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高效位点特异性链霉菌φC31噬菌体整合酶的研究进展 被引量:2

Advance on φC31 integrase Research as a High Efficiency Tool for Site-Special Integation
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摘要 链霉菌φC31噬菌体整合酶(φC31-int)属于位点特异性重组酶的解离酶/转化酶系,该家族催化机制由丝氨酸介导,能识别噬菌体附着位点(attP)和宿主基因组上的细菌附着位点(attB),介导同源序列之间的位点特异性重组。实验证实,φC31-int是一种高效位点特异性整合工具酶,与其他整合策略相比,具有集高效和安全于一体的优点,通过介导位点特异性整合,将外源基因特异地整合到宿主基因组,使目的基因得以持续、高效的表达,并且具有DNA容量方面的优势。随着研究的深入,人们对φC31-int介导整合作用机制和影响因素有了进一步的认识。通过一系列成功应用φC31-int进行的基因治疗的动物学实验,为今后如何利用非病毒载体系统进行基因治疗及转基因动物模型的建立提供了一种新的选择。 φC31 integrase(φC31-int) belongs to the serine recombinase family that can catalyses the recombination reaction between the phage attachment site(attP) and the bacterial attachment site(attB). Studies prove that φC31-int is a valuable site-special integration tool enzyme because of its efficiency and safety. This integrase can perform an site-special chromosomal integration of aimed DNA into host genomes that results in long-term and efficient transgene expression, which also has the DNA capacity dominance. With further study, researchers know more about the mechanism and influ- ence factors on the integration reaction mediated by φC31-int and serial successful animal gene therapy studies by using φC31-int suggest the possible utility of nonvirus vectors as φC31-int for gene therapy and constructing transgene animal model.
出处 《生物技术通讯》 CAS 2007年第6期1036-1038,共3页 Letters in Biotechnology
关键词 噬菌体整合酶 位点特异性整合 基因治疗 φC31 integrase site-special integration gene therapy
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参考文献17

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二级参考文献6

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共引文献1

同被引文献109

  • 1盛卫忠,沈坤堂,秦新裕.应用整合酶ΦC31治疗1型糖尿病的实验研究[J].中国临床医学,2004,11(3):397-399. 被引量:2
  • 2徐焕宇,马晴雯.φC31整合酶与生物医学[J].医学分子生物学杂志,2007,4(4):339-342. 被引量:2
  • 3Woodard LE,Hillman RT,Keravala A,Lee S,Calos MP.Effect of nuclear localization and hydrodynamic delivery-induced cell division on φC31 integrase activityNLS addition,cell division,and φC31 integrase.Gene Ther,2010,17(2):217-226.
  • 4Bischof J,Maeda RK,Hediger M,Karch F,Basler K.An optimized transgenesis system for Drosophila using germ-line-specific φC31 integrases.Proc Natl Acad Sci U SA,2007,104(9):3312-3317.
  • 5Chen JZ,Ji CN,Xu GL,Pang RY,Yao JH,Zhu HZ,Xue JL,Jia W.DAXX interacts with phage φC31 integrase and inhibits recombination.Nucleic Acids Res,2006,34(21):6298-6304.
  • 6Wang BY,Xu GL,Zhou CH,Tian L,Xue JL,Chen JZ,Jia W.φC31 integrase interacts with TTRAP and inhibits NFκB activation.Mol Biol Rep,2010,37(6):2809-2816.
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  • 8Nishiumi F,Sone T,Kishine H,Thyagarajan B,Kogure T,Miyawaki A,Chesnut JD,Imamoto F.Simultaneous single cell stable expression of 2-4 cDNAs in HeLaS3 using φC31integrase system.Cell Struct Funct,2009,34(1):47-59.
  • 9Venken KJT,He YC,Hoskins RA,Bellen HJ.P[acman]:a BAC transgenic platform for targeted insertion of large DNA fragments in D.melanogaster.Science,2006,314(5806):1747-1751.
  • 10Chalberg TW,Portlock JL,Olivares EC,Thyagarajan B,Kirby PJ,Hillman RT,Hoelters J,Calos MP.Integration specificity of phage φC31 integrase in the human genome.J Mol Biol,2006,357(1):28-48.

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