PDHA1 (pyruvate dehydrogenase E1 subunit alpha 1)

symbol:
PDHA1
locus group:
protein-coding gene
location:
Xp22.12
gene_family:
alias symbol:
E1alpha
alias name:
pyruvate dehydrogenase E1 componen…
entrez id:
5160
ensembl gene id:
ENSG00000131828
ucsc gene id:
uc011mjc.3
refseq accession:
NM_000284
hgnc_id:
HGNC:8806
approved reserved:
1989-06-30
Xp22.12
基因染色体位置图

PDHA1(丙酮酸脱氢酶E1α亚基)基因位于X染色体(Xp22.12),编码丙酮酸脱氢酶复合体(PDC)的关键组分,负责将丙酮酸转化为乙酰辅酶A,连接糖酵解与三羧酸循环(TCA循环),是细胞能量代谢的核心酶。其表达产物为PDHA1蛋白,与PDHB(E1β亚基)共同形成E1组分,依赖硫胺素焦磷酸(TPP)催化丙酮酸脱羧。PDHA1的活性受磷酸化调控(PDK激酶抑制,PDP磷酸酶激活),主要在线粒体基质发挥作用。突变(如R263H、R349C)会导致PDHA1缺乏症,表现为乳酸酸中毒、神经退行性变(Leigh综合征样症状)及发育迟缓,属于X连锁遗传病。该基因过表达可能增强糖代谢流但罕见报道,而表达降低或功能缺失会阻断丙酮酸氧化,迫使细胞依赖无氧糖酵解(类似Warburg效应),影响ATP生成并累积乳酸。PDHA1属于丙酮酸脱氢酶复合体基因家族,该家族还包括PDHB、DLAT(E2)、DLD(E3)等,共同构成多酶复合体,其共性是通过协同作用完成丙酮酸氧化脱羧。PDHA1还与癌症相关(某些肿瘤中表达下调),并可能通过代谢重编程影响免疫细胞功能(如T细胞活化)。

The pyruvate dehydrogenase (PDH) complex is a nuclear-encoded mitochondrial multienzyme complex that catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2), and provides the primary link between glycolysis and the tricarboxylic acid (TCA) cycle. The PDH complex is composed of multiple copies of three enzymatic components: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and lipoamide dehydrogenase (E3). The E1 enzyme is a heterotetramer of two alpha and two beta subunits. This gene encodes the E1 alpha 1 subunit containing the E1 active site, and plays a key role in the function of the PDH complex. Mutations in this gene are associated with pyruvate dehydrogenase E1-alpha deficiency and X-linked Leigh syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2010]

的丙酮酸脱氢酶(PDH)复合物是核编码的线粒体多酶复合催化丙酮酸的总转化为乙酰-CoA和CO(2),并提供了糖酵解和三羧酸(TCA)之间的主链路周期。 PDH复合物是由三个酶组分的多个拷贝:丙酮酸脱氢酶(E1),二氢硫辛酰胺乙酰转移酶(E2)和硫辛酰胺脱氢酶(E3)。将E1酶是两个α和两个β亚基的异四聚体。该基因编码含有E1的活性部位的E1的α1亚单位,并播放在PDH复合物的功能的关键的作用。在这种基因突变与丙酮酸脱氢酶的E1-α缺乏和X-连锁Leigh综合征有关。另外剪接转录变体编码不同亚型也发现了这种基因。[由RefSeq的,2010年3月提供]

PDHA1基因的碱基序列:[NCBI]
Loading Gene Browser...
PDHA1基因的碱基突变:           仅显示部分snp
rs781681212       rs781301068       rs781441358       rs781171460       rs781176856       rs781121875       rs781061388       rs780973496       rs780856898       rs780865791       rs780847301       rs780672353       rs780572519       rs780521730       rs780413596       rs780183383       rs780298971      

