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ACO1
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 2B3X, 2B3Y
Identifiers
Aliases	ACO1, ACONS, HEL60, IREB1, IREBP, IREBP1, IRP1, aconitase 1
External IDs	OMIM: 100880; MGI: 87879; HomoloGene: 1657; GeneCards: ACO1; OMA:ACO1 - orthologs
Gene location (Human) Chr. Chromosome 9 (human) Band 9p21.1 Start 32,384,603 bp End 32,454,769 bp
Gene location (Mouse) Chr. Chromosome 4 (mouse) Band 4 A5|4 20.24 cM Start 40,143,081 bp End 40,198,338 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in right lobe of liver stromal cell of endometrium right adrenal gland right adrenal cortex adipose tissue left adrenal gland kidney tubule subcutaneous adipose tissue duodenum jejunal mucosa Top expressed in tunica adventitia of aorta external carotid artery internal carotid artery migratory enteric neural crest cell dermis efferent ductule carotid body tunica media of zone of aorta submandibular gland proximal tubule More reference expression data BioGPS n/a
Gene ontology Molecular function iron-sulfur cluster binding metal ion binding protein binding lyase activity RNA binding aconitate hydratase activity iron-responsive element binding 3 iron, 4 sulfur cluster binding 4 iron, 4 sulfur cluster binding Cellular component Golgi apparatus endoplasmic reticulum mitochondrion extracellular exosome cytoplasm cytosol Biological process response to iron(II) ion tricarboxylic acid cycle post-embryonic development regulation of gene expression intestinal absorption metabolism regulation of translation citrate metabolic process cellular iron ion homeostasis Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 48 11428 Ensembl ENSG00000122729 ENSMUSG00000028405 UniProt P21399 P28271 RefSeq (mRNA) NM_001278352 NM_002197 NM_001362840 NM_007386 RefSeq (protein) NP_001265281 NP_002188 NP_001349769 NP_031412 Location (UCSC) Chr 9: 32.38 – 32.45 Mb Chr 4: 40.14 – 40.2 Mb PubMed search
Wikidata
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Aconitase 1, soluble is a protein that in humans is encoded by the ACO1 gene.

Function

The protein encoded by this gene is a bifunctional, cytosolic protein that functions as an essential enzyme in the TCA cycle and interacts with mRNA to control the levels of iron inside cells. When cellular iron levels are high, this protein binds to a 4Fe-4S cluster and functions as an aconitase. Aconitases are iron-sulfur proteins that function to catalyze the conversion of citrate to isocitrate. When cellular iron levels are low, the protein binds to iron-responsive elements (IREs), which are stem-loop structures found in the 5' UTR of ferritin mRNA, and in the 3' UTR of transferrin receptor mRNA. When the protein binds to IRE, it results in repression of translation of ferritin mRNA, and inhibition of degradation of the otherwise rapidly degraded transferrin receptor mRNA. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. Alternative splicing results in multiple transcript variants.

References

1. ^ GRCh38: Ensembl release 89: ENSG00000122729 – Ensembl, May 2017
2. ^ GRCm38: Ensembl release 89: ENSMUSG00000028405 – 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: Aconitase 1, soluble".

External links

• Human ACO1 genome location and ACO1 gene details page in the UCSC Genome Browser.

Further reading

• Wang W, Di X, D'Agostino RB, Torti SV, Torti FM (Aug 2007). "Excess capacity of the iron regulatory protein system". The Journal of Biological Chemistry. 282 (34): 24650–9. doi:10.1074/jbc.M703167200. PMID 17604281.
• Martelli A, Salin B, Dycke C, Louwagie M, Andrieu JP, Richaud P, Moulis JM (Feb 2007). "Folding and turnover of human iron regulatory protein 1 depend on its subcellular localization". The FEBS Journal. 274 (4): 1083–92. doi:10.1111/j.1742-4658.2007.05657.x. PMID 17244191. S2CID 8412580.
• Hu J, Connor JR (Aug 1996). "Demonstration and characterization of the iron regulatory protein in human brain". Journal of Neurochemistry. 67 (2): 838–44. doi:10.1046/j.1471-4159.1996.67020838.x. PMID 8764614. S2CID 35872879.
• Popovic Z, Templeton DM (Jun 2007). "Inhibition of an iron-responsive element/iron regulatory protein-1 complex by ATP binding and hydrolysis". The FEBS Journal. 274 (12): 3108–19. doi:10.1111/j.1742-4658.2007.05843.x. PMID 17521334. S2CID 22629034.
• Wang J, Fillebeen C, Chen G, Biederbick A, Lill R, Pantopoulos K (Apr 2007). "Iron-dependent degradation of apo-IRP1 by the ubiquitin-proteasome pathway". Molecular and Cellular Biology. 27 (7): 2423–30. doi:10.1128/MCB.01111-06. PMC 1899896. PMID 17242182.
• Liu CY, Liu YF, Zeng L, Zhang SG, Xu H (Apr 2007). "". Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi. 28 (4): 255–8. PMID 17877204.
• Zimmer M, Lamb J, Ebert BL, Lynch M, Neil C, Schmidt E, Golub TR, Iliopoulos O (Apr 2010). "The connectivity map links iron regulatory protein-1-mediated inhibition of hypoxia-inducible factor-2a translation to the anti-inflammatory 15-deoxy-delta12,14-prostaglandin J2". Cancer Research. 70 (8): 3071–9. doi:10.1158/0008-5472.CAN-09-2877. PMC 2861799. PMID 20354189.
• Gu JM, Lim SO, Oh SJ, Yoon SM, Seong JK, Jung G (May 2008). "HBx modulates iron regulatory protein 1-mediated iron metabolism via reactive oxygen species". Virus Research. 133 (2): 167–77. doi:10.1016/j.virusres.2007.12.014. PMID 18262302.
• Popovic Z, Templeton DM (Oct 2004). "Iron accumulation and iron-regulatory protein activity in human hepatoma (HepG2) cells". Molecular and Cellular Biochemistry. 265 (1–2): 37–45. doi:10.1023/b:mcbi.0000044313.19574.c6. PMID 15543932. S2CID 19363206.

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

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