Identification of the Nef-associated kinase as p21-activated kinase 2

被引:117
作者
Renkema, GH
Manninen, A
Mann, DA
Harris, M
Saksela, K [1 ]
机构
[1] Univ Tampere, Inst Med Technol, FIN-33101 Tampere, Finland
[2] Southampton Gen Hosp, Southampton SO9 4XY, Hants, England
[3] Univ Leeds, Sch Biochem & Mol Biol, Div Microbiol, Leeds, W Yorkshire, England
[4] Tampere Univ Hosp, Dept Clin Chem, FIN-33521 Tampere, Finland
关键词
D O I
10.1016/S0960-9822(00)80086-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Nef protein of primate immunodeficiency viruses plays an important role in the pathogenesis of acquired immunodeficiency syndrome (AIDS) [1,2]. The interaction of Nef with the Nef-associated kinase (NAK) is one of the most conserved properties of different human and simian immunodeficiency virus (HIV and SIV) Nef alleles. The role of NAK association is currently not known but it has been implicated in enhanced viral infectivity in cell culture and in disease progression in SIV-infected macaques [3]. Previous studies have indicated that NAK shares many features with the p21-activated kinases (PAKs) [3], but the molecular identity of NAK has remained unknown. We have generated specific antisera against PAKs 1-3, and expressed these kinases individually as epitope-tagged proteins. By using these reagents in experiments involving partial proteolytic mapping, and exploiting the unique ability of PAK2 to serve as a caspase substrate, we have positively identified NAK as PAK2. Interestingly, although ectopic PAK2 overexpression efficiently replaced endogenous PAK2 from the complex with Nef, the total Nef-associated PAK2 activity was not increased, indicating the abundance of another cellular factor(s) as the limiting factor in Nef-PAK2 complex formation. Identification of NAK as PAK2 should now facilitate elucidation of its role as a mediator of the pathogenic effects of Nef.
引用
收藏
页码:1407 / 1410
页数:4
相关论文
共 15 条
[1]   Interaction of the Nck adapter protein with p21-activated kinase (PAK1) [J].
Bokoch, GM ;
Wang, Y ;
Bohl, BP ;
Sells, MA ;
Quilliam, LA ;
Knaus, UG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (42) :25746-25749
[2]   Caspases: the executioners of apoptosis [J].
Cohen, GM .
BIOCHEMICAL JOURNAL, 1997, 326 :1-16
[3]   Multisite autophosphorylation of p21-activated protein kinase γ-PAK as a function of activation [J].
Gatti, A ;
Huang, ZD ;
Tuazon, PT ;
Traugh, JA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (12) :8022-8028
[4]   IMPORTANCE OF THE NEF GENE FOR MAINTENANCE OF HIGH VIRUS LOADS AND FOR DEVELOPMENT OF AIDS [J].
KESTLER, HW ;
RINGLER, DJ ;
MORI, K ;
PANICALI, DL ;
SEHGAL, PK ;
DANIEL, MD ;
DESROSIERS, RC .
CELL, 1991, 65 (04) :651-662
[5]   BRIEF REPORT - ABSENCE OF INTACT NEF SEQUENCES IN A LONG-TERM SURVIVOR WITH NONPROGRESSIVE HIV-1 INFECTION [J].
KIRCHHOFF, F ;
GREENOUGH, TC ;
BRETTLER, DB ;
SULLIVAN, JL ;
DESROSIERS, RC .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (04) :228-232
[6]   The p21Rac/Cdc42-activated kinases (PAKs) [J].
Knaus, UG ;
Bokoch, GM .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1998, 30 (08) :857-862
[7]   Activation of Pak by membrane localization mediated by an SH3 domain from the adaptor protein Nck [J].
Lu, WG ;
Katz, S ;
Gupta, R ;
Mayer, BJ .
CURRENT BIOLOGY, 1997, 7 (02) :85-94
[8]   CDC42 and Rac1 are implicated in the activation of the Nef-associated kinase and replication of HIV-1 [J].
Lu, XB ;
Wu, XN ;
Plemenitas, A ;
Yu, HF ;
Sawai, ET ;
Abo, A ;
Peterlin, BM .
CURRENT BIOLOGY, 1996, 6 (12) :1677-1684
[9]   SH3-domain binding function of HIV-1 Nef is required for association with a PAK-related kinase [J].
Manninen, A ;
Hiipakka, M ;
Vihinen, M ;
Lu, WG ;
Mayer, BJ ;
Saksela, K .
VIROLOGY, 1998, 250 (02) :273-282
[10]   Human immunodeficiency virus type 1 Nef associates with a member of the p21-activated kinase family [J].
Nunn, MF ;
Marsh, JW .
JOURNAL OF VIROLOGY, 1996, 70 (09) :6157-6161