Rig is a novel Ras-related protein and potential neural tumor suppressor

被引:48
作者
Ellis, CA
Vos, MD
Howell, H
Vallecorsa, T
Fults, DW
Clark, GJ
机构
[1] NCI, Dept Cell & Canc Biol, NIH, Rockville, MD 20850 USA
[2] Univ Utah, Sch Med, Dept Neurosurg, Salt Lake City, UT 84132 USA
[3] Huntsman Canc Inst, Salt Lake City, UT 84132 USA
关键词
D O I
10.1073/pnas.142193799
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Ras superfamily consists of a large group of monomeric GTPases demonstrating homology to Ras oncoproteins. Although structurally similar, Ras-superfamily proteins are functionally diverse. Whereas some members exhibit oncogenic properties, others may serve as tumor suppressors. We have identified a novel Ras-related protein that suppresses cell growth and have designated it Rig (Ras-related inhibitor of cell growth). Overexpression of Rig inhibited Ras-mediated cellular transformation and activation of downstream signaling in NIH 3T3 cells. rig mRNA is expressed at high levels in normal cardiac and neural tissue. However, Rig protein expression is frequently lost or down-regulated in neural tumor-derived cell lines and primary human neural tumors. Moreover, expression of exogenous Rig in human astrocytoma cells suppressed growth. Rig has a C-terminal CAAX motif that codes for posttranslational modification by both farnesyl and geranylgeranyl isoprenoid lipids. Consequently, Rig may play a role in the cellular response to farnesyl transferase inhibitors. Rig bears 63% overall sequence homology to a recently described Ras-family member Noey2, a tumor suppressor in breast and ovarian tissue. Therefore, Rig and Noey2 may represent a new subfamily of Ras-like tumor suppressors.
引用
收藏
页码:9876 / 9881
页数:6
相关论文
共 45 条
  • [1] A PUTATIVE MURINE ECOTROPIC RETROVIRUS RECEPTOR GENE ENCODES A MULTIPLE MEMBRANE-SPANNING PROTEIN AND CONFERS SUSCEPTIBILITY TO VIRUS-INFECTION
    ALBRITTON, LM
    TSENG, L
    SCADDEN, D
    CUNNINGHAM, JM
    [J]. CELL, 1989, 57 (04) : 659 - 666
  • [2] DNA hypermethylation in tumorigenesis - epigenetics joins genetics
    Baylin, SB
    Herman, JG
    [J]. TRENDS IN GENETICS, 2000, 16 (04) : 168 - 174
  • [3] BOS JL, 1997, BIOCHIM BIOPHYS ACTA, V1333, P19
  • [4] THE COOH-TERMINAL DOMAIN OF THE RAP1A (KREV-1) PROTEIN IS ISOPRENYLATED AND SUPPORTS TRANSFORMATION BY AN H-RAS-RAP1A CHIMERIC PROTEIN
    BUSS, JE
    QUILLIAM, LA
    KATO, K
    CASEY, PJ
    SOLSKI, PA
    WONG, G
    CLARK, R
    MCCORMICK, F
    BOKOCH, GM
    DER, CJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (03) : 1523 - 1530
  • [5] Increasing complexity of Ras signaling
    Campbell, SL
    Khosravi-Far, R
    Rossman, KL
    Clark, GJ
    Der, CJ
    [J]. ONCOGENE, 1998, 17 (11) : 1395 - 1413
  • [6] CHARDIN P, 1991, CANCER CELL-MON REV, V3, P117
  • [7] Clark GJ, 1997, J BIOL CHEM, V272, P10608
  • [8] CLARK GJ, 1995, METHOD ENZYMOL, V255, P395
  • [9] Collins VP, 1998, CANCER SURV, V32, P37
  • [10] COX AD, 1997, BIOCHIM BIOPHYS ACTA, V1333, P51