PYCR2

Pyrroline-5-carboxylate reductase family, member 2 is a protein that in humans is encoded by the PYCR2 gene.[5]

PYCR2
Identifiers
AliasesPYCR2, P5CR2, HLD10, pyrroline-5-carboxylate reductase family member 2, pyrroline-5-carboxylate reductase 2
External IDsOMIM: 616406 MGI: 1277956 HomoloGene: 8343 GeneCards: PYCR2
Orthologs
SpeciesHumanMouse
Entrez

29920

69051

Ensembl

ENSG00000143811

ENSMUSG00000026520

UniProt

Q96C36

Q922Q4

RefSeq (mRNA)

NM_013328
NM_001271681

NM_133705

RefSeq (protein)

NP_001258610
NP_037460

NP_598466

Location (UCSC)Chr 1: 225.92 – 225.92 MbChr 1: 180.73 – 180.74 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

This gene belongs to the pyrroline-5-carboxylate reductase family. The encoded mitochondrial protein catalyzes the conversion of pyrroline-5-carboxylate to proline, which is the last step in proline biosynthesis.[5] Loss of PYCR2 does not lead to a gross defect in mitochondrial protein synthesis, but loss of function of PYCR2 leads to increased apoptosis under oxidative stress.[6]

Clinical significance

Mutations in the PYCR2 gene have been identified as the cause of a unique syndrome characterized by postnatal microcephaly, hypomyelination, and reduced cerebral white-matter volume. Hypomyelination and the absence of wrinkly skin makes this condition distinct from that caused by previously reported mutations in the gene encoding PYCR2’s isozyme, PYCR1, suggesting a unique and indispensable role for PYCR2 in the human CNS during development. This is substantiated by the fact that PYCR2 mRNA is moderately expressed in the developing human brain, and in much higher forms than either of the other two isoforms. Although PYCR2 is an enzyme for proline biosynthesis, systemic deprivation of proline does not appear to be the pathogenetic mechanism of this condition, given that plasma amino acid analysis in two affected individuals did not show low proline levels. Furthermore, mitochondrial protein synthesis was not affected in PYCR2-deficient cells. Therefore, deficiency of proline, as a building block of proteins, might not be the major pathophysiology. However, proline has been reported as a non-enzymatic antioxidant that suppresses apoptosis, and therefore local proline biosynthesis in neurons might be important for neuronal protection against oxidative stress.[6]

The PYCR family also has been correlated with melanoma cells. PYCR2 as well as PYCR are abundant in melanoma cells but not detected in melanocytes.[7]

References

  1. GRCh38: Ensembl release 89: ENSG00000143811 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000026520 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: Pyrroline-5-carboxylate reductase family, member 2".
  6. Nakayama, T; Al-Maawali, A; El-Quessny, M; Rajab, A; Khalil, S; Stoler, JM; Tan, WH; Nasir, R; Schmitz-Abe, K; Hill, RS; Partlow, JN; Al-Saffar, M; Servattalab, S; LaCoursiere, CM; Tambunan, DE; Coulter, ME; Elhosary, PC; Gorski, G; Barkovich, AJ; Markianos, K; Poduri, A; Mochida, GH (7 May 2015). "Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination". American Journal of Human Genetics. 96 (5): 709–19. doi:10.1016/j.ajhg.2015.03.003. PMC 4570282. PMID 25865492.
  7. De Ingeniis, J; Ratnikov, B; Richardson, AD; Scott, DA; Aza-Blanc, P; De, SK; Kazanov, M; Pellecchia, M; Ronai, Z; Osterman, AL; Smith, JW (2012). "Functional specialization in proline biosynthesis of melanoma". PLOS ONE. 7 (9): e45190. Bibcode:2012PLoSO...745190D. doi:10.1371/journal.pone.0045190. PMC 3443215. PMID 23024808.

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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