期刊文献+

LRP16编码蛋白的信息学分析及亚细胞定位研究 被引量:25

Bioinformatic analysis and subcellular distribution of LRP16 protein
下载PDF
导出
摘要 目的 :探讨LRP16基因编码蛋白的基本生物学特征及其在真核细胞中的分布。方法 :以Internet为操作平台、以国际公共生物数据库为实验材料、应用生物学软件为研究工具对LRP16编码蛋白进行了全方位的生物信息学分析。在此基础上 ,将该基因的编码序列重组到pEGFP N1真核表达中 ,融合在绿色荧光蛋白 (GFP)的N端转染HeLa细胞 ,激光共聚焦显微镜观察荧光分布。结果 :LRP16编码产物主要与一些RNA病毒产生的与核酸结合的非结构蛋白有较高相似性 ,含有与功能未知的Motif:Hismacro、DUF2 7、A1pp相似的结构域。激光共聚焦显微镜扫描发现GFP分布于细胞核内。结论 :LRP16基因编码一种起源古老、进化缓慢的核蛋白因子 。 Objective:To explore the basic biologically characteristics and the intracellular distribution of LRP16 protein cloned by us. Methods: The primarily structural sequence of LRP16 protein was thoroughly analysed using public databases provided by Internet and biological softwares. On the basis of bioinformatical hint, LRP16 was recombined in pEGFP-N1 vector, inserting in the N-termini of GFP(green fluorescence protein),and then transferred into HeLa cell line. Fluorescent signal was detected using confocal.Results: LRP16 protein has relatively higher similarity with some non-structural proteins coded by RNA virus, which are nucleic acid binding proteins. In addition,LRP16 has similar motif to the function-unknown Hismacro,DUF27 and A1pp.The green fluorescence was inspired from cellular nucleolus. Conclusion:LRP16 protein is a nuclear factor, which originated prior to the appearance of eukaryotes, and its evolution velocity is relatively slow and its motif has retained the basic function of ancestral gene. The motif feature provide a clue that LRP16 protein maybe play an important function in cellular multiple behavior.
出处 《军医进修学院学报》 CAS 2002年第4期277-279,共3页 Academic Journal of Pla Postgraduate Medical School
基金 国家自然科学基金资助项目 ( 39970 82 )
关键词 亚细胞定位 LRP16蛋白 NF-ΚΒ 医学信息学 蛋白质公共数据库 LRP16 protein NF-kappa B medical informatics
  • 相关文献

参考文献8

二级参考文献23

  • 11,Caligiuri MA,Strout MP,Gilliand DG.Molecular biology of acute myeloid leukemia[J].Semin Oncol,1997,24(1)32-44.
  • 22,Sambrook J,Fritsch EF,Maniatis T.Molecular Cloning:A laboratory manual[C].Cold Spring Harbor Lab Press:Plainview NY,1989.
  • 33,Okazaki Y.A linkage map of the mouse using an expanded production system of the restriction landmark genomic scanning (RLGS Ver 1.8)[J].Biochem Biophys Res Comm,1995,205(3):1922-1928.
  • 44,Costello JF,Plass C,Arap W et al.Cyclin dependent kinase 6 (CDK6) amplification in human glioblastomas identified using two-dimensional separation of genomic DNA[J].Cancer Res,1997,57(7):1250-1254.
  • 55,Smiraglia DJ,Fruhwald MC,Costello JF et al.A new tool for the rapid cloning of amplified and hypermethylated human DNA sequences from restriction landmark genome scanning gels[J].Genomics,1999,58(3):254-262.
  • 66,Newell W,Beck S,Lehrach H et al.Estimation of distances and map construction using radiation hybrids[J].Genome Res,1998,8(5):493-508.
  • 77,Plass C,Yu F,Yu L et al.Restriction landmark genome scanning for aberrant methylation in primary refractory and relapsed acute myeloid leukemia;invilvement of the WIT-1 gene[J].Oncogene,1999,18(20):3159-3165.
  • 88,Schaefer BC.Revolutions in rapid amplification of cDNA ends:new strategies for polymerase chain reaction cloning of full-length cDNA ends[J].Anal Biochem,1995,227(2):255-273.
  • 99,Baylin SB,Herman JG,Graff JR.Alterations in methylation:A fundamental aspect of neoplasia[J].Adv Cancer Res,1998,72:141-196.
  • 1010,Issa JPJ,Baylin S B,Herman JG.DNA methylation changes in hematologic malignancies:biologic and clinical implication[J].Leukemia,1997,11(Suppl):S7-S11.

共引文献90

同被引文献90

引证文献25

二级引证文献91

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