PER2 (period circadian regulator 2)

symbol:
PER2
locus group:
protein-coding gene
location:
2q37.3
gene_family:
alias symbol:
KIAA0347
alias name:
None
entrez id:
8864
ensembl gene id:
ENSG00000132326
ucsc gene id:
uc002vyc.4
refseq accession:
NM_022817
hgnc_id:
HGNC:8846
approved reserved:
1999-06-11
2q37.3
基因染色体位置图

PER2(Period Circadian Regulator 2)是生物钟调控的核心基因之一,属于Period基因家族(包括PER1、PER2和PER3),该家族成员在维持昼夜节律中起关键作用。PER2通过与其他生物钟蛋白(如CLOCK和BMAL1)相互作用,形成负反馈环路,抑制自身转录,从而调控24小时周期的基因表达节律。其表达产物PER2蛋白在细胞核和细胞质之间穿梭,通过磷酸化和泛素化修饰调节稳定性,进而影响睡眠-觉醒周期、代谢、免疫功能和细胞增殖等生理过程。PER2主要在中枢神经系统(如视交叉上核)和外周组织(如肝脏、心脏)中表达,协调局部与全身节律。突变或表达异常会导致昼夜节律紊乱,例如家族性睡眠相位提前综合征(FASPS)与PER2的S662G突变相关,该突变加速蛋白降解,缩短生物钟周期。PER2还与多种疾病有关,包括失眠、抑郁症、代谢综合征和癌症(如乳腺癌和结直肠癌),其低表达可能促进肿瘤细胞增殖。过表达PER2可增强节律振幅并改善代谢异常,但可能抑制细胞生长;而表达降低会导致节律失调、糖代谢紊乱和免疫功能下降。PER基因家族的共性在于均含有PAS结构域(介导蛋白相互作用)和核定位信号,通过类似的负反馈机制参与生物钟调控,但各成员在组织分布和功能上存在差异,例如PER3对光敏感性较低。PER2还通过调控下游基因(如CCGs)影响体温、激素分泌等生理功能,其表达受光照、饮食等环境因素调节。

This gene is a member of the Period family of genes and is expressed in a circadian pattern in the suprachiasmatic nucleus, the primary circadian pacemaker in the mammalian brain. Genes in this family encode components of the circadian rhythms of locomotor activity, metabolism, and behavior. This gene is upregulated by CLOCK/ARNTL heterodimers but then represses this upregulation in a feedback loop using PER/CRY heterodimers to interact with CLOCK/ARNTL. Polymorphisms in this gene may increase the risk of getting certain cancers and have been linked to sleep disorders. [provided by RefSeq, Jan 2014]

该基因是时期基因家族的成员,并在视交叉上核,在哺乳动物脑的主要昼夜起搏器昼夜图案表示。基因的活动能力,代谢和行为的昼夜节律的这个家族编码的组件。该基因是由时钟/ ARNTL异上调但随后压制这种上调使用PER / CRY异与时钟/ ARNTL互动反馈环路。在这种基因多态性可能增加得到某些癌症的风险,并已与睡眠障碍。 [由RefSeq的,2014年1月提供]

CCND1基因的碱基序列:[NCBI]
Loading Gene Browser...
PER2基因的碱基突变:           仅显示部分snp
rs744837       rs880140       rs934944       rs934945       rs1972874       rs2119022       rs2304668       rs2304669       rs2304670       rs2304671       rs2304672       rs2304673       rs2304674       rs2304675       rs2304676       rs2304677       rs3217472      

