共 25 条
Acidic domain is indispensable for MDM2 to negatively regulate the acetylation of p53
被引:8
作者:

Wang, Qian
论文数: 0 引用数: 0
h-index: 0
机构:
Fudan Univ, Sch Life Sci, Inst Genet, State Key Lab Genet Engn, Shanghai 200433, Peoples R China Fudan Univ, Sch Life Sci, Inst Genet, State Key Lab Genet Engn, Shanghai 200433, Peoples R China

Yang, Ying
论文数: 0 引用数: 0
h-index: 0
机构:
Fudan Univ, Sch Life Sci, Inst Genet, State Key Lab Genet Engn, Shanghai 200433, Peoples R China Fudan Univ, Sch Life Sci, Inst Genet, State Key Lab Genet Engn, Shanghai 200433, Peoples R China

Wang, Lan
论文数: 0 引用数: 0
h-index: 0
机构:
Fudan Univ, Sch Life Sci, Inst Genet, State Key Lab Genet Engn, Shanghai 200433, Peoples R China Fudan Univ, Sch Life Sci, Inst Genet, State Key Lab Genet Engn, Shanghai 200433, Peoples R China

Zhang, Ping-zhao
论文数: 0 引用数: 0
h-index: 0
机构:
Fudan Univ, Sch Life Sci, Inst Genet, State Key Lab Genet Engn, Shanghai 200433, Peoples R China Fudan Univ, Sch Life Sci, Inst Genet, State Key Lab Genet Engn, Shanghai 200433, Peoples R China

Yu, Long
论文数: 0 引用数: 0
h-index: 0
机构:
Fudan Univ, Sch Life Sci, Inst Genet, State Key Lab Genet Engn, Shanghai 200433, Peoples R China Fudan Univ, Sch Life Sci, Inst Genet, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
机构:
[1] Fudan Univ, Sch Life Sci, Inst Genet, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
关键词:
p53;
acetylation;
MDM2;
acidic domain;
p300;
HDAC1;
D O I:
10.1016/j.bbrc.2008.07.038
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:
MDM2 is the most important negative regulator of tumor suppressor p53. Both RING finger domain and acidic domain of MDM2 contribute to the ubiquitination of p53. The crosstalk between ubiquitination and acetylation of p53 prompts us to examine whether acidic domain is essential for MDM2 to regulate the acetylation of p53. We find that the acidic domain of MDM2 is necessary to inhibit p300-mediated acetylation of p53 as well as to mediate the deacetylation of p53. Our results indicate that acidic domain of MDM2 Provides essential information for acetyltransferase p300 and deacetylase HDAC1 and is indispensable for MDM2 to negatively regulate the acetylation of p53. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:437 / 441
页数:5
相关论文
共 25 条
[1]
Post-translational modification of p53 in tumorigenesis
[J].
Bode, AM
;
Dong, ZG
.
NATURE REVIEWS CANCER,
2004, 4 (10)
:793-805

Bode, AM
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Minnesota, Hormel Inst, Austin, MN 55912 USA Univ Minnesota, Hormel Inst, Austin, MN 55912 USA

Dong, ZG
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Minnesota, Hormel Inst, Austin, MN 55912 USA Univ Minnesota, Hormel Inst, Austin, MN 55912 USA
[2]
Ubiquitination, phosphorylation and acetylation: the molecular basis for p53 regulation
[J].
Brooks, CL
;
Gu, W
.
CURRENT OPINION IN CELL BIOLOGY,
2003, 15 (02)
:164-171

Brooks, CL
论文数: 0 引用数: 0
h-index: 0
机构: Columbia Univ, Inst Canc Genet, New York, NY 10032 USA

Gu, W
论文数: 0 引用数: 0
h-index: 0
机构: Columbia Univ, Inst Canc Genet, New York, NY 10032 USA
[3]
Inhibiting the p53-MDM2 interaction:: An important target for cancer therapy
[J].
Chène, P
.
NATURE REVIEWS CANCER,
2003, 3 (02)
:102-109

Chène, P
论文数: 0 引用数: 0
h-index: 0
机构:
Novartis, CH-4002 Basel, Switzerland Novartis, CH-4002 Basel, Switzerland
[4]
Mdm2 is a RING finger-dependent ubiquitin protein ligase for itself and p53
[J].
Fang, SY
;
Jensen, JP
;
Ludwig, RL
;
Vousden, KH
;
Weissman, AM
.
JOURNAL OF BIOLOGICAL CHEMISTRY,
2000, 275 (12)
:8945-8951

Fang, SY
论文数: 0 引用数: 0
h-index: 0
机构: NCI, Lab Immune Cell Biol, Div Basic Sci, NIH, Bethesda, MD 20892 USA

Jensen, JP
论文数: 0 引用数: 0
h-index: 0
机构: NCI, Lab Immune Cell Biol, Div Basic Sci, NIH, Bethesda, MD 20892 USA

Ludwig, RL
论文数: 0 引用数: 0
h-index: 0
机构: NCI, Lab Immune Cell Biol, Div Basic Sci, NIH, Bethesda, MD 20892 USA

Vousden, KH
论文数: 0 引用数: 0
h-index: 0
机构: NCI, Lab Immune Cell Biol, Div Basic Sci, NIH, Bethesda, MD 20892 USA

