Fibrillin

Not to be confused with Fibrin.

fibrillin 1
File:2W86 (Fibrillin).png Crystallographic structure of the cbEGF9-hybrid2-cbEGF10 region of human fibrillin 1.
Identifiers
Symbol	FBN1
Alt. symbols	FBN, MFS1, WMS
NCBI gene	2200
HGNC	3603
OMIM	134797
PDB	2W86
RefSeq	NM_000138
UniProt	P35555
Other data
Locus	Chr. 15 q21.1
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fibrillin 2
Identifiers
Symbol	FBN2
Alt. symbols	CCA
NCBI gene	2201
HGNC	3604
OMIM	121050
RefSeq	NM_001999
UniProt	P35556
Other data
Locus	Chr. 5 q23-q31
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fibrillin 3
Identifiers
Symbol	FBN3
NCBI gene	84467
HGNC	18794
OMIM	608529
RefSeq	NM_032447
UniProt	Q75N90
Other data
Locus	Chr. 19 p13
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Fibrillin is a glycoprotein, which is essential for the formation of elastic fibers found in connective tissue. Fibrillin is secreted into the extracellular matrix by fibroblasts and becomes incorporated into the insoluble microfibrils, which appear to provide a scaffold for deposition of elastin.

Clinical aspects

Marfan syndrome is a genetic disorder of the connective tissue caused by defected FBN1 gene. Mutations in FBN1 and FBN2 are also sometimes associated with adolescent idiopathic scoliosis.

Types

Fibrillin-1

Fibrillin-1 is a major component of the microfibrils that form a sheath surrounding the amorphous elastin. It is believed that the microfibrils are composed of end-to-end polymers of fibrillin. To date, 3 forms of fibrillin have been described. The fibrillin-1 protein was isolated by Engvall in 1986, and mutations in the FBN1 gene cause Marfan syndrome.

This protein is found in humans, and its gene is found on chromosome 15. At present more than 1500 different mutations have been described.

Structure

There is no complete, high-resolution structure of fibrillin-1. Instead, short fragments have been produced recombinantly and their structures solved by X-ray crystallography or using NMR spectroscopy. A recent example is the structure of the fibrillin-1 hybrid2 domain, in context of its flanking calcium binding epidermal growth factor domains, which was determined using X-ray crystallography to a resolution of 1.8 Å. The microfibrils that are made up of fibrillin protein are responsible for different cell-matrix interactions in the human body.

Fibrillin-2

Fibrillin-2 was isolated in 1994 by Zhang and is thought to play a role in early elastogenesis. Mutations in the fibrillin-2 gene have been linked to Beals syndrome.

Fibrillin-3

More recently, fibrillin-3 was described and is believed to be located mainly in the brain. Along with the brain, fibrillin-3 has been localized in the gonads and ovaries of field mice.

Fibrillin-4

Fibrillin-4 was first discovered in zebrafish, and has a sequence similar to fibrillin-2.

External links

• Fibrillin at the U.S. National Library of Medicine Medical Subject Headings (MeSH)