Dysfunctionality of a tobacco mosaic virus movement protein mutant mimicking threonine 104 phosphorylation.

Summary, in English

Replication of tobacco mosaic virus (TMV) is connected with endoplasmic reticulum (ER)-associated membranes at early stages of infection. This study reports that TMV movement protein (MP)-specific protein kinases (PKs) associated with the ER of tobacco were capable of phosphorylating Thr104 in TMV MP. The MP-specific PKs with apparent molecular masses of about 45–50 kDa and 38 kDa were revealed by gel PK assays. Two types of mutations were introduced in TMV MP gene of wild-type TMV U1 genome to substitute Thr104 by neutral Ala or by negatively charged Asp. Mutation of Thr104 to Ala did not affect the size of necrotic lesions induced by the mutant virus in Nicotiana tabacum Xanthi nc. plants. Conversely, mutation of Thr to Asp mimicking Thr104 phosphorylation strongly inhibited cell-to-cell movement. The possible role of Thr104 phosphorylation in TMV MP function is discussed. © 2003 Society for General Microbiology

• Author: E M Karger; O Yu Frolova; N V Fedorova; L A Baratova; T V Ovchinnikova; P Susi; K Makinen; Lars Rönnstrand; Yu L Dorokhov; J G Atabekov
• Publishing year: 2003
• Language: English
• Pages: 32-727
• Publication/Series: Journal of General Virology
• Volume: 84
• Issue: Pt 3
• Full text: - 318 kB; Download statistics
• Links: http://dx.doi.org/10.1099/vir.0.18972-0
• Document type: Journal article
• Publisher: Microbiology Society
• Topic: Medicinal Chemistry
• Keywords: Comparative Study; Support; Amino Acid Substitution; Biological Transport; Non-U.S. Gov't; Viral Proteins: metabolism; U.S. Gov't; P.H.S.; Threonine: metabolism; Tobacco: virology; Tobacco Mosaic Virus: metabolism; Endoplasmic Reticulum: enzymology; Molecular Weight; Mutation; Phosphorylation; Protein Kinases: chemistry; Protein Kinases: metabolism
• Status: Published
• ISBN/ISSN/Other: ISSN: 1465-2099