Sea urchin insulator protects lentiviral vector from silencing by maintaining active chromatin structure

被引:43
作者
Hino, S
Fan, J
Taguwa, S
Akasaka, K
Matsuoka, M
机构
[1] Kyoto Univ, Inst Virus Res, Lab Virus Immunol, Kyoto 6068507, Japan
[2] Hiroshima Univ, Fac Sci, Grad Dept Gene Sci, Higashihiroshima 724, Japan
关键词
D O I
10.1038/sj.gt.3302227
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Suppressed expression of transgenes in vivo is the major obstacle in the gene therapy. For the long-term expression, we utilized a chromatin insulator from sea urchin arylsulfatase (Ars) gene locus ( Ars insulator, ArsI), which has been shown to epigenetically regulate gene expression across species. ArsI was able to prevent silencing of the transgene in a myeloid cell line, HL-60, and a murine embryonic stem cell line, CCE, in an orientation-dependent manner, but not in Huh-7, K562 and MCF-7 cells, indicating that the effect of ArsI on gene silencing was cell type dependent. Although anti-silencing effect of ArsI was almost equivalent to that of chicken beta-globin insulator, incorporation of ArsI into lentiviral vector had little effect on the virus titer compared with chicken beta-globin insulator. Clonal analysis of transduced HL-60 cells revealed that ArsI protects the lentiviral vector from position effects regardless of its orientation. Furthermore, chromatin immunoprecipitation assays revealed that a high acetylation level was observed in the promoter of the insulated vector, whereas that of ArsI was independent of its anti-silencing capacity. In addition to it having little deteriorative effect on the virus titer, the identified anti-silencing effect of ArsI suggested its possibility for application in gene therapy.
引用
收藏
页码:819 / 828
页数:10
相关论文
共 55 条
[1]  
Akasaka K, 1999, CELL MOL BIOL, V45, P555
[2]   The 5′ boundary of the human apolipoprotein B chromatin domain in intestinal cells [J].
Antes, TJ ;
Namciu, SJ ;
Fournier, REK ;
Levy-Wilson, B .
BIOCHEMISTRY, 2001, 40 (23) :6731-6742
[3]   Gene silencing as a threat to the success of gene therapy [J].
Bestor, TH .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (04) :409-411
[4]   Gene therapy for SCID - a complication after remarkable progress [J].
Buckley, RH .
LANCET, 2002, 360 (9341) :1185-1186
[5]   Tissue-specific nuclear architecture and gene expession regulated by SATB1 [J].
Cai, ST ;
Han, HJ ;
Kohwi-Shigematsu, T .
NATURE GENETICS, 2003, 34 (01) :42-51
[6]  
Chen SQ, 2001, GENETICS, V159, P1649
[7]   Characterization of the chicken beta-globin insulator [J].
Chung, JH ;
Bell, AC ;
Felsenfeld, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (02) :575-580
[8]   A 5' ELEMENT OF THE CHICKEN BETA-GLOBIN DOMAIN SERVES AS AN INSULATOR IN HUMAN ERYTHROID-CELLS AND PROTECTS AGAINST POSITION EFFECT IN DROSOPHILA [J].
CHUNG, JH ;
WHITELEY, M ;
FELSENFELD, G .
CELL, 1993, 74 (03) :505-514
[9]   TERMINAL DIFFERENTIATION OF HUMAN PROMYELOCYTIC LEUKEMIA-CELLS INDUCED BY DIMETHYL-SULFOXIDE AND OTHER POLAR COMPOUNDS [J].
COLLINS, SJ ;
RUSCETTI, FW ;
GALLAGHER, RE ;
GALLO, RC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (05) :2458-2462
[10]   Molecular mechanisms of gene silencing mediated by DNA methylation [J].
Curradi, M ;
Izzo, A ;
Badaracco, G ;
Landsberger, N .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (09) :3157-3173