Effect of the Compaction and the Size of DNA on the Nuclear Transfer Efficiency after Microinjection in Synchronized Cells

被引:22
作者
Akita, Hidetaka [1 ]
Kurihara, Dai [1 ]
Schmeer, Marco [2 ]
Schleef, Martin [2 ]
Harashima, Hideyoshi [1 ]
机构
[1] Hokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Kita 12,Nishi 6, Sapporo, Hokkaido 0600812, Japan
[2] PlasmidFactory GmbH & Co KG, D-33607 Bielefeld, Germany
关键词
DNA; nuclear transfer; size; microinjection;
D O I
10.3390/pharmaceutics7020064
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The nuclear transfer process is one of the critical rate-limiting processes in transgene expression. In the present study, we report on the effect of compaction and the size of the DNA molecule on nuclear transfer efficiency by microinjection. A DNA/protamine complex-or variously-sized naked DNA molecules were injected into the cytoplasm or nucleus of synchronized HeLa cells. To evaluate the nuclear transfer process, a nuclear transfer score (NT score), calculated based on transgene expression after cytoplasmic microinjection divided by that after nuclear microinjection, was employed. The compaction of DNA with protamine decreased the NT score in comparison with the injection of naked DNA when the N/P ratio was increased to >2.0. Moreover, when naked DNA was microinjected, gene expression increased in parallel with the size of the DNA in the following order: minicircle DNA (MC07. CMV-EGFP; 2257 bp) > middle-sized plasmid DNA (pBS-EGFP; 3992 bp) > conventional plasmid DNA (pcDNA3.1-EGFP; 6172 bp), while the level of gene expression was quite comparable among them when the DNAs were injected into the nucleus. The above findings suggest that the intrinsic size of the DNA molecule is a major determinant for nuclear entry and that minicircle DNA has a great advantage in nuclear transfer.
引用
收藏
页码:64 / 73
页数:10
相关论文
共 30 条
[1]   Evaluation of the nuclear delivery and intra-nuclear transcription of plasmid DNA condensed with μ (mu) and NLS-μ by cytoplasmic and nuclear microinjection:: a comparative study with poly-L-lysine [J].
Akita, H ;
Tanimoto, M ;
Masuda, T ;
Kogure, K ;
Hama, S ;
Ninomiya, K ;
Futaki, S ;
Harashima, H .
JOURNAL OF GENE MEDICINE, 2006, 8 (02) :198-206
[2]  
Allen TD, 2000, J CELL SCI, V113, P1651
[3]   Transcription factor plasmid binding modulates microtubule interactions and intracellular trafficking during gene transfer [J].
Badding, M. A. ;
Vaughan, E. E. ;
Dean, D. A. .
GENE THERAPY, 2012, 19 (03) :338-346
[4]   Gradient of increasing affinity of importin β for nucleoporins along the pathway of nuclear import [J].
Ben-Efraim, I ;
Gerace, L .
JOURNAL OF CELL BIOLOGY, 2001, 152 (02) :411-417
[5]   Cell cycle dependence of gene transfer by lipoplex polyplex and recombinant adenovirus [J].
Brunner, S ;
Sauer, T ;
Carotta, S ;
Cotten, M ;
Saltik, M ;
Wagner, E .
GENE THERAPY, 2000, 7 (05) :401-407
[6]   Supramolecular structure and nuclear targeting efficiency determine the enhancement of transfection by modified polylysines [J].
Chan, CK ;
Senden, T ;
Jans, DA .
GENE THERAPY, 2000, 7 (19) :1690-1697
[7]   Enhancement of polylysine-mediated transferrinfection by nuclear localization sequences: Polylysine does not function as a nuclear localization sequence [J].
Chan, CK ;
Jans, DA .
HUMAN GENE THERAPY, 1999, 10 (10) :1695-1702
[8]   Import of plasmid DNA into the nucleus is sequence specific [J].
Dean, DA .
EXPERIMENTAL CELL RESEARCH, 1997, 230 (02) :293-302
[9]   Sequence requirements for plasmid nuclear import [J].
Dean, DA ;
Dean, BS ;
Muller, S ;
Smith, LC .
EXPERIMENTAL CELL RESEARCH, 1999, 253 (02) :713-722
[10]   Minicircle DNA vectors for gene therapy: advances and applications [J].
Gaspar, Vitor ;
de Melo-Diogo, Duarte ;
Costa, Elisabete ;
Moreira, Andre ;
Queiroz, Joao ;
Pichon, Chantal ;
Correia, Ilidio ;
Sousa, Fani .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2015, 15 (03) :353-379