期刊文献+

PiggyBac转座子:人类基因编码研究的新工具 被引量:3

PiggyBac transposon vectors: The new tools of the human gene encoding
在线阅读 下载PDF
导出
摘要 转座子是一种不依赖于同源性重组即可在宿主基因组中发生基因座位置改变的DNA片段。PiggyBac(PB)转座子是一种可移动的遗传元素,并通过"剪切-黏贴"机制在有效载体和染色体之间调换。在换位过程中,PB转座子识别具体转座子的反向末端重复序列(inverted terminal repeat sequences,ITRS)位于转座子载体的2端,有效地移动原来位置的内容,并整合到TTAA染色体。PB转座子系统强大的活动使在PB载体上位于2个ITRS之间的基因容易地动员到靶基因。PB转座子因其高转座活性,转座安全、稳定与无痕移除的特性而备受关注,在分子医学研究中有较好的应用前景。针对其特性,PiggyBac转座子可被用于基因转移载体、癌基因筛选工具和基因治疗的载体。文中就其在基因编码研究中的应用作一综述。 A transposon is a DNA segment which can change its relative position within the genome of a cell. The PiggyBac (PB) transposon is a mobile genetic element that efficiently transposes between vectors and chromosomes via a "cut and paste" mechanism. During the transposition, the PB transposase recognizes transposon-specific inverted terminal repeat sequences (ITRs) located on both ends of the transposon vector and efficiently moves the contents from the original sites and efficiently integrates them into TTAA chromosomal sites. PiggyBac has drawn much attention because of its transposition efficiency, safety and stability. Due to its priorities, PiggyBac can be used as a new genetic vehicle, a new tool for oncogene screening and a new method for gene therapy. PiggyBac has created a new outlook for molecular medicine.
出处 《医学研究生学报》 CAS 北大核心 2014年第2期199-202,共4页 Journal of Medical Postgraduates
基金 国家自然科学基金(81272260) 江苏省六大人才高峰基金(BK2009284)
关键词 PIGGYBAC 转座子 转基因 PiggyBac Transposon Transgene
作者简介 南京军区南京总医院肿瘤内科医学博士
  • 相关文献

参考文献21

二级参考文献79

  • 1李永文,姚毅冰,万海粟,周清华.“睡美人”转座子及其在肿瘤研究中的应用[J].中国肺癌杂志,2008,11(6):816-820. 被引量:1
  • 2曹五七,谢林,童海燕.生物基因组中的转座因子[J].四川农业大学学报,1994,12(1):149-152. 被引量:2
  • 31,OBrochta D A,Atkinson P W.Transposable elements and gene transformation in non-dnosophilid insects.Insect Biochem.Molecular.Biol,1996,26(8~9):739~753
  • 42,Lobo N,Li X,Fraser M J.Transposition of the piggBac element in embryos of Drosophila melanogaster,Aedes aegypti and Trichoplusia ni.Mol Gen Genetic,1999,(261):803~810
  • 53,Elick T A,Bauser C A,Fraser M J.Excision of the piggBac transposable element in vitro is a precise event that is enhanced by the expression of its enconded transposase.Genetica,1996,(98):33~41
  • 64,Bauser C A,Elick T A,Fraser M J.Proteins from nuclear extracts of two lepidopteran cell lines recognize the ends of TTAA-specific ttransposons piggyBac and tagalong.Insect Mol Biol,1999,8(2):223~230
  • 75,Elick T A,Lobo N,Fraser M J.Analysis of cis-acting DNA elements required for piggyBac transposable element excision.Mol Gen Genetic,1997,(255):605~610
  • 86,Cary L C,Goebel M,Gcorsaro B,et al.Transposon mutagenesis of Baculoviruses:Analysis of Trichoplusia ni transposon IFP2 insertions within the FP-locus of nuclear polyhedrosis viruses.Virology,1989,(172):156~169
  • 97,Fraser M J,Cary L,Boonvisudhi K,et al.Assay for movement of the lepidopteran transposon IFP2 in insect cells using a baculovirus genome as a target DNA.Virolobgy,1995,(211):397~407
  • 108,Fraser M J,Ciszczon T,Elick T.et al.Precise excision of TTAA-specific lepidopteran transposons TFP3 and IFP2 from the baculovirus genome in cell lines from two species of lepidoptera.J.Insect Mol.Bio.,1996,(5):141~151

共引文献10

同被引文献28

引证文献3

二级引证文献2

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