CREB-binding protein transcription activation domain for enhanced transgene expression by a positive feedback system

被引:4
作者
Kanda, Genki [2 ]
Ochiai, Hiroshi [2 ]
Harashima, Hideyoshi [2 ,3 ]
Kamiya, Hiroyuki [1 ,2 ,3 ]
机构
[1] Ehime Univ, Grad Sch Sci & Engn, Matsuyama, Ehime 7908577, Japan
[2] Hokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Sapporo, Hokkaido 0600812, Japan
[3] Japan Sci & Technol, CREST, Tokyo, Japan
基金
日本学术振兴会;
关键词
Artificial transcription factor; Positive feedback system; CREB-binding protein; NONVIRAL GENE DELIVERY; CBP-INDUCED STIMULATION; IN-VIVO; KIX DOMAIN; P53; COACTIVATORS; P300/CBP; COFACTOR; MEDIATOR; THERAPY;
D O I
10.1016/j.jbiotec.2011.09.016
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The positive feedback system using a fusion protein of the sequence-specific DNA binding domain of yeast GAL4 and the transcription activation domain of herpes simplex virus VP16 (GAL4-VP16), in which GAL4-VP16 promotes its own expression as well as that of a reporter gene product, is useful for efficient transgene expression from plasmid DNA. In this study, the transcription activation domains of endogenous proteins, instead of VP16, were fused to the GAL4 DNA binding domain, and the positive feedback systems employing the novel fusion proteins were examined. Plasmid DNAs encoding the transcription factors were introduced into mouse Hepa 1-6 cells by electroporation and lipofection. Among CREB-binding protein (226-460), sterol regulatory element-binding protein-1 (1-140), p53 (1-70), and Med15 (9-73), the CREB-binding protein functioned efficiently as an activator. These results indicated that the GAL4-CREB-binding protein is useful for enhanced transgene expression by the positive feedback system. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:7 / 11
页数:5
相关论文
共 30 条
  • [1] An essential role for p300/CBP in the cellular response to hypoxia
    Arany, Z
    Huang, LE
    Eckner, R
    Bhattacharya, S
    Jiang, C
    Goldberg, MA
    Bunn, HF
    Livingston, DM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (23) : 12969 - 12973
  • [2] CBP-INDUCED STIMULATION OF C-FOS ACTIVITY IS ABROGATED BY E1A
    BANNISTER, AJ
    KOUZARIDES, T
    [J]. EMBO JOURNAL, 1995, 14 (19) : 4758 - 4762
  • [3] Bannister AJ, 1995, ONCOGENE, V11, P2509
  • [4] Cooperation of Stat2 and p300/CBP in signalling induced by interferon-alpha
    Bhattacharya, S
    Eckner, R
    Grossman, S
    Oldread, E
    Arany, Z
    DAndrea, A
    Livingston, DM
    [J]. NATURE, 1996, 383 (6598) : 344 - 347
  • [5] CBP as a transcriptional coactivator of c-Myb
    Dai, P
    Akimaru, H
    Tanaka, Y
    Hou, DX
    Yasukawa, T
    KaneiIshii, C
    Takahashi, T
    Ishii, S
    [J]. GENES & DEVELOPMENT, 1996, 10 (05) : 528 - 540
  • [6] Solution structure of the TAZ2 (CH3) domain of the transcriptional adaptor protein CBP
    De Guzman, RN
    Liu, HY
    Martinez-Yamout, M
    Dyson, HJ
    Wright, PE
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2000, 303 (02) : 243 - 253
  • [7] Demeneix B, 2004, CURR GENE THER, V4, P445
  • [8] Activator-Mediator binding regulates Mediator-cofactor interactions
    Ebmeier, Christopher C.
    Taatjes, Dylan J.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (25) : 11283 - 11288
  • [9] Nonviral gene delivery: What we know and what is next
    Gao, Xiang
    Kim, Keun-Sik
    Liu, Dexi
    [J]. AAPS JOURNAL, 2007, 9 (01) : E92 - E104
  • [10] Time course of gene expression after plasmid DNA gene transfer to the liver
    Herweijer, H
    Zhang, GF
    Subbotin, VM
    Budker, V
    Williams, P
    Wolff, JA
    [J]. JOURNAL OF GENE MEDICINE, 2001, 3 (03) : 280 - 291