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    Topic review

    CARD11 Gene

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    Submitted by: Vicky Zhou
    (This entry belongs to Entry Collection "MedlinePlus ")

    Definition

    caspase recruitment domain family member 11

    1. Normal Function

    The CARD11 gene provides instructions for making a protein involved in the function of immune system cells called lymphocytes, particularly certain types called T cells and B cells. These cells identify foreign substances such as bacteria, viruses, and fungi and defend the body against infection. When T or B cells recognize a foreign substance, the CARD11 protein is turned on (activated) and attaches (binds) to two other proteins, BCL10 and MALT1, to form the CBM signalosome complex. This complex in turn activates other protein complexes called nuclear factor-kappa-B (NF-κB) and mTOR complex 1 (mTORC1), which are important for cellular signaling. NF-κB and mTORC1 signaling direct the development and function of T and B cells so they can support an immune response against foreign invaders.

    2. Health Conditions Related to Genetic Changes

    2.1. Atopic Dermatitis

    At least five CARD11 gene mutations have been identified in people with a skin disorder called atopic dermatitis (also known as atopic eczema). This condition is characterized by dry, itchy skin and red rashes. The word "atopic" indicates an association with allergies. While atopic dermatitis is not always due to an allergic reaction, it is commonly associated with other allergic disorders. People with atopic dermatitis caused by CARD11 gene mutations often have additional allergic disorders, such as asthma and environmental (such as pollen) or food allergies. Many of these individuals also have recurrent infections due to problems with the immune system (immunodeficiency).

    Atopic dermatitis is generally thought of as a complex condition that is influenced by multiple genetic and environmental factors, which each contribute only a small amount to the overall risk of developing the condition. However, CARD11 gene mutations appear to cause atopic dermatitis without other factors. These mutations likely account for only a small percentage of cases of the condition.

    A mutation in one of the two copies of the CARD11 gene in each cell is sufficient to cause atopic dermatitis. These mutations result in the production of an altered protein that does not function normally. The altered protein produced from the mutated copy of the gene interferes with the normal protein produced from the non-mutated copy of the gene (such mutations are described as "dominant-negative"), so the amount of functioning CARD11 protein in cells is reduced. These genetic changes are thought to prevent formation of the CBM signalosome complex, impairing signaling by NF-κB and mTORC1. Without these signals, T cells do not develop or function properly. The number of these cells is normal, but their response to foreign invaders is diminished, leading to recurrent infections.

    It is not clear how the immune dysfunction caused by CARD11 gene mutations leads to atopic dermatitis and allergic disorders. Atopic dermatitis is not initially caused by an allergic reaction, although sometimes substances that can cause allergic reactions (allergens) are thought to contribute to flare-ups of the rashes.

    2.2. Omenn Syndrome

    Omenn syndrome

    2.3. Other Disorders

    CARD11 gene mutations can cause other immune system disorders. At least 3 mutations in the gene have been found to cause a type of severe combined immunodeficiency (SCID) known as immunodeficiency 11. SCID is a group of disorders characterized by an almost total lack of immune protection from foreign invaders. Immunodeficiency 11 is characterized by recurrent severe infections in the respiratory tract, particularly pneumonia caused by a fungus known as Pneumocystis jirovecii. Immunodeficiency 11 occurs when both copies of the CARD11 gene are mutated. The mutations are described as "loss of function" because they lead to production of an abnormally short, nonfunctional CARD11 protein. The lack of CARD11 function diminishes T cells' ability to fight foreign invaders, despite normal numbers of the cells, leading to recurrent infections. Individuals with immunodeficiency 11 do not appear to have an increased risk of atopic dermatitis (described above) or allergies.

    At least four mutations in the CARD11 gene cause another immune cell disorder called B-cell expansion with NF-κB and T-cell anergy (BENTA). This condition is characterized by an excess of immune system cells called B cells (B-cell lymphocytosis), an increased risk of B-cell lymphoma, and susceptibility to infection. The mutations that cause BENTA are inherited and occur in one copy of the CARD11 gene. Like those involved in B-cell and T-cell cancers (described above), the genetic changes that cause BENTA are "gain-of-function" mutations; they lead to production of an altered CARD11 protein that is always turned on, resulting in constant NF-κB signaling. Overactive NF-κB promotes the proliferation of B cells, which can lead to B-cell lymphoma. These abnormal cells, however, cannot respond to infections. T cells are also abnormal and unable to fight foreign invaders (a phenomenon known as anergy). These immune cell problems lead to the increased risk of infection in people with BENTA.

    2.4. Cancers

    Mutations in the CARD11 gene are also associated with cancers of B cells (primarily diffuse large B-cell lymphoma) and T cells (adult T-cell leukemia/lymphoma). These mutations are not inherited; instead, they arise during a person's lifetime and are found only in B or T cells that give rise to cancer. These genetic changes are called "gain-of-function" mutations because they lead to production of an altered CARD11 protein that is always turned on, even without recognition of foreign substances by the B or T cell. As a result, NF-κB is constantly activated. Unregulated NF-κB signaling allows these cells to grow and divide without control, contributing to the development of cancer.

