TMPRSS6 Gene: History
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Transmembrane serine protease 6: The TMPRSS6 gene provides instructions for making a protein called matriptase-2.

  • genes

1. Normal Function

The TMPRSS6 gene provides instructions for making a protein called matriptase-2. This protein is part of a signaling pathway that controls the levels of another protein called hepcidin, which is a key regulator of iron balance in the body. When blood iron levels are low, this signaling pathway reduces hepcidin production, allowing more iron from the diet to be absorbed through the intestines and transported out of storage sites (particularly in the liver and spleen) into the bloodstream. Iron is an essential component of hemoglobin, which is the molecule in red blood cells that carries oxygen.

2. Health Conditions Related to Genetic Changes

2.1. Iron-refractory iron deficiency anemia

At least 40 mutations in the TMPRSS6 gene have been found to cause an inherited form of anemia called iron-refractory iron deficiency anemia. This condition is characterized by a shortage (deficiency) of iron in the bloodstream that is resistant (refractory) to treatment with iron.

TMPRSS6 gene mutations greatly reduce the amount of functional matriptase-2, preventing it from controlling hepcidin levels. The resulting elevation in hepcidin activity blocks the absorption of iron through the intestines and the release of iron from storage. When not enough iron is available in the bloodstream, less hemoglobin is produced and red blood cells cannot carry oxygen to the body's cells and tissues effectively. The shortage of oxygen causes the signs and symptoms of anemia, which can include tiredness (fatigue), weakness, and pale skin.

3. Other Names for This Gene

  • matriptase 2
  • matriptase-2
  • membrane-bound mosaic serine proteinase matriptase-2
  • transmembrane protease serine 6
  • transmembrane protease, serine 6
  • type II transmembrane serine protease 6

This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/tmprss6

References

  1. Camaschella C, Silvestri L. Molecular mechanisms regulating hepcidin revealed by hepcidin disorders. ScientificWorldJournal. 2011 Jul 7;11:1357-66. doi:10.1100/tsw.2011.130. Review.
  2. De Falco L, Totaro F, Nai A, Pagani A, Girelli D, Silvestri L, Piscopo C,Campostrini N, Dufour C, Al Manjomi F, Minkov M, Van Vuurden DG, Feliu A,Kattamis A, Camaschella C, Iolascon A. Novel TMPRSS6 mutations associated withiron-refractory iron deficiency anemia (IRIDA). Hum Mutat. 2010May;31(5):E1390-405. doi: 10.1002/humu.21243.
  3. Du X, She E, Gelbart T, Truksa J, Lee P, Xia Y, Khovananth K, Mudd S, Mann N, Moresco EM, Beutler E, Beutler B. The serine protease TMPRSS6 is required tosense iron deficiency. Science. 2008 May 23;320(5879):1088-92. doi:10.1126/science.1157121.
  4. Meynard D, Vaja V, Sun CC, Corradini E, Chen S, López-Otín C, Grgurevic L,Hong CC, Stirnberg M, Gütschow M, Vukicevic S, Babitt JL, Lin HY. Regulation ofTMPRSS6 by BMP6 and iron in human cells and mice. Blood. 2011 Jul21;118(3):747-56. doi: 10.1182/blood-2011-04-348698.
  5. Ramsay AJ, Hooper JD, Folgueras AR, Velasco G, López-Otín C. Matriptase-2(TMPRSS6): a proteolytic regulator of iron homeostasis. Haematologica. 2009Jun;94(6):840-9. doi: 10.3324/haematol.2008.001867.
  6. Stirnberg M, Gütschow M. Matriptase-2, a regulatory protease of ironhomeostasis: possible substrates, cleavage sites and inhibitors. Curr Pharm Des. 2013;19(6):1052-61. Review.
  7. Zhao N, Zhang AS, Enns CA. Iron regulation by hepcidin. J Clin Invest. 2013Jun;123(6):2337-43. doi: 10.1172/JCI67225.
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