TNNT3

TNNT3
Identifiers
Aliases	TNNT3, TNTF, troponin T3, fast skeletal type, beta-TnTF, DA2B2
External IDs	OMIM: 600692; MGI: 109550; HomoloGene: 31405; GeneCards: TNNT3; OMA:TNNT3 - orthologs
Gene location (Human) Chr. Chromosome 11 (human)[1] Band 11p15.5 Start 1,919,703 bp[1] End 1,938,706 bp[1]
Gene location (Mouse) Chr. Chromosome 7 (mouse)[2] Band 7 F5|7 87.94 cM Start 142,498,836 bp[2] End 142,516,009 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in muscle of thigh skeletal muscle tissue gastrocnemius muscle apex of heart left ventricle testicle placenta right uterine tube right auricle subcutaneous adipose tissue Top expressed in sternocleidomastoid muscle temporal muscle digastric muscle triceps brachii muscle extensor digitorum longus muscle plantaris muscle tibialis anterior muscle triceps surae muscle of thigh extraocular muscle More reference expression data BioGPS n/a
Gene ontology Molecular function calcium-dependent ATPase activity actin binding tropomyosin binding troponin I binding calcium-dependent protein binding troponin C binding calcium ion binding protein binding Cellular component cytosol troponin complex Biological process regulation of muscle contraction skeletal muscle contraction regulation of striated muscle contraction regulation of ATP-dependent activity muscle filament sliding muscle contraction sarcomere organization cardiac muscle contraction Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 7140 21957 Ensembl ENSG00000130595 ENSG00000288250 ENSMUSG00000061723 UniProt P45378 Q9QZ47 RefSeq (mRNA) NM_001042780 NM_001042781 NM_001042782 NM_001297646 NM_006757 NM_001363561 NM_001367842 NM_001367843 NM_001367844 NM_001367845 NM_001367846 NM_001367847 NM_001367848 NM_001367849 NM_001367850 NM_001367851 NM_001367852 NM_001163664 NM_001163665 NM_001163666 NM_001163667 NM_001163668 NM_001163669 NM_001163670 NM_011620 NM_001347546 NM_001347547 NM_001347548 NM_001347549 NM_001347550 NM_001347551 NM_001347552 NM_001360157 NM_001360158 RefSeq (protein) NP_001036245 NP_001036246 NP_001036247 NP_001284575 NP_006748 NP_001350490 NP_001354771 NP_001354772 NP_001354773 NP_001354774 NP_001354775 NP_001354776 NP_001354777 NP_001354778 NP_001354779 NP_001354780 NP_001354781 NP_001157136 NP_001157137 NP_001157138 NP_001157139 NP_001157140 NP_001157141 NP_001157142 NP_001334475 NP_001334476 NP_001334477 NP_001334478 NP_001334479 NP_001334480 NP_001334481 NP_035750 NP_001347086 NP_001347087 Location (UCSC) Chr 11: 1.92 – 1.94 Mb Chr 7: 142.5 – 142.52 Mb PubMed search [3] [4]
Wikidata
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Fast skeletal muscle troponin T (fTnT) is a protein that in humans is encoded by the TNNT3 gene.^[5][6]

The TNNT3 gene is located at 11p15.5 in the human genome, encoding the fast skeletal muscle isoform of troponin T (fsTnT). fsTnT is an ~31-kDa protein consisting of 268 amino acids including the first methionine with an isoelectric point (pI) of 6.21 (embryonic form). fsTnT is the tropomyosin-binding and thin filament anchoring subunit of the troponin complex in the sarcomeres of fast twitch skeletal muscle.^[7][8][9] TNNT3 gene is specifically expressed in vertebrate fast twitch skeletal muscles.^[8][9][10]

TNNT3 gene evolved as one of the three TnT isoform genes in vertebrates. Each of the TnT isoform genes is linked to an upstream troponin I (TnI, one of the other two subunits of the troponin complex) isoform gene, and fsTnT is linked with fsTnI genes (Fig. 1). Sequence homology and protein epitope allosteric similarity data suggest that TnT gene was originated by duplication of a TnI-like ancestor gene and fsTnT was the first TnT emerged.^[11] Whereas significantly diverged from the slow skeletal muscle TnT (ssTnT encoded by TNNT1) and cardiac TnT (cTnT encoded by TNNT2), Structure of fsTnT is conserved among vertebrate species (Fig. 2), reflecting specialized functional features of the different muscle fiber types.^[7][8][9]

Mammalian TNNT3 gene contains 19 exons. Alternative RNA splicing of 8 of them significantly increases structural variations of fsTnT.^[12] Two variable regions of the fsTnT protein are generated by alternative splicing (Fig. 3).

