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FBLN1

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Protein-coding gene in the species Homo sapiens

FBLN1
Identifiers
AliasesFBLN1, FBLN, FIBL1, fibulin 1
External IDsOMIM: 135820; MGI: 95487; HomoloGene: 21295; GeneCards: FBLN1; OMA:FBLN1 - orthologs
Gene location (Human)
Chromosome 22 (human)
Chr.Chromosome 22 (human)
Chromosome 22 (human)Genomic location for FBLN1Genomic location for FBLN1
Band22q13.31Start45,502,238 bp
End45,601,135 bp
Gene location (Mouse)
Chromosome 15 (mouse)
Chr.Chromosome 15 (mouse)
Chromosome 15 (mouse)Genomic location for FBLN1Genomic location for FBLN1
Band15|15 E2Start85,090,150 bp
End85,170,736 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • canal of the cervix

  • gallbladder

  • vena cava

  • pericardium

  • gastric mucosa

  • ectocervix

  • vagina

  • left uterine tube

  • right auricle

  • tendon of biceps brachii
Top expressed in
  • aortic valve

  • otic vesicle

  • ascending aorta

  • otic placode

  • ciliary body

  • external carotid artery

  • saccule

  • mandibular prominence

  • internal carotid artery

  • maxillary prominence
More reference expression data
BioGPS




More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

2192

14114

Ensembl

ENSG00000077942

ENSMUSG00000006369

UniProt

P23142

Q08879

RefSeq (mRNA)

NM_006487
NM_001996
NM_006485
NM_006486

NM_010180
NM_001347088

RefSeq (protein)

NP_001987
NP_006476
NP_006477
NP_006478

NP_001334017
NP_034310

Location (UCSC)Chr 22: 45.5 – 45.6 MbChr 15: 85.09 – 85.17 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

FBLN1 is the gene encoding fibulin-1, an extracellular matrix and plasma protein.

Function

Fibulin-1 is a secreted glycoprotein that is found in association with extracellular matrix structures including fibronectin-containing fibers, elastin-containing fibers and basement membranes. Fibulin-1 binds to a number of extracellular matrix constituents including fibronectin, nidogen-1, and the proteoglycan, versican. Fibulin-1 is also a blood protein capable of binding to fibrinogen.

Structure

Fibulin-1 has modular domain structure and includes a series of nine epidermal growth factor-like modules followed by a fibulin-type module, a module found in all members of the fibulin gene family.

The human fibulin-1 gene, FBLN1, encodes four splice variants designated fibulin-1A, B, C and D, which differ in their carboxy terminal regions. In mouse, chicken and the nematode, C. elegans, only two fibulin-1 variants are produced, fibulin-1C and fibulin-1D.

Interactions

FBLN1 has been shown to interact with:

See also

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000077942Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000006369Ensembl, 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: FBLN1 fibulin 1".
  6. ^ Argraves WS, Tran H, Burgess WH, Dickerson K (Dec 1990). "Fibulin is an extracellular matrix and plasma glycoprotein with repeated domain structure". The Journal of Cell Biology. 111 (6 Pt 2): 3155–64. doi:10.1083/jcb.111.6.3155. PMC 2116371. PMID 2269669.
  7. ^ Balbona K, Tran H, Godyna S, Ingham KC, Strickland DK, Argraves WS (Oct 1992). "Fibulin binds to itself and to the carboxyl-terminal heparin-binding region of fibronectin". The Journal of Biological Chemistry. 267 (28): 20120–5. doi:10.1016/S0021-9258(19)88674-X. PMID 1400330.
  8. Timpl R, Sasaki T, Kostka G, Chu ML (Jun 2003). "Fibulins: a versatile family of extracellular matrix proteins". Nature Reviews Molecular Cell Biology. 4 (6): 479–89. doi:10.1038/nrm1130. PMID 12778127. S2CID 8442153.
  9. ^ Argraves WS, Tanaka A, Smith EP, Twal WO, Argraves KM, Fan D, Haudenschild CC (Nov 2009). "Fibulin-1 and fibrinogen in human atherosclerotic lesions". Histochemistry and Cell Biology. 132 (5): 559–65. doi:10.1007/s00418-009-0628-7. PMID 19693531. S2CID 13501440.
  10. Perbal B, Martinerie C, Sainson R, Werner M, He B, Roizman B (Feb 1999). "The C-terminal domain of the regulatory protein NOVH is sufficient to promote interaction with fibulin 1C: a clue for a role of NOVH in cell-adhesion signaling". Proceedings of the National Academy of Sciences of the United States of America. 96 (3): 869–74. Bibcode:1999PNAS...96..869P. doi:10.1073/pnas.96.3.869. PMC 15317. PMID 9927660.
  11. Ohsawa I, Takamura C, Kohsaka S (Mar 2001). "Fibulin-1 binds the amino-terminal head of beta-amyloid precursor protein and modulates its physiological function". Journal of Neurochemistry. 76 (5): 1411–20. doi:10.1046/j.1471-4159.2001.00144.x. PMID 11238726. S2CID 83321033.
  12. Adam S, Göhring W, Wiedemann H, Chu ML, Timpl R, Kostka G (Sep 1997). "Binding of fibulin-1 to nidogen depends on its C-terminal globular domain and a specific array of calcium-binding epidermal growth factor-like (EG) modules". Journal of Molecular Biology. 272 (2): 226–36. doi:10.1006/jmbi.1997.1244. PMID 9299350.
  13. Tran H, VanDusen WJ, Argraves WS (Sep 1997). "The self-association and fibronectin-binding sites of fibulin-1 map to calcium-binding epidermal growth factor-like domains". The Journal of Biological Chemistry. 272 (36): 22600–6. doi:10.1074/jbc.272.36.22600. PMID 9278415.
  14. Pan TC, Kluge M, Zhang RZ, Mayer U, Timpl R, Chu ML (Aug 1993). "Sequence of extracellular mouse protein BM-90/fibulin and its calcium-dependent binding to other basement-membrane ligands". European Journal of Biochemistry. 215 (3): 733–40. doi:10.1111/j.1432-1033.1993.tb18086.x. PMID 8354280.
  15. Deeney JT, Tornheim K, Korchak HM, Prentki M, Corkey BE (Oct 1992). "Acyl-CoA esters modulate intracellular Ca2+ handling by permeabilized clonal pancreatic beta-cells". The Journal of Biological Chemistry. 267 (28): 19840–5. doi:10.1016/S0021-9258(19)88631-3. PMID 1400300.

Further reading

Cell signaling: calcium signaling and calcium metabolism
Cell membrane
Adhesion molecules
Calcium channels
Calcium pumps
GPCRs
Annexins
Intracellular signaling
Second messengers
Intracellular channels
Intracellular pumps
Sensors and chelators
Calcium-dependent chaperones
Calcium-dependent kinases
Calcium-dependent proteases
Indirect regulators
Extracellular chelators
Extracellular matrix proteins
Secreted hormones
Calcium-binding domains
Category: