FGF8

FGF8
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 2FDB
Identifiers
Aliases	FGF8, AIGF, FGF-8, HBGF-8, HH6, KAL6, fibroblast growth factor 8
External IDs	MGI: 99604 HomoloGene: 7715 GeneCards: FGF8
Gene ontology Molecular function • type 1 fibroblast growth factor receptor binding • receptor binding • type 2 fibroblast growth factor receptor binding • growth factor activity • fibroblast growth factor receptor binding • chemoattractant activity • protein tyrosine kinase activity • 1-phosphatidylinositol-3-kinase activity • phosphatidylinositol-4,5-bisphosphate 3-kinase activity • Ras guanyl-nucleotide exchange factor activity Cellular component • extracellular region • extracellular space • intracellular • external side of plasma membrane Biological process • negative regulation of neuron apoptotic process • cell migration involved in mesendoderm migration • male genitalia development • epithelial to mesenchymal transition involved in endocardial cushion formation • outflow tract morphogenesis • embryonic heart tube development • mesonephros development • heart looping • forebrain neuron development • blood vessel remodeling • central nervous system neuron development • positive regulation of ERK1 and ERK2 cascade • metanephros development • cell proliferation in forebrain • positive regulation of mitotic nuclear division • gonad development • pharyngeal system development • branching involved in salivary gland morphogenesis • apoptotic process • dopaminergic neuron differentiation • cell fate commitment • limb morphogenesis • kidney development • lung development • anatomical structure morphogenesis • signal transduction involved in regulation of gene expression • regulation of odontogenesis of dentin-containing tooth • response to oxidative stress • embryo development ending in birth or egg hatching • forebrain morphogenesis • heart development • telencephalon development • branching involved in ureteric bud morphogenesis • midbrain-hindbrain boundary development • branching involved in blood vessel morphogenesis • thyroid-stimulating hormone-secreting cell differentiation • positive chemotaxis • mesodermal cell migration • cell differentiation • dorsal/ventral axon guidance • corticotropin hormone secreting cell differentiation • organ induction • neural plate morphogenesis • positive regulation of organ growth • negative regulation of apoptotic process • BMP signaling pathway • outflow tract septum morphogenesis • odontogenesis • thyroid gland development • pallium development • gastrulation • canonical Wnt signaling pathway • phosphatidylinositol-mediated signaling • subpallium development • lung morphogenesis • response to organic cyclic compound • otic vesicle formation • forebrain dorsal/ventral pattern formation • heart morphogenesis • aorta morphogenesis • generation of neurons • MAPK cascade • neuroepithelial cell differentiation • multicellular organism development • fibroblast growth factor receptor signaling pathway • positive regulation of gene expression • negative regulation of cardiac muscle tissue development • determination of left/right symmetry • inner ear morphogenesis • positive regulation of cell proliferation • bone development • motor neuron axon guidance • positive regulation of cell division • response to drug • embryonic hindlimb morphogenesis • positive regulation of GTPase activity • phosphatidylinositol phosphorylation • phosphatidylinositol-3-phosphate biosynthetic process • peptidyl-tyrosine phosphorylation • regulation of phosphatidylinositol 3-kinase signaling Sources:Amigo / QuickGO
RNA expression pattern
More reference expression data
Orthologs
Species	Human	Mouse
Entrez	2253	14179
Ensembl	ENSG00000107831	ENSMUSG00000025219
UniProt	P55075	P37237
RefSeq (mRNA)	NM_001206389 NM_006119 NM_033163 NM_033164 NM_033165	NM_001166361 NM_001166362 NM_001166363 NM_010205
RefSeq (protein)	NP_006110.1 NP_149353.1 NP_149354.1 NP_149355.1	NP_001159834.1 NP_001159835.1 NP_034335.1
Location (UCSC)	Chr 10: 101.77 – 101.78 Mb	Chr 19: 45.74 – 45.74 Mb
PubMed search	[1]	[2]
Wikidata

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Fibroblast growth factor 8 is a protein that in humans is encoded by the FGF8 gene.^[3][4]

Function

The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion.^[4]

