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    HOXA13 Gene

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    Submitted by: Dean Liu
    (This entry belongs to Entry Collection "MedlinePlus ")

    Definition

    Homeobox A13

    1. Introduction

    The HOXA13 gene provides instructions for producing a protein that attaches (binds) to specific regions of DNA and regulates the activity of other genes. On the basis of this role, the HOXA13 gene is called a transcription factor. The HOXA13 gene is part of a larger family of transcription factors called homeobox genes, which act during early embryonic development to control the formation of many body structures. Specifically, the HOXA13 protein appears to be critical for the formation and development of the limbs (particularly the hands and feet), urinary tract, and reproductive system.

    The HOXA13 gene contains three areas where a protein building block (amino acid) called alanine is repeated multiple times. These stretches of alanines are known as polyalanine tracts or poly(A) tracts. The role of polyalanine tracts in normal HOXA13 function is unknown.

    2. Health Conditions Related to Genetic Changes

    2.1. Hand-Foot-Genital Syndrome

    At least 14 mutations in the HOXA13 gene have been found to cause hand-foot-genital syndrome. More than half of these mutations affect one of the polyalanine tracts in the HOXA13 gene. These mutations add extra alanines to these tracts, making them abnormally long and unstable. The resulting altered protein is degraded by the cell, so it is unavailable to regulate the activity of other genes during early development. These changes affect the development of the hands, feet, urinary tract, and reproductive system.

    Other HOXA13 mutations result in the production of an abnormally short, nonfunctional version of the HOXA13 protein or change single amino acids in the protein. Mutations that substitute one amino acid for another amino acid may change the way the HOXA13 protein is folded. The altered protein may or may not function or bind to DNA normally. Mutations that result in an altered but functional HOXA13 protein may cause more severe signs and symptoms of hand-foot-genital syndrome than mutations that lead to a nonfunctional version of this protein.

    2.2. Cancers

    Chromosomal rearrangements (translocations) involving the short (p) arm of chromosome 7 have been associated with rare cases of leukemia, a cancer of blood-forming cells. These translocations disrupt the region of chromosome 7 that contains several similar homeobox genes, including HOXA13.

    Within cancer cells, researchers have found translocations between chromosome 7 and chromosome 11 in several people with leukemia. These rearrangements abnormally fuse part of HOXA13 or a similar gene on chromosome 7 to part of the NUP98 gene on chromosome 11. The protein produced from the fused gene probably signals abnormal cells to continue dividing without control or order, which likely contributes to the development of cancer.

    3. Other Names for This Gene

    • homeo box 1J

    • homeo box A13

    • Homeobox protein Hox-A13

    • homeobox protein HOXA13

    • Hox-1J

    • HOX1

    • HOX1J

    • HXA13_HUMAN

    • transcription factor HOXA13

    The entry is from https://medlineplus.gov/genetics/gene/hoxa13

    References

    1. Fujino T, Suzuki A, Ito Y, Ohyashiki K, Hatano Y, Miura I, Nakamura T.Single-translocation and double-chimeric transcripts: detection of NUP98-HOXA9 inmyeloid leukemias with HOXA11 or HOXA13 breaks of the chromosomal translocationt(7;11)(p15;p15). Blood. 2002 Feb 15;99(4):1428-33.
    2. Goodman FR, Bacchelli C, Brady AF, Brueton LA, Fryns JP, Mortlock DP, InnisJW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ.Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.Am J Hum Genet. 2000 Jul;67(1):197-202.
    3. Goodman FR, Scambler PJ. Human HOX gene mutations. Clin Genet. 2001Jan;59(1):1-11. Review.
    4. Goodman FR. Limb malformations and the human HOX genes. Am J Med Genet. 2002Oct 15;112(3):256-65. Review.
    5. Innis JW, Mortlock D, Chen Z, Ludwig M, Williams ME, Williams TM, Doyle CD,Shao Z, Glynn M, Mikulic D, Lehmann K, Mundlos S, Utsch B. Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model. Hum Mol Genet. 2004 Nov 15;13(22):2841-51.
    6. Innis JW. Hand-Foot-Genital Syndrome. 2006 Jul 11 [updated 2019 Aug 8]. In:Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A,editors. GeneReviews® [Internet]. Seattle (WA): University of Washington,Seattle; 1993-2020. Available from http://www.ncbi.nlm.nih.gov/books/NBK1423/
    7. Mortlock DP, Innis JW. Mutation of HOXA13 in hand-foot-genital syndrome. NatGenet. 1997 Feb;15(2):179-80.
    8. Taketani T, Taki T, Ono R, Kobayashi Y, Ida K, Hayashi Y. The chromosometranslocation t(7;11)(p15;p15) in acute myeloid leukemia results in fusion of theNUP98 gene with a HOXA cluster gene, HOXA13, but not HOXA9. Genes ChromosomesCancer. 2002 Aug;34(4):437-43.
    9. Utsch B, Becker K, Brock D, Lentze MJ, Bidlingmaier F, Ludwig M. A novelstable polyalanine [poly(A)] expansion in the HOXA13 gene associated withhand-foot-genital syndrome: proper function of poly(A)-harbouring transcriptionfactors depends on a critical repeat length? Hum Genet. 2002 May;110(5):488-94.
    10. Utsch B, McCabe CD, Galbraith K, Gonzalez R, Born M, Dötsch J, Ludwig M,Reutter H, Innis JW. Molecular characterization of HOXA13 polyalanine expansionproteins in hand-foot-genital syndrome. Am J Med Genet A. 2007 Dec15;143A(24):3161-8.
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