FBLN1

Protein-coding gene in the species Homo sapiens

Failed to serialize data. FBLN1 is the gene encoding fibulin-1, an extracellular matrix and plasma protein.^[1]^[2]^[3]

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,^[3] nidogen-1, and the proteoglycan, versican.^[3]^[4] Fibulin-1 is also a blood protein capable of binding to fibrinogen.^[5]

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.^[2]

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.^[1]

Interactions

FBLN1 has been shown to interact with:

NOV/CCN3,^[6]
amyloid precursor protein,^[7]
entactin,^[8]^[9]^[10]
fibrinogen,^[5] and
fibronectin.^[11]

References

^ ^a ^b "Entrez Gene: FBLN1 fibulin 1".
^ ^a ^b 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.
^ ^a ^b ^c 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.
^ 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.
^ ^a ^b 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.
^ 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.
^ 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.
^ 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.
^ 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.
^ 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.
^ 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.

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.
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.
Argraves WS, Dickerson K, Burgess WH, Ruoslahti E (Aug 1989). "Fibulin, a novel protein that interacts with the fibronectin receptor beta subunit cytoplasmic domain". Cell. 58 (4): 623–9. doi:10.1016/0092-8674(89)90097-4. PMID 2527614. S2CID 24834825.
Sasaki T, Göhring W, Pan TC, Chu ML, Timpl R (Dec 1995). "Binding of mouse and human fibulin-2 to extracellular matrix ligands". Journal of Molecular Biology. 254 (5): 892–9. doi:10.1006/jmbi.1995.0664. PMID 7500359.
Roark EF, Keene DR, Haudenschild CC, Godyna S, Little CD, Argraves WS (Apr 1995). "The association of human fibulin-1 with elastic fibers: an immunohistological, ultrastructural, and RNA study". The Journal of Histochemistry and Cytochemistry. 43 (4): 401–11. doi:10.1177/43.4.7534784. PMID 7534784.
Tran H, Tanaka A, Litvinovich SV, Medved LV, Haudenschild CC, Argraves WS (Aug 1995). "The interaction of fibulin-1 with fibrinogen. A potential role in hemostasis and thrombosis". The Journal of Biological Chemistry. 270 (33): 19458–64. doi:10.1074/jbc.270.33.19458. PMID 7642629.
Mattei MG, Pan TC, Zhang RZ, Timpl R, Chu ML (Jul 1994). "The fibulin-1 gene (FBLN1) is located on human chromosome 22 and on mouse chromosome 15". Genomics. 22 (2): 437–8. doi:10.1006/geno.1994.1406. PMID 7806231.
Korenberg JR, Chen XN, Tran H, Argraves WS (1995). "Localization of the human gene for fibulin-1 (FBLN1) to chromosome band 22q13.3". Cytogenetics and Cell Genetics. 68 (3–4): 192–3. doi:10.1159/000133911. PMID 7842734.
Brown JC, Wiedemann H, Timpl R (Jan 1994). "Protein binding and cell adhesion properties of two laminin isoforms (AmB1eB2e, AmB1sB2e) from human placenta". Journal of Cell Science. 107 (1): 329–38. doi:10.1242/jcs.107.1.329. PMID 8175920.
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.
Clinton GM, Rougeot C, Derancourt J, Roger P, Defrenne A, Godyna S, Argraves WS, Rochefort H (Jan 1996). "Estrogens increase the expression of fibulin-1, an extracellular matrix protein secreted by human ovarian cancer cells". Proceedings of the National Academy of Sciences of the United States of America. 93 (1): 316–20. Bibcode:1996PNAS...93..316C. doi:10.1073/pnas.93.1.316. PMC 40229. PMID 8552629.
Miosge N, Götz W, Sasaki T, Chu ML, Timpl R, Herken R (Feb 1996). "The extracellular matrix proteins fibulin-1 and fibulin-2 in the early human embryo". The Histochemical Journal. 28 (2): 109–16. doi:10.1007/BF02331415. PMID 8737292. S2CID 25996538.
Godyna S, Diaz-Ricart M, Argraves WS (Oct 1996). "Fibulin-1 mediates platelet adhesion via a bridge of fibrinogen". Blood. 88 (7): 2569–77. doi:10.1182/blood.V88.7.2569.bloodjournal8872569. PMID 8839849.
Tran H, Mattei M, Godyna S, Argraves WS (Mar 1997). "Human fibulin-1D: molecular cloning, expression and similarity with S1-5 protein, a new member of the fibulin gene family". Matrix Biology. 15 (7): 479–93. doi:10.1016/S0945-053X(97)90021-4. PMID 9106159.
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.
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.
Qing J, Maher VM, Tran H, Argraves WS, Dunstan RW, McCormick JJ (Oct 1997). "Suppression of anchorage-independent growth and matrigel invasion and delayed tumor formation by elevated expression of fibulin-1D in human fibrosarcoma-derived cell lines". Oncogene. 15 (18): 2159–68. doi:10.1038/sj.onc.1201385. PMID 9393974.
Hayashido Y, Lucas A, Rougeot C, Godyna S, Argraves WS, Rochefort H (Feb 1998). "Estradiol and fibulin-1 inhibit motility of human ovarian- and breast-cancer cells induced by fibronectin". International Journal of Cancer. 75 (4): 654–8. doi:10.1002/(SICI)1097-0215(19980209)75:4<654::AID-IJC26>3.0.CO;2-7. PMID 9466671.
Roger P, Pujol P, Lucas A, Baldet P, Rochefort H (Nov 1998). "Increased immunostaining of fibulin-1, an estrogen-regulated protein in the stroma of human ovarian epithelial tumors". The American Journal of Pathology. 153 (5): 1579–88. doi:10.1016/S0002-9440(10)65746-X. PMC 1853396. PMID 9811350.
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.

