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Liu, R. TSC2 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5831 (accessed on 13 June 2024).
Liu R. TSC2 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5831. Accessed June 13, 2024.
Liu, Rui. "TSC2 Gene" Encyclopedia, https://encyclopedia.pub/entry/5831 (accessed June 13, 2024).
Liu, R. (2020, December 25). TSC2 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5831
Liu, Rui. "TSC2 Gene." Encyclopedia. Web. 25 December, 2020.
TSC2 Gene
Edit

TSC complex subunit 2

genes

1. Normal Function

The TSC2 gene provides instructions for producing a protein called tuberin, whose function is not fully understood. Within cells, tuberin interacts with a protein called hamartin, which is produced from the TSC1 gene. These two proteins help control cell growth and size. Proteins that normally prevent cells from growing and dividing too fast or in an uncontrolled way are known as tumor suppressors. Hamartin and tuberin carry out their tumor suppressor function by interacting with and regulating a wide variety of other proteins.

2. Health Conditions Related to Genetic Changes

2.1. Lymphangioleiomyomatosis

Mutations in the TSC2 gene cause most cases of a disorder called lymphangioleiomyomatosis (LAM). This destructive lung disease is characterized by the abnormal overgrowth of smooth muscle-like tissue in the lungs. It occurs almost exclusively in women, causing coughing, shortness of breath, chest pain, and lung collapse.

LAM can occur alone (isolated or sporadic LAM) or in combination with a condition called tuberous sclerosis complex (described below). Researchers suggest that sporadic LAM is caused by a random mutation in the TSC2 gene that occurs very early in development. As a result, some of the body's cells have a normal version of the gene, while others have the mutated version. This situation is called mosaicism. When a mutation occurs in the other copy of the TSC2 gene in certain cells during a woman's lifetime (a somatic mutation), she may develop LAM.

2.2. Tuberous sclerosis complex

More than 1,100 mutations in the TSC2 gene have been identified in individuals with tuberous sclerosis complex, a condition characterized by developmental problems and the growth of noncancerous tumors in many parts of the body. Most of these mutations insert or delete a small number of DNA building blocks (base pairs) in the TSC2 gene. Other mutations change a single base pair in the TSC2 gene or create a premature stop signal in the instructions for making tuberin.

People with TSC2-related tuberous sclerosis complex are born with one mutated copy of the TSC2 gene in each cell. This mutation prevents the cell from making functional tuberin from that copy of the gene. However, enough tuberin is usually produced from the other, normal copy of the TSC2 gene to regulate cell growth effectively. For some types of tumors to develop, a second mutation involving the other copy of the gene must occur in certain cells during a person's lifetime.

When both copies of the TSC2 gene are mutated in a particular cell, that cell cannot produce any functional tuberin. The loss of this protein allows the cell to grow and divide in an uncontrolled way to form a tumor. A shortage of tuberin also interferes with the normal development of certain cells. In people with TSC2-related tuberous sclerosis complex, a second TSC2 gene mutation typically occurs in multiple cells over an affected person's lifetime. The loss of tuberin in different types of cells disrupts normal development and leads to the growth of tumors in many different organs and tissues.

3. Other Names for This Gene

  • PPP1R160
  • TSC2_HUMAN
  • tuberin
  • tuberous sclerosis 2

References

  1. Carsillo T, Astrinidis A, Henske EP. Mutations in the tuberous sclerosiscomplex gene TSC2 are a cause of sporadic pulmonary lymphangioleiomyomatosis.Proc Natl Acad Sci U S A. 2000 May 23;97(11):6085-90.
  2. Chorianopoulos D, Stratakos G. Lymphangioleiomyomatosis and tuberous sclerosiscomplex. Lung. 2008 Jul-Aug;186(4):197-207. doi: 10.1007/s00408-008-9087-5.
  3. Goncharova EA, Krymskaya VP. Pulmonary lymphangioleiomyomatosis (LAM):progress and current challenges. J Cell Biochem. 2008 Feb 1;103(2):369-82.Review.
  4. Huang J, Manning BD. The TSC1-TSC2 complex: a molecular switchboardcontrolling cell growth. Biochem J. 2008 Jun 1;412(2):179-90. doi:10.1042/BJ20080281. Review.
  5. Juvet SC, McCormack FX, Kwiatkowski DJ, Downey GP. Molecular pathogenesis oflymphangioleiomyomatosis: lessons learned from orphans. Am J Respir Cell MolBiol. 2007 Apr;36(4):398-408.
  6. Mak BC, Yeung RS. The tuberous sclerosis complex genes in tumor development.Cancer Invest. 2004;22(4):588-603. Review.
  7. Martignoni G, Pea M, Reghellin D, Gobbo S, Zamboni G, Chilosi M, Bonetti F.Molecular pathology of lymphangioleiomyomatosis and other perivascularepithelioid cell tumors. Arch Pathol Lab Med. 2010 Jan;134(1):33-40. doi:10.1043/2008-0542-RAR1.1.
  8. Narayanan V. Tuberous sclerosis complex: genetics to pathogenesis. PediatrNeurol. 2003 Nov;29(5):404-9. Review.
  9. Rosner M, Hanneder M, Siegel N, Valli A, Hengstschläger M. The tuberoussclerosis gene products hamartin and tuberin are multifunctional proteins with a wide spectrum of interacting partners. Mutat Res. 2008 Mar-Apr;658(3):234-46.doi: 10.1016/j.mrrev.2008.01.001.
  10. Sampson JR. TSC1 and TSC2: genes that are mutated in the human geneticdisorder tuberous sclerosis. Biochem Soc Trans. 2003 Jun;31(Pt 3):592-6.
  11. Yeung RS. Multiple roles of the tuberous sclerosis complex genes. GenesChromosomes Cancer. 2003 Dec;38(4):368-75. Review.
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