An immune-suppressing protein in human endogenous retroviruses

Author:

Zhang Huan1,Ni Shengliang1,Frith Martin C123ORCID

Affiliation:

1. Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences, University of Tokyo , Chiba 277-8568, Japan

2. Artificial Intelligence Research Center, AIST , Tokyo 135-0064, Japan

3. CBBD-OIL, AIST , Tokyo 169-8555, Japan

Abstract

Abstract Motivation Retroviruses are important contributors to disease and evolution in vertebrates. Sometimes, retrovirus DNA is heritably inserted in a vertebrate genome: an endogenous retrovirus (ERV). Vertebrate genomes have many such virus-derived fragments, usually with mutations disabling their original functions. Results Some primate ERVs appear to encode an overlooked protein. This protein is homologous to protein MC132 from Molluscum contagiosum virus, which is a human poxvirus, not a retrovirus. MC132 suppresses the immune system by targeting NF-κB, and it had no known homologs until now. The ERV homologs of MC132 in the human genome are mostly disrupted by mutations, but there is an intact copy on chromosome 4. We found homologs of MC132 in ERVs of apes, monkeys and bushbaby, but not tarsiers, lemurs or non-primates. This suggests that some primate retroviruses had, or have, an extra immune-suppressing protein, which underwent horizontal genetic transfer between unrelated viruses. Contact mcfrith@edu.k.u-tokyo.ac.jp

Funder

University of Tokyo World-leading Innovative Graduate Study Program on Global Leadership for Social Design and Management

Japan Science and Technology Agency

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Embryology,Anatomy

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