PDHA1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
GAATGGGAACGTCTGTTGAG
59
ATTCCATCCACTCTCAGCC
59
TGCTCTAGCCTGTAAGTATAATGG
60
ATATCTGGCCCTGGTTAGC
59
TGCTCTAGCCTGTAAGTATAATGG
60
ATATCTGGCCCTGGTTAGC
59
GTGTGATGGTCAGGAAGCT
60
GGTGAAAGTAAAGCCGTGAG
59
TAAAGGGAAAGGAGGATCGA
58
CTTCGAATATCTGGCCCTG
58
TGCTCTAGCCTGTAAGTATAATGG
60
ATATCTGGCCCTGGTTAGC
59
GAGTTGAAAGCAGATCAGCT
58
AGGAAGGAGAAACTGACCA
58
GTGTGATGGTCAGGAAGCT
60
GGTGAAAGTAAAGCCGTGAG
59
CTTCTCAGAAGCCGTTTGC
60
CTGGGCACTTTCAAAGGTG
59
GTGTGATGGTCAGGAAGCT
60
GGTGAAAGTAAAGCCGTGAG
59
转录因子
影响基因
影响类型
参考文献链接(PubMed)
FOS
PDHA1
Unknown
JUN
PDHA1
Unknown
SP1
PDHA1
Unknown

PDHA1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

PDHA1基因的本体(GO)信息:

GO库代码
对应的蛋白质
来源代码
GO:0004738
P08559 (UniProtKB)
IDA
GO:0004739
P08559 (UniProtKB)
IEA
GO:0005634
P08559 (UniProtKB)
IDA
GO:0005739
P08559 (UniProtKB)
IDA
GO:0005759
P08559 (UniProtKB)
TAS
GO:0005759
P08559 (UniProtKB)
TAS
GO:0005759
P08559 (UniProtKB)
TAS
GO:0005759
P08559 (UniProtKB)
TAS
GO:0006006
P08559 (UniProtKB)
IEA
GO:0006086
P08559 (UniProtKB)
IDA
GO:0006090
P08559 (UniProtKB)
TAS
GO:0006099
P08559 (UniProtKB)
IDA
GO:0010510
P08559 (UniProtKB)
TAS
GO:0034604
P08559 (UniProtKB)
IEA
GO:0043209
P08559 (UniProtKB)
IEA
GO:0045254
P08559 (UniProtKB)
IDA
GO:0046487
P08559 (UniProtKB)
TAS
GO:0061732
P08559 (UniProtKB)
IEA
GO:0016624
Q5JPT9 (UniProtKB)
IEA
GO:0055114
Q5JPT9 (UniProtKB)
IEA
GO:0016624
Q5JPU0 (UniProtKB)
IEA
GO:0055114
Q5JPU0 (UniProtKB)
IEA
GO:0016624
Q5JPU1 (UniProtKB)
IEA
GO:0055114
Q5JPU1 (UniProtKB)
IEA
GO:0016624
Q5JPU3 (UniProtKB)
IEA
GO:0055114
Q5JPU3 (UniProtKB)
IEA

可能调控 PDHA1基因的相关microRNA:     

Reactome

MINT

BioGrid

IntAct

mentha

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
Pyruvate Dehydrogenase E1 Alpha Deficiency 0.24 11 2 ORPHANET_UNIPROT
Pyruvate Dehydrogenase Complex Deficiency Disease 0.124071628 16 0 BeFree_CTD_human
Acidosis, Lactic 0.120814326 4 0 BeFree_CTD_human
Pyruvate Metabolism, Inborn Errors 0.12 1 0 CTD_human
Stomach Neoplasms 0.12 1 0 CTD_human
Degenerative polyarthritis 0.12 1 0 CTD_human
Disease Progression 0.12 1 0 CTD_human
Myocardial Ischemia 0.12 1 0 CTD_human
Prostatic Neoplasms 0.12 1 0 CTD_human
Ataxia 0.000542884 2 0 BeFree

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