Human PLU-1 has transcriptional repression properties and interacts with the developmental transcription factors BF-1 and PAX9

被引:78
作者
Tan, K
Shaw, AL
Madsen, B
Jensen, K
Taylor-Papadimitriou, J
Freemont, PS
机构
[1] Univ London Imperial Coll Sci Technol & Med, Ctr Struct Biol, Dept Sci Biol, London SW7 2AZ, England
[2] Lincolns Inn Fields, Mol Struct & Funct Lab, Canc Res UK, London WC2A 3PX, England
[3] Guys Hosp, Breast Canc Biol Grp, Canc Res UK, London SE1 9RT, England
关键词
D O I
10.1074/jbc.M301994200
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
PLU-1 is a large ( 1544 amino acids) nuclear protein that is highly expressed in breast cancers and is proposed to function as a regulator of gene expression. A yeast two-hybrid screen using PLU-1 as bait has identified two unrelated PLU-1 interacting proteins, namely brain factor-1 (BF-1) and paired box 9 (PAX9), both of which are developmental transcription factors. BF-1 and PAX9 interact with PLU-1 via a novel conserved sequence motif ( Ala-X-Ala-Ala-X-Val-Pro-X-4-Val-Pro-X(8)Pro, termed the VP motif), because deletion or site-directed mutagenesis of this motif in either protein abolishes PLU-1 interaction in vivo. In a reporter assay system, PLU-1 has potent transcriptional repression activity. BF-1 and PAX9 also represses transcription in the same assay, but co-expression of PLU-1 with BF-1 or PAX9 significantly enhances this repression. Mutation of the PLU-1 binding motifs in BF-1 and PAX9 abolishes the observed PLU-1 co-repression activity. These data support a role for PLU-1 acting as a transcriptional corepressor of two unrelated developmental transcription factors. Because both BF-1 and PAX proteins interact with members of the groucho co-repressor family, it is plausible that PLU-1 has a role in groucho-mediated transcriptional repression.
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页码:20507 / 20513
页数:7
相关论文
共 42 条
  • [1] THE PHD FINGER - IMPLICATIONS FOR CHROMATIN-MEDIATED TRANSCRIPTIONAL REGULATION
    AASLAND, R
    GIBSON, TJ
    STEWART, AF
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (02) : 56 - 59
  • [2] Evidence of domain swapping within the jumonji family of transcription factors
    Balciunas, D
    Ronne, H
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (06) : 274 - 276
  • [3] HPC3 is a new human polycomb orthologue that interacts and associates with RING1 and Bmi1 and Has transcriptional repression properties
    Bárdos, JI
    Saurin, AJ
    Tissot, C
    Duprez, E
    Freemont, PS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (37) : 28785 - 28792
  • [4] PLU-1 nuclear protein, which is upregulated in breast cancer, shows restricted expression in normal human adult tissues: A new cancer/testis antigen?
    Barrett, A
    Madsen, B
    Copier, J
    Lu, PJ
    Cooper, L
    Scibetta, AG
    Burchell, J
    Taylor-Papadimitriou, J
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2002, 101 (06) : 581 - 588
  • [5] BERDICHEVSKY F, 1994, J CELL SCI, V107, P3557
  • [6] Retinoblastoma-binding protein 2 (Rbp2) potentiates nuclear hormone receptor-mediated transcription
    Chan, SW
    Hong, WJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (30) : 28402 - 28412
  • [7] Chang HW, 1996, ONCOGENE, V13, P441
  • [8] A functional interaction between the histone deacetylase Rpd3 and the corepressor Groucho in Drosophila development
    Chen, GQ
    Fernandez, J
    Mische, S
    Courey, AJ
    [J]. GENES & DEVELOPMENT, 1999, 13 (17) : 2218 - 2230
  • [9] The homeodomain protein NK-3 recruits Groucho and a histone deacetylase complex to repress transcription
    Choi, CY
    Kim, YH
    Kwon, HJ
    Kim, Y
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (47) : 33194 - 33197
  • [10] JmjC:: cupin metalloenzyme-like domains in jumonji, hairless and phospholipase A2β
    Clissold, PM
    Ponting, CP
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (01) : 7 - 9