Fgf8 is important and necessary for setting up and maintaining the midbrain/hindbrain border (or mesencephalon/met-encephalon border) which plays the vital role of “organizer” in development, like the Spemann “organizer” of the gastrulating embryo. Fgf8 is expressed in the region where Otx2 and Gbx2 cross inhibit each other and is maintained expression by this interaction. Once expressed, the Fgf8 induces other transcription factors to form cross-regulatory loops between cells, thus the border is established. Through development, the Fgf8 goes to regulate the growth and differentiation of progenitor cells in this region to produce ultimate structure of midbrain and hindbrain.^[5] Crossely’s experiment proves that the Fgf8 is sufficient to induce the repatterning of midbrain and hindbrain structure.^[6]

In the development of forebrain, cortical patterning centers are the boundaries or poles of cortical primordium, where multiple BMP and WNT genes are expressed. Besides, at the anterior pole several FGF family including Fgf3, 8,17 and 18 overlap in expression.^[7] The similarity in cortical gene expression in Emx2 mutants and mice in which the anterior FGF8 source is augmented suggests that FGF8 controls the graded expression(low anterior, high posterior) of Emx2 in the cortical primordium. Emx2 is one of the protomap molecular determinants that prove to be closely interacted with Pax6. Emx2 and Pax6 are expressed in opposing gradients along the A/P axis of the cortical primordium and cooperate to set up area pattern. Fgf8 and Emx2 antagonize each other to create the development map. Fgf8 promotes the development of anterior part and suppresses posterior fate, while the Emx2 does the reverse. What's more, FGF8 manipulations suggest FGF8 controls the cortical graded expression of COUP-TF1.^[8] Moreover, the sharpness of both COUPTF1 and COUP-TF2 expression borders would be expected of genes involved in boundary specification.Thus, the interaction between them regulates the A/P axis of cortical primordium and directs the development map of cortical area.

Clinical signficance

This protein is known to be a factor that supports androgen and anchorage independent growth of mammary tumor cells. Overexpression of this gene has been shown to increase tumor growth and angiogenesis. The adult expression of this gene is restricted to testes and ovaries. Temporal and spatial pattern of this gene expression suggests its function as an embryonic epithelial factor. Studies of the mouse and chick homologs reveal roles in midbrain and limb development, organogenesis, embryo gastrulation and left-right axis determination. The alternative splicing of this gene results in four transcript variants.^[4]

References

1. "Human PubMed Reference:".
2. "Mouse PubMed Reference:".
3. White RA, Dowler LL, Angeloni SV, Pasztor LM, MacArthur CA (Apr 1996). "Assignment of FGF8 to human chromosome 10q25-q26: mutations in FGF8 may be responsible for some types of acrocephalosyndactyly linked to this region". Genomics. 30 (1): 109–11. doi:10.1006/geno.1995.0020. PMID 8595889.
4. "Entrez Gene: FGF8 fibroblast growth factor 8 (androgen-induced)".
5. Harris WA, Sanes DH, Reh TA (2011). Development of the Nervous System, Third Edition. Boston: Academic Press. pp. 33–34. ISBN 0-12-374539-X.
6. Crossley PH, Martin GR (February 1995). "The mouse Fgf8 gene encodes a family of polypeptides and is expressed in regions that direct outgrowth and patterning in the developing embryo". Development. 121 (2): 439–51. PMID 7768185.
7. Grove EA, Fukuchi-Shimogori T (2003). "Generating the cerebral cortical area map". Annu. Rev. Neurosci. 26: 355–80. doi:10.1146/annurev.neuro.26.041002.131137. PMID 14527269.
8. Rebsam A, Seif I, Gaspar P (October 2002). "Refinement of thalamocortical arbors and emergence of barrel domains in primary somatosensory cortex: a study of normal and monoamine oxidase A knock-out mice". J.Neurosci. 22 (19): 8541–8552. PMID 12351728.

