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TTN
Available structures PDB Ortholog search: A2ASS6%20or%20Q8WZ42%20or%20 A2ASS6%20or%20H0Y4J7 PDBe A2ASS6,Q8WZ42, A2ASS6,H0Y4J7 RCSB List of PDB id codes 4UOW, 1BPV, 1G1C, 1NCT, 1NCU, 1TIT, 1TIU, 1TKI, 1TNM, 1TNN, 1WAA, 1YA5, 2A38, 2BK8, 2F8V, 2ILL, 2J8H, 2J8O, 2NZI, 2RQ8, 2WP3, 2WWK, 2WWM, 2Y9R, 3KNB, 3LCY, 3LPW, 3PUC, 3Q5O, 3QP3, 4C4K, 4JNW, 4O00, 4QEG, 5BS0
Identifiers
Aliases	TTN, CMD1G, CMH9, CMPD4, EOMFC, HMERF, LGMD2J, MYLK5, TMD, titin, SALMY, LGMDR10
External IDs	OMIM: 188840; MGI: 98864; HomoloGene: 130650; GeneCards: TTN; OMA:TTN - orthologs
EC number	2.7.11.1
Gene location (Human) Chr. Chromosome 2 (human) Band 2q31.2 Start 178,525,989 bp End 178,830,802 bp
Gene location (Mouse) Chr. Chromosome 2 (mouse) Band 2 C3|2 45.13 cM Start 76,703,980 bp End 76,982,547 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in glutes Skeletal muscle tissue of biceps brachii triceps brachii muscle Skeletal muscle tissue of rectus abdominis right ventricle thoracic diaphragm body of tongue vastus lateralis muscle deltoid muscle myocardium of left ventricle Top expressed in vastus lateralis muscle digastric muscle triceps brachii muscle sternocleidomastoid muscle knee joint body of femur temporal muscle atrium intercostal muscle medial head of gastrocnemius muscle More reference expression data BioGPS More reference expression data
Gene ontology Molecular function transferase activity nucleotide binding calcium ion binding protein kinase activity actinin binding muscle alpha-actinin binding structural molecule activity conferring elasticity metal ion binding telethonin binding protease binding protein self-association actin filament binding protein serine/threonine kinase activity kinase activity protein binding identical protein binding enzyme binding protein tyrosine kinase activity structural constituent of muscle ATP binding protein kinase binding calmodulin binding structural constituent of cytoskeleton ankyrin binding Cellular component cytoplasm cytosol I band striated muscle thin filament condensed nuclear chromosome extracellular region Z discdkac muscle myosin complex extracellular exosome nucleus M band sarcomere A band myofibril Biological process sarcomerogenesis muscle contraction mitotic chromosome condensation cardiac muscle contraction phosphorylation cardiac muscle hypertrophy platelet degranulation cardiac muscle tissue morphogenesis skeletal muscle thin filament assembly detection of muscle stretch response to calcium ion cardiac myofibril assembly protein phosphorylation muscle filament sliding regulation of protein kinase activity regulation of catalytic activity sarcomere organization skeletal muscle myosin thick filament assembly striated muscle contraction peptidyl-tyrosine phosphorylation positive regulation of gene expression protein kinase A signaling positive regulation of protein secretion somitogenesis ventricular system development in utero embryonic development heart morphogenesis striated muscle cell development heart growth adult heart development forward locomotion heart development regulation of relaxation of cardiac muscle actin filament organization striated muscle myosin thick filament assembly Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 7273 22138 Ensembl ENSG00000155657 ENSMUSG00000051747 UniProt Q8WZ42 Q8WZ42 RefSeq (mRNA) NM_001256850 NM_001267550 NM_003319 NM_133378 NM_133379 NM_133432 NM_133437 NM_011652 NM_028004 RefSeq (protein) NP_001243779 NP_001254479 NP_003310 NP_596869 NP_596870 NP_597676 NP_597681 NP_035782 NP_082280 NP_001372637 NP_001243779 NP_001254479 NP_003310 NP_596869 NP_596870 NP_597676 NP_597681 NP_035782 NP_082280 NP_001372637 Location (UCSC) Chr 2: 178.53 – 178.83 Mb Chr 2: 76.7 – 76.98 Mb PubMed search
Wikidata
View/Edit Human View/Edit Mouse

Titin /ˈtaɪtɪn/ (contraction for Titan protein) (also called connectin) is a protein that in humans is encoded by the TTN gene. The protein, which is over 1 μm in length, functions as a molecular spring that is responsible for the passive elasticity of muscle. It comprises 244 individually folded protein domains connected by unstructured peptide sequences. These domains unfold when the protein is stretched and refold when the tension is removed.

