Identification of Herpes TATT-binding protein

被引:47
作者
Wyrwicz, Lucjan S.
Rychlewski, Leszek
机构
[1] BioInfoBank Inst, PL-60744 Poznan, Poland
[2] Marie Sklodowska Curie Mem Canc Ctr, Dept Gastroenterol, PL-02781 Warsaw, Poland
[3] Inst Oncol, PL-02781 Warsaw, Poland
[4] Adam Mickiewicz Univ Poznan, Fac Phys, PL-61614 Poznan, Poland
关键词
Herpesviridae; regulation of transcription; promoter; protein structure prediction; bioinformatics;
D O I
10.1016/j.antiviral.2007.03.002
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The regulation of viral gene expression is a compilation of virus and host factors influencing the transcription machinery. In Epstein-Barr Virus (EBV) a distinct regulatory element utilizing the TATT-box was described. The motif is present in promoters of lytic cycle genes and resembles a crucial host genome motif (TATA-box). Since the binding specificity of eukaryotic proteins recognizing TATA-box (TBP) was determined and no specific preference for interaction with TATT motif was found, we performed a genome-wide fold recognition search to identify viral proteins potentially recognizing the TATT-box. By applying profile-profile comparisons and homology-based protein structure prediction we identified a protein of unknown function from Gammaherpesvirinae (BcRF1 of EBV) and their Betaherpesvirinae homologs (UL87 of CMV) as proteins encoding TBP fold. Although overall sequence identity is very low (circa 10%), the saddle-like fold and presence of important residues on a surface of DNA-protein interface marked both proteins as distantly related to TBP and permitted the characterization of a putative molecular basis of selective recognition of TATT-motif by BcRF1. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:167 / 172
页数:6
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