GenAge entry for PYCR1 (Homo sapiens)
Gene name (HAGRID: 280)
- HGNC symbol
- PYCR1
- Aliases
- P5C
- Common name
- pyrroline-5-carboxylate reductase 1
Potential relevance to the human ageing process
- Main reason for selection
- Entry selected based on indirect or inconclusive evidence linking the gene product to ageing in humans or in one or more model systems
- Description
The PYCR1 gene encodes an enzyme that catalyzes the NAD(P)H-dependent conversion of pyrroline-5-carboxylate to proline. It appears that mutations in PYCR1 result in altered mitochondrial function and progeroid changes in connective tissues. Defects in the PYCR1 gene are the cause of cutis laxa autosomal recessive type 2B, a syndromal disorder characterized by the appearance of premature ageing, wrinkled and lax skin with reduced elasticity, joint laxity, craniofacial dysmorphic features, growth retardation and developmental delay. Homozygosity or compound heterozygosity for mutations in the PYCR1 gene were found in consanguineous human families, and knockdown of the orthologous genes in Xenopus and zebrafish resulted in epidermal hypoplasia and blistering, accompanied by a massive increase of apoptosis [2202]. Further research is needed in order to fully understand the link between PYCR1 and human ageing.
Cytogenetic information
- Cytogenetic band
- 17q25.3
- Location
- 81,932,386 bp to 81,937,257 bp
- Orientation
- Minus strand
Protein information
- Gene Ontology
-
Process: GO:0006561; proline biosynthetic process
GO:0008652; cellular amino acid biosynthetic process
GO:0034599; cellular response to oxidative stress
GO:0051881; regulation of mitochondrial membrane potential
GO:0055114; oxidation-reduction process
GO:0055129; L-proline biosynthetic process
GO:1903206; negative regulation of hydrogen peroxide-induced cell death
Cellular component: GO:0005739; mitochondrion
GO:0005759; mitochondrial matrix
Function: GO:0004735; pyrroline-5-carboxylate reductase activity
GO:0005515; protein binding
GO:0042802; identical protein binding