Positional cloning of ZNF217 and NABC1:: Genes amplified at 20q13.2 and overexpressed in breast carcinoma

被引:270
作者
Collins, C
Rommens, JM
Kowbel, D
Godfrey, T
Tanner, M
Hwang, S
Polikoff, D
Nonet, G
Cochran, J
Myambo, K
Jay, KE
Froula, J
Cloutier, T
Kuo, WL
Yaswen, P
Dairkee, S
Giovanola, J
Hutchinson, GB
Isola, J
Kallioniemi, OP
Palazzolo, M
Martin, C
Ericsson, C
Pinkel, D
Albertson, D
Li, WB
Gray, JW
机构
[1] Univ Calif San Francisco, Ctr Canc, San Francisco, CA 94143 USA
[2] Lawrence Berkeley Lab, Div Life Sci, Berkeley, CA 94720 USA
[3] Univ Toronto, Dept Genet, Toronto, ON M5G 1X8, Canada
[4] Tampere Univ Hosp, Canc Genet Lab, FIN-33521 Tampere, Finland
[5] Inst Med Technol, FIN-33521 Tampere, Finland
[6] Univ British Columbia, Dept Med Genet, Vancouver, BC V6T 2B5, Canada
[7] NHGRI, Canc Genet Lab, NIH, Bethesda, MD 20892 USA
[8] Life Technol Inc, Rockville, MD 20850 USA
[9] Calif Pacific Med Ctr, Brush Canc Res Inst, San Francisco, CA 94619 USA
关键词
D O I
10.1073/pnas.95.15.8703
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
We report here the molecular cloning of an approximate to 1-Mb region of recurrent amplification at 20q13.2 in breast cancer and other tumors and the delineation of a 260-kb common region of amplification. Analysis of the I-Mb region produced evidence for five genes, ZNF217, ZNF218, and NABC1, PIC1L (PIC1-like), CYP24, and a pseudogene CRP (Cyclophillin Related Pseudogene). ZNF217 and NABC1 emerged as strong candidate oncogenes and were characterized in detail. NABC1 is predicted to encode a 585-aa protein of unknown function and is overexpressed in most but not all breast cancer cell lints in which it was amplified. ZNF217 is centrally located in the 260-kb common region of amplification, transcribed in multiple normal tissues, and overexpressed in all cell lines and tumors in which it is amplified and in two in which it is not. ZNF217 is predicted to encode alternately spliced, Kruppel-like transcription factors of 1,062 and 1,108 aa, each having a DNA-binding domain (eight C2H2 zinc fingers) and a proline-rich transcription activation domain.
引用
收藏
页码:8703 / 8708
页数:6
相关论文
共 45 条
  • [1] ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
  • [2] AIB1, a steroid receptor coactivator amplified in breast and ovarian cancer
    Anzick, SL
    Kononen, J
    Walker, RL
    Azorsa, DO
    Tanner, MM
    Guan, XY
    Sauter, G
    Kallioniemi, OP
    Trent, JM
    Meltzer, PS
    [J]. SCIENCE, 1997, 277 (5328) : 965 - 968
  • [3] ONCOGENE AMPLIFICATION AND PROGNOSIS IN BREAST-CANCER - RELATIONSHIP WITH SYSTEMIC TREATMENT
    BERNS, EMJJ
    FOEKENS, JA
    VANSTAVEREN, IL
    VANPUTTEN, WLJ
    DEKONING, HYWCM
    PORTENGEN, H
    KLIJN, JGM
    [J]. GENE, 1995, 159 (01) : 11 - 18
  • [4] Genetic screening of head and neck cancer by Comparative Genomic Hybridization (CGH)
    Bockmuhl, U
    Petersen, I
    Schwendel, A
    Dietel, M
    [J]. LARYNGO-RHINO-OTOLOGIE, 1996, 75 (07) : 408 - 414
  • [5] Boddy MN, 1996, ONCOGENE, V13, P971
  • [6] C-MYC AMPLIFICATION IS AN INDEPENDENT PROGNOSTIC FACTOR IN POSTMENOPAUSAL BREAST-CANCER
    BORG, A
    BALDETORP, B
    FERNO, M
    OLSSON, H
    SIGURDSSON, H
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1992, 51 (05) : 687 - 691
  • [7] BORG A, 1991, ONCOGENE, V6, P137
  • [8] The human CAS (cellular apoptosis susceptibility) gene mapping on chromosome 20q13 is amplified in BT474 breast cancer cells and part of aberrant chromosomes in breast and colon cancer cell lines
    Brinkmann, U
    Gallo, M
    Polymeropoulos, MH
    Pastan, I
    [J]. GENOME RESEARCH, 1996, 6 (03) : 187 - 194
  • [9] EXON AMPLIFICATION - A STRATEGY TO ISOLATE MAMMALIAN GENES BASED ON RNA SPLICING
    BUCKLER, AJ
    CHANG, DD
    GRAW, SL
    BROOK, JD
    HABER, DA
    SHARP, PA
    HOUSMAN, DE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) : 4005 - 4009
  • [10] AU-RICH ELEMENTS - CHARACTERIZATION AND IMPORTANCE IN MESSENGER-RNA DEGRADATION
    CHEN, CYA
    SHYU, AB
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (11) : 465 - 470