Loss of the INI1 tumor suppressor does not impair the expression of multiple BRG1-dependent genes or the assembly of SWI/SNF enzymes

被引:62
作者
Doan, DN
Veal, TM
Yan, ZJ
Wang, WD
Jones, SN
Imbalzano, AN
机构
[1] Univ Massachusetts, Sch Med, Dept Cell Biol, Worcester, MA 01655 USA
[2] NIA, Genet Lab, NIH, Baltimore, MD 21224 USA
关键词
INI1; BRG1; SWI/SNF; tumor suppressor; gene regulation;
D O I
10.1038/sj.onc.1207472
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
The INI1/hSNF5 tumor suppressor is an integral component of mammalian SWI/SNF chromatin remodeling enzymes that contain SNF2 family ATPases BRM (Brahma) or BRG1 (Brahma Related Gene 1) and that contribute to the regulation of many genes. Genetic studies of yeast SWI/SNF enzyme revealed similar phenotypes when single or multiple components of the enzyme were deleted, indicating a requirement for each subunit. To address the contribution of INI1 in the regulation of SWI/SNF-dependent genes in mammalian cells, we examined the expression of multiple BRG1-dependent, constitutively expressed genes in INI1-deficient cancer cell lines. At least one INI1-deficient line expressed each gene, and reintroduction of INI1 had negligible effects on expression levels. Lack of INI1 also did not prevent interferon gamma (IFNc)-mediated induction of CIITA, which is BRG1 dependent, and GBP-1, which is BRG1 enhanced, and reintroduction of INI1 had minimal effects. Chromatin immunoprecipitation experiments revealed that BRG1 inducibly binds to the CIITA promoter despite the absence of INI1. Unlike yeast deleted for the INI1 homologue, SWI/SNF enzymes in INI1-deficient cells were largely intact. Thus in human cells, SWI/SNF enzyme complex formation and the expression of many BRG1-dependent genes are independent of INI1.
引用
收藏
页码:3462 / 3473
页数:12
相关论文
共 73 条
  • [1] Adler HT, 1999, MOL CELL BIOL, V19, P7050
  • [2] Chromatin remodeling factor encoded by ini1 induces G1 arrest and apoptosis in ini1-deficient cells
    Ae, K
    Kobayashi, N
    Sakuma, R
    Ogata, T
    Kuroda, H
    Kawaguchi, N
    Shinomiya, K
    Kitamura, Y
    [J]. ONCOGENE, 2002, 21 (20) : 3112 - 3120
  • [3] Ordered recruitment of chromatin modifying and general transcription factors to the IFN-β promoter
    Agalioti, T
    Lomvardas, S
    Parekh, B
    Yie, JM
    Maniatis, T
    Thanos, D
    [J]. CELL, 2000, 103 (04) : 667 - 678
  • [4] A SWI/SNF-related chromatin remodeling complex, E-RC1, is required for tissue-specific transcriptional regulation by EKLF in vitro
    Armstrong, JA
    Bieker, JJ
    Emerson, BM
    [J]. CELL, 1998, 95 (01) : 93 - 104
  • [5] ATP-dependent nucleosomere modeling
    Becker, PB
    Hörz, W
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 2002, 71 : 247 - 273
  • [6] Re-expression of hSNF5/INI1/BAF47 in pediatric tumor cells leads to G1 arrest associated with induction of p16ink4a and activation of RB
    Betz, BL
    Strobeck, MW
    Reisman, DN
    Knudsen, ES
    Weissman, BE
    [J]. ONCOGENE, 2002, 21 (34) : 5193 - 5203
  • [7] Biegel JA, 2000, CLIN CANCER RES, V6, P2759
  • [8] Cellular responses to interferon-gamma
    Boehm, U
    Klamp, T
    Groot, M
    Howard, JC
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1997, 15 : 749 - 795
  • [9] A Brg1 null mutation in the mouse reveals functional differences among mammalian SWI/SNF complexes
    Bultman, S
    Gebuhr, T
    Yee, D
    La Mantia, C
    Nicholson, J
    Gilliam, A
    Randazzo, F
    Metzger, D
    Chambon, P
    Crabtree, G
    Magnuson, T
    [J]. MOLECULAR CELL, 2000, 6 (06) : 1287 - 1295
  • [10] A MULTISUBUNIT COMPLEX CONTAINING THE SWI1/ADR6, SWI2/SNF2, SWI3, SNF5, AND SNF6 GENE-PRODUCTS ISOLATED FROM YEAST
    CAIRNS, BR
    KIM, YJ
    SAYRE, MH
    LAURENT, BC
    KORNBERG, RD
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (05) : 1950 - 1954