Marek's Disease Virus-Encoded MicroRNA 155 Ortholog Critical for the Induction of Lymphomas Is Not Essential for the Proliferation of Transformed Cell Lines

Author:

Zhang Yaoyao12,Tang Na13,Luo Jun45,Teng Man4,Moffat Katy1,Shen Zhiqiang3,Watson Mick6ORCID,Nair Venugopal178,Yao Yongxiu1

Affiliation:

1. The Pirbright Institute & UK-China Centre of Excellence for Research on Avian Diseases, Pirbright, Guildford, Surrey, United Kingdom

2. School of Animal Science and Technology, Guangxi University, Nanning, China

3. Binzhou Animal Science and Veterinary Medicine Academy & UK-China Centre of Excellence for Research on Avian Diseases, Binzhou, China

4. Key Laboratory of Animal Immunology of the Ministry of Agriculture, Henan Provincial Key Laboratory of Animal Immunology, Henan Academy of Agricultural Sciences, Zhengzhou, China

5. College of Animal Science and Technology, Henan University of Science and Technology, Luoyang, China

6. The Roslin Institute, R(D)SVS, University of Edinburgh, Midlothian, United Kingdom

7. The Jenner Institute Laboratories, University of Oxford, Oxford, United Kingdom

8. Department of Zoology, University of Oxford, Oxford, United Kingdom

Abstract

Marek’s disease virus (MDV) is an alphaherpesvirus associated with Marek’s disease (MD), a highly contagious neoplastic disease of chickens. MD serves as an excellent model for studying virus-induced T-cell lymphomas in the natural chicken hosts. Among the limited set of genes associated with MD oncogenicity, MDV-miR-M4, a highly expressed viral ortholog of the oncogenic miR-155, has received extensive attention due to its direct role in the induction of lymphomas. Using a targeted CRISPR-Cas9-based gene editing approach in MDV-transformed lymphoblastoid cell lines, we show that MDV-miR-M4, despite its critical role in the induction of tumors, is not essential for maintaining the transformed phenotype and continuous proliferation. As far as we know, this was the first study in which precise editing of an oncogenic miRNA was carried out in situ in MD lymphoma-derived cell lines to demonstrate that it is not essential in maintaining the transformed phenotype.

Funder

PhD placement programme of UK-China Joint Research and Innovation Partnership Fund

BBSRC Newton Fund Joint Centre Awards

Fund for Distinguished Young Scholars from Henan Academy of Agricultural Sciences

National Natural Science Foundation of China

RCUK | Biotechnology and Biological Sciences Research Council

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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