GLS2

Source: Wikipedia, the free encyclopedia.
GLS2
Available structures
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_001280796
NM_001280797
NM_001280798
NM_013267
NM_138566

NM_001033264
NM_001285777
NM_001285779

RefSeq (protein)

NP_001267725
NP_001267726
NP_001267727
NP_037399

NP_001028436
NP_001272706
NP_001272708

Location (UCSC)Chr 12: 56.47 – 56.49 MbChr 10: 128.03 – 128.05 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Glutaminase 2 (liver, mitochondrial) is a protein that in humans is encoded by the GLS2 gene.[5]

Structure

The GLS2 gene is on the 12th chromosome in humans, with its specific location being 12q13.3. It contains 19 exons.[5]

Function

GLS2 is a part of the glutaminase family. The protein encoded by this gene is a mitochondrial phosphate-activated glutaminase that catalyzes the hydrolysis of glutamine to stoichiometric amounts of glutamate and ammonia. Originally thought to be liver-specific, this protein has been found in other tissues as well. Alternative splicing results in multiple transcript variants that encode different isoforms.

Clinical significance

GLS2 has interesting molecular relationships with tumor progression and cancer. Glutaminase 2 negatively regulates the PI3K/AKT signaling and shows tumor suppression activity in human hepatocellular carcinoma.[6] Additionally, silencing of GLS and overexpression of GLS2 genes cooperate in decreasing the proliferation and viability of glioblastoma cells.[7]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000135423Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000044005Ensembl, 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. ^ a b "Entrez Gene: Glutaminase 2 (liver, mitochondrial)".
  6. PMID 24797434
    .
  7. .

Further reading

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


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