Titin is important in the contraction of striated muscle tissues. It connects the Z disc to the M line in the sarcomere. The protein contributes to force transmission at the Z disc and resting tension in the I band region. It limits the range of motion of the sarcomere in tension, thus contributing to the passive stiffness of muscle. Variations in the sequence of titin between different types of striated muscle (cardiac or skeletal) have been correlated with differences in the mechanical properties of these muscles.

Titin is the third most abundant protein in muscle (after myosin and actin), and an adult human contains approximately 0.5 kg of titin. With its length of ~27,000 to ~35,000 amino acids (depending on the splice isoform), titin is the largest known protein. Furthermore, the gene for titin contains the largest number of exons (363) discovered in any single gene, as well as the longest single exon (17,106 bp).

Discovery

In 1954, Reiji Natori proposed the existence of an elastic structure in muscle fiber to account for the return to the resting state when muscles are stretched and then released. In 1977, Koscak Maruyama and coworkers isolated an elastic protein from muscle fiber that they called connectin. Two years later, Kuan Wang and coworkers identified a doublet band on electrophoresis gel corresponding to a high molecular weight, elastic protein that they named titin.

In 1990, Siegfried Labeit isolated a partial cDNA clone of titin. Five years later, Labeit and Bernhard Kolmerer determined the cDNA sequence of human cardiac titin. In 2001, Labeit and colleagues determined the complete sequence of the human titin gene.

Genetics

The human gene encoding for titin is located on the long arm of chromosome 2 and contains 363 exons, which together code for 38,138 amino acid residues (4200 kDa). Within the gene are found a large number of PEVK (proline-glutamate-valine-lysine -abundant structural motifs) exons 84 to 99 nucleotides in length, which code for conserved 28- to 33-residue motifs that may represent structural units of the titin PEVK spring. The number of PEVK motifs in the titin gene appears to have increased during evolution, apparently modifying the genomic region responsible for titin's spring properties.

Isoforms

A number of titin isoforms are produced in different striated muscle tissues as a result of alternative splicing. All but one of these isoforms are in the range of ~27,000 to ~36,000 amino acid residues in length. The exception is the small cardiac novex-3 isoform, which is only 5,604 amino acid residues in length. The following table lists the known titin isoforms:

Structure

Titin is the largest known protein; its human variant consists of 34,350 amino acids, with the molecular weight of the mature "canonical" isoform of the protein being approximately 3,816,030.05 Da. Its mouse homologue is even larger, comprising 35,213 amino acids with a molecular weight of 3,906,487.6 Da. It has a theoretical isoelectric point of 6.02. The protein's empirical chemical formula is C_169,719H_270,466N_45,688O_52,238S₉₁₁. It has a theoretical instability index (II) of 42.38, classifying the protein as unstable. The protein's in vivo half-life, the time it takes for half of the amount of protein in a cell to break down after its synthesis in the cell, is predicted to be approximately 30 hours (in mammalian reticulocytes).

The Titin protein is located between the myosin thick filament and the Z disk. Titin consists primarily of a linear array of two types of modules, also referred to as protein domains (244 copies in total): type I fibronectin type III domain (132 copies) and type II immunoglobulin domain (112 copies). However, the exact number of these domains is different in different species. This linear array is further organized into two regions:

• N-terminal I-band: acts as the elastic part of the molecule and is composed mainly of type II modules. More specifically the I-band contains two regions of tandem type II immunoglobulin domains on either side of a PEVK region that is rich in proline (P), glutamate (E), valine (V) and lysine (K).
• C-terminal A-band: is thought to act as a protein-ruler and is composed of alternating type I (Fn3) and II (Ig) modules with super-repeat segments. These have been shown to align to the 43 nm axial repeats of myosin thick filaments with immunoglobulin domains correlating to myosin crowns.

