HINT2

Last updated
HINT2
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases HINT2 , HIT-17, histidine triad nucleotide binding protein 2
External IDs OMIM: 609997 MGI: 1916167 HomoloGene: 13072 GeneCards: HINT2
Gene location (Human)
Ideogram human chromosome 9.svg
Chr. Chromosome 9 (human) [1]
Human chromosome 9 ideogram.svg
HSR 1996 II 3.5e.svg
Red rectangle 2x18.png
Band 9p13.3Start35,812,960 bp [1]
End35,815,354 bp [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_032593

NM_026871

RefSeq (protein)

NP_115982

NP_081147

Location (UCSC) Chr 9: 35.81 – 35.82 Mb Chr 4: 43.65 – 43.66 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

Histidine triad nucleotide binding protein 2 (HINT2) is a mitochondrial protein that in humans is encoded by the HINT2 gene on chromosome 9. This protein is an AMP-lysine hydrolase and phosphoamidase and may contribute to tumor suppression. [5] [6] [7] [8] [9]

Contents

Structure

As a member of the histidine triad nucleotide-binding (Hint) protein family, which is a subfamily of the histidine triad (HIT) family, HINT2 contains a conserved histidine and HIT sequence motif (His-X-His-X-His-X-X), and the latter two histidines contribute to a catalytic triad. [6] [8] The 163-amino acid protein encoded by this gene forms a 17-kDa homodimer. [6] [7] [8] Compared to other members of the Hint family, HINT2 has a 61% sequence homology to HINT1 and 28% sequence homology to HINT3. [6] When compared with HINT1, the 35–amino acid extension at the HINT2 N-terminal corresponds to a predicted mitochondria import signal. [8]

Function

HINT2 is a member of the HIT superfamily and Hint subfamily, which are characterized as nucleotide hydrolases and transferases that act on the alpha-phosphate of ribonucleotides. [5] The Hint family is the oldest within the HIT superfamily and thus, its members are highly conserved among eukaryotes and archaebacteria. [6] The Hint proteins function as AMP-lysine hydrolases and phosphoramidases. [6] [7] [8] [9] In mammals, HINT2 is expressed in the liver, adrenal cortex, and pancreas and localizes to the mitochondria within their cells. [7] [8] Specifically, the protein is located in the inner mitochondrial membrane, facing the mitochondrial matrix. This positioning likely facilitates the transport of cholesterol from the cytosol to the matrix, which is necessary for steroidogenesis, by providing a contact site for the hydrophobic molecule and allowing it to cross the mitochondrial intermembrane space. HINT2 regulates steroidogenesis through calcium-dependent and calcium-independent signalling pathways that may serve to maintain a favorable mitochondrial potential. Its role in calcium homeostasis may also contribute to its proapoptotic function in hepatocytes and other non-steroidogenic cells, though the exact mechanism remains unclear. [7]

Clinical significance

Hint2, one of the three members of the Hint family of proteins, is localized to mitochondria of various cell types. In human adrenocarcinoma cells, Hint2 modulates Ca2+ handling by mitochondria. In all living organisms, intracellular calcium controls a wide variety of physiological processes. Extracellular stimuli generate temporally organized Ca2+ signals, which most of the time occur as repetitive spikes. The frequency of these oscillations controls the nature and the extent of the cellular response. Ca2+ oscillations originate from the repetitive opening of the inositol 1,4,5-trisphosphate (InsP3) receptors that are Ca2+ channels embedded in the membrane of the endoplasmic reticulum (ER). Opening of these channels is initiated by the stimulus-induced rise in InsP3; because their activity is biphasically regulated by the level of cytoplasmic Ca2+, oscillations can occur. Mitochondria also affect cytoplasmic Ca2+ signals. They can both buffer cytosolic Ca2+ changes (7 and 8) and release Ca2+. At rest, intramitochondrial ([Ca2+]m) and cytosolic Ca2+ concentration ([Ca2+]i) are similar, of the order of 100 nM (9).

