Wikipedia

IRX1

Iroquois-class homeodomain protein IRX-1, also known as Iroquois homeobox protein 1, is a protein that in humans is encoded by the IRX1 gene.[5][6] All members of the Iroquois (IRO) family of proteins share two highly conserved features, encoding both a homeodomain and a characteristic IRO sequence motif.[7] Members of this family are known to play numerous roles in early embryo patterning.[5] IRX1 has also been shown to act as a tumor suppressor gene in several forms of cancer.[8][9][10][11]

IRX1
Identifiers
AliasesIRX1, IRX-5, IRXA1, iroquois homeobox 1
External IDsOMIM: 606197; MGI: 1197515; HomoloGene: 19065; GeneCards: IRX1; OMA:IRX1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

79192

16371

Ensembl

ENSG00000170549

ENSMUSG00000060969

UniProt

P78414

P81068

RefSeq (mRNA)

NM_024337

NM_010573

RefSeq (protein)

NP_077313

NP_034703

Location (UCSC)Chr 5: 3.6 – 3.6 MbChr 13: 72.11 – 72.11 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Role in development

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IRX1 is a member of the Iroquois homeobox gene family. Members of this family play multiple roles during pattern formation in embryos of numerous vertebrate and invertebrate species.[5][12] IRO genes are thought to function early in development to define large territories, and again later in development for further patterning specification.[7] Experimental data suggest roles for IRX1 in vertebrates may include development and patterning of lungs, limbs, heart, eyes, and nervous system.[13][14][15][16][17][18]

Gene

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Overview

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IRX1 is located on the forward DNA strand (see Sense (molecular biology)) of chromosome 5, from position 3596054 - 3601403 at the 5p15.3 location.[5] The human gene product is a 1858 base pair mRNA with 4 predicted exons in humans.[19] Promoter analysis was performed using El Dorado through the Genomatix software page.[20] The predicted promoter region spans 1040 base pairs from position 3595468 through 3595468 on the forward strand of chromosome 5.

Gene neighborhood

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IRX1 is relatively isolated, with no other protein coding genes found from position 3177835 – 5070004.[5]

Expression

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Microarray and RNA seq data suggest that IRX1 is ubiquitously expressed at low levels in adult tissues, with the highest relative levels of expression occurring in the heart, adipose, kidney, and breast tissues.[21][22] Moderate to high levels are also indicated in the lung, prostate and stomach.[22][23] Promoter analysis with the El Dorado program from Genomatix predicted that IRX1 expression is regulated by factors that include E2F cell cycle regulators, NRF1, and ZF5,[24] and brachyury.[20] Expression data from human, mouse, and developing mouse brains are available though the Allen Brain Atlas.[25]

Protein

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Properties and characteristics

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The mature IRX1 protein has 480 amino acid residues, with a molecular mass of 49,600 daltons and an isoelectric point of 5.7. A BLAST search revealed that IRX1 contains two highly conserved domains: a homeodomain and a characteristic IRO motif of unknown function.[26] The homeodomain belongs to the TALE (three amino acid loop extension) class of homeodomains, and is characterized by the addition of three extra amino acids between the first and second helix of three alpha helices that comprise the domain.[27] The presence of this well characterized homeodomain strongly suggests that IRX1 acts as a transcription factor. This is further supported by the predicted localization of IRX1 to the nucleus.[28] The IRO motif is a region downstream of the homeodomain that is found only in members of the Iroquois-class homeodomain proteins, though its function is poorly understood. However, its similarity to an internal region of the Notch receptor protein suggests that it may be involved with protein-protein interaction.[7] In addition to these two characteristic domains, IRX1 contains a third domain from the HARE-HTH superfamily[29] fused to the C-terminal end of the homeodomain.[30] This domain adopts a winged helix-turn-helix fold predicted to bind DNA, and is thought to play a role in recruiting effector activities to DNA.[29] Several forms of post-translational modification are predicted, including SUMOylation, C-mannosylation, and phosphorylation, using bioinformatics tools from ExPASy.[31] Bioinformatic analysis of IRX1 with the NetPhos tool predicted 71 potential phosphorylation sites throughout the protein.[32]

