SMOX (spermine oxidase)

symbol:
SMOX
locus group:
protein-coding gene
location:
20p13
gene_family:
alias symbol:
FLJ20746|dJ779E11.1|PAO|PAOh1|MGC1010|SMO
alias name:
None
entrez id:
54498
ensembl gene id:
ENSG00000088826
ucsc gene id:
uc002wkm.2
refseq accession:
NM_175842
hgnc_id:
HGNC:15862
approved reserved:
2001-06-21
20p13
基因染色体位置图

SMOX(精胺氧化酶,spermine oxidase)是一种催化多胺代谢的关键酶,主要功能是将精胺(spermine)氧化降解为亚精胺(spermidine),同时产生过氧化氢(H2O2)和3-氨基丙醛(3-AP)。这一反应在多胺稳态调控中起重要作用,影响细胞增殖、分化、凋亡等过程。SMOX主要表达于肝脏、肾脏、前列腺等组织,其活性与氧化应激密切相关,因为其反应副产物H2O2可能造成DNA损伤或激活信号通路。SMOX属于多胺氧化酶(PAO)基因家族,该家族成员均含黄素腺嘌呤二核苷酸(FAD)辅基,通过氧化反应调控多胺代谢平衡。SMOX功能异常与多种疾病相关:过表达会导致细胞内氧化应激水平升高,与前列腺癌、肝纤维化等疾病进展正相关,可能通过促进细胞增殖或炎症反应;而表达降低可能影响组织再生能力。基因突变可能引起酶活性改变,如某些错义突变导致催化效率下降,进而扰乱多胺代谢稳态。在肿瘤中,SMOX过表达可能通过持续产生H2O2促进基因组不稳定性,同时消耗具有细胞保护作用的精胺;而抑制其表达可减少氧化损伤但可能影响正常细胞周期调控。该基因与邻近的PAOX基因存在功能冗余,但SMOX对精胺的特异性更高。研究还发现SMOX参与免疫调节,其表达受转录因子Nrf2调控,与抗氧化应激通路相互作用。目前针对SMOX的抑制剂(如MDL72527)正在研究中,可能为相关疾病治疗提供新靶点。

Polyamines are ubiquitous polycationic alkylamines which include spermine, spermidine, putrescine, and agmatine. These molecules participate in a broad range of cellular functions which include cell cycle modulation, scavenging reactive oxygen species, and the control of gene expression. These molecules also play important roles in neurotransmission through their regulation of cell-surface receptor activity, involvement in intracellular signalling pathways, and their putative roles as neurotransmitters. This gene encodes an FAD-containing enzyme that catalyzes the oxidation of spermine to spermadine and secondarily produces hydrogen peroxide. Multiple transcript variants encoding different isoenzymes have been identified for this gene, some of which have failed to demonstrate significant oxidase activity on natural polyamine substrates. The characterized isoenzymes have distinctive biochemical characteristics and substrate specificities, suggesting the existence of additional levels of complexity in polyamine catabolism. [provided by RefSeq, Jul 2012]

多胺是普遍存在的聚阳离子烷基胺,其中包括精胺,亚精胺,腐胺,和胍丁胺。这些分子参与广泛的细胞功能,包括细胞周期调节,清除活性氧物质,以及基因表达的控制。这些分子也在神经传递通过其调节细胞表面受体活性,在细胞内信号通路参与,和它们的推定的角色神经递质发挥重要作用。该基因编码一种催化精胺对spermadine的氧化和二次产生过氧化氢的含FAD-酶。编码不同同功酶的多个转录物变体已确定该基因,其中一些已未能证明对天然多胺底显著氧化酶活性。的特征在于同工酶具有独特的生化特征和底物特异性,这表明在多胺分解代谢复杂的附加级别的存在。 [由RefSeq的,2012年7月提供]

CCND1基因的碱基序列:[NCBI]
Loading Gene Browser...
SMOX基因的碱基突变:           仅显示部分snp
rs880648       rs910954       rs927091       rs945771       rs945772       rs1051904       rs1124983       rs1310180       rs1310181       rs1337281       rs1535225       rs1538071       rs1538072       rs1538073       rs1538074       rs1538075       rs1611939      

SMOX基因在不同组织中的表达:    [UniProt]

基因在不同组织中的表达图
正向引物序列
正向Tm值
反向引物序列
反向Tm值
评分
AGAGTGTGAAACTTGGACAC
58
AGATGATAGATAGGGTTCCCA
57
AGTACCTGAAGGTGGAGAG
58
GTTTCCCTAGCTGGATGAC
58
CAGTACCTGAAGGGAACCC
59
ACCTGCGTGTATGAATAGGA
59
TGCTACCTTACCAACCACG
60
TGGGTCAAGTTATAGACCTCG
59
TGGAATGGAACCCATCTTCC
60
TCTAGGAACCACGAACATCC
59
TATTCATACACGCAGGTGG
57
GAATAGTACTTGCGGTGGG
58
GGAATGGAACCCATCTTCCT
60
TTCTAGGAACCACGAACATCC
60
CTGCTACCTTACCAACCAC
58
GGGTCAAGTTATAGACCTCG
57
CAGTACCTGAAGGGAACCC
59
CTGCGTGTATGAATAGGAGC
59
TATTCATACACGCAGGTGG
57
AATAGTACTTGCGGTGGGT
59
      尚未收录相关数据

