TRPM5 (transient receptor potential cation channel subfamily M member 5)

symbol:
TRPM5
locus group:
protein-coding gene
location:
11p15.5
gene_family:
Transient receptor potential cation channels
alias symbol:
LTRPC5|MTR1
alias name:
None
entrez id:
29850
ensembl gene id:
ENSG00000070985
ucsc gene id:
uc001lwm.5
refseq accession:
NM_014555
hgnc_id:
HGNC:14323
approved reserved:
2002-01-11
11p15.5
基因染色体位置图

TRPM5(瞬时受体电位阳离子通道亚家族M成员5)是一种钙离子(Ca²⁺)激活的非选择性阳离子通道,属于TRP(瞬时受体电位)基因家族中的TRPM亚家族。TRP通道是一类广泛存在于生物体内的膜蛋白,主要参与感知外界刺激(如温度、味道、机械力等)和细胞内信号传导。TRPM5在味觉信号转导中起关键作用,主要表达于舌部的味蕾细胞中,尤其是甜味、鲜味(umami)和苦味感受细胞。当味觉受体被激活后,细胞内钙离子浓度升高,TRPM5通道开放,导致细胞去极化并触发神经信号传递至大脑。此外,TRPM5也存在于肠道、胰腺和呼吸道等组织,可能参与激素分泌和免疫调节。TRPM5的功能特点是其高度依赖细胞内钙离子(Ca²⁺)激活,但对电压变化不敏感,且对单价阳离子(如Na⁺、K⁺)的通透性高于二价阳离子。TRPM5基因突变可能导致味觉功能障碍,例如对甜味或苦味的感知异常。研究发现,TRPM5与代谢性疾病(如糖尿病、肥胖)有关,因为味觉信号异常可能影响食欲和能量摄入。在呼吸道中,TRPM5的异常表达可能与哮喘等炎症性疾病相关。TRPM5过表达可能增强味觉敏感度或导致细胞过度兴奋,而表达降低可能导致味觉迟钝或信号转导障碍。TRPM5属于TRPM基因家族,该家族共有8个成员(TRPM1-8),其共性是均含有TRP结构域(负责通道形成和调控)和多个跨膜区,主要参与温度感知、离子稳态和细胞增殖等生理过程。TRPM亚家族成员通常对二价阳离子(如Mg²⁺、Ca²⁺)有一定通透性,但TRPM5是其中的例外,主要通透单价离子。TRPM5的研究为开发针对味觉障碍或代谢性疾病的药物提供了潜在靶点。

This gene encodes a member of the transient receptor potential (TRP) protein family, which is a diverse group of proteins with structural features typical of ion channels. This protein plays an important role in taste transduction, and has characteristics of a calcium-activated, non-selective cation channel that carries Na+, K+, and Cs+ ions equally well, but not Ca(2+) ions. It is activated by lower concentrations of intracellular Ca(2+), and inhibited by higher concentrations. It is also a highly temperature-sensitive, heat activated channel showing a steep increase of inward currents at temperatures between 15 and 35 degrees Celsius. This gene is located within the Beckwith-Wiedemann syndrome critical region-1 on chromosome 11p15.5, and has been shown to be imprinted, with exclusive expression from the paternal allele. [provided by RefSeq, Oct 2010]

该基因编码的瞬时受体电位(TRP)家族蛋白,这与典型的离子通道的结构特征的蛋白质的不同群体的成员。这种蛋白在味觉转导中起重要作用,并具有携带的Na +,K +和Cs +离子同样一钙激活,非选择性阳离子通道的特征,但不是钙离子的离子。它是由低浓度的细胞内钙离子的激活,并通过较高浓度的抑制。这也显示出内向电流在温度摄氏15至35度之间的急剧增加高温度敏感,热激活通道。该基因位于染色体11p15.5贝克威-威德曼综合征关键区域-1内,并已被证明是印迹与来自父亲的等位基因排他性表达。 [由RefSeq的,2010年10月提供]

TRPM5基因的碱基序列:[NCBI]
Loading Gene Browser...
TRPM5基因的碱基突变:           仅显示部分snp
rs1859080       rs1978125       rs11022821       rs12292286       rs61873488       rs61873489       rs61873490       rs74050572       rs74396926       rs75191383       rs79000975       rs114694740       rs114985294       rs115690918       rs116189615       rs116812595       rs118043325      

TRPM5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
GACTTCATTGCCAAGTACCTC
59
GCAGTAGTTGATCTGTGACTC
58
GACTTCATTGCCAAGTACCT
57
GCAGTAGTTGATCTGTGACTC
58
GGACTTCATTGCCAAGTACC
59
CAGTAGTTGATCTGTGACTCCA
59
      尚未收录相关数据

TRPM5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

TRPM5基因的本体(GO)信息:

GO库代码
对应的蛋白质
来源代码
GO:0005216
A0A0C4DGF4 (UniProtKB)
IEA
GO:0016021
A0A0C4DGF4 (UniProtKB)
IEA
GO:0034220
A0A0C4DGF4 (UniProtKB)
IEA
GO:0005227
E9PQF7 (UniProtKB)
IEA
GO:0016021
E9PQF7 (UniProtKB)
IEA
GO:0050909
E9PQF7 (UniProtKB)
IEA
GO:0098655
E9PQF7 (UniProtKB)
IEA
GO:0005227
E9PRW0 (UniProtKB)
IEA
GO:0016021
E9PRW0 (UniProtKB)
IEA
GO:0050909
E9PRW0 (UniProtKB)
IEA
GO:0098655
E9PRW0 (UniProtKB)
IEA
GO:0005216
Q9NZQ8 (UniProtKB)
TAS
GO:0005227
Q9NZQ8 (UniProtKB)
IEA
GO:0005244
Q9NZQ8 (UniProtKB)
IEA
GO:0005267
Q9NZQ8 (UniProtKB)
IEA
GO:0005272
Q9NZQ8 (UniProtKB)
TAS
GO:0005886
Q9NZQ8 (UniProtKB)
TAS
GO:0016021
Q9NZQ8 (UniProtKB)
IEA
GO:0030425
Q9NZQ8 (UniProtKB)
IEA
GO:0034765
Q9NZQ8 (UniProtKB)
IEA
GO:0035725
Q9NZQ8 (UniProtKB)
IEA
GO:0043025
Q9NZQ8 (UniProtKB)
IEA
GO:0050909
Q9NZQ8 (UniProtKB)
IEA
GO:0070588
Q9NZQ8 (UniProtKB)
TAS
GO:0071805
Q9NZQ8 (UniProtKB)
IEA

可能调控 TRPM5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
Diabetes Mellitus, Non-Insulin-Dependent 0.000814326 3 0 BeFree
Adenocarcinoma 0.000271442 1 0 BeFree
Rhabdomyosarcoma 0.000271442 1 0 BeFree
Metabolic Syndrome X 0.000271442 1 0 BeFree
Breast Carcinoma 0.000271442 1 0 BeFree
Malignant neoplasm of breast 0.000271442 1 0 BeFree

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