Protein Interactions

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Potential protein interacting partners for IRX1 were found using computational tools. The STRING database lists nine putative interacting partners supported by text mining evidence, though closer analysis of the results shows little support for most of these predicted interactions.[33] However, it is possible that one of these proteins, CDKN1A, is involved in the predicted regulation of IRX1 by E2F cell cycle regulators.[20][33]

Conservation

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Orthologs

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IRX1 has a high degree of conservation across vertebrate and invertebrate species. The entire protein is more fully conserved through vertebrate species, while only the homeodomain and IRO motif are conserved in more distant homologs.[12] Homologous sequences were found in species as distantly related to humans as the pig roundworm Ascaris suum, from the family Ascarididae, using BLAST and the ALIGN tool through the San Diego Super Computer Biology Workbench.[26] The following is a table describing the evolutionary conservation of IRX1.

Genus Species Organism Common Name Divergence from Humans (MYA) [34] NCBI Protein Accession Number Sequence Identity [26] Protein Length Common Gene Name
Homo sapiens[30] Humans -- NP_077313 100% 480 IRX-1
Pongo abelii[35] Sumatran Orangutan 15.7 XP_002815448 99% 480 IRX-1
Bos taurus[36] Cattle 94.2 XP_002696496 92.3% 476 IRX-1
Mus musculus[37] House Mouse 92.3 NP_034703 91.5% 480 IRX-1
Rattus norvegicus[38] Brown rat 92.3 NP_001100801 90.4% 480 IRX-1
Gallus gallus[39] Red Junglefowl 296 NP_001025509 72.9% 467 IRX-1
Xenopus tropicalis[40] Western clawed frog 371.2 NP_001188351 68% 467 IRX-1
Latimeria chalumnae[41] West Indian Ocean coelacanth 441.9 XP_006002089 65.1% 460 Irx-1-A-like isoform X1
Danio rerio[42] Zebrafish 400.1 NP_997067 61.1% 426 Irx-1 isoform 1
Taeniopygia guttata[43] Zebra finch 296 XP_002189063 59.7% 400 Irx-1-A-like
Astyanax mexicanus[44] Mexican tetra 400.1 XP_007254591.1 58% 450 IRX-1
Ophiophagus hannah[45] King cobra 296 ETE68928 54.5% 387 Irx-1-A partial
Ovis aries[46] Sheep 94.2 XP_004017207 43.3% 260 IRX-1
Condylura cristata[47] Star-nosed mole 94.2 XP_004678440 41.7% 342 IRX-1
Branchiostoma floridae[48] Lancelet 713.2 ACF10237.1 35.5% 461 Iroquois A isoform 1
Strongylocentrotus purpuratus[49] Purple sea urchin 742.9 NP_001123285 31.7% 605 Iroquois homeobox A
Ascaris suum[50] Pig roundworm 937.5 F1KXE6 29% 444 IRX-1
Caenorhabditis elegans[51] Nematode roundworm 937.5 NP_492533.2 28.6% 377 IRX-1
Drosophila melanogaster[52] Fruit fly 782.7 NP_524045 27% 717 Araucan isoform A

Paralogs

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IRX1 is one of six members of the Iroquois-class homeodomain proteins found in humans: IRX2, IRX3, IRX4, IRX5, and IRX6. IRX1, IRX2, and IRX4 are found on human chromosome 5, and their orientation corresponds to that of IRX3, IRX5, and IRX6 found on human chromosome 16.[7] It is thought that the genomic organization of IRO genes in conserved gene clusters allows for coregulation and enhancer sharing during development.