The C-terminal region also contains a serine kinase domain that is primarily known for adapting the muscle to mechanical strain. It is “stretch-sensitive” and helps repair overstretching of the sarcomere. The N-terminal (the Z-disc end) contains a "Z repeat" that recognizes Actinin alpha 2.

The elasticity of the PEVK region has both entropic and enthalpic contributions and is characterized by a polymer persistence length and a stretch modulus. At low to moderate extensions PEVK elasticity can be modeled with a standard worm-like chain (WLC) model of entropic elasticity. At high extensions PEVK stretching can be modeled with a modified WLC model that incorporates enthalpic elasticity. The difference between low-and high- stretch elasticity is due to electrostatic stiffening and hydrophobic effects.

Embedded between the PEVK and Ig residues are N2A domains.

Evolution

The titin domains have evolved from a common ancestor through many gene duplication events. Domain duplication was facilitated by the fact that most domains are encoded by single exons. Other giant sarcomeric proteins made out of Fn3/Ig repeats include obscurin and myomesin. Throughout evolution, titin mechanical strength appears to decrease through the loss of disulfide bonds as the organism becomes heavier.

Titin A-band has homologs in invertebrates, such as twitchin (unc-22) and projectin, which also contain Ig and FNIII repeats and a protein kinase domain. The gene duplication events took place independently but were from the same ancestral Ig and FNIII domains. It is said that the protein titin was the first to diverge out of the family. Drosophila projectin, officially known as bent (bt), is associated with lethality by failing to escape the egg in some mutations as well as dominant changes in wing angles.

Drosophila Titin, also known as Kettin or sallimus (sls), is kinase-free. It has roles in the elasticity of both muscle and chromosomes. It is homologous to vertebrate titin I-band and contains Ig PEVK domains, the many repeats being a hot target for splicing. There also exists a titin homologue, ttn-1, in C. elegans. It has a kinase domain, some Ig/Fn3 repeats, and PEVT repeats that are similarly elastic.

Function

Titin is a large abundant protein of striated muscle. Titin's primary functions are to stabilize the thick filament, center it between the thin filaments, prevent overstretching of the sarcomere, and to recoil the sarcomere like a spring after it is stretched. An N-terminal Z-disc region and a C-terminal M-line region bind to the Z-line and M-line of the sarcomere, respectively, so that a single titin molecule spans half the length of a sarcomere. Titin also contains binding sites for muscle-associated proteins so it serves as an adhesion template for the assembly of contractile machinery in muscle cells. It has also been identified as a structural protein for chromosomes. Considerable variability exists in the I-band, the M-line and the Z-disc regions of titin. Variability in the I-band region contributes to the differences in elasticity of different titin isoforms and, therefore, to the differences in elasticity of different muscle types. Of the many titin variants identified, five are described with complete transcript information available.

Dominant mutation in TTN causes predisposition to hernias.

Titin interacts with many sarcomeric proteins including:

• Z line region: telethonin and alpha-actinin
• I band region: calpain-3 and obscurin
• M line region: myosin-binding protein C, calmodulin 1, CAPN3, and MURF1

Clinical relevance

Mutations anywhere within the unusually long sequence of this gene can cause premature stop codons or other defects. Titin mutations are associated with hereditary myopathy with early respiratory failure, early-onset myopathy with fatal cardiomyopathy, core myopathy with heart disease, centronuclear myopathy, limb-girdle muscular dystrophy type 2J, familial dilated cardiomyopathy 9, hypertrophic cardiomyopathy and tibial muscular dystrophy. Further research also suggests that no genetically linked form of any dystrophy or myopathy can be safely excluded from being caused by a mutation on the TTN gene. Truncating mutations in dilated cardiomyopathy patients are most commonly found in the A region; although truncations in the upstream I region might be expected to prevent translation of the A region entirely, alternative splicing creates some transcripts that do not encounter the premature stop codon, ameliorating its effect. mRNA splicing factors such as RBM20 and SLM2 (KHDRBS3) were shown to mediated alternative mRNA splicing of titin mRNA contributing to the development of heart failure due to cardiomyopathies.