PER2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
GAGAGTCAGAAGCAGGAGC
60
TAAACACATTCTGCCACGTC
59
AGTGGACATGAGACCAACG
60
AAAGGTATCTGGACTCTGGC
59
TGTGGATGAAAGTCCTGCA
59
GATGTACTCTCCGTTCCGG
60
AGTGGACATGAGACCAACG
60
AAAGGTATCTGGACTCTGGC
59
AAATCTCCTTCATCATTGGGAG
58
AAACACGTCCTCATTCAAAGG
59
GTGGACATGAGACCAACGA
60
AAAGGTATCTGGACTCTGGC
59
GGAGAGTCAGAAGCAGGAG
59
AAACACATTCTGCCACGTC
59
GGATGAAAGTCCTGCAGTC
58
GTGATGTACTCTCCGTTCC
57
GTGGACATGAGACCAACGA
60
AAAGGTATCTGGACTCTGGC
59
AATCTCCTTCATCATTGGGAG
58
AAACACGTCCTCATTCAAAGG
59
转录因子
影响基因
影响类型
参考文献链接(PubMed)
ARNTL
PER2
Activation
ARNTL
PER2
Unknown
CLOCK
PER2
Activation
CLOCK
PER2
Unknown
NPAS2
PER2
Unknown
PER2
SNAI2
Repression
PER2
TWIST1
Repression

PER2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

PER2基因的本体(GO)信息:

GO库代码
对应的蛋白质
来源代码
GO:0000122
O15055 (UniProtKB)
ISS
GO:0000122
O15055 (UniProtKB)
ISS
GO:0000976
O15055 (UniProtKB)
ISS
GO:0000989
O15055 (UniProtKB)
ISS
GO:0002931
O15055 (UniProtKB)
ISS
GO:0003713
O15055 (UniProtKB)
ISS
GO:0005515
O15055 (UniProtKB)
IPI
GO:0005634
O15055 (UniProtKB)
ISS
GO:0005634
O15055 (UniProtKB)
IDA
GO:0005654
O15055 (UniProtKB)
IDA
GO:0005730
O15055 (UniProtKB)
IEA
GO:0005737
O15055 (UniProtKB)
IDA
GO:0005978
O15055 (UniProtKB)
ISS
GO:0006094
O15055 (UniProtKB)
ISS
GO:0006351
O15055 (UniProtKB)
IEA
GO:0006631
O15055 (UniProtKB)
ISS
GO:0007623
O15055 (UniProtKB)
TAS
GO:0019229
O15055 (UniProtKB)
ISS
GO:0019249
O15055 (UniProtKB)
ISS
GO:0031397
O15055 (UniProtKB)
ISS
GO:0032922
O15055 (UniProtKB)
ISS
GO:0042752
O15055 (UniProtKB)
ISS
GO:0042754
O15055 (UniProtKB)
ISS
GO:0043130
O15055 (UniProtKB)
ISS
GO:0045892
O15055 (UniProtKB)
ISS
GO:0048471
O15055 (UniProtKB)
IEA
GO:0050767
O15055 (UniProtKB)
ISS
GO:0050796
O15055 (UniProtKB)
ISS
GO:0050872
O15055 (UniProtKB)
ISS
GO:0051726
O15055 (UniProtKB)
ISS
GO:0051946
O15055 (UniProtKB)
ISS
GO:0070345
O15055 (UniProtKB)
ISS
GO:0070932
O15055 (UniProtKB)
ISS
GO:0097167
O15055 (UniProtKB)
ISS
GO:2000678
O15055 (UniProtKB)
ISS

可能调控 PER2基因的相关microRNA:     

Reactome

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
Advanced Sleep-Phase Syndrome, Familial 0.242442977 9 1 BeFree_CLINVAR_CTD_human
Substance Withdrawal Syndrome 0.12 2 0 CTD_human
ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1 0.12 1 0 UNIPROT
Alcoholic Intoxication 0.12 1 0 CTD_human
Myeloid Leukemia, Chronic 0.12 1 0 CTD_human
Bipolar Disorder 0.005905708 4 0 BeFree_GAD_LHGDN
Sleep Disorders 0.005276948 4 0 BeFree_GAD
Lymphoma 0.003810118 4 0 BeFree_LHGDN
Mental Depression 0.003724241 5 0 BeFree_GAD
Leukemia, Myelocytic, Acute 0.003267234 2 0 BeFree_LHGDN

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