TPM2
| TPM2 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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| Aliases | TPM2, AMCD1, DA1, DA2B, HEL-S-273, NEM4, TMSB, tropomyosin 2 (beta), tropomyosin 2, DA2B4 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | OMIM: 190990; MGI: 98810; HomoloGene: 134045; GeneCards: TPM2; OMA:TPM2 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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β-Tropomyosin, also known as tropomyosin beta chain is a protein that in humans is encoded by the TPM2 gene.[5][6] β-tropomyosin is striated muscle-specific coiled coil dimer that functions to stabilize actin filaments and regulate muscle contraction.
Structure
[edit]β-tropomyosin is roughly 32 kDa in molecular weight (284 amino acids), but multiple splice variants exist.[7][8][9][10] Tropomysin is a flexible protein homodimer or heterodimer composed of two alpha-helical chains, which adopt a bent coiled coil conformation to wrap around the seven actin molecules in a functional unit of muscle. It is polymerized end to end along the two grooves of actin filaments and provides stability to the filaments.[11] Tropomyosin dimers are composed of varying combinations of tropomyosin isoforms; human striated muscles express protein from the TPM1 (α-tropoomyosin), TPM2 (β-tropomyosin) and TPM3 (γ-tropomyosin) genes, with α-tropomyosin being the predominant isoform in striated muscle. Fast skeletal muscle and cardiac muscle contain more αα-homodimers, and slow skeletal muscle contains more ββ-homodimers.[12] In human cardiac muscle the ratio of α-tropomyosin to β-tropomyosin is roughly 5:1.[13][14] It has been shown that different combinations of tropomyosin isoforms bind troponin T with differing affinities, demonstrating that isoform combinations are used to impart a specific functional impact.[12]
Function
[edit]β-tropomyosin functions in association with α-tropomyosin and the troponin complex—composed of troponin I, troponin C and troponin T—to modulated the actin and myosin interaction. In diastole, the tropomyosin-troponin complex inhibits this interaction, and during systole the rise in intracellular calcium from sarcoplasmic reticulum binds to troponin C and induces a conformational change in the troponin-tropomyosin complex that disinhibits the actomyosin ATPase and permits contraction.[12]
Specific functional insights into the function of the β-tropomyosin isoform have come from studies employing transgenesis. A study overexpressing β-tropomyosin in adult cardiac muscle evoked a 34-fold increase in expression of β-tropomyosin, resulting in preferential formation of the αβ-tropomyosin heterodimer. Transgenic hearts showed a significant delay in relaxation time as well as a decrease in the maximum rate of left ventricular relaxation.[12] A more aggressive overexpression of β-tropomyosin (to over 75% of total tropomyosin) in the heart causes death of mice 10–14 days old, along with cardiac abnormalities, suggesting that the normal distribution of tropomyosin isoforms is critical to normal cardiac function.[15]
In a disease model of cardiac hypertrophy, β-tropomyosin was shown to be reexpressed within two days following induction of pressure overload.[16]
Studies from mice, which express 98% α-tropomyosin, have shown that α-tropomyosin can be phosphorylated at Serine-283, which is one amino acid away from the C-terminus. β-tropomyosin also has a Serine residue at position 283,[17] thus, it is likely that β-tropomyosin is also phosphorylated. Mouse transgenic studies in which the phosphorylation site in α-tropomyosin is mutated to Alanine have shown that phosphorylation may function to modulate tropomyosin polymerization, head-to-tail interactions between adjacent tropomyosin molecules, cooperativity, myosin ATPase activity, and the cardiac response to stress.[18]
Clinical significance
[edit]A decrease in β-tropomyosin in patients with heart failure was demonstrated, as failing ventricles expressed solely α-tropomyosin.[19]
Heterozygous mutations in TPM2 have been identified in patients with congenital cap myopathy, a rare disorder defined by cap-like structures in muscle fiber periphery.[20][21][22][23]
Mutations in TPM2 have also been associated with nemaline myopathy, a rare disorder characterized by muscle weakness and nemaline bodies,[24][25][26]
as well as distal arthrogryposis.[27][28]
The muscle weakness observed in these patients may be due to a change in mutated TPM2 affinity for actin or decreased calcium-induced activation of contractility.[29][30][31] Moreover, studies unveiled alterations in cross-bridge attachment and detachment rates,[32] as well as changes in ATPase rates.[30][33]
Interactions
[edit]TPM2 has been shown to interact with:
References
[edit]- ^ a b c GRCh38: Ensembl release 89: ENSG00000198467 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028464 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
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- ^ "Entrez Gene: TPM2 tropomyosin 2 (beta)".
