Mutation analysis of the coding sequences of MEK-1 and MEK-2 genes in human lung cancer cell lines

被引:20
作者
Bansal, A
Ramirez, RD
Minna, JD
机构
[1] UNIV TEXAS,SW MED CTR,HAMON CTR THERAPEUT ONCOL RES,DALLAS,TX 75235
[2] UNIV TEXAS,SW MED CTR,DEPT INTERNAL MED,DALLAS,TX 75235
[3] UNIV TEXAS,SW MED CTR,DEPT PHARMACOL,DALLAS,TX 75235
关键词
MAP kinase pathway; MEK; human lung cancer;
D O I
10.1038/sj.onc.1200947
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
Recently, constitutively active mutants of MEK (MAP/ ERI( kinase) were shown to be capable of transforming cells to tumorigenicity suggesting that MEK can function as a dominant oncogene and potentially play a role in human carcinogenesis, Human lung cancer cells exhibit mutations in other components of the MAP kinase signaling pathway such as the Her-2/neu and ras oncogenes. Thus, the coding sequences of both MEK-1 and MEK-2 cDNAs from human lung cancer cell lines were screened by single strand conformation polymorphism analysis and DNA sequencing for alterations in these two genes. In 37 lung cancer cell lines we found: an allelic variant in MEK-1 cDNA, nt 783 G-->A, (no amino acid change); a MEK-2 cDNA change (nt 977 C-->T mutation leading to 298 Pro-->Leu change); a MEK-2 cDNA change nt 537 C-->T (no amino acid change); and a frequent MEK-2 cDNA germline polymorphism nt 744, A-->C (no amino acid change) with an allele frequency of 0.5 for each form. These results suggest that mutations in the MEK-1 and MEK-2 gene occur at a very low frequency in human lung cancer.
引用
收藏
页码:1231 / 1234
页数:4
相关论文
共 26 条
  • [1] MAMMALIAN MITOGEN-ACTIVATED PROTEIN-KINASE KINASE KINASE (MEKK) CAN FUNCTION IN A YEAST MITOGEN-ACTIVATED PROTEIN-KINASE PATHWAY DOWNSTREAM OF PROTEIN-KINASE-C
    BLUMER, KJ
    JOHNSON, GL
    LANGECARTER, CA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (11) : 4925 - 4929
  • [2] ERKS - A FAMILY OF PROTEIN-SERINE THREONINE KINASES THAT ARE ACTIVATED AND TYROSINE PHOSPHORYLATED IN RESPONSE TO INSULIN AND NGF
    BOULTON, TG
    NYE, SH
    ROBBINS, DJ
    IP, NY
    RADZIEJEWSKA, E
    MORGENBESSER, SD
    DEPINHO, RA
    PANAYOTATOS, N
    COBB, MH
    YANCOPOULOS, GD
    [J]. CELL, 1991, 65 (04) : 663 - 675
  • [3] BRUNET A, 1994, ONCOGENE, V9, P3379
  • [4] EXTRACELLULAR SIGNAL-REGULATED KINASES - ERKS IN PROGRESS
    COBB, MH
    BOULTON, TG
    ROBBINS, DJ
    [J]. CELL REGULATION, 1991, 2 (12): : 965 - 978
  • [5] COBB MH, 1994, SEMIN CANCER BIOL, V5, P261
  • [6] ACTIVATION OF MAP KINASE KINASE IS NECESSARY AND SUFFICIENT FOR PC12 DIFFERENTIATION AND FOR TRANSFORMATION OF NIH 3T3 CELLS
    COWLEY, S
    PATERSON, H
    KEMP, P
    MARSHALL, CJ
    [J]. CELL, 1994, 77 (06) : 841 - 852
  • [7] THE PRIMARY STRUCTURE OF MEK, A PROTEIN-KINASE THAT PHOSPHORYLATES THE ERK GENE-PRODUCT
    CREWS, CM
    ALESSANDRINI, A
    ERIKSON, RL
    [J]. SCIENCE, 1992, 258 (5081) : 478 - 480
  • [8] DAVIS RJ, 1993, J BIOL CHEM, V268, P14553
  • [9] MOLECULAR-GENETIC CHANGES FOUND IN HUMAN LUNG-CANCER AND ITS PRECURSOR LESIONS
    GAZDAR, AF
    BADER, S
    HUNG, J
    KISHIMOTO, Y
    SEKIDO, Y
    SUGIO, K
    VIRMANI, A
    FLEMING, J
    CARBONE, DP
    MINNA, JD
    [J]. COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1994, 59 : 565 - 572
  • [10] MULTIPLE MECHANISMS FOR TRANSCRIPTIONAL REGULATION OF THE MYC GENE FAMILY IN SMALL-CELL LUNG-CANCER
    KRYSTAL, G
    BIRRER, M
    WAY, J
    NAU, M
    SAUSVILLE, E
    THOMPSON, C
    MINNA, J
    BATTEY, J
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (08) : 3373 - 3381