Autoantibodies to titin are produced in patients with the autoimmune disease Myasthenia gravis.

Interactions

Titin has been shown to interact with:

• ANK1,
• ANKRD1,
• ANKRD23
• CAPN3,
• FHL2,
• OBSCN,
• TCAP, and
• TRIM63.

Linguistic significance

The name titin is derived from the Greek Titan (a giant deity, anything of great size).

As the largest known protein, titin also has the longest IUPAC name of a protein. The full chemical name of the human canonical form of titin, which starts methionyl... and ends ...isoleucine, contains 189,819 letters and is sometimes stated to be the longest word in the English language, or of any language. However, lexicographers regard generic names of chemical compounds as verbal formulae rather than English words.

See also

• PKZILLA-1 - new largest known protein with 45,212 amino acids

References

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Further reading

• Tskhovrebova L, Trinick J (September 2003). "Titin: properties and family relationships". Nature Reviews. Molecular Cell Biology. 4 (9): 679–689. doi:10.1038/nrm1198. PMID 14506471. S2CID 12293932.
• Kinbara K, Sorimachi H, Ishiura S, Suzuki K (August 1998). "Skeletal muscle-specific calpain, p49: structure and physiological function". Biochemical Pharmacology. 56 (4): 415–420. doi:10.1016/S0006-2952(98)00095-1. PMID 9763216.
• Kolmerer B, Witt CC, Freiburg A, Millevoi S, Stier G, Sorimachi H, et al. (1999). "The titin cDNA sequence and partial genomic sequences: insights into the molecular genetics, cell biology and physiology of the titin filament system". Reviews of Physiology, Biochemistry and Pharmacology. 138: 19–55. doi:10.1007/BF02346659. PMID 10396137.
• Trinick J, Tskhovrebova L (October 1999). "Titin: a molecular control freak". Trends in Cell Biology. 9 (10): 377–380. doi:10.1016/S0962-8924(99)01641-4. PMID 10481174.
• Sorimachi H, Ono Y, Suzuki K (2000). "Skeletal Muscle-Specific Calpain, p94, and Connectin/Titin: Their Physiological Functions and Relationship to Limb-Girdle Muscular Dystrophy Type 2A". Elastic Filaments of the Cell. Advances in Experimental Medicine and Biology. Vol. 481. pp. 383–95, discussion 395–7. doi:10.1007/978-1-4615-4267-4_23. ISBN 978-1-4613-6916-5. PMID 10987085.
• Tskhovrebova L, Trinick J (February 2002). "Role of titin in vertebrate striated muscle". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 357 (1418): 199–206. doi:10.1098/rstb.2001.1028. PMC 1692937. PMID 11911777.
• Sela BA (July 2002). "". Harefuah. 141 (7): 631–5, 665. PMID 12187564.
• Tskhovrebova L, Trinick J (November 2004). "Properties of titin immunoglobulin and fibronectin-3 domains". The Journal of Biological Chemistry. 279 (45): 46351–46354. doi:10.1074/jbc.R400023200. PMID 15322090.
• Wu Y, Labeit S, Lewinter MM, Granzier H (December 2002). "Titin: an endosarcomeric protein that modulates myocardial stiffness in DCM". Journal of Cardiac Failure. 8 (6 Suppl): S276–S286. doi:10.1054/jcaf.2002.129278. PMID 12555133.

External links

• GeneReviews/NIH/NCBI/UW entry on Familial Hypertrophic Cardiomyopathy Overview
• GeneReviews/NCBI/NIH/UW entry on Udd Distal Myopathy, Tibial Muscular Dystrophy, Udd Myopathy
• GeneReviews/NIH/NCBI/UW entry on Salih Myopathy or Early-Onset Myopathy with Fatal Cardiomyopathy
• InterPro domain organization of titin

• Biology

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

• Genes on human chromosome 2
• Structural proteins
• EC 2.7.11
• Muscular system
• Long words