The Hint family has been implicated in tumor suppression. [6] Int2, a member of the superfamily of histidine triad proteins, has been localized exclusively in mitochondria, near the contact sites of the inner membrane. This enzyme is highly expressed in the liver, where it has been shown to stimulate mitochondrial lipid metabolism, respiration, and glucose homeostasis. Hint2 modulates cytoplasmic and mitochondrial Ca2+ dynamics by stimulating the activity of the mitochondrial respiratory chain. It appears that the absence of Hint2 leads to a premature opening of the mitochondrial permeability transition pore (mPTP) in mitochondrial suspensions. As such, HINT2 plays a prominent role in mitochondrial cell death signaling (e.g. apoptosis) and in ischemia-reperfusion injury (for instance during heart attacks) through calcium homeostasis.

In particular, HINT2 is also observed to be upregulated in breast, pancreatic, and colon cancer cells, while it is downregulated in hepatocellular carcinoma and endometrial cancer. Its exact role in tumor suppression remains unknown, though studies suggest it may promote apoptosis in hepatocellular carcinoma and endometrial cancer. [6] [7] [8] [9] In double knockout Hint2 mice, higher acylation and morphological alterations were observed in the mitochondria, suggesting that Hint2 may regulate glucose and lipid metabolism. [10]

Interactions

Currently, HINT2 has no known protein-protein interaction partners. [6]

See also

Related Research Articles

TRAIL mammalian protein found in Homo sapiens

In the field of cell biology, TNF-related apoptosis-inducing ligand (TRAIL), is a protein functioning as a ligand that induces the process of cell death called apoptosis.

Gelsolin (cellular) protein-coding gene in the species Homo sapiens

Gelsolin is an actin-binding protein that is a key regulator of actin filament assembly and disassembly. Gelsolin is one of the most potent members of the actin-severing gelsolin/villin superfamily, as it severs with nearly 100% efficiency.

Calcium-binding proteins are proteins that participate in calcium cell signalling pathways by binding to Ca2+, the calcium ion that plays an important role in many cellular processes. Calcium-binding proteins have specific domains that bind to calcium and are known to be heterogeneous.

HSP60

Heat shock proteins are generally responsible for preventing damage to proteins in response to high levels of heat. Heat shock proteins are classified into six major families based on their molecular mass: small HSPs, HSP40, HSP60, HSP70, HSP90, and HSP110

HSPA1A protein-coding gene in the species Homo sapiens

Heat shock 70 kDa protein 1, also termed Hsp72, is a protein that in humans is encoded by the HSPA1A gene. As a member of the heat shock protein 70 family and a chaperone protein, it facilitates the proper folding of newly translated and misfolded proteins, as well as stabilize or degrade mutant proteins. In addition, Hsp72 also facilitates DNA repair. Its functions contribute to biological processes including signal transduction, apoptosis, protein homeostasis, and cell growth and differentiation. It has been associated with an extensive number of cancers, neurodegenerative diseases, cell senescence and aging, and inflammatory diseases such as Diabetes mellitus type 2 and rheumatoid arthritis.

Peptidylprolyl isomerase A protein-coding gene in the species Homo sapiens

Peptidylprolyl isomerase A (PPIA), also known as cyclophilin A (CypA) or rotamase A is an enzyme that in humans is encoded by the PPIA gene on chromosome 7. As a member of the peptidyl-prolyl cis-trans isomerase (PPIase) family, this protein catalyzes the cis-trans isomerization of proline imidic peptide bonds, which allows it to regulate many biological processes, including intracellular signaling, transcription, inflammation, and apoptosis. Due to its various functions, PPIA has been implicated in a broad range of inflammatory diseases, including atherosclerosis and arthritis, and viral infections.

