-
Je něco špatně v tomto záznamu ?
Effective inhibition of mRNA accumulation and protein expression of H5N1 avian influenza virus NS1 gene in vitro by small interfering RNAs
H. Jiao, L. Du, Y. Hao, Y. Cheng, J. Luo, W. Kuang, D. Zhang, M. Lei, X. Jia, X. Zhang, C. Qi, H. He, F. Wang
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- buněčné linie MeSH
- faktory virulence antagonisté a inhibitory genetika MeSH
- kvantitativní polymerázová řetězová reakce MeSH
- lidé MeSH
- malá interferující RNA * MeSH
- průtoková cytometrie MeSH
- rekombinantní fúzní proteiny analýza genetika MeSH
- reportérové geny MeSH
- umělá fúze genů MeSH
- virové nestrukturální proteiny antagonisté a inhibitory genetika MeSH
- virus chřipky A, podtyp H5N1 genetika růst a vývoj MeSH
- western blotting MeSH
- zelené fluorescenční proteiny analýza genetika MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Avian influenza has emerged as a devastating disease and may cross species barrier and adapt to a new host, causing enormous economic loss and great public health threats, and non-structural protein 1 (NS1) is a multifunctional non-structural protein of avian influenza virus (AIV) that counters cellular antiviral activities and is a virulence factor. RNA interference (RNAi) provides a powerful promising approach to inhibit viral infection specifically. To explore the possibility of using RNAi as a strategy against AIV infection, after the fusion protein expression plasmids pNS1-enhanced green fluorescent protein (EGFP), which contain the EGFP reporter gene and AIV NS1 as silencing target, were constructed and NS1-EGFP fusion protein expressing HEK293 cell lines were established, four small interfering RNAs (siRNAs) targeting NS1 gene were designed, synthesized, and used to transfect the stable cell lines. Flow cytometry, real-time quantitative polymerase chain reaction, and Western blot were performed to assess the expression level of NS1. The results suggested that sequence-dependent specific siRNAs effectively inhibited mRNA accumulation and protein expression of AIV NS1 in vitro. These findings provide useful information for the development of RNAi-based prophylaxis and therapy for AIV infection.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc14046065
- 003
- CZ-PrNML
- 005
- 20140415095546.0
- 007
- ta
- 008
- 140212s2013 xr f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s12223-012-0212-8 $2 doi
- 035 __
- $a (PubMed)23192525
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Jiao, Hanwei $u College of Agriculture, Hainan Key Laboratory of Tropical Animal Reproduction & Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Laboratory of Haikou, Hainan University, Haidian Island, Haikou, People's Republic of China
- 245 10
- $a Effective inhibition of mRNA accumulation and protein expression of H5N1 avian influenza virus NS1 gene in vitro by small interfering RNAs / $c H. Jiao, L. Du, Y. Hao, Y. Cheng, J. Luo, W. Kuang, D. Zhang, M. Lei, X. Jia, X. Zhang, C. Qi, H. He, F. Wang
- 520 9_
- $a Avian influenza has emerged as a devastating disease and may cross species barrier and adapt to a new host, causing enormous economic loss and great public health threats, and non-structural protein 1 (NS1) is a multifunctional non-structural protein of avian influenza virus (AIV) that counters cellular antiviral activities and is a virulence factor. RNA interference (RNAi) provides a powerful promising approach to inhibit viral infection specifically. To explore the possibility of using RNAi as a strategy against AIV infection, after the fusion protein expression plasmids pNS1-enhanced green fluorescent protein (EGFP), which contain the EGFP reporter gene and AIV NS1 as silencing target, were constructed and NS1-EGFP fusion protein expressing HEK293 cell lines were established, four small interfering RNAs (siRNAs) targeting NS1 gene were designed, synthesized, and used to transfect the stable cell lines. Flow cytometry, real-time quantitative polymerase chain reaction, and Western blot were performed to assess the expression level of NS1. The results suggested that sequence-dependent specific siRNAs effectively inhibited mRNA accumulation and protein expression of AIV NS1 in vitro. These findings provide useful information for the development of RNAi-based prophylaxis and therapy for AIV infection.
