PER3
PER3 | |||
---|---|---|---|
Identifiers | |||
Gene ontology | |||
Molecular function | |||
Cellular component | |||
Biological process |
| ||
Sources:Amigo / QuickGO |
Ensembl | |||||||||
---|---|---|---|---|---|---|---|---|---|
UniProt | |||||||||
RefSeq (mRNA) |
| ||||||||
RefSeq (protein) |
| ||||||||
Location (UCSC) | Chr 1: 7.78 – 7.85 Mb | Chr 4: 151 – 151.04 Mb | |||||||
PubMed search | [3] | [4] |
View/Edit Human | View/Edit Mouse |
The PER3
History
The Per3 gene was independently cloned by two research groups (Kobe University School of Medicine and Harvard Medical School) who both published their discovery in June 1998.[7][8] The mammalian Per3 was discovered by searching for homologous cDNA sequences to Per2. The amino acid sequence of the mouse PERIOD3 protein (mPER3) is between 37-56% similar to the other two PER proteins.[8][7]
Function
This gene is a member of the Period family of genes. It is expressed in a
Role in chronobiology
The
The mPER3 protein contains a PAS domain, similar to mPER1 and mPER2. Likely, mPER3 binds to other proteins using this domain.[8] However, while PER1/2 have been shown to be important in the transcription-translation feedback loop involved in the intracellular circadian clock, the influence of PER3 in this loop has not yet been fully elucidated, given that mPER3 does not appear to be functionally redundant to mPER1 and mPER2.[12] mPer3 may not be a member of the core clock loop at all.[12]
Animal studies
While the Per3 gene is a
Per3 knockout mice experience a slightly shortened period of locomotor activity (by 0.5 hr[13]) and are less sensitive to light, in that they entrain more slowly to changes in the light-dark cycle. PER3 may be involved in the suppression of behavioral activity in response to light, although mPer3 expression is not necessary for circadian rhythms.[14][15]
Clinical significance
The PER3 “length” polymorphism in the 54-bp repeat sequence in exon 18 (GenBank accession no. AB047686) is a structural polymorphism due to an insertion or deletion of 18 amino acids in a region encoding a putative phosphorylation domain. The polymorphism has been associated with diurnal preference and
Gene
Orthologs
The following is a list of some orthologs of the PER3 gene in other species:[17]
- PER3 (P. troglodytes)
- PER3 (M. mulatta)
- PER3 (C. lupus)
- PER3 (H. sapiens)
- PER3 (B. taurus)
- Per3 (M. musculus)
- Per3 (R. norvegicus)
- PER3 (G. gallus)
- per3 (X. tropicalis)
- per3 (D. rerio)
Paralogs
- PER1
- PER2
Gene location
The human PER3 gene is located on chromosome 1 at the following location:[18]
- Start: 7,784,320 bp
- Finish: 7,845,181 bp
- Length: 60,862 bases
- Exons: 25
PER3 has 19 transcripts (splice variants).
Protein structure
The PER3 protein has been identified to have the following features:[19]
- Size: 1201 amino acids
- Molecular mass: 131888 Da
- Quaternary structure: Homodimer
Post translational modifications
The following are some known post transcriptional modifications to the Per3 gene:[19]
- Phosphorylation by CSNK1E is weak and appears to require association with PER1 and translocation to the nucleus.
- Ubiquitinated.
- Modification sites at PhosphoSitePlus
- Modification sites at neXtProt
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000049246 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028957 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- S2CID 10059149.
- ^ PMID 12841365.
- ^ PMID 9707434.
- ^ S2CID 14797914.
- ^ "Entrez Gene: PER3 period homolog 3 (Human)".
- PMID 22253927.
- ^ PMID 26903630.
- ^ S2CID 219582.
- ^ PMID 10938103.
- S2CID 770136.
- PMID 24982860.
- S2CID 36626446.
- ^ "PER3". Homologene. NCBI. 2017. Retrieved 12 Apr 2017.
- ^ "PER3". Entrez Gene. NCBI. 2017. Retrieved 12 Apr 2017.
- ^ a b "Per3 Gene". GeneCards. Weizmann Institute of Science. Retrieved April 12, 2017.
External links
- PER3+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
This article incorporates text from the United States National Library of Medicine, which is in the public domain.