DNAJA3 protein-coding gene in the species Homo sapiens

DnaJ homolog subfamily A member 3, mitochondrial, also known as Tumorous imaginal disc 1 (TID1), is a protein that in humans is encoded by the DNAJA3 gene on chromosome 16. This protein belongs to the DNAJ/Hsp40 protein family, which is known for binding and activating Hsp70 chaperone proteins to perform protein folding, degradation, and complex assembly. As a mitochondrial protein, it is involved in maintaining membrane potential and mitochondrial DNA (mtDNA) integrity, as well as cellular processes such as cell movement, growth, and death. Furthermore, it is associated with a broad range of diseases, including neurodegenerative diseases, inflammatory diseases, and cancers.

Diablo homolog protein-coding gene in the species Homo sapiens

Diablo homolog (DIABLO) is a mitochondrial protein that in humans is encoded by the DIABLO gene on chromosome 12. DIABLO is also referred to as second mitochondria-derived activator of caspases or SMAC. This protein binds inhibitor of apoptosis proteins (IAPs), thus freeing caspases to activate apoptosis. Due to its proapoptotic function, SMAC is implicated in a broad spectrum of tumors, and small molecule SMAC mimetics have been developed to enhance current cancer treatments.

DLC1 protein-coding gene in the species Homo sapiens

Deleted in Liver Cancer 1 also known as DLC1 and StAR-related lipid transfer protein 12 (STARD12) is a protein which in humans is encoded by the DLC1 gene.

HINT1 protein-coding gene in the species Homo sapiens

Histidine triad nucleotide-binding protein 1 is a protein that in humans is encoded by the HINT1 gene. It is a haploinsufficient tumor suppressor gene that inhibits the Wnt/β-catenin pathway in colon cancer cells and microphthalmia-associated transcription factor (MITF) activity in human mast cells. In the LysRS-Ap4A-MITF signaling pathway, HINT1 inhibits the MITF transcriptional activity by direct association. Upon pathway activation, HINT1 is released from MITF by diadenosine tetraphosphate (Ap4A), produced by LysRS.

FATE1 protein-coding gene in the species Homo sapiens

Fetal and Adult Testis-Expressed 1, encoded by the FATE1 gene in humans, is a protein identified as a cancer-testis antigen (CTA) in hepatocellular carcinomas and gastric and colon cancers. It is testis-specific in the fetus. In adults, it is expressed predominantly in the testis and adrenal glands, with some expression in the lungs, heart, kidneys and throughout the brain.

RHOT1 protein-coding gene in the species Homo sapiens

Mitochondrial Rho GTPase 1 (MIRO1) is an enzyme that in humans is encoded by the RHOT1 gene on chromosome 17. As a Miro protein isoform, the protein facilitates mitochondrial transport by attaching the mitochondria to the motor/adaptor complex. Through its key role in mitochondrial transport, RHOT1 is involved in mitochondrial homeostasis and apoptosis, as well as Parkinson’s disease (PD) and cancer.

RHOT2 protein-coding gene in the species Homo sapiens

Mitochondrial Rho GTPase 2 is an enzyme that in humans is encoded by the RHOT2 gene. As a Miro protein isoform, the protein facilitates mitochondrial transport by attaching the mitochondria to the motor/adaptor complex. Through its key role in mitochondrial transport, RHOT2 is involved in mitochondrial homeostasis and apoptosis, as well as Parkinson’s disease (PD).

ADP/ATP translocase 4 protein-coding gene in the species Homo sapiens

ADP/ATP translocase 4 (ANT4) is an enzyme that in humans is encoded by the SLC25A31 gene on chromosome 4. This enzyme inhibits apoptosis by catalyzing ADP/ATP exchange across the mitochondrial membranes and regulating membrane potential. In particular, ANT4 is essential to spermatogenesis, as it imports ATP into sperm mitochondria to support their development and survival. Outside this role, the SLC25AC31 gene has not been implicated in any human disease.

