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Epstein-Barr Virus BHRF1 Micro- and Stable RNAs During Latency III and After Induction of Replication

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Journal J Virol
Date 2007 Jul 13
PMID 17626073
Citations 59
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Abstract

Epstein-Barr virus (EBV) microRNAs miR-BHRF1-1, -2, and -3 have been detected in latency III-infected lymphoblasts, where they are encoded within EBNA transcripts (X. Cai, A. Schafer, S. Lu, J. P. Bilello, R. C. Desrosiers, R. Edwards, N. Raab-Traub, and B. R. Cullen, PLoS Pathog. 2:e23, 2006). In latency III-infected lymphoblasts, we have also identified a stable 1.3-kb RNA, which begins 3' to miR-BHRF1-1, includes the BHRF1 open reading frame, and ends near miR-BHRF1-2. This 1.3-kb RNA is the residue of Drosha cleavage of the BHRF1 microRNAs from EBNA transcripts. Early after induction of EBV replication in latency I-infected Akata lymphoblasts, BHRF1 spliced 1.4-kb mRNA accumulated along with low levels of miR-BHRF1-2 and -3 and a 0.9-kb Drosha or miR-BHRF1-2 cleavage product of BHRF1 mRNA. The turning on of latency III infection at 48 to 72 h after induction of EBV replication was associated with higher miR-BHRF1-1, -2, and -3 levels; accumulation of the 1.3-kb RNA residue in the nucleus; abundant BHRF1 spliced 1.4-kb mRNA in the cytoplasm; and more abundant 0.9-kb mRNA cleavage product in the cytoplasm. These findings implicate miR-BHRF1-2 in 3' cleavage of BHRF1 mRNA in the cytoplasm and Drosha in cleavage of latency III EBNA and EBV replication-associated BHRF1 transcripts in the nucleus.

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References
1.
Russo J, Bohenzky R, Chien M, Chen J, Yan M, Maddalena D . Nucleotide sequence of the Kaposi sarcoma-associated herpesvirus (HHV8). Proc Natl Acad Sci U S A. 1996; 93(25):14862-7. PMC: 26227. DOI: 10.1073/pnas.93.25.14862. View

2.
Liu M, Shih Y, Chou S, Chen C, Sheen T, Yang C . Antibody against the Epstein-Barr virus BHRF1 protein, a homologue of Bcl-2, in patients with nasopharyngeal carcinoma. J Med Virol. 1998; 56(3):179-85. DOI: 10.1002/(sici)1096-9071(199811)56:3<179::aid-jmv1>3.0.co;2-4. View

3.
Kaiser C, Laux G, Eick D, Jochner N, Bornkamm G, Kempkes B . The proto-oncogene c-myc is a direct target gene of Epstein-Barr virus nuclear antigen 2. J Virol. 1999; 73(5):4481-4. PMC: 104340. DOI: 10.1128/JVI.73.5.4481-4484.1999. View

4.
Cheung S, Huang D, Hui A, Lo K, Ko C, Tsang Y . Nasopharyngeal carcinoma cell line (C666-1) consistently harbouring Epstein-Barr virus. Int J Cancer. 1999; 83(1):121-6. DOI: 10.1002/(sici)1097-0215(19990924)83:1<121::aid-ijc21>3.0.co;2-f. View

5.
Johannsen E, Luftig M, Chase M, Weicksel S, Cahir-McFarland E, Illanes D . Proteins of purified Epstein-Barr virus. Proc Natl Acad Sci U S A. 2004; 101(46):16286-91. PMC: 528973. DOI: 10.1073/pnas.0407320101. View