P53


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p53是一系列被称为腫瘤抑制蛋白(也稱為p53蛋白或p53腫瘤蛋白)的同源异构蛋白的统称。由TP53(人体)及Trp53(老鼠)基因编码。该蛋白是最早发现的肿瘤抑制基因所编码的蛋白之一。p53蛋白能調節細胞週期,促使細胞出現凋亡或細胞衰老(cell senescence)等現象,从而避免细胞癌变發生。p53蛋白能保持基因組的穩定性,避免或减少突變的發生。因此被稱為基因組守護者。

P53
已知的結構
PDB直系同源搜索: PDBe RCSB
PDBID列表

4QO1、​1A1U、​1AIE、​1C26、​1DT7、​1GZH、​1H26、​1HS5、​1KZY、​1MA3、​1OLG、​1OLH、​1PES、​1PET、​1SAE、​1SAF、​1SAK、​1SAL、​1TSR、​1TUP、​1UOL、​1XQH、​1YC5、​1YCQ、​1YCR、​1YCS、​2AC0、​2ADY、​2AHI、​2ATA、​2B3G、​2BIM、​2BIN、​2BIO、​2BIP、​2BIQ、​2FEJ、​2FOJ、​2FOO、​2GS0、​2H1L、​2H2D、​2H2F、​2H4F、​2H4H、​2H4J、​2H59、​2J0Z、​2J10、​2J11、​2J1W、​2J1X、​2J1Y、​2J1Z、​2J20、​2J21、​2K8F、​2L14、​2LY4、​2MEJ、​2MWO、​2MWP、​2MZD、​2OCJ、​2PCX、​2RUK、​2VUK、​2WGX、​2X0U、​2X0V、​2X0W、​2XWR、​2YBG、​2YDR、​2Z5S、​2Z5T、​3D05、​3D06、​3D07、​3D08、​3D09、​3D0A、​3DAB、​3DAC、​3IGK、​3IGL、​3KMD、​3KZ8、​3LW1、​3OQ5、​3PDH、​3Q01、​3Q05、​3Q06、​3SAK、​3TG5、​3TS8、​3ZME、​4AGL、​4AGM、​4AGN、​4AGO、​4AGP、​4AGQ、​4BUZ、​4BV2、​4HFZ、​4HJE、​4IBQ、​4IBS、​4IBT、​4IBU、​4IBV、​4IBW、​4IBY、​4IBZ、​4IJT、​4KVP、​4LO9、​4LOE、​4LOF、​4MZI、​4MZR、​4X34、​4ZZJ、​5AOL、​5ABA、​5AOK、​2MWY、​5A7B、​5AOJ、​5AOI、​5ECG、​5AB9、​4FZ3、​4RP6、​4XR8、​5AOM、​4RP7、​5HOU、​5HP0、​5HPD、​5LGY、​5G4M、​5G4O、​5G4N、​5BUA

識別號
别名TP53;, BCC7, LFS1, P53, TRP53, tumor protein p53, BMFS5, Genes, p53
外部IDOMIM191170 MGI98834 HomoloGene460 GeneCardsTP53
相關疾病
基底細胞癌(BCC)、​头颈部鳞状细胞癌、​李-佛美尼症候群、​Li-Fraumeni syndrome 1、​B細胞慢性淋巴性白血病、​liver carcinoma、​急性骨髓性白血病、​breast adenocarcinoma、​gastric adenocarcinoma、​肺腺癌、​骨肉瘤、​prostate adenocarcinoma、​lung small cell carcinoma、​肺鱗狀上皮癌、​large intestine cancer、​pancreatic adenocarcinoma[1]
基因位置(人类
17號染色體
染色体17號染色體[2]

17號染色體

P53的基因位置

P53的基因位置

基因座17p13.1起始7,661,779 bp[2]
终止7,687,538 bp[2]
基因位置(小鼠
小鼠11号染色体
染色体小鼠11号染色体[3]

