Identification of cellular proteins interacting with equine infectious anemia virus S2 protein

被引:11
作者
Covaleda, Lina [1 ]
Gno, Bich-Ty [1 ]
Fuller, Fredrick J. [2 ]
Payne, Susan L. [1 ]
机构
[1] Texas A&M Univ, Texas Vet Med Coll, Dept Pathobiol, College Stn, TX 77843 USA
[2] N Carolina State Univ, Coll Vet Med, Dept Publ Hlth & Pathobiol, Raleigh, NC 27606 USA
关键词
Equine infectious anemia virus; EIAV; OS-9; PSMC3; TBP-1; Lentivirus; TAT-BINDING PROTEIN-1; ENDOPLASMIC-RETICULUM; VIRAL REPLICATION; 26S PROTEASOME; OS-9; GENE; LOCALIZATION; EXPRESSION; TRANSLATION; FAMILY;
D O I
10.1016/j.virusres.2010.04.007
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The macrophage-tropic lentivirus, equine infectious anemia virus (EIAV), encodes the small auxiliary protein S2 from a short open reading frame that overlaps the amino terminus of env EIAV S2 is dispensable for virus replication in cultured cells but is required for disease production. S2 is approximately 7 kDa and has no overall amino acid sequence homology to other cellular or viral proteins. Therefore it is likely that S2 plays a role as an adaptor protein. To further investigate S2 function we performed a yeast-2-hybrid screen to identify cellular proteins that interact with EIAV S2. The screen identified two human cellular proteins, amplified in osteosarcoma (OS-9) and proteasome 26S ATPase subunit 3 (PSMC3) that interact with S2. The equine homologues of these proteins were cloned and their interactions with S2 confirmed using co-immunoprecipitation assays. We identified two OS-9 isoforms that interact with S2 and a third splice variant that does not, indicating a region of OS-9 apparently required for the S2 interaction. The roles of these cellular proteins during EIAV infection have not been determined. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:235 / 239
页数:5
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