Detection and subcellular localization of the turnip yellow mosaic virus 66K replication protein in infected cells

被引:75
作者
Prod'homme, D
Le Panse, S
Drugeon, G
Jupin, I
机构
[1] Univ Paris 06, Mol Virol Lab, F-75251 Paris 05, France
[2] Univ Paris 07, Mol Virol Lab, F-75251 Paris 05, France
[3] Univ Paris 06, Serv Commun Microscopie Elect, Inst Jacques Monod, CNRS,UMR 7592, F-75251 Paris 05, France
[4] Univ Paris 07, Serv Commun Microscopie Elect, Inst Jacques Monod, CNRS,UMR 7592, F-75251 Paris 05, France
关键词
viral replication; RdRp; transient accumulation; membrane vesicles; chloroplast envelope;
D O I
10.1006/viro.2000.0769
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Turnip yellow mosaic virus (TYMV) encodes a 206-kDa (206K) polyprotein with domains of methyltransferase, proteinase, NTPase/helicase, and RNA-dependent RNA polymerase (RdRp). In vitro, the 206K protein has been shown to undergo proteolytic processing, giving rise to the synthesis of 140-kDa (140K) and 66-kDa (66K) proteins, the latter comprising the RdRp protein domain. Antibodies were raised against the 66K protein and were used to detect the corresponding viral protein in infected cells; both leaf tissues and protoplasts were examined. The antiserum specifically recognized a protein of similar to 66 kDa, indicating that the cleavage observed in vitro is also functional in vivo. The 66K protein accumulates transiently during protoplast infection and localizes to cellular membrane fractions. Indirect immunoflorescence assays and electron microscopy of immunogold-decorated ultrathin sections of infected leaf tissue using anti-66K-specific antibody revealed labeling of membrane vesicles located at the chloroplast envelope. (C) 2001 Academic Press.
引用
收藏
页码:88 / 101
页数:14
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