期刊文献+

铜绿假单胞菌噬菌体PaP3基因组的初步注释 被引量:7

Primary annotation of gnome of Pseudomonas aeruginosa phage PaP3
下载PDF
导出
摘要 目的 对已完成测序的铜绿假单胞菌噬菌体PaP3基因组进行初步注释。方法 利用生物信息学软件和网上工具对噬菌体PaP3进行开发阅读框 (Openreadingframe ,ORFs)检索 ;编码序列鉴定 ;对公共数据库进行BLAST查询 ,分析基因的可能功能 ;对存在高度同源性序列的推定蛋白进行多重序列比对和系统发生树分析。结果 利用生物信息学软件在PaP3基因组中检索到2 5 2个大于 10 0bp的ORFs ,其中有 69个ORFs可确认为推定基因 ;核苷酸对核苷酸的BLASTn分析未发现有意义的同源性核苷酸序列 ;核苷酸对蛋白质的BLASTx分析共发现了 4个在公共数据库中有高度同源性序列的ORFs ,根据其同源性蛋白的功能推定ORF13 0 5 2 14 761编码产物为引物酶 解旋酶 ,ORF40 2 80 4172 8编码产物为末端酶大亚单位 ,ORF4172 8 42 2 2 5编码产物为溶菌酶 ,ORF16912 185 49编码产物为DNA聚合酶 ;绘制出了上述这四种蛋白的系统发生树。结论 噬菌体PaP3具有 2 5 2个大于 10 0bp的ORFs ,其中 69个为推定基因 ,有 4个推定基因的功能被确认为分别编码引物酶 解旋酶 ,末端酶大亚单位 ,溶菌酶及DNA聚合酶。 Objective To primarily annotate the genome of Pseudomonas areuginosa phage PaP3 after its sequencing. Methods The primary annotation items of the genome of the bacteriophage PaP3, including identification of open reading frames (ORFs) and coding sequence, BLAST query of each ORF, multiple alignment of homology sequences and phylogenetic analysis, were carried out with bioinformatic software and analysis tool in internet. Results A total of 252 of >100 bp ORFs and 69 coding sequences were detected in the phage PaP3 genome. BLASTn did not find any homology sequence, but BLASTx found out 4 high homology sequences, that is, ORF13052-14761 coding for primase/helicase, ORF40280 41728 for terminase large subunit, ORF41728 42225 for lysozyme and ORF16912 18549 for DNA polymerase. Multiple alignment of those 4 homology sequences was completed and their phylogenetic trees were obtained. Conclusion The 252 > 100 bp ORFs and 69 coding sequences are detected, and 4 functional genes, coding for primase/helicase, terminase large subunit, lysozyme and DNA polymerase respectively, are predicated in the phage PaP3 genome.
出处 《第三军医大学学报》 CAS CSCD 北大核心 2002年第4期381-384,共4页 Journal of Third Military Medical University
基金 国家自然科学基金资助项目 ( 30 0 70 0 37) 重庆市攻关课题资助项目 ( 2 0 0 0 )
关键词 噬菌体 基因组 一级注释 铜绿假单胞菌 bacteriophage PaP3 genome annotation
  • 相关文献

参考文献1

二级参考文献3

共引文献8

同被引文献49

  • 1申晓冬,胡福泉,李明,胡晓梅,周莹冰,张克斌.噬菌体PaP3推定基因tls核酸内切酶活性的初步验证[J].解放军医学杂志,2006,31(3):196-198. 被引量:2
  • 2申晓冬,张克斌,李明,周莹冰,蹇锐,胡晓梅,陈志瑾,饶贤才,胡福泉.铜绿假单胞菌噬菌体PaP3末端酶大亚单位DNA结合能力的测定[J].第三军医大学学报,2006,28(22):2205-2208. 被引量:2
  • 3Becker A, Murialdo H. Bacteriophage lambda DNA: the beginning of the end[J]. J Bacteriol, 1990,172(6) :2819 -2824.
  • 4Smith D E, Tans S J, Smith S B, et al. The bacteriophage straight phi29 portal motor can package DNA against a large internal force [ J]. Nature, 2001, 413(6857) : 748 752.
  • 5Bogner E. Human cytomegalovirus terminase as a target for antiviral chemotherapy[J]. Rev Med Virol, 2002, 12(2): 115 -127.
  • 6Cue D, Feiss M. Genetic analysis of cosB, the binding site for terminase, the DNA packaging enzyme of bacteriophage lambda[ J]. J Mol Biol, 1992, 228(1) :58 -71.
  • 7Gottesman M E, Weisberg R A. Little lambda, who made thee? [ J]. Microbiol Mol Biol Rev, 2004, 68(4): 796-813.
  • 8de-Beer T, Fang J, Ortega M, et al. Insights into specific DNA recognition during the assembly of a viral genome packaging machine [J]. Mol Cell, 2002, 9(5):981-991.
  • 9Hwang Y, Felss M. Mutations affecting Lysine-35 of gpNul, the small subunit of bacteriophage lambda terminase, alter the strength and specificity of holoterminase interactions with DNA[J]. Virology, 1997, 231(2): 216-230.
  • 10Kondabagil K R, Rao V B. A critical coiled coil motif in the small terminase, gp16, from bacteriophage T4: insights into DNA packaging initiation and assembly of packaging motor [ J ]. J Mol Biol, 2006, 358(1): 67-82.

引证文献7

二级引证文献7

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部