    3. Other Names for This Gene

    • bcl10-interacting maguk protein 3
    • BENTA
    • BIMP3
    • CARD-containing MAGUK protein 1
    • carma 1
    • CARMA1
    • caspase recruitment domain-containing protein 11
    • IMD11
    • IMD11A
    • PPBL

    The entry is from https://medlineplus.gov/genetics/gene/card11

    References

    1. Dadi H, Jones TA, Merico D, Sharfe N, Ovadia A, Schejter Y, Reid B, Sun M,Vong L, Atkinson A, Lavi S, Pomerantz JL, Roifman CM. Combined immunodeficiencyand atopy caused by a dominant negative mutation in caspase activation andrecruitment domain family member 11 (CARD11). J Allergy Clin Immunol. 2018May;141(5):1818-1830.e2. doi: 10.1016/j.jaci.2017.06.047.
    2. Greil J, Rausch T, Giese T, Bandapalli OR, Daniel V, Bekeredjian-Ding I, StützAM, Drees C, Roth S, Ruland J, Korbel JO, Kulozik AE. Whole-exome sequencinglinks caspase recruitment domain 11 (CARD11) inactivation to severe combinedimmunodeficiency. J Allergy Clin Immunol. 2013 May;131(5):1376-83.e3. doi:10.1016/j.jaci.2013.02.012.
    3. Kogure Y, Kataoka K. Genetic alterations in adult T-cell leukemia/lymphoma.Cancer Sci. 2017 Sep;108(9):1719-1725. doi: 10.1111/cas.13303.Review.
    4. Lamason RL, McCully RR, Lew SM, Pomerantz JL. Oncogenic CARD11 mutationsinduce hyperactive signaling by disrupting autoinhibition by the PKC-responsiveinhibitory domain. Biochemistry. 2010 Sep 28;49(38):8240-50. doi:10.1021/bi101052d.
    5. Lenz G, Davis RE, Ngo VN, Lam L, George TC, Wright GW, Dave SS, Zhao H, Xu W, Rosenwald A, Ott G, Muller-Hermelink HK, Gascoyne RD, Connors JM, Rimsza LM,Campo E, Jaffe ES, Delabie J, Smeland EB, Fisher RI, Chan WC, Staudt LM.Oncogenic CARD11 mutations in human diffuse large B cell lymphoma. Science. 2008 Mar 21;319(5870):1676-9. doi: 10.1126/science.1153629.
    6. Ma CA, Stinson JR, Zhang Y, Abbott JK, Weinreich MA, Hauk PJ, Reynolds PR,Lyons JJ, Nelson CG, Ruffo E, Dorjbal B, Glauzy S, Yamakawa N, Arjunaraja S, VossK, Stoddard J, Niemela J, Zhang Y, Rosenzweig SD, McElwee JJ, DiMaggio T,Matthews HF, Jones N, Stone KD, Palma A, Oleastro M, Prieto E, Bernasconi AR,Dubra G, Danielian S, Zaiat J, Marti MA, Kim B, Cooper MA, Romberg N, Meffre E,Gelfand EW, Snow AL, Milner JD. Germline hypomorphic CARD11 mutations in severeatopic disease. Nat Genet. 2017 Aug;49(8):1192-1201. doi: 10.1038/ng.3898.
    7. Shi JH, Sun SC. TCR signaling to NF-κB and mTORC1: Expanding roles of theCARMA1 complex. Mol Immunol. 2015 Dec;68(2 Pt C):546-57. doi:10.1016/j.molimm.2015.07.024.
    8. Snow AL, Xiao W, Stinson JR, Lu W, Chaigne-Delalande B, Zheng L, Pittaluga S, Matthews HF, Schmitz R, Jhavar S, Kuchen S, Kardava L, Wang W, Lamborn IT, JingH, Raffeld M, Moir S, Fleisher TA, Staudt LM, Su HC, Lenardo MJ. Congenital Bcell lymphocytosis explained by novel germline CARD11 mutations. J Exp Med. 2012 Nov 19;209(12):2247-61. doi: 10.1084/jem.20120831.
    9. Thome M, Charton JE, Pelzer C, Hailfinger S. Antigen receptor signaling toNF-kappaB via CARMA1, BCL10, and MALT1. Cold Spring Harb Perspect Biol. 2010Sep;2(9):a003004. doi: 10.1101/cshperspect.a003004.
    10. Turvey SE, Durandy A, Fischer A, Fung SY, Geha RS, Gewies A, Giese T, Greil J,Keller B, McKinnon ML, Neven B, Rozmus J, Ruland J, Snow AL, Stepensky P, WarnatzK. The CARD11-BCL10-MALT1 (CBM) signalosome complex: Stepping into the limelight of human primary immunodeficiency. J Allergy Clin Immunol. 2014Aug;134(2):276-84. doi: 10.1016/j.jaci.2014.06.015. Review.
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