In the N-terminal region of fsTnT, exons 4, 5, 6, 7 and 8 are alternatively spliced in adult skeletal muscle cells.^[12][13][14] A fetal fsTnT exon located between exons 8 and 9 is specifically expressed in embryonic muscle (Briggs and Schachat 1993). Exons 16 and 17, previously designated as α and β exons, in the C-terminal region of fsTnT are alternatively spliced in a mutually exclusive manner.^[15]

Avian Tnnt3 gene has evolved with additional alternatively spliced exons, w, P1-7(x) and y, encoding the N-terminal variable region (Fig. 3).^[16][17][18] Reflecting the power of combined alternative splicing of multiple exons to generate fsTnT variants, two-dimensional gel electrophoresis detected more than 40 different fsTnT splice forms in chicken leg muscle.^[19]

Through alternative splicing of the fetal exon and other alternative exons in the N-terminal variable region, the expression of fsTnT during mammalian and avian development undergoes a high molecular to low molecular weight isoform switch in both fast and slow fiber dominant skeletal muscles.^[20] The inclusion of more N-terminal exons increases the negative charge that tunes the overall molecular conformation of fsTnT and alters interaction with TnI, TnC and tropomyosin.^[21][22][23] The alternative splicing-based addition of N-terminal negative charge in fsTnT also contributes to the tolerance to acidosis.^[24]

Alternative splicing of the two C-terminal mutually exclusive exons 16 and 17 appears also regulated during development.^[14] Exon 17 with a sequence more similar to the counterpart segment in ssTnT and cTnT is predominantly expressed in embryonic and neonatal fsTnT.^[14][25] Exon 16 of fsTnT was only found in adult skeletal muscles. Exons 16 and 17 both encode a 14 amino acids peptide fragment residing in the α-helix interfacing with TnI and TnC. Protein interaction studies revealed that incorporation of exon 17 weakened binding of fsTnT to TnC and tropomyosin.^[26] Therefore, alternative splicing of exons 16 and 17 regulates the binding of fsTnT with TnI, possibly TnC, and thus tunes the function of the troponin complex and skeletal muscle contractility during development.

Avian Tnnt3 gene with additional alternatively spliced exons has unique expression pattern. The seven P exons are specifically expressed in pectoral muscles but not leg muscles.^[24] During post hatch development of the avian pectoral muscles, the segment encoded by the P exons (named Tx from the original annotation of the coding exons as an x exon) is up-regulated and included predominantly in fsTnT of adult pectoral muscles.^[27] Each P exon encodes a pentapeptide AHH(A/E)A. The Tx segment of adult fsTnT in avian orders of Galliformes and Craciformes contains 7-9 H(A/E)AAH repeats that possess high affinity binding to transition metal ions Cu(II), Ni(II), Zn(II) and Co(II).^[27] The Tx segment of chicken breast muscle fsTnT also a binding capacity for calcium, presumably serves as a calcium reservoir in avian fast pectoral muscles.^[28] Together with more N-terminal negative charges, this function may contribute to the higher calcium sensitivity of chicken breast muscle than that of leg muscle.^[29]

The switch of high to low molecular weight splice forms occurs in avian leg muscles during post hatching development similar to that in developing mammalian skeletal muscles. Early during post hatch development of chicken pectoral muscles, fsTnT also shows a high to low molecular weight switch. However, around 28 days after hatch, fsTnT with Tx segment spliced-in is rapidly up-regulated and becomes the major fsTnT splice form in adult pectoral muscles.^[27]

Deficiency of ssTnT did not affect the developmental switch of fsTnT splice forms in ssTnT-null mice, indicating that the developmental alternative splicing of the fsTnT pre-mRNA is regulated independent of skeletal muscle fiber type abnormality and adaptation.^[20]

The 2016 version of this article was updated by an external expert under a dual publication model. The corresponding academic peer reviewed article was published in Gene and can be cited as: Bin Wei; J-P Jin (13 January 2016). "TNNT1, TNNT2, and TNNT3: Isoform genes, regulation, and structure-function relationships". Gene. Gene Wiki Review Series. 582 (1): 1–13. doi:10.1016/J.GENE.2016.01.006. ISSN 0378-1119. PMC 5325693. PMID 26774798. Wikidata Q37666010.