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000170549 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000060969 – 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. ^ a b c d e "Entrez Gene: iroquois homeobox 1".
  6. ^ Ogura K, Matsumoto K, Kuroiwa A, Isobe T, Otoguro T, Jurecic V, et al. (2001). "Cloning and chromosome mapping of human and chicken Iroquois (IRX) genes". Cytogenetics and Cell Genetics. 92 (3–4): 320–325. doi:10.1159/000056921. PMID 11435706. S2CID 46509502.
  7. ^ a b c d Cavodeassi F, Modolell J, Gómez-Skarmeta JL (August 2001). "The Iroquois family of genes: from body building to neural patterning". Development. 128 (15): 2847–2855. doi:10.1242/dev.128.15.2847. hdl:10261/198505. PMID 11532909.
  8. ^ Bennett KL, Karpenko M, Lin MT, Claus R, Arab K, Dyckhoff G, et al. (June 2008). "Frequently methylated tumor suppressor genes in head and neck squamous cell carcinoma". Cancer Research. 68 (12): 4494–4499. doi:10.1158/0008-5472.CAN-07-6509. PMID 18559491.
  9. ^ Marcinkiewicz KM, Gudas LJ (January 2014). "Altered epigenetic regulation of homeobox genes in human oral squamous cell carcinoma cells". Experimental Cell Research. 320 (1): 128–143. doi:10.1016/j.yexcr.2013.09.011. PMC 3880227. PMID 24076275.
  10. ^ Guo X, Liu W, Pan Y, Ni P, Ji J, Guo L, et al. (July 2010). "Homeobox gene IRX1 is a tumor suppressor gene in gastric carcinoma". Oncogene. 29 (27): 3908–3920. doi:10.1038/onc.2010.143. PMID 20440264. S2CID 6638457.
  11. ^ Park SH, Kim SK, Choe JY, Moon Y, An S, Park MJ, et al. (April 2013). "Hypermethylation of EBF3 and IRX1 genes in synovial fibroblasts of patients with rheumatoid arthritis". Molecules and Cells. 35 (4): 298–304. doi:10.1007/s10059-013-2302-0. PMC 3887890. PMID 23456299.
  12. ^ a b Kerner P, Ikmi A, Coen D, Vervoort M (April 2009). "Evolutionary history of the iroquois/Irx genes in metazoans". BMC Evolutionary Biology. 9 (74): 74. Bibcode:2009BMCEE...9...74K. doi:10.1186/1471-2148-9-74. PMC 2674049. PMID 19368711.
  13. ^ Choy SW, Cheng CW, Lee ST, Li VW, Hui MN, Hui CC, et al. (December 2010). "A cascade of irx1a and irx2a controls shh expression during retinogenesis". Developmental Dynamics. 239 (12): 3204–3214. doi:10.1002/dvdy.22462. PMID 21046643. S2CID 38099649.
  14. ^ Cheng CW, Yan CH, Choy SW, Hui MN, Hui CC, Cheng SH (September 2007). "Zebrafish homologue irx1a is required for the differentiation of serotonergic neurons". Developmental Dynamics. 236 (9): 2661–2667. doi:10.1002/dvdy.21272. PMID 17685478. S2CID 142831.
  15. ^ Becker MB, Zülch A, Bosse A, Gruss P (August 2001). "Irx1 and Irx2 expression in early lung development". Mechanisms of Development. 106 (1–2): 155–158. doi:10.1016/S0925-4773(01)00412-9. PMID 11472847. S2CID 16857354.
  16. ^ Bosse A, Zülch A, Becker MB, Torres M, Gómez-Skarmeta JL, Modolell J, et al. (December 1997). "Identification of the vertebrate Iroquois homeobox gene family with overlapping expression during early development of the nervous system". Mechanisms of Development. 69 (1–2): 169–181. doi:10.1016/S0925-4773(97)00165-2. hdl:11858/00-001M-0000-0012-FE9F-5. PMID 9486539. S2CID 9655500.
  17. ^ Christoffels VM, Keijser AG, Houweling AC, Clout DE, Moorman AF (August 2000). "Patterning the embryonic heart: identification of five mouse Iroquois homeobox genes in the developing heart". Developmental Biology. 224 (2): 263–274. doi:10.1006/dbio.2000.9801. PMID 10926765.
