Table of Contents

    Topic review

    FRAS1 Gene

    View times: 11
    Submitted by: Vivi Li
    (This entry belongs to Entry Collection "MedlinePlus ")

    Definition

    Fraser extracellular matrix complex subunit 1

    1. Normal Function

    The FRAS1 gene provides instructions for making a protein that is part of a group of proteins called the FRAS/FREM complex. This complex is found in basement membranes, which are thin, sheet-like structures that separate and support cells in many tissues. The FRAS/FREM complex is particularly important during development before birth. One of its roles is to anchor the top layer of skin by connecting the basement membrane of the top layer to the layer of skin below. The FRAS/FREM complex is also involved in the proper development of certain other organs and tissues, including the kidneys, although the mechanism is unclear.

    2. Health Conditions Related to Genetic Changes

    2.1 Fraser Syndrome

    At least 24 mutations in the FRAS1 gene cause a condition called Fraser syndrome; FRAS1 gene mutations account for about half of cases of this condition. Fraser syndrome affects development before birth and is characterized by eyes that are completely covered by skin (cryptophthalmos), fusion of the skin between the fingers and toes (cutaneous syndactyly), and abnormalities of the kidneys and other organs and tissues.

    Most mutations in the FRAS1 gene involved in Fraser syndrome lead to production of an abnormal protein with little or no function. The abnormal protein is likely broken down quickly, preventing formation of the FRAS/FREM complex. Lack of the FRAS/FREM complex in the basement membrane of the skin leads to detachment of the top layer, causing blisters to form during development. These blisters likely prevent the proper formation of certain structures before birth, leading to cryptophthalmos and cutaneous syndactyly. It is unknown how lack of the FRAS/FREM complex leads to kidney abnormalities and other problems in Fraser syndrome.

    2.2 Coloboma

    2.3 Congenital Anomalies of Kidney and Urinary Tract

    2.4 Other Disorders

    Mutations in the FRAS1 gene have also been found in people with abnormalities of the kidneys and urinary tract but no other signs and symptoms of Fraser syndrome (described above). Such abnormalities are grouped together as congenital anomalies of the kidney and urinary tract (CAKUT). A common abnormality in people with FRAS1 gene mutations is the absence of one of the kidneys (a condition called renal agenesis). The FRAS1 gene mutations involved in CAKUT typically change single protein building blocks (amino acids) in the FRAS1 protein. Researchers speculate that the effects of these mutations are milder than those of mutations that cause Fraser syndrome; some FRAS1 protein function may still remain. How these gene mutations affect the FRAS/FREM complex or lead to renal agenesis and other CAKUT is unknown.

    3. Other Names for This Gene

    • extracellular matrix protein FRAS1

    • FLJ14927

    • FLJ22031

    • Fraser syndrome 1

    • KIAA1500

    The entry is from https://medlineplus.gov/genetics/gene/fras1

    References

    1. Kohl S, Hwang DY, Dworschak GC, Hilger AC, Saisawat P, Vivante A, Stajic N,Bogdanovic R, Reutter HM, Kehinde EO, Tasic V, Hildebrandt F. Mild recessivemutations in six Fraser syndrome-related genes cause isolated congenitalanomalies of the kidney and urinary tract. J Am Soc Nephrol. 2014Sep;25(9):1917-22. doi: 10.1681/ASN.2013101103.
    2. Pavlakis E, Chiotaki R, Chalepakis G. The role of Fras1/Frem proteins in thestructure and function of basement membrane. Int J Biochem Cell Biol. 2011Apr;43(4):487-95. doi: 10.1016/j.biocel.2010.12.016.
    3. Petrou P, Makrygiannis AK, Chalepakis G. The Fras1/Frem family ofextracellular matrix proteins: structure, function, and association with Frasersyndrome and the mouse bleb phenotype. Connect Tissue Res. 2008;49(3):277-82.doi: 10.1080/03008200802148025.
    4. Short K, Wiradjaja F, Smyth I. Let's stick together: the role of the Fras1 andFrem proteins in epidermal adhesion. IUBMB Life. 2007 Jul;59(7):427-35. Review.
    5. van Haelst MM, Maiburg M, Baujat G, Jadeja S, Monti E, Bland E, Pearce K;Fraser Syndrome Collaboration Group, Hennekam RC, Scambler PJ. Molecular study of33 families with Fraser syndrome new data and mutation review. Am J Med Genet A. 2008 Sep 1;146A(17):2252-7. doi: 10.1002/ajmg.a.32440.
    More

    Keywords