- 650 _2
- $a umělá fúze genů $7 D019677
- 650 _2
- $a western blotting $7 D015153
- 650 _2
- $a buněčné linie $7 D002460
- 650 _2
- $a průtoková cytometrie $7 D005434
- 650 _2
- $a reportérové geny $7 D017930
- 650 _2
- $a zelené fluorescenční proteiny $x analýza $x genetika $7 D049452
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a virus chřipky A, podtyp H5N1 $x genetika $x růst a vývoj $7 D053124
- 650 12
- $a malá interferující RNA $7 D034741
- 650 _2
- $a kvantitativní polymerázová řetězová reakce $7 D060888
- 650 _2
- $a rekombinantní fúzní proteiny $x analýza $x genetika $7 D011993
- 650 _2
- $a virové nestrukturální proteiny $x antagonisté a inhibitory $x genetika $7 D017361
- 650 _2
- $a faktory virulence $x antagonisté a inhibitory $x genetika $7 D037521
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Du, Li $u College of Agriculture, Hainan Key Laboratory of Tropical Animal Reproduction & Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Laboratory of Haikou, Hainan University, Haidian Island, Haikou, People's Republic of China
- 700 1_
- $a Hao, Yongchang $u College of Agriculture, Hainan Key Laboratory of Tropical Animal Reproduction & Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Laboratory of Haikou, Hainan University, Haidian Island, Haikou, People's Republic of China
- 700 1_
- $a Cheng, Ying $u College of Agriculture, Hainan Key Laboratory of Tropical Animal Reproduction & Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Laboratory of Haikou, Hainan University, Haidian Island, Haikou, People's Republic of China
- 700 1_
- $a Luo, Jing $u Key Laboratory of Animal Ecology and Conservation Biology, National Research Center for Wildlife Born Diseases, Institute of Zoology, Chinese Academy of Scienses, Beijing, People's Republic of China
- 700 1_
- $a Kuang, Wenhua $u College of Life Scienses, Huazhong Normal University, Wuhan, People's Republic of China
- 700 1_
- $a Zhang, Donglin $u College of Agriculture, Hainan Key Laboratory of Tropical Animal Reproduction & Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Laboratory of Haikou, Hainan University, Haidian Island, Haikou, People's Republic of China
- 700 1_
- $a Lei, Ming $u College of Agriculture, Hainan Key Laboratory of Tropical Animal Reproduction & Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Laboratory of Haikou, Hainan University, Haidian Island, Haikou, People's Republic of China
- 700 1_
- $a Jia, Xiaoxiao $u College of Agriculture, Hainan Key Laboratory of Tropical Animal Reproduction & Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Laboratory of Haikou, Hainan University, Haidian Island, Haikou, People's Republic of China
- 700 1_
- $a Zhang, Xiaoru $u College of Life Scienses, Huazhong Normal University, Wuhan, People's Republic of China
- 700 1_
- $a Qi, Chao $u College of Life Scienses, Huazhong Normal University, Wuhan, People's Republic of China
- 700 1_
- $a He, Hongxuan $u Key Laboratory of Animal Ecology and Conservation Biology, National Research Center for Wildlife Born Diseases, Institute of Zoology, Chinese Academy of Scienses, Beijing, People's Republic of China
- 700 1_
- $a Wang, Fengyang $u College of Agriculture, Hainan Key Laboratory of Tropical Animal Reproduction & Breeding and Epidemic Disease Research, Animal Genetic Engineering Key Laboratory of Haikou, Hainan University, Haidian Island, Haikou, People's Republic of China
- 773 0_
- $w MED00011005 $t Folia microbiologica $x 1874-9356 $g Roč. 58, č. 4 (2013), s. 335-342
- 856 41
- $u http://link.springer.com/journal/12223/58/4/page/1 $y domovská stránka časopisu
- 910 __
- $a ABA008 $b online $c sign $y a $z 0
- 990 __
- $a 20140212 $b ABA008
- 991 __
- $a 20140415095644 $b ABA008
- 999 __
- $a ok $b bmc $g 1019652 $s 844599
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2013 $b 58 $c 4 $d 335-342 $i 1874-9356 $m Folia microbiologica $n Folia microbiol. (Prague) $x MED00011005
- LZP __
- $b NLK111 $a Pubmed-20140212