Use of conditionally active Ras fusion proteins to study epidermal growth, differentiation, and neoplasia

被引:4
作者
Reuter, Jason A. [1 ]
Khavari, Paul A.
机构
[1] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Program Epithelial Biol, Stanford, CA 94305 USA
来源
REGULATORS AND EFFECTORS OF SMALL GTPASES: RAS FAMILY | 2006年 / 407卷
关键词
D O I
10.1016/S0076-6879(05)07054-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Ras proteins are membrane-bound GTPases that play a central role in transmitting signals from the cell surface to the nucleus and affect a wide array of biological processes. The overall cellular response to Ras activation varies with cell type, experimental conditions, signal strength, and signal duration. Most current studies, however, rely on expression of constitutively active protein to study Ras function and thus ignore temporal variables, as well as signal strength. These experiments may provide contradictory results, as seen in the case of epidermal keratinocytes. In this setting, Ras has been shown to both promote and oppose proliferation and differentiation. By providing control over timing, duration, and signal magnitude, conditional systems allow for more precise investigation of the role of Ras in carcinogenesis, as well as normal cellular physiology. This chapter focuses on use of a ligand-responsive steroid hormone receptor fusion of Ras, ER-Ras, to study aspects of cellular transformation in epidermal keratinocytes.
引用
收藏
页码:691 / 702
页数:12
相关论文
共 25 条
  • [1] PHENOL RED IN TISSUE-CULTURE MEDIA IS A WEAK ESTROGEN - IMPLICATIONS CONCERNING THE STUDY OF ESTROGEN-RESPONSIVE CELLS IN CULTURE
    BERTHOIS, Y
    KATZENELLENBOGEN, JA
    KATZENELLENBOGEN, BS
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (08) : 2496 - 2500
  • [2] Increasing complexity of Ras signaling
    Campbell, SL
    Khosravi-Far, R
    Rossman, KL
    Clark, GJ
    Der, CJ
    [J]. ONCOGENE, 1998, 17 (11) : 1395 - 1413
  • [3] Transglutaminase 1 delivery to lamellar ichthyosis keratinocytes
    Choate, KA
    Kinsella, TM
    Williams, ML
    Nolan, GP
    Khavari, PA
    [J]. HUMAN GENE THERAPY, 1996, 7 (18) : 2247 - 2253
  • [4] NF-κB blockade and oncogenic Ras trigger invasive human epidermal neoplasia
    Dajee, M
    Lazarov, M
    Zhang, JY
    Cai, T
    Green, CL
    Russell, AJ
    Marinkovich, MP
    Tao, SY
    Lin, Q
    Kubo, Y
    Khavari, PA
    [J]. NATURE, 2003, 421 (6923) : 639 - 643
  • [5] Epidermal Ras blockade demonstrates spatially localized Ras promotion of proliferation and inhibition of differentiation
    Dajee, M
    Tarutani, M
    Deng, H
    Cai, T
    Khavari, PA
    [J]. ONCOGENE, 2002, 21 (10) : 1527 - 1538
  • [6] High-efficiency gene transfer and pharmacologic selection of genetically engineered human keratinocytes
    Deng, H
    Choate, KA
    Lin, Q
    Khavari, PA
    [J]. BIOTECHNIQUES, 1998, 25 (02) : 274 - +
  • [7] Minimal Ras-binding domain of Raf1 can be used as an activation-specific probe for Ras
    deRooij, J
    Bos, JL
    [J]. ONCOGENE, 1997, 14 (05) : 623 - 625
  • [8] CHIMERAS OF MYC ONCOPROTEIN AND STEROID-RECEPTORS CAUSE HORMONE-DEPENDENT TRANSFORMATION OF CELLS
    EILERS, M
    PICARD, D
    YAMAMOTO, KR
    BISHOP, JM
    [J]. NATURE, 1989, 340 (6228) : 66 - 68
  • [9] Ewen M E, 2000, Prog Cell Cycle Res, V4, P1
  • [10] Episomal vectors rapidly and stably produce high-titer recombinant retrovirus
    Kinsella, TM
    Nolan, GP
    [J]. HUMAN GENE THERAPY, 1996, 7 (12) : 1405 - 1413