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Liu, R. TNNI2 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/5806 (accessed on 26 December 2024).
Liu R. TNNI2 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/5806. Accessed December 26, 2024.
Liu, Rui. "TNNI2 Gene" Encyclopedia, https://encyclopedia.pub/entry/5806 (accessed December 26, 2024).
Liu, R. (2020, December 25). TNNI2 Gene. In Encyclopedia. https://encyclopedia.pub/entry/5806
Liu, Rui. "TNNI2 Gene." Encyclopedia. Web. 25 December, 2020.
TNNI2 Gene
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This entry is adapted from the peer-reviewed paper https://medlineplus.gov/genetics/gene/tnni2

Troponin I2, fast skeletal type: The TNNI2 gene provides instructions for making one form of a protein called troponin I.

genes

1. Normal Function

The TNNI2 gene provides instructions for making one form of a protein called troponin I. The troponin I protein produced from the TNNI2 gene is found in skeletal muscles, which are the muscles used for movement. Troponin I is one of three proteins that make up the troponin complex in muscle cells. The troponin complex, along with calcium, helps regulate muscle tensing (contraction).

The troponin complex is part of a structure called the sarcomere, which is the basic unit of muscle contraction. Sarcomeres contain thick and thin filaments. The overlapping thick and thin filaments attach (bind) to each other and release, which allows the filaments to move relative to one another so that muscles can contract.

When calcium levels are low, the troponin complex blocks the binding between the thick and thin filaments that is needed for muscle contraction. An increase in calcium levels causes structural changes in the troponin complex, which exposes the binding sites and allows the thick and thin filaments to interact, leading to muscle contraction.

2. Health Conditions Related to Genetic Changes

2.1. Sheldon-Hall syndrome

At least eight TNNI2 gene mutations have been identified in people with Sheldon-Hall syndrome. This disorder affects muscle and skeletal development before birth and is characterized by joint deformities (contractures) that restrict movement in the hands and feet. Researchers suggest that the TNNI2 gene mutations that cause Sheldon-Hall syndrome may prevent the troponin complex from blocking thick and thin filament binding to control muscle contractions, resulting in the contractures and other muscle and skeletal abnormalities associated with Sheldon-Hall syndrome.

3. Other Names for This Gene

  • AMCD2B
  • DA2B
  • FSSV
  • fsTnI
  • troponin I fast twitch 2
  • troponin I type 2 (skeletal, fast)
  • troponin I, fast skeletal muscle
  • troponin I, fast skeletal muscle isoform 1
  • troponin I, fast skeletal muscle isoform 2
  • troponin I, fast-twitch isoform
  • troponin I, fast-twitch skeletal muscle isoform
  • troponin I, skeletal, fast

References

  1. Beck AE, McMillin MJ, Gildersleeve HI, Kezele PR, Shively KM, Carey JC,Regnier M, Bamshad MJ. Spectrum of mutations that cause distal arthrogryposistypes 1 and 2B. Am J Med Genet A. 2013 Mar;161A(3):550-5. doi:10.1002/ajmg.a.35809.
  2. Drera B, Zoppi N, Barlati S, Colombi M. Recurrence of the p.R156X TNNI2mutation in distal arthrogryposis type 2B. Clin Genet. 2006 Dec;70(6):532-4.
  3. Ochala J. Thin filament proteins mutations associated with skeletalmyopathies: defective regulation of muscle contraction. J Mol Med (Berl). 2008Nov;86(11):1197-204. doi: 10.1007/s00109-008-0380-9.
  4. Toydemir RM, Bamshad MJ. Sheldon-Hall syndrome. Orphanet J Rare Dis. 2009 Mar 23;4:11. doi: 10.1186/1750-1172-4-11. Review.
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Subjects: Genetics & Heredity
Contributor MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Rui Liu
View Times: 512
Entry Collection: MedlinePlus
Revision: 1 time (View History)
Update Date: 25 Dec 2020
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