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Journal of Virology, March 2000, p. 2907-2912, Vol. 74, No. 6
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Nef-Induced Major Histocompatibility Complex Class
I Down-Regulation Is Functionally Dissociated from Its Virion
Incorporation, Enhancement of Viral Infectivity, and CD4
Down-Regulation
Hirofumi
Akari,1,*
Stefan
Arold,1,
Tomoharu
Fukumori,1
Toshiyuki
Okazaki,1
Klaus
Strebel,2 and
Akio
Adachi1
Department of Virology, The University of
Tokushima School of Medicine, Tokushima, Tokushima 770-8503, Japan,1 and Laboratory of Molecular
Microbiology, National Institute of Allergy and Infectious
Diseases, Bethesda, Maryland 20892-04402
Received 1 June 1999/Accepted 2 December 1999
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.
*
Corresponding author. Mailing address: Department of
Virology, The University of Tokushima School of Medicine, 3 Kuramoto, Tokushima, Tokushima 770-8503, Japan. Phone: 81-88-633-7079. Fax: 81-88-633-7080. E-mail:
akari{at}basic.med.tokushima-u.ac.jp.

Present address: Laboratory of Molecular Biophysics, Oxford, United
Kingdom.
Journal of Virology, March 2000, p. 2907-2912, Vol. 74, No. 6
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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