A novel cofactor for p300 that regulates the p53 response

被引:176
作者
Shikama, N [1 ]
Lee, CW [1 ]
France, S [1 ]
Delavaine, L [1 ]
Lyon, J [1 ]
Krstic-Demonacos, M [1 ]
La Thangue, NB [1 ]
机构
[1] Univ Glasgow, Div Biochem & Mol Biol, Glasgow G12 8QQ, Lanark, Scotland
基金
英国医学研究理事会;
关键词
D O I
10.1016/S1097-2765(00)80338-X
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 ability of p53 to function as a transcription factor is instrumental in facilitating the response to cellular stress, and p300/CBP proteins, which act as coactivators for diverse transcription factors, participate in regulating p53 activity. We report a novel cofactor for p300 that facilitates the p53 response by augmenting p53-dependent transcription and apoptosis. JMY and p300 associate in physiological conditions, and, during the cellular stress response, the p300/JMY complex is recruited to activated p53. The bar gene is efficiently activated by JMY, and protein isoforms that arise through alternative splicing alter the functional outcome of the p53 response. The results provide compelling evidence that the p300/JMY coactivator complex plays a central role in facilitating the p53 response.
引用
收藏
页码:365 / 376
页数:12
相关论文
共 51 条
  • [1] A FAMILY OF TRANSCRIPTIONAL ADAPTER PROTEINS TARGETED BY THE E1A ONCOPROTEIN
    ARANY, Z
    NEWSOME, D
    OLDREAD, E
    LIVINGSTON, DM
    ECKNER, R
    [J]. NATURE, 1995, 374 (6517) : 81 - 84
  • [2] Transcriptional activation by p53, but not induction of the p21 gene, is essential for oncogene-mediated apoptosis
    Attardi, LD
    Lowe, SW
    Brugarolas, J
    Jacks, T
    [J]. EMBO JOURNAL, 1996, 15 (14) : 3693 - 3701
  • [3] Recruitment of p300/CBP in p53-dependent signal pathways
    Avantaggiati, ML
    Ogryzko, V
    Gardner, K
    Giordano, A
    Levine, AS
    Kelly, K
    [J]. CELL, 1997, 89 (07) : 1175 - 1184
  • [4] The CBP co-activator is a histone acetyltransferase
    Bannister, AJ
    Kouzarides, T
    [J]. NATURE, 1996, 384 (6610) : 641 - 643
  • [5] THE CALIFORNIA MODEL - A COOPERATIVE SOLUTION FOR LAND REUSE AND ENVIRONMENTAL TECHNOLOGY COMMERCIALIZATION
    BUCKLES, R
    GLADDEN, J
    LOONEY, B
    [J]. JOURNAL OF URBAN TECHNOLOGY, 1995, 2 (02) : 31 - 49
  • [6] P53-DEPENDENT APOPTOSIS IN THE ABSENCE OF TRANSCRIPTIONAL ACTIVATION OF P53-TARGET GENES
    CAELLES, C
    HELMBERG, A
    KARIN, M
    [J]. NATURE, 1994, 370 (6486) : 220 - 223
  • [7] A multiplicity of mediators: alternative forms of transcription complexes communicate with transcriptional regulators
    Chang, MP
    Jaehning, JA
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (24) : 4861 - 4865
  • [8] Nuclear receptor coactivator ACTR is a novel histone acetyltransferase and forms a multimeric activation complex with P/CAF and CBP/p300
    Chen, HW
    Lin, RJ
    Schiltz, RL
    Chakravarti, D
    Nash, A
    Nagy, L
    Privalsky, ML
    Nakatani, Y
    Evans, RM
    [J]. CELL, 1997, 90 (03) : 569 - 580
  • [9] p53 levels, functional domains, and DNA damage determine the extent of the apoptotic response of tumor cells
    Chen, XB
    Ko, LJ
    Jayaraman, L
    Prives, C
    [J]. GENES & DEVELOPMENT, 1996, 10 (19) : 2438 - 2451
  • [10] CRYSTAL-STRUCTURE OF A P53 TUMOR-SUPPRESSOR DNA COMPLEX - UNDERSTANDING TUMORIGENIC MUTATIONS
    CHO, YJ
    GORINA, S
    JEFFREY, PD
    PAVLETICH, NP
    [J]. SCIENCE, 1994, 265 (5170) : 346 - 355