Epstein-Barr Virus BHRF1 Micro- and Stable RNAs During Latency III and After Induction of Replication
Overview
Authors
Affiliations
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.
Inter-regulatory role of microRNAs in interaction between viruses and stem cells.
Afshari A, Yaghobi R, Rezaei G World J Stem Cells. 2021; 13(8):985-1004.
PMID: 34567421 PMC: 8422934. DOI: 10.4252/wjsc.v13.i8.985.
SoRelle E, Dai J, Bonglack E, Heckenberg E, Zhou J, Giamberardino S Elife. 2021; 10.
PMID: 33501914 PMC: 7867410. DOI: 10.7554/eLife.62586.
Li C, Romero-Masters J, Huebner S, Ohashi M, Hayes M, Bristol J PLoS Pathog. 2020; 16(6):e1008590.
PMID: 32542010 PMC: 7316346. DOI: 10.1371/journal.ppat.1008590.
Oncogenic Properties of the EBV ZEBRA Protein.
Germini D, Sall F, Shmakova A, Wiels J, Dokudovskaya S, Drouet E Cancers (Basel). 2020; 12(6).
PMID: 32517128 PMC: 7352903. DOI: 10.3390/cancers12061479.
Crosstalk Between Mammalian Antiviral Pathways.
Watson S, Knol L, Witteveldt J, Macias S Noncoding RNA. 2019; 5(1).
PMID: 30909383 PMC: 6468734. DOI: 10.3390/ncrna5010029.