SMOX基因(以及对应的蛋白质)的细胞分布位置:

[UniProt]     [GenomeNet]

" d="M482.414,245.296c3.539,4.293,4.455,10.009,0.202,11 c-4.244,0.996-4.983-10.983-8.293-8.438c-5.271,4.08,9.834,12.271,5.144,17.287c-3.717,3.607-6.172-5.75-10.839-1.976 c-4.673,3.776,6.781,7.299,2.831,11.326c-4.354,4.045-6.979-1.449-9.837-5.517c-1.193-1.742-2.059-3.851-3.595-2.748 c-1.516,1.078-1.854,1.795-0.938,3.666c2.374,4.854,9.235,10.119,5.156,12.535c-5.636,3.346-5.044-8.871-9.426-7.574 c-4.388,1.291,2.557,10.66-1.245,11.141c-4.089,0.545-3.483-10.239-6.979-8.575c-2.522,1.206-0.929,3.071-0.938,4.899 c0.004,1.32-0.964,3.6-2.372,4.062c-3.593,1.171-8.544-1.065-10.251-3.59c-6.04-8.93,0.396-15.997,4.639-7.015 c3.023,4.642,5.182,0.834,2.839-2.219c-1.032-1.354-4.309-5.901-0.781-7.252c2.904-1.113,4.271,1.941,5.985,4.592 c2.61,4.016,5.485,0.117,3.031-3.414c-1.828-2.633-2.74-3.803,3.156-7.42c6.405-4.369,6.52,3.869,10.077,0.646 c2.309-1.832-4.783-5.149,0.06-8.995c2.896-2.293,5.18,6.207,7.961,3.516c3.523-2.737-7.717-7.369,0.117-11.736 C473.413,240.77,480.519,242.891,482.414,245.296z"/> Extracellular space Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi Apparatus Nucleus Mitochondrion 0 1 2 3 4 5 Confidence
  • 质膜
  • 细胞质
  • 细胞外
  • 高尔基体
  • 囊泡
  • 细胞骨架
  • 内质网
  • 细胞核
  • 内体
  • 溶酶体
  • 线粒体

SMOX基因的本体(GO)信息:

GO库代码
对应的蛋白质
来源代码
GO:0016491
Q5TE25 (UniProtKB)
IEA
GO:0055114
Q5TE25 (UniProtKB)
IEA
GO:0005634
Q9NWM0 (UniProtKB)
IEA
GO:0005634
Q9NWM0 (UniProtKB)
IDA
GO:0005634
Q9NWM0 (UniProtKB)
IDA
GO:0005634
Q9NWM0 (UniProtKB)
IDA
GO:0005737
Q9NWM0 (UniProtKB)
IDA
GO:0005737
Q9NWM0 (UniProtKB)
IDA
GO:0005737
Q9NWM0 (UniProtKB)
IDA
GO:0005737
Q9NWM0 (UniProtKB)
IDA
GO:0005829
Q9NWM0 (UniProtKB)
TAS
GO:0006596
Q9NWM0 (UniProtKB)
TAS
GO:0006598
Q9NWM0 (UniProtKB)
IDA
GO:0046208
Q9NWM0 (UniProtKB)
IEA
GO:0046208
Q9NWM0 (UniProtKB)
IDA
GO:0046208
Q9NWM0 (UniProtKB)
IDA
GO:0046208
Q9NWM0 (UniProtKB)
IDA
GO:0046592
Q9NWM0 (UniProtKB)
IDA
GO:0046592
Q9NWM0 (UniProtKB)
IDA
GO:0046592
Q9NWM0 (UniProtKB)
IDA
GO:0046592
Q9NWM0 (UniProtKB)
IDA
GO:0052894
Q9NWM0 (UniProtKB)
IEA
GO:0052895
Q9NWM0 (UniProtKB)
IEA
GO:0052901
Q9NWM0 (UniProtKB)
TAS
GO:0055114
Q9NWM0 (UniProtKB)
IEA
GO:0055114
Q9NWM0 (UniProtKB)
IEA
GO:0055114
Q9NWM0 (UniProtKB)
IEA
GO:0055114
Q9NWM0 (UniProtKB)
IEA

可能调控 SMOX基因的相关microRNA:     

String

基因与其他基因之间的相互作用关系图
序号 作用方式 资源库来源/分值 基因名称 基因名称
疾病名称 关系值 NofPmids NofSnps 来源
疾病名称 关系值 NofPmids NofSnps 来源
Cerebrovascular accident 0.12 1 0 CTD_human
Alzheimer's Disease 0.12 1 1 GWASCAT
Dementia 0.12 1 1 GWASCAT
Prostatic Intraepithelial Neoplasias 0.00272435 1 0 LHGDN
Prostatic Neoplasms 0.00272435 1 0 LHGDN
Mammary Neoplasms 0.00272435 1 0 LHGDN
Tobacco Use Disorder 0.002367032 1 0 GAD
Panic Disorder 0.002367032 1 1 GAD
Cystic Fibrosis 0.001900093 7 0 BeFree
Experimental Organism Basal Cell Carcinoma 0.001628651 6 0 BeFree

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