Arenobufagin chemical compound

Arenobufagin is a cardiotoxic bufanolide steroid secreted by the Argentine toad Bufo arenarum. It has effects similar to digitalis, blocking the Na+/K+ pump in heart tissue.

Regucalcin protein-coding gene in the species Homo sapiens

Regucalcin is a protein that in humans is encoded by the RGN gene

ADP/ATP translocase 2 protein-coding gene in the species Homo sapiens

ADP/ATP translocase 2 is a protein that in humans is encoded by the SLC25A5 gene on the X chromosome.

FASTKD1 protein-coding gene in the species Homo sapiens

FAST kinase domain-containing protein 1 is a protein that in humans is encoded by the FASTKD1 gene on chromosome 2. This protein is part of the FASTKD family, which is known for regulating the energy balance of mitochondria under stress. FASTKD1 is also an RNA-binding protein and has been associated with endometrial cancer.

RMDN3 protein-coding gene in the species Homo sapiens

Regulator of microtubule dynamics protein 3 (RMDN3), more commonly known as Protein tyrosine phosphatase interacting protein 51 (PTPIP51), is a protein that in humans is encoded by the RMDN3 gene on chromosome 15. This protein contributes to multiple biological functions, including cellular differentiation, proliferation, motility, cytoskeleton formation, and apoptosis, and has been associated with numerous cancers.

CHCHD2 protein-coding gene in the species Homo sapiens

Coiled-coil-helix-coiled-coil-helix domain containing 2 is a protein that in humans is encoded by the CHCHD2 gene.

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000137133 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000028470 - 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. 1 2 "Entrez Gene: HINT2 histidine triad nucleotide binding protein 2".
  6. 1 2 3 4 5 6 7 8 9 Maize KM, Wagner CR, Finzel BC (Jul 2013). "Structural characterization of human histidine triad nucleotide-binding protein 2, a member of the histidine triad superfamily". The FEBS Journal. 280 (14): 3389–98. doi:10.1111/febs.12330. PMC   3703500 . PMID   23659632.
  7. 1 2 3 4 5 6 Lenglet S, Antigny F, Vetterli L, Dufour JF, Rossier MF (Nov 2008). "Hint2 is expressed in the mitochondria of H295R cells and is involved in steroidogenesis". Endocrinology. 149 (11): 5461–9. doi: 10.1210/en.2008-0400 . PMID   18653718.
  8. 1 2 3 4 5 6 7 Martin J, Magnino F, Schmidt K, Piguet AC, Lee JS, Semela D, St-Pierre MV, Ziemiecki A, Cassio D, Brenner C, Thorgeirsson SS, Dufour JF (Jun 2006). "Hint2, a mitochondrial apoptotic sensitizer down-regulated in hepatocellular carcinoma". Gastroenterology. 130 (7): 2179–88. doi:10.1053/j.gastro.2006.03.024. PMC   2569837 . PMID   16762638.
  9. 1 2 3 Lee LR, Teng PN, Nguyen H, Hood BL, Kavandi L, Wang G, Turbov JM, Thaete LG, Hamilton CA, Maxwell GL, Rodriguez GC, Conrads TP, Syed V (Jul 2013). "Progesterone enhances calcitriol antitumor activity by upregulating vitamin D receptor expression and promoting apoptosis in endometrial cancer cells". Cancer Prevention Research. 6 (7): 731–43. doi: 10.1158/1940-6207.CAPR-12-0493 . PMID   23682076.
  10. Martin, Juliette; Maurhofer, Olivier; Bellance, Nadège; Benard, Giovanni; Graber, Franziska; Hahn, Dagmar; Galinier, Anne; Hora, Caroline; Gupta, Anirudh (2013-05-01). "Disruption of the histidine triad nucleotide-binding hint2 gene in mice affects glycemic control and mitochondrial function". Hepatology. 57 (5): 2037–2048. doi:10.1002/hep.26060. ISSN   1527-3350. PMID   22961760.