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Four and a half LIM domains 1

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Entry Collection: MedlinePlus
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Update Date: 25 Dec 2020
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    1. Normal Function

    The FHL1 gene provides instructions for making three versions (isoforms) of a protein that plays an important role in muscles used for movement (skeletal muscles) and in the heart (cardiac muscle). The full-length isoform is known as FHL1A, or sometimes just FHL1. The other two isoforms, which are shorter, are called FHL1B and FHL1C.

    FHL1A is the best-studied of the three FHL1 isoforms. Studies suggest that interactions between FHL1A and other proteins play a critical role in the assembly of sarcomeres, which are structures within muscle cells that are necessary for muscle tensing (contraction). These interactions also appear to be involved in chemical signaling within muscle cells, maintaining the structure of these cells, and influencing muscle growth and size.

    Less is known about the FHL1B and FHL1C isoforms. FHL1B moves in and out of the nucleus and is also part of the nuclear envelope, which is a structure that surrounds the nucleus in cells. The protein's function in this structure is unknown. FHL1B and FHL1C are suspected to play roles in the normal structure and function of skeletal and cardiac muscles.

    2. Health Conditions Related to Genetic Changes

    2.1 Emery-Dreifuss Muscular Dystrophy

    At least seven mutations in the FHL1 gene have been found to cause Emery-Dreifuss muscular dystrophy. This condition affects skeletal and cardiac muscle, causing joint deformities called contractures, which restrict the movement of certain joints; muscle weakness and wasting that worsen over time; and heart problems, including an increased risk of sudden death.

    Some of the FHL1 gene mutations that cause Emery-Dreifuss muscular dystrophy change single protein building blocks (amino acids) in the FHL1 protein, while others insert or delete a small amount of DNA from the FHL1 gene. All of the known mutations affect the FHL1A isoform. Depending on where the mutations occur, they may affect one or both of the other isoforms as well.

    Studies suggest that mutations reduce the amount of functional FHL1 protein produced in cells or lead to the production of an abnormally short, nonfunctional version of the protein. A shortage of this protein disrupts the normal structure and function of cardiac and skeletal muscle cells. However, the exact mechanism by which these changes cause joint contractures, muscle weakness and wasting, and heart problems remains unknown.

    2.2 Other Disorders

    Several other muscle disorders also result from mutations in the FHL1 gene. These include reducing body myopathy, X-linked scapuloperoneal myopathy, X-linked myopathy with postural muscle atrophy (XMPMA), and rigid spine syndrome. Together with Emery-Dreifuss muscular dystrophy, these conditions are known as FHL1-related myopathies or FHL1opathies. Features common among these disorders include skeletal muscle weakness, particularly in the shoulders and lower legs; contractures involving the joints of the spine (rigid spine); and heart abnormalities. However, the disorders differ in their age of onset, the severity of muscle weakness, and how quickly the signs and symptoms worsen.

    More than 50 FHL1 gene mutations have been associated with the FHL1-related myopathies. Each of these mutations affects some or all of the FHL1 isoforms. In general, mutations that affect all three isoforms cause more severe signs and symptoms than mutations that affect only one or two isoforms. Researchers have proposed several possible mechanisms by which FHL1 mutations lead to the FHL1-related myopathies. In some cases, mutations lead to the production of a nonfunctional version of the protein or no protein at all. In others, mutations may result in the production of an abnormal version of the protein that can form clumps (called reducing bodies) within muscle cells. Reducing bodies have been found in people with reducing body myopathy, X-linked scapuloperoneal myopathy, and rigid spine syndrome, but it is unclear how they are related to the major features of these disorders.

