Expression profiles of microRNAs encoded by the oncogenic Marek's disease virus reveal two distinct expression patterns in vivo during different phases of disease

被引:24
|
作者
Luo, Jun [1 ]
Sun, Ai-Jun [2 ]
Teng, Man [1 ]
Zhou, Hui [3 ]
Cui, Zhi-Zhong [2 ]
Qu, Liang-Hu [3 ]
Zhang, Gai-Ping [1 ]
机构
[1] Henan Acad Agr Sci, Minist Agr, Henan Prov Key Lab Anim Immunol, Key Lab Anim Immunol, Zhengzhou 450002, Peoples R China
[2] Shandong Agr Univ, Coll Anim Sci & Vet Med, Tai An 271018, Shandong, Peoples R China
[3] Sun Yat Sen Zhongshan Univ, Minist Educ, Sch Life Sci, Key Lab Gene Engn,State Key Lab Biocontrol, Guangzhou 510275, Guangdong, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
RETICULOENDOTHELIOSIS VIRUS; SEQUENCE CONSERVATION; FIELD STRAIN; HERPESVIRUS; GENOMICS;
D O I
10.1099/vir.0.024158-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Marek's disease virus (MDV) is a long-recognized oncogenic herpesvirus, which induces lymphoma in its natural host that can be prevented by vaccination. MDV infection provides an excellent biological model for investigating the biology, genetics and immunology of viral oncogenesis. Recently discovered microRNAs (miRNAs) in the MDV genome have been suggested to have regulatory roles during MDV oncogenesis. We have examined the expression profiles of all 22 previously reported miRNAs encoded by MDV-1 in chickens artificially challenged with MDV-GX0101. We found that a subset of the miRNAs was differentially expressed during different phases of the developing disease. These miRNAs show early or late expression during disease progression, accompanied by obvious tissue-specific and differential expression patterns. This temporal and differential tissue distribution suggest that these miRNAs may perform different regulatory roles in switching from latency to lytic replication, immunosupression, neoplastic transformation or other aspects of lymphoma formation. These reported in vivo expression profiles indicate the potentially functional MDV-1-encoded miRNAs that should be selected for further investigation of their functions in MDV oncogenesis.
引用
收藏
页码:608 / 620
页数:13
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