小鼠11号染色体

P53的基因位置

P53的基因位置

基因座11 B3|11 42.83 cM起始69,471,185 bp[3]
终止69,482,699 bp[3]
RNA表达模式

查阅更多表达数据
基因本體
分子功能 protein N-terminus binding
DNA结合转录因子活性
蛋白質自締合
core promoter sequence-specific DNA binding
DNA-binding transcription factor activity, RNA polymerase II-specific
protein phosphatase binding
ATP結合
转录因子结合
金屬離子結合
protein phosphatase 2A binding
酶结合
鋅離子結合
chromatin binding
蛋白酶結合
damaged DNA binding
血浆蛋白结合
histone acetyltransferase binding
copper ion binding
protein kinase binding
chaperone binding
DNA-binding transcription activator activity, RNA polymerase II-specific
receptor tyrosine kinase binding
p53 binding
相同蛋白质结合
protein heterodimerization activity
泛素蛋白连接酶结合
RNA polymerase II transcription regulatory region sequence-specific DNA binding
DNA结合
RNA polymerase II cis-regulatory region sequence-specific DNA binding
TFIID-class transcription factor complex binding
mRNA 3'-UTR binding
histone deacetylase binding
无序域特异性结合
promoter-specific chromatin binding
histone deacetylase regulator activity
protein homodimerization activity
MDM2/MDM4 family protein binding
細胞組分 細胞質
線粒體
细胞核
nuclear body
transcription factor TFIID complex
nuclear matrix
replication fork
核仁
内质网
核质
线粒体基质
PML body
细胞质基质
胞內
轉錄調節複合物
大分子复合体
site of double-strand break
生物學過程 positive regulation of histone deacetylation
DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest
rhythmic process
replicative senescence
negative regulation of telomerase activity
oligodendrocyte apoptotic process
cellular response to DNA damage stimulus
intrinsic apoptotic signaling pathway
positive regulation of neuron apoptotic process
regulation of mitochondrial membrane permeability
positive regulation of reactive oxygen species metabolic process
cellular response to ionizing radiation
positive regulation of thymocyte apoptotic process
negative regulation of helicase activity
細胞週期
Ras protein signal transduction
細胞增殖
cellular response to hypoxia
negative regulation of cell population proliferation
核苷酸切除修复
cellular response to glucose starvation
regulation of transcription, DNA-templated
response to antibiotic
transcription, DNA-templated
ER overload response
positive regulation of transcription, DNA-templated
negative regulation of cell growth
intrinsic apoptotic signaling pathway by p53 class mediator
positive regulation of peptidyl-tyrosine phosphorylation
viral process
response to gamma radiation
negative regulation of fibroblast proliferation
positive regulation of intrinsic apoptotic signaling pathway
细胞分化
determination of adult lifespan
positive regulation of transcription from RNA polymerase II promoter in response to endoplasmic reticulum stress
cellular response to UV
DNA damage response, signal transduction by p53 class mediator
negative regulation of apoptotic process
protein tetramerization
oxidative stress-induced premature senescence
positive regulation of release of cytochrome c from mitochondria
circadian behavior
negative regulation of transcription, DNA-templated
protein localization
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator
positive regulation of execution phase of apoptosis
multicellular organism development
positive regulation of protein insertion into mitochondrial membrane involved in apoptotic signaling pathway
positive regulation of gene expression
mitotic G1 DNA damage checkpoint signaling
positive regulation of protein oligomerization
positive regulation of apoptotic process
entrainment of circadian clock by photoperiod
response to X-ray
positive regulation of transcription by RNA polymerase II
base-excision repair
DNA damage response, signal transduction by p53 class mediator resulting in transcription of p21 class mediator
regulation of cell cycle G2/M phase transition
proteasome-mediated ubiquitin-dependent protein catabolic process
regulation of signal transduction by p53 class mediator
细胞凋亡
transcription by RNA polymerase II
positive regulation of protein export from nucleus
细胞程序性死亡
regulation of apoptotic process
protein deubiquitination
phosphatidylinositol-mediated signaling
negative regulation of transcription by RNA polymerase II
自噬
mRNA transcription
cytokine-mediated signaling pathway
positive regulation of RNA polymerase II transcription preinitiation complex assembly
RNA polymerase II preinitiation complex assembly
protein homotetramerization
protein-containing complex assembly
cellular response to gamma radiation
signal transduction by p53 class mediator
cellular response to actinomycin D
positive regulation of pri-miRNA transcription by RNA polymerase II
positive regulation of production of miRNAs involved in gene silencing by miRNA
in utero embryonic development
somitogenesis
release of cytochrome c from mitochondria
hematopoietic progenitor cell differentiation
T cell proliferation involved in immune response
B cell lineage commitment
T cell lineage commitment
response to ischemia
double-strand break repair
regulation of transcription by RNA polymerase II
protein import into nucleus
response to oxidative stress
transforming growth factor beta receptor signaling pathway
原腸胚形成
negative regulation of neuroblast proliferation
central nervous system development
心脏发育
昼夜节律
negative regulation of DNA replication
rRNA transcription
response to UV
response to salt stress
embryo development ending in birth or egg hatching
negative regulation of gene expression
positive regulation of cardiac muscle cell apoptotic process
cerebellum development
negative regulation of transforming growth factor beta receptor signaling pathway
T cell differentiation in thymus
regulation of tissue remodeling
multicellular organism growth
positive regulation of mitochondrial membrane permeability
positive regulation of transcription from RNA polymerase II promoter in response to stress
regulation of cell population proliferation
mitochondrial DNA repair
regulation of DNA damage response, signal transduction by p53 class mediator
regulation of neuron apoptotic process
negative regulation of proteolysis
negative regulation of mitotic cell cycle
bone marrow development
embryonic organ development
protein stabilization
chromosome organization
neuron apoptotic process
regulation of cell cycle
hematopoietic stem cell differentiation
interferon-gamma-mediated signaling pathway
cardiac septum morphogenesis
positive regulation of transcription from RNA polymerase II promoter in response to hypoxia
positive regulation of programmed necrotic cell death
intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress
regulation of thymocyte apoptotic process
程序性坏死
cellular response to UV-C
negative regulation of mitophagy
regulation of mitochondrial membrane permeability involved in apoptotic process
regulation of intrinsic apoptotic signaling pathway by p53 class mediator
negative regulation of production of miRNAs involved in gene silencing by miRNA
negative regulation of glucose catabolic process to lactate via pyruvate
intrinsic apoptotic signaling pathway in response to hypoxia
regulation of fibroblast apoptotic process
negative regulation of reactive oxygen species metabolic process
regulation of cellular senescence
Sources:Amigo / QuickGO
直系同源
物種人類小鼠
Entrez

