期刊文献+

Functional analysis of a miRNA‐like small RNA derived from Bombyx mori cytoplasmic polyhedrosis virus 被引量:7

原文传递
导出
摘要 Bombyx mori cytoplasmic polyhedrosis virus(BmCPV)is a major pathogen of the economic insect silkworm,Bombyx mori.Virus‐encoded microRNAs(miRNAs)have been proven to play important roles in host–pathogen interactions.In this study we identified a BmCPV‐derived miRNA‐like 21 nt small RNA,BmCPV‐miR‐1,from the small RNA deep sequencing of BmCPV‐infected silkworm larvae by stem‐loop quantitative real‐time PCR(qPCR)and investigated its functions with qPCR and lentiviral expression systems.Bombyx mori inhibitor of apoptosis protein(BmIAP)gene was predicted by both target prediction software miRanda and Targetscan to be one of its target genes with a binding site for BmCPV‐miR‐1 at the 5′untranslated region.It was found that the expression of BmCPV‐miR‐1 and its target gene BmIAP were both up‐regulated in BmCPV‐infected larvae.At the same time,it was confirmed that BmCPV‐miR‐1 could up‐regulate the expression of BmIAP gene in HEK293T cells with lentiviral expression systems and in BmN cells by transfecting mimics.Furthermore,BmCPV‐miR‐1 mimics could up‐regulate the expression level of BmIAP gene in midgut and fat body in the silkworm.In the midgut of BmCPV‐infected larvae,BmCPV‐miR‐1 mimics could be further up‐regulated and inhibitors could lower the virus‐mediated expression of BmIAP gene.With the viral genomic RNA segments S1 and S10 as indicators,BmCPV‐miR‐1 mimics could up‐regulate and inhibitors down‐regulate their replication in the infected silkworm.These results implied that BmCPV‐miR‐1 could inhibit cell apoptosis in the infected silkworm through up‐regulating BmIAP expression,providing the virus with a better cell circumstance for its replication.
出处 《Insect Science》 SCIE CAS CSCD 2020年第3期449-462,共14页 昆虫科学(英文版)
基金 This work was financially supported by the National Natural Science Foundation of China(Grant No.31572463).
  • 相关文献

参考文献5

二级参考文献92

  • 1孙延波,李菁华,史红艳.mIL-4昆虫表达载体pIZT/V5-His的构建及其高效表达[J].吉林大学学报(医学版),2006,32(2):194-195. 被引量:3
  • 2石艳春,梁浩,旭日干.融合表达IL-2和EGFP逆转录病毒载体的构建[J].中国生物制品学杂志,2006,19(1):1-4. 被引量:3
  • 3王星,罗光彬,刘永,肖焕星,姜卓.哺乳动物颗粒细胞凋亡研究进展[J].安徽农业科学,2007,35(12):3554-3555. 被引量:4
  • 4Aris K, Michael T, Oliver G, et al. Discovery and analysis of the first endogenous lentivirus. PNAS, 2007, 104 (15): 6261-6265.
  • 5Parolin C, Sodroski L A defective HIV-1 vector for gene transfer to human lymphocytes. J Mol Med, 1995, 73 (6): 279-288.
  • 6Curran MA, Kaiser SM, Achacoso PL, et al. Efficient transduction of nondividing cells by optimized feline immunodeficiency virus vectors. Mol Ther, 2000, 1 ( 1 ): 31-38.
  • 7Mitrophanous K, Yoon S, Rohll J, etal. Stable gene transfer to the nervous system using a non-primate lentiviral vector. Gene Ther. 1999, 6 (11): 1808-1818.
  • 8Mselli-Lakhal L, Favier C, Da Silva Teixeira MF, et al. Defective RNA packaging is responsible for low transduction efficiency of CAEV-based vectors. Arch Virol, 1998, 143 (4): 681-695.
  • 9Berkowitz R, Ilves H, Lin WY, etal. Construction and molecular analysis of gene transfer systems derived from bovine immunodeficiency virus. J Virol, 2001, 75 (7): 3371-3382.
  • 10Berkowitz RD, Ilves H, Plavec I, et al. Gene transfer systems derived from Visna virus: analysis of virus production and infectivity. Virology, 2001, 279 (1): 116-129.

共引文献42

同被引文献45

引证文献7

二级引证文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部