    3. Other Names for This Gene

    • bA5A


    1. Bertrand AT, Bönnemann CG, Bonne G; FHL1 myopathy consortium. 199th ENMCinternational workshop: FHL1 related myopathies, June 7-9, 2013, Naarden, TheNetherlands. Neuromuscul Disord. 2014 May;24(5):453-62. doi:10.1016/j.nmd.2014.02.002.
    2. Cowling BS, Cottle DL, Wilding BR, D'Arcy CE, Mitchell CA, McGrath MJ. Fourand a half LIM protein 1 gene mutations cause four distinct human myopathies: acomprehensive review of the clinical, histological and pathological features.Neuromuscul Disord. 2011 Apr;21(4):237-51. doi: 10.1016/j.nmd.2011.01.001.Review.
    3. Gueneau L, Bertrand AT, Jais JP, Salih MA, Stojkovic T, Wehnert M,Hoeltzenbein M, Spuler S, Saitoh S, Verschueren A, Tranchant C, Beuvin M, Lacene E, Romero NB, Heath S, Zelenika D, Voit T, Eymard B, Ben Yaou R, Bonne G.Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy. Am J HumGenet. 2009 Sep;85(3):338-53. doi: 10.1016/j.ajhg.2009.07.015.
    4. Quinzii CM, Vu TH, Min KC, Tanji K, Barral S, Grewal RP, Kattah A, Camaño P,Otaegui D, Kunimatsu T, Blake DM, Wilhelmsen KC, Rowland LP, Hays AP, Bonilla E, Hirano M. X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1. Am J Hum Genet. 2008Jan;82(1):208-13. doi: 10.1016/j.ajhg.2007.09.013.
    5. Schessl J, Feldkirchner S, Kubny C, Schoser B. Reducing body myopathy andother FHL1-related muscular disorders. Semin Pediatr Neurol. 2011Dec;18(4):257-63. doi: 10.1016/j.spen.2011.10.007. Review.
    6. Schessl J, Taratuto AL, Sewry C, Battini R, Chin SS, Maiti B, Dubrovsky AL,Erro MG, Espada G, Robertella M, Saccoliti M, Olmos P, Bridges LR, Standring P,Hu Y, Zou Y, Swoboda KJ, Scavina M, Goebel HH, Mitchell CA, Flanigan KM, Muntoni F, Bönnemann CG. Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1. Brain. 2009 Feb;132(Pt 2):452-64. doi:10.1093/brain/awn325.
    7. Shalaby S, Hayashi YK, Goto K, Ogawa M, Nonaka I, Noguchi S, Nishino I. Rigid spine syndrome caused by a novel mutation in four-and-a-half LIM domain 1 gene(FHL1). Neuromuscul Disord. 2008 Dec;18(12):959-61. doi:10.1016/j.nmd.2008.09.012.
    8. Wilding BR, McGrath MJ, Bonne G, Mitchell CA. FHL1 mutants that causeclinically distinct human myopathies form protein aggregates and impair myoblast differentiation. J Cell Sci. 2014 May 15;127(Pt 10):2269-81. doi:10.1242/jcs.140905.
    9. Windpassinger C, Schoser B, Straub V, Hochmeister S, Noor A, Lohberger B,Farra N, Petek E, Schwarzbraun T, Ofner L, Löscher WN, Wagner K, Lochmüller H,Vincent JB, Quasthoff S. An X-linked myopathy with postural muscle atrophy andgeneralized hypertrophy, termed XMPMA, is caused by mutations in FHL1. Am J HumGenet. 2008 Jan;82(1):88-99. doi: 10.1016/j.ajhg.2007.09.004.
    10. Ziat E, Mamchaoui K, Beuvin M, Nelson I, Azibani F, Spuler S, Bonne G,Bertrand AT. FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Laminaand is Misregulated in Emery-Dreifuss Muscular Dystrophy. J Neuromuscul Dis. 2016Nov 29;3(4):497-510.
    Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to :
    View Times: 188
    Entry Collection: MedlinePlus
    Revisions: 2 times (View History)
    Update Date: 25 Dec 2020
    Table of Contents


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      Li, V. FHL1 Gene. Encyclopedia. Available online: (accessed on 22 March 2023).
      Li V. FHL1 Gene. Encyclopedia. Available at: Accessed March 22, 2023.
      Li, Vivi. "FHL1 Gene" Encyclopedia, (accessed March 22, 2023).
      Li, V. (2020, December 25). FHL1 Gene. In Encyclopedia.
      Li, Vivi. "FHL1 Gene." Encyclopedia. Web. 25 December, 2020.