7157

22059

Ensembl

ENSG00000141510

ENSMUSG00000059552

UniProt

P04637

P02340

mRNA​序列
NM_001276761
​NM_000546
​NM_001126112
​NM_001126113
​NM_001126114

​NM_001126115
​NM_001126116
​NM_001126117
​NM_001126118
​NM_001276695
​NM_001276696
​NM_001276697
​NM_001276698
​NM_001276699
​NM_001276760

NM_001127233
​NM_011640

蛋白序列
NP_000537
​NP_001119584
​NP_001119585
​NP_001119586
​NP_001119587

​NP_001119588
​NP_001119589
​NP_001119590
​NP_001263624
​NP_001263625
​NP_001263626
​NP_001263627
​NP_001263628
​NP_001263689
​NP_001263690

NP_001120705
​NP_035770

基因位置​(UCSC)Chr 17: 7.66 – 7.69 MbChr 11: 69.47 – 69.48 Mb
PubMed​查找[4][5]
維基數據
檢視/編輯人類檢視/編輯小鼠

p53得名于1979年,因为其的分子量SDS凝膠電泳中測得約為53kDa。不过依據胺基酸序列进行計算后发现p53蛋白的分子量應為43.7kDa.兩者所測得之分子量差別是因为该蛋白中存在大量的脯胺酸殘基,減緩了其在SDS膠電泳中的遷移速度。而此遷移速度減緩的效應在跨物種的p53蛋白皆已被觀察,如人類,嚙齒動物,青蛙和魚類。