Further reading

• Powers CJ, McLeskey SW, Wellstein A (2000). "Fibroblast growth factors, their receptors and signaling.". Endocr. Relat. Cancer. 7 (3): 165–97. doi:10.1677/erc.0.0070165. PMID 11021964.
• Mattila MM, Härkönen PL (2007). "Role of fibroblast growth factor 8 in growth and progression of hormonal cancer.". Cytokine Growth Factor Rev. 18 (3–4): 257–66. doi:10.1016/j.cytogfr.2007.04.010. PMID 17512240.
• Duester G (2007). "Retinoic acid regulation of the somitogenesis clock". Birth Defects Res. C Embryo Today. 81 (2): 84–92. doi:10.1002/bdrc.20092. PMC 2235195. PMID 17600781.
• Tanaka A, Miyamoto K, Matsuo H, et al. (1995). "Human androgen-induced growth factor in prostate and breast cancer cells: its molecular cloning and growth properties". FEBS Lett. 363 (3): 226–30. doi:10.1016/0014-5793(95)00324-3. PMID 7737407.
• Gemel J, Gorry M, Ehrlich GD, MacArthur CA (1996). "Structure and sequence of human FGF8". Genomics. 35 (1): 253–7. doi:10.1006/geno.1996.0349. PMID 8661131.
• Ornitz DM, Xu J, Colvin JS, et al. (1996). "Receptor specificity of the fibroblast growth factor family". J. Biol. Chem. 271 (25): 15292–7. doi:10.1074/jbc.271.25.15292. PMID 8663044.
• Payson RA, Wu J, Liu Y, Chiu IM (1996). "The human FGF-8 gene localizes on chromosome 10q24 and is subjected to induction by androgen in breast cancer cells". Oncogene. 13 (1): 47–53. PMID 8700553.
• Ghosh AK, Shankar DB, Shackleford GM, et al. (1997). "Molecular cloning and characterization of human FGF8 alternative messenger RNA forms". Cell Growth Differ. 7 (10): 1425–34. PMID 8891346.
• Yoshiura K, Leysens NJ, Chang J, et al. (1997). "Genomic structure, sequence, and mapping of human FGF8 with no evidence for its role in craniosynostosis/limb defect syndromes". Am. J. Med. Genet. 72 (3): 354–62. doi:10.1002/(SICI)1096-8628(19971031)72:3<354::AID-AJMG21>3.0.CO;2-R. PMID 9332670.
• Chellaiah A, Yuan W, Chellaiah M, Ornitz DM (2000). "Mapping ligand binding domains in chimeric fibroblast growth factor receptor molecules. Multiple regions determine ligand binding specificity". J. Biol. Chem. 274 (49): 34785–94. doi:10.1074/jbc.274.49.34785. PMID 10574949.
• Loo BB, Darwish KK, Vainikka SS, et al. (2001). "Production and characterization of the extracellular domain of recombinant human fibroblast growth factor receptor 4". Int. J. Biochem. Cell Biol. 32 (5): 489–97. doi:10.1016/S1357-2725(99)00145-4. PMID 10736564.
• Xu J, Liu Z, Ornitz DM (2000). "Temporal and spatial gradients of Fgf8 and Fgf17 regulate proliferation and differentiation of midline cerebellar structures". Development. 127 (9): 1833–43. PMID 10751172.
• Tanaka S, Ueo H, Mafune K, et al. (2001). "A novel isoform of human fibroblast growth factor 8 is induced by androgens and associated with progression of esophageal carcinoma". Dig. Dis. Sci. 46 (5): 1016–21. doi:10.1023/A:1010753826788. PMID 11341643.
• Ruohola JK, Viitanen TP, Valve EM, et al. (2001). "Enhanced invasion and tumor growth of fibroblast growth factor 8b-overexpressing MCF-7 human breast cancer cells". Cancer Res. 61 (10): 4229–37. PMID 11358849.
• Mattila MM, Ruohola JK, Valve EM, et al. (2001). "FGF-8b increases angiogenic capacity and tumor growth of androgen-regulated S115 breast cancer cells". Oncogene. 20 (22): 2791–804. doi:10.1038/sj.onc.1204430. PMID 11420691.
• Zammit C, Coope R, Gomm JJ, et al. (2002). "Fibroblast growth factor 8 is expressed at higher levels in lactating human breast and in breast cancer". Br. J. Cancer. 86 (7): 1097–103. doi:10.1038/sj.bjc.6600213. PMC 2364190. PMID 11953856.
• Brondani V, Klimkait T, Egly JM, Hamy F (2002). "Promoter of FGF8 reveals a unique regulation by unliganded RARalpha". J. Mol. Biol. 319 (3): 715–28. doi:10.1016/S0022-2836(02)00376-5. PMID 12054865.
• Gnanapragasam VJ, Robson CN, Neal DE, Leung HY (2002). "Regulation of FGF8 expression by the androgen receptor in human prostate cancer". Oncogene. 21 (33): 5069–80. doi:10.1038/sj.onc.1205663. PMID 12140757.

External links

• GeneReviews/NCBI/NIH/UW entry on Kallmann syndrome
• FGF8 human gene location in the UCSC Genome Browser.
• FGF8 human gene details in the UCSC Genome Browser.