Bacteriophage T4 genome

被引:551
作者
Miller, ES
Kutter, E
Mosig, G
Arisaka, F
Kunisawa, T
Rüger, W
机构
[1] N Carolina State Univ, Dept Microbiol, Raleigh, NC 27696 USA
[2] Evergreen State Coll, Olympia, WA 98505 USA
[3] Vanderbilt Univ, Dept Sci Biol, Nashville, TN 37232 USA
[4] Tokyo Inst Technol, Dept Mol & Cellular Assembly, Yokohama, Kanagawa 2268501, Japan
[5] Tokyo Univ Sci, Dept Appl Biol Sci, Noda, Chiba 2788510, Japan
[6] Ruhr Univ Bochum, Fac Biol, D-44780 Bochum, Germany
关键词
SINGLE-STRANDED-DNA; COLI RNA-POLYMERASE; T4; ENDONUCLEASE-V; GENE; 32; PROTEIN; AMINO-ACID-SEQUENCE; GROUP-I INTRON; UVSY RECOMBINATION PROTEIN; THYMIDYLATE SYNTHASE GENE; PYRIMIDINE DIMER-DNA; GP45 SLIDING CLAMP;
D O I
10.1128/MMBR.67.1.86-156.2003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Phage T4 has provided countless contributions to the paradigms of genetics and biochemistry. Its complete genome sequence of 168,903 bp encodes about 300 gene products. T4 biology and its genomic sequence provide the best-understood model for modem functional genomics and proteomics. Variations on gene expression, including overlapping genes, internal translation initiation, spliced genes, translational bypassing, and RNA processing, alert us to the caveats of purely computational methods. The T4 transcriptional pattern reflects its dependence on the host RNA polymerase and the use of phage-encoded proteins that sequentially modify RNA polymerase; transcriptional activator proteins, a phage sigma factor, anti-sigma, and sigma decoy proteins also act to specify early, middle, and late promoter recognition. Posttranscriptional controls by T4 provide excellent systems for the study of RNA-dependent processes, particularly at the structural level. The redundancy of DNA replication and recombination systems of T4 reveals how phage and other genomes are stably replicated and repaired in different environments, providing insight into genome evolution and adaptations to new hosts and growth environments. Moreover, genomic sequence analysis has provided new insights into tail fiber variation, lysis, gene duplications, and membrane localization of proteins, while high-resolution structural determination of the "cell-puncturing device," combined with the three-dimensional image reconstruction of the baseplate, has revealed the mechanism of penetration during infection. Despite these advances, nearly 130 potential T4 genes remain uncharacterized. Current phage-sequencing initiatives are now revealing the similarities and differences among members of the T4 family, including those that infect bacteria other than Escherichia coli. T4 functional genomics will aid in the interpretation of these newly sequenced T4-related genomes and in broadening our understanding of the complex evolution and ecology of phages-the most abundant and among the most ancient biological entities on Earth.
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页码:86 / +
页数:72
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