Weissman, AM
论文数: 0 引用数: 0
h-index: 0
机构: NCI, Lab Immune Cell Biol, Div Basic Sci, NIH, Bethesda, MD 20892 USA
[5]
p300/MDM2 complexes participate in MDM2-mediated p53 degradation
[J].
Grossman, SR
;
Perez, M
;
Kung, AL
;
Joseph, M
;
Mansur, C
;
Xiao, ZX
;
Kumar, S
;
Howley, PM
;
Livingston, DM
.
MOLECULAR CELL,
1998, 2 (04)
:405-415

Grossman, SR
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA

Perez, M
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA

Kung, AL
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA

Joseph, M
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA

Mansur, C
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA

Xiao, ZX
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA

Kumar, S
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA

Howley, PM
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA

Livingston, DM
论文数: 0 引用数: 0
h-index: 0
机构: Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02115 USA
[6]
Activity of MDM2, a ubiquitin Ligase, toward p53 or itself is dependent on the RING finger domain of the ligase
[J].
Honda, R
;
Yasuda, H
.
ONCOGENE,
2000, 19 (11)
:1473-1476

Honda, R
论文数: 0 引用数: 0
h-index: 0
机构:
Tokyo Univ Pharm & Life Sci, Sch Life Sci, Hachioji, Tokyo 1920392, Japan Tokyo Univ Pharm & Life Sci, Sch Life Sci, Hachioji, Tokyo 1920392, Japan

Yasuda, H
论文数: 0 引用数: 0
h-index: 0
机构:
Tokyo Univ Pharm & Life Sci, Sch Life Sci, Hachioji, Tokyo 1920392, Japan Tokyo Univ Pharm & Life Sci, Sch Life Sci, Hachioji, Tokyo 1920392, Japan
[7]
p300/CBP-mediated p53 acetylation is commonly induced by p53-activating agents and inhibited by MDM2
[J].
Ito, A
;
Lai, CH
;
Zhao, X
;
Saito, S
;
Hamilton, MH
;
Appella, E
;
Yao, TP
.
EMBO JOURNAL,
2001, 20 (06)
:1331-1340

Ito, A
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA

Lai, CH
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA

Zhao, X
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA

Saito, S
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA

Hamilton, MH
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA

Appella, E
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA

Yao, TP
论文数: 0 引用数: 0
h-index: 0
机构:
Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
[8]
MDM2-HDAC1-mediated deacetylation of p53 is required for its degradation
[J].
Ito, A
;
Kawaguchi, Y
;
Lai, CH
;
Kovacs, JJ
;
Higashimoto, Y
;
Appella, E
;
Yao, TP
.
EMBO JOURNAL,
2002, 21 (22)
:6236-6245

Ito, A
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA

Kawaguchi, Y
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA

Lai, CH
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA

Kovacs, JJ
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA

Higashimoto, Y
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA

Appella, E
论文数: 0 引用数: 0
h-index: 0
机构: Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA

Yao, TP
论文数: 0 引用数: 0
h-index: 0
机构:
Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA Duke Univ, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
[9]
Mutation at p53 serine 389 does not rescue the embryonic lethality in mdm2 or mdm4 null mice
[J].
Iwakuma, T
;
Parant, JM
;
Fasulo, M
;
Zwart, E
;
Jacks, T
;
de Vries, A
;
Lozano, G
.
ONCOGENE,
2004, 23 (46)
:7644-7650

Iwakuma, T
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Sect Canc Genet, Houston, TX 77030 USA

Parant, JM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Sect Canc Genet, Houston, TX 77030 USA

Fasulo, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Sect Canc Genet, Houston, TX 77030 USA

Zwart, E
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Sect Canc Genet, Houston, TX 77030 USA

Jacks, T
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Sect Canc Genet, Houston, TX 77030 USA

de Vries, A
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Sect Canc Genet, Houston, TX 77030 USA

Lozano, G
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Sect Canc Genet, Houston, TX 77030 USA Univ Texas, MD Anderson Canc Ctr, Dept Mol Genet, Sect Canc Genet, Houston, TX 77030 USA
[10]
MDM2 inhibits PCAF (p300/CREB-binding protein-associated factor)-mediated p53 acetylation
[J].
Jin, YT
;
Zeng, SX
;
Dai, MS
;
Yang, XJ
;
Lu, H
.
JOURNAL OF BIOLOGICAL CHEMISTRY,
2002, 277 (34)
:30838-30843

Jin, YT
论文数: 0 引用数: 0
h-index: 0
机构: Oregon Hlth & Sci Univ, Dept Biochem & Mol Biol, Portland, OR 97201 USA

Zeng, SX
论文数: 0 引用数: 0
h-index: 0
机构: Oregon Hlth & Sci Univ, Dept Biochem & Mol Biol, Portland, OR 97201 USA

Dai, MS
论文数: 0 引用数: 0
h-index: 0
机构: Oregon Hlth & Sci Univ, Dept Biochem & Mol Biol, Portland, OR 97201 USA

Yang, XJ
论文数: 0 引用数: 0
h-index: 0
机构: Oregon Hlth & Sci Univ, Dept Biochem & Mol Biol, Portland, OR 97201 USA

Lu, H
论文数: 0 引用数: 0
h-index: 0
机构: Oregon Hlth & Sci Univ, Dept Biochem & Mol Biol, Portland, OR 97201 USA