Cell signaling: calcium signaling and calcium metabolism

Cell membrane

Adhesion molecules	Cadherins CDH1 CDH2 CDH3 CDH4 CDH5 CDH6 CDH7 CDH8 CDH9 CDH10 CDH11 CDH12 CDH13 CDH14 CDH15 CDH16 CDH17
Calcium channels	Ligand-gated 5-HT3 receptor Ionotropic glutamate receptors AMPA receptors Kainate receptors NMDA receptors P2X receptors Voltage-gated L N P R T TRP channels TRPA TRPC TRPV
Calcium pumps	Sodium-calcium exchangers SLC3A2 SLC8A1
GPCRs	Calcium-sensing receptor
Annexins	A1 A2 A3 A4 A5 A6 A7 A8 A8-L2 A9 A10 A11 A12 A13

Intracellular signaling

Second messengers	IP3 NAADP cADPR
Intracellular channels	IP3 receptor Ryanodine receptor Calcium-induced calcium release
Intracellular pumps	SERCA ATP2A1 ATP2A2 ATP2A3 Sodium-calcium exchangers SLC8B1 SLC24A5
Sensors and chelators	Calbindin Calmodulin CALM1 CALM2 CALM3 CALML3 CALML5 Calsequestrin Calretinin Gelsolin Neuronal calcium sensors Calsenilin Frequenin GUCA 1A 1B Hippocalcin Neurocalcin Recoverin Visinin Parvalbumin Phospholamban Sarcalumenin Synaptotagmins SYT1 SYT2 SYT3 SYT4 SYT5 SYT6 SYT7 SYT9 SYT11 SYT13 SYT14 S100 S100P Troponin C TNNC1 TNNC2
Calcium-dependent chaperones	Calreticulin Calnexin HSPA5 HSP90B1
Calcium-dependent kinases	CaM kinases CAMK1 CAMK2 A B D G CAMK3 CAMK4 Protein kinase C
Calcium-dependent proteases	Calpains CAPN1 CAPN2 CAPN3 CAPN4 CAPN5 CAPN6 CAPN7 CAPN8 CAPN9 CAPN10
Indirect regulators	Calcitonin Parathyroid hormone Vitamin D Vitamin K

Extracellular chelators

Extracellular matrix proteins	Fibulins FBLN1 FBLN2 FBLN3 FBLN4 FBLN5 Hemicentin 1 Matrix gla protein Osteonectin SIBLINGs Bone sialoprotein Dentin matrix phosphoprotein Dentin sialophosphoprotein Osteopontin
Secreted hormones	Osteocalcin