Nef-Induced Major Histocompatibility Complex Class I Down-Regulation Is Functionally Dissociated from Its Virion Incorporation, Enhancement of Viral Infectivity, and CD4 Down-Regulation

Author:

Akari Hirofumi1,Arold Stefan1,Fukumori Tomoharu1,Okazaki Toshiyuki1,Strebel Klaus2,Adachi Akio1

Affiliation:

1. Department of Virology, The University of Tokushima School of Medicine, Tokushima, Tokushima 770-8503, Japan,1 and

2. Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892-04402

Abstract

ABSTRACT The N-terminal alpha-helix domain of the human immunodeficiency virus type 1 (HIV-1) Nef protein plays important roles in enhancement of viral infectivity, virion incorporation of Nef, and the down-regulation of major histocompatibility complex class I (MHC-I) expression on cell surfaces. In this study, we demonstrated that Met 20 in the alpha-helix domain was indispensable for the ability of Nef to modulate MHC-I expression but not for other events. We also showed that Met 20 was unnecessary for the down-regulation of CD4. These findings indicate that the region governing MHC-I down-regulation is proximate in the alpha-helix domain but is dissociated functionally from that determining enhancement of viral infectivity, virion incorporation of Nef, and CD4 down-regulation.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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