 strains associated with hand,foot,and mouth disease epidemics in Hubei province of China,in 2010 and 2011
Coxsackievirus A16(CA16),a RNA virus of the family Picornaviridae,is cocirculating with Human enterovirus 71(H...
Liu Wanhong~1,Dong Lanlan~1,Shi Yingying~1,Liu Yongjuan~1,Zhou Bingfei~1,Fu Chong~1,He Xiaohua~(1,2) 1.School of Basic Medical Sciences,Wuhan University 2.Wuhan Center for Medical Treatment
关键词:HFMDVP1
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The long non-coding RNA expression profile of Coxsackievirus A16 infected RD cells identified by RNA-seq被引量:4
2016年
Coxsackievirus A16(CVA16) is one of major pathogens of hand, foot and mouth disease(HFMD) in children. Long non-coding RNAs(Inc RNAs) have been implicated in various biological processes,but they have not been associated with CVA16 infection. In this study, we comprehensively characterized the landscape of Inc RNAs of normal and CVA16 infected rhabdomyosarcoma(RD)cells using RNA-Seq to investigate the functional relevance of Inc RNAs. We showed that a total of 760 Inc RNAs were upregulated and 1210 Inc RNAs were downregulated. Out of these dysregulated Inc RNAs, 43.64% were intergenic, 22.31% were sense, 15.89% were intronic, 8.67% were bidirectional, 5.59% were antisense, 3.85% were s RNA host Inc RNAs and 0.05% were enhancer. Six dysregulated Inc RNAs were validated by quantitative PCR assays and the secondary structures of these Inc RNAs were projected. Moreover, we conducted a bioinformatics analysis of an Inc RNAs(ENST00000602478) to elucidate the diversity of modification and functions of Inc RNAs. In summary, the current study compared the dysregulated Inc RNAs profile upon CVA16 challenge and illustrated the intricate relationship between coding and Inc RNAs transcripts. These results may not only provide a complete picture of transcription in CVA16 infected cells but also provide novel molecular targets for treatments of HFMD.
Yingying ShiHuilin TuXiong ChenYingying ZhangLiujun ChenZhongchun LiuJiqun ShengSong HanJun YinBiwen PengXiaohua HeWanhong Liu
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