目前在人体内发现的p53同源异构蛋白有15种;另外由於FOXO4可和p53結合以促進細胞衰老之故[6],因此一些和FOXO4有競爭效應的胜肽,可藉由將p53屏除於細胞核之外而成為返老藥(Senolytic)。[6]

p53蛋白在避免癌症發生機制上扮演重要的角色,例如,細胞凋亡 (apoptosis) 、細胞衰老(cell senescence)、基因組穩定性 (genetic stability) 、抑制血管新生 (angiogenesis)。 p53蛋白通過下列之機構達成避免癌症發生:

  • 當DNA受損時,p53蛋白能活化DNA修復蛋白 (DNA repair proteins)。
  • p53蛋白能抑制細胞生長,通过使细胞周期停留於G1/S的節律點上,以達成DNA損壞辨識。 (若能將細胞於此節律點上停留夠久,DNA修复蛋白將有更充裕的時間修復DNA損壞部位,並繼續細胞的生長週期。)
  • 若細胞的DNA受損已不能修復,p53蛋白能起始細胞凋亡程序,避免擁有不正常遺傳資訊的細胞繼續分裂生長。

活化的p53蛋白能接合於DNA,促使多個基因表現,包括基因WAF1/CIP1,其為p21蛋白之編碼基因。 p21 (WAF1)接合於G1-S/CDK (CDK2) 和S/CDK複合體 (此蛋白在G1/S細胞週期節律點上有重要功能) 以抑制該複合體的活性。 當p21蛋白 (WAF1) 與CDK2形成複合體時,細胞將無法進入到細胞分裂的階段。 而突變後的p53蛋白將可能喪失與DNA形成有效結合的能力,造成p21蛋白將無法形成,以發出停止細胞分裂的信號。 因此,受損細胞將不受控制的進行細胞分裂,最終形成腫瘤。 根據最近的研究,p53蛋白與RB1程序經由p14ARF蛋白相互調節的可能性更加提高。

p53蛋白藉由許多不同的壓力形式而激發其活性,其中包括但不僅僅侷限於DNA損傷 (包括 UV, IR或化學物質如過氧化氫 (hydrogen peroxide)所造成的損傷),氧化壓力 (oxidative stress),滲透壓力 (osmotic stress),核糖核苷酸缺乏 (nucleotide depletion) 和喪失調節癌基因表現能力。這些活性激發可由兩個主要的事件得出。首先,在受到壓力的細胞中,p53蛋白的半衰期 (half-life) 會突然的增加,造成p53蛋白在細胞中的累積。再來則是構型變化 (conformational change) 使得p53蛋白被激發成為轉錄調節因子 (transcription regulator)。

  1. ^ 與P53相關的疾病;在維基數據上查看/編輯參考.
  2. ^ 2.0 2.1 2.2 GRCh38: Ensembl release 89: ENSG00000141510 - Ensembl, May 2017
  3. ^ 3.0 3.1 3.2 GRCm38: Ensembl release 89: ENSMUSG00000059552 - Ensembl, May 2017
  4. ^ Human PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Mouse PubMed Reference:. National Center for Biotechnology Information, U.S. National Library of Medicine.
  6. ^ 6.0 6.1 Baar, Marjolein P.; Brandt, Renata M.C.; Putavet, Diana A.; Klein, Julian D.D.; Derks, Kasper W.J.; Bourgeois, Benjamin R.M.; Stryeck, Sarah; Rijksen, Yvonne; van Willigenburg, Hester; Feijtel, Danny A.; van der Pluijm, Ingrid; Essers, Jeroen; van Cappellen, Wiggert A.; van IJcken, Wilfred F.; Houtsmuller, Adriaan B.; Pothof, Joris; de Bruin, Ron W.F.; Madl, Tobias; Hoeijmakers, Jan H.J.; Campisi, Judith; de Keizer, Peter L.J. Targeted Apoptosis of Senescent Cells Restores Tissue Homeostasis in Response to Chemotoxicity and Aging. Cell. March 2017, 169 (1): 132–147.e16. PMC 5556182 . PMID 28340339. doi:10.1016/j.cell.2017.02.031.