  18. ^ Díaz-Hernández ME, Bustamante M, Galván-Hernández CI, Chimal-Monroy J (March 11, 2013). "Irx1 and Irx2 are coordinately expressed and regulated by retinoic acid, TGFβ and FGF signaling during chick hindlimb development". PLOS ONE. 8 (3): e58549. Bibcode:2013PLoSO...858549D. doi:10.1371/journal.pone.0058549. PMC 3594311. PMID 23505533.
  19. ^ "NCBI Nucleotide: IRX1". Retrieved May 17, 2014.
  20. ^ a b c "El Dorado". Genomatix. Retrieved May 17, 2014.[permanent dead link]
  21. ^ "BioGPS: IRX1". Retrieved 17 May 2014.
  22. ^ a b "GeneCards: IRX1". Retrieved 17 May 2014.
  23. ^ "GEO Profile: IRX1". Retrieved May 17, 2014.
  24. ^ Numoto M, Yokoro K, Koshi J (March 1999). "ZF5, which is a Kruppel-type transcriptional repressor, requires the zinc finger domain for self-association". Biochemical and Biophysical Research Communications. 256 (3): 573–578. doi:10.1006/bbrc.1999.0375. PMID 10080939.
  25. ^ "Allen Brain Atlas". Retrieved May 17, 2014.
  26. ^ a b c "IRX1 Analysis". Biology Workbench. San Diego Supercomputing Center- University of California San Diego. Retrieved 8 May 2014.[permanent dead link]
  27. ^ Bürglin TR (November 1997). "Analysis of TALE superclass homeobox genes (MEIS, PBC, KNOX, Iroquois, TGIF) reveals a novel domain conserved between plants and animals". Nucleic Acids Research. 25 (21): 4173–4180. doi:10.1093/nar/25.21.4173. PMC 147054. PMID 9336443.
  28. ^ "Expasy: Psort". Retrieved 18 May 2014.[permanent dead link]
  29. ^ a b Aravind L, Iyer LM (January 2012). "The HARE-HTH and associated domains: novel modules in the coordination of epigenetic DNA and protein modifications". Cell Cycle. 11 (1): 119–131. doi:10.4161/cc.11.1.18475. PMC 3272235. PMID 22186017.
  30. ^ a b "NCBI Protein: IRX1". Retrieved 18 May 2014.
  31. ^ "ExPASy: Bioinformatics Resource Portal". Retrieved 18 May 2014.
  32. ^ "NetPhos". Retrieved 18 May 2014.
  33. ^ a b "STRING Database". Retrieved 5 May 2014.
  34. ^ "Time Tree".
  35. ^ "NCBI Nucleotide: XP_002815448". Retrieved 18 May 2014.
  36. ^ "NCBI Nucleotide: XP_002696496". Retrieved 18 May 2014.
  37. ^ "NCBI Nucleotide: NP_034703". Retrieved 18 May 2014.
  38. ^ "NCBI Nucleotide: NP_001100801". Retrieved 18 May 2014.
  39. ^ "NCBI Nucleotide: NP_001025509". Retrieved 18 May 2014.
  40. ^ "NCBI Nucleotide: NP_001188351". Retrieved 18 May 2014.
  41. ^ "NCBI Nucleotide: XP_006002089". Retrieved 18 May 2014.
  42. ^ "NCBI Nucleotide: NP_997067". Retrieved 18 May 2014.
  43. ^ "NCBI Nucleotide: XP_002189063". Retrieved 18 May 2014.
  44. ^ "NCBI Nucleotide: XP_007254591.1". Retrieved 18 May 2014.
  45. ^ "NCBI Nucleotide: ETE68928". Retrieved 18 May 2014.
  46. ^ "NCBI Nucleotide: XP_004017207". Retrieved 18 May 2014.
  47. ^ "NCBI Nucleotide: XP_004678440". Retrieved 18 May 2014.
  48. ^ "NCBI Nucleotide: ACF10237.1". Retrieved 18 May 2014.
  49. ^ "NCBI Nucleotide: NP_001123285". Retrieved 18 May 2014.
  50. ^ "UniProt: F1KXE6". Retrieved 18 May 2014.
  51. ^ "NCBI Nucleotide: NP_492533.2". Retrieved 18 May 2014.
  52. ^ "NCBI Nucleotide: NP_524045". Retrieved 18 May 2014.

Further reading

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

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