haracterization of a membrane protein (VP001L) from infectious spleen and kidney necrosis virus (ISKNV)

被引:5
作者
Xu, Xiaopeng [1 ]
Lu, Jing [2 ]
Lu, Qingxia [1 ]
Zhong, Hui [1 ]
Weng, Shaoping [1 ]
He, Jianguo [1 ]
机构
[1] Sun Yat Sen Univ, Sch Life Sci, State Key Lab Biocontrol, Guangzhou 510275, Peoples R China
[2] Chinese Acad Sci, GIBH, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
ISKNV; VP001L; membrane protein; cellular localization;
D O I
10.1007/s11262-007-0177-x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Infectious spleen and kidney necrosis virus (ISKNV) is the type species of megalocytivirus, Iridoviridae. A novel membrane protein corresponding to the first open reading frame (ORF001L) of ISKNV genome was identified. This 378-residue protein, termed the VP001L protein, has a high content of hydrophobic sequences and contains 10-11 putative transmembrane domains, indicating it may be a membrane protein. The VP001L mRNA start site was extended 433 bp upstream of the start codon and the temporal analysis showed that the VP001L gene was first transcribed at 8 h post-infection (h.p.i.). VP001L protein was detected on the plasma membrane of ISKNV infected cells by immunofluresence. In order to further investigate different transmembrane domains' influence on subcellular localization of VP001L, series of truncated or deleted mutants were constructed with GFP at the C terminus. The transfection results indicated that the second putative transmembrane domain played a determinative role in VP001L's membrane localization and the translocation of the first and third transmembrane domains depended on their interactions with the second one. Therefore, this novel VP001L protein is considered to serve as a model for analyzing the topology and roles of different hydrophobic regions in multi-transmembrane proteins.
引用
收藏
页码:157 / 167
页数:11
相关论文
共 63 条
[1]   Cotranslational membrane protein biogenesis at the endoplasmic reticulum [J].
Alder, NN ;
Johnson, AE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (22) :22787-22790
[2]  
[Anonymous], 1993, Biol. Chem. Hoppe Seyler, DOI DOI 10.1515/BCHM3.1993.374.1-6.143
[3]   Outbreaks of an iridovirus disease in maricultured large yellow croaker, Larimichthys crocea (Richardson), in China [J].
Chen, XH ;
Lin, KB ;
Wang, XW .
JOURNAL OF FISH DISEASES, 2003, 26 (10) :615-619
[4]   Identification of cytoplasmic residues of Sec61p involved in ribosome binding and cotranslational translocation [J].
Cheng, ZL ;
Jiang, Y ;
Mandon, EC ;
Gilmore, R .
JOURNAL OF CELL BIOLOGY, 2005, 168 (01) :67-77
[5]  
CHINCHAR VG, 2005, BALL VIRUS TAXONOMY, P145
[6]   Isolation and characterization of a pathogenic iridovirus from cultured grouper (Epinephelus sp.) in Taiwan [J].
Chou, HY ;
Hsu, CC ;
Peng, TY .
FISH PATHOLOGY, 1998, 33 (04) :201-206
[7]   INVESTIGATION OF OUTBREAKS OF A NOVEL DISEASE, SLEEPY GROUPER DISEASE, AFFECTING THE BROWN-SPOTTED GROUPER, EPINEPHELUS-TAUVINA FORSKAL [J].
CHUA, FHC ;
NG, ML ;
NG, KL ;
LOO, JJ ;
WEE, JY .
JOURNAL OF FISH DISEASES, 1994, 17 (04) :417-427
[8]  
CLAROS MG, 1994, COMPUT APPL BIOSCI, V10, P685
[9]  
Danayadol Y., 1996, AAHRI AQUATIC ANIMAL, V5, P6
[10]   ANALYSIS OF THE GENOME OF FISH LYMPHOCYSTIS DISEASE VIRUS ISOLATED DIRECTLY FROM EPIDERMAL TUMORS OF PLEURONECTES [J].
DARAI, G ;
ANDERS, K ;
KOCH, HG ;
DELIUS, H ;
GELDERBLOM, H ;
SAMALECOS, C ;
FLUGEL, RM .
VIROLOGY, 1983, 126 (02) :466-479