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- ^ "Protein sequence of human TPM2 (Uniprot ID: P07951)". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB). Retrieved 1 July 2015.
- ^ "Protein sequence of human TPM2 (Uniprot ID: P07951-2)". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB). Retrieved 1 July 2015.
- ^ "Protein sequence of human TPM2 (Uniprot ID: P07951-3)". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB). Retrieved 1 July 2015.
- ^ Brown JH, Kim KH, Jun G, Greenfield NJ, Dominguez R, Volkmann N, Hitchcock-DeGregori SE, Cohen C (Jul 2001). "Deciphering the design of the tropomyosin molecule". Proceedings of the National Academy of Sciences of the United States of America. 98 (15): 8496–501. Bibcode:2001PNAS...98.8496B. doi:10.1073/pnas.131219198. PMC 37464. PMID 11438684.
- ^ a b c d Muthuchamy M, Grupp IL, Grupp G, O'Toole BA, Kier AB, Boivin GP, Neumann J, Wieczorek DF (Dec 1995). "Molecular and physiological effects of overexpressing striated muscle beta-tropomyosin in the adult murine heart". The Journal of Biological Chemistry. 270 (51): 30593–603. doi:10.1074/jbc.270.51.30593. PMID 8530495.
- ^ Dube DK, McLean MD, Dube S, Poiesz BJ (Sep 2014). "Translational control of tropomyosin expression in vertebrate hearts". Anatomical Record. 297 (9): 1585–95. doi:10.1002/ar.22978. PMID 25125172. S2CID 19982025.
- ^ Yin Z, Ren J, Guo W (Jan 2015). "Sarcomeric protein isoform transitions in cardiac muscle: a journey to heart failure". Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1852 (1): 47–52. doi:10.1016/j.bbadis.2014.11.003. PMC 4268308. PMID 25446994.
- ^ Muthuchamy M, Boivin GP, Grupp IL, Wieczorek DF (Aug 1998). "Beta-tropomyosin overexpression induces severe cardiac abnormalities". Journal of Molecular and Cellular Cardiology. 30 (8): 1545–57. doi:10.1006/jmcc.1998.0720. PMID 9737941.
- ^ Izumo S, Nadal-Ginard B, Mahdavi V (Jan 1988). "Protooncogene induction and reprogramming of cardiac gene expression produced by pressure overload". Proceedings of the National Academy of Sciences of the United States of America. 85 (2): 339–43. Bibcode:1988PNAS...85..339I. doi:10.1073/pnas.85.2.339. PMC 279543. PMID 2963328.
- ^ "Protein sequence alignment of human TPM1 and TPM2". Uniprot Knowledgebase. Retrieved 2 July 2015.
- ^ Schulz, EM; Wieczorek, DF (August 2013). "Tropomyosin de-phosphorylation in the heart: what are the consequences?". Journal of Muscle Research and Cell Motility. 34 (3–4): 239–46. doi:10.1007/s10974-013-9348-7. PMID 23793376. S2CID 15297144.
- ^ Purcell IF, Bing W, Marston SB (Sep 1999). "Functional analysis of human cardiac troponin by the in vitro motility assay: comparison of adult, foetal and failing hearts". Cardiovascular Research. 43 (4): 884–91. doi:10.1016/s0008-6363(99)00123-6. PMID 10615415.
- ^ Ohlsson M, Quijano-Roy S, Darin N, Brochier G, Lacène E, Avila-Smirnow D, Fardeau M, Oldfors A, Tajsharghi H (Dec 2008). "New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutations". Neurology. 71 (23): 1896–901. doi:10.1212/01.wnl.0000336654.44814.b8. PMID 19047562. S2CID 24356825.
- ^ Tajsharghi H, Ohlsson M, Lindberg C, Oldfors A (Sep 2007). "Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2)". Archives of Neurology. 64 (9): 1334–8. doi:10.1001/archneur.64.9.1334. PMID 17846275.
- ^ Lehtokari VL, Ceuterick-de Groote C, de Jonghe P, Marttila M, Laing NG, Pelin K, Wallgren-Pettersson C (Jun 2007). "Cap disease caused by heterozygous deletion of the beta-tropomyosin gene TPM2". Neuromuscular Disorders. 17 (6): 433–42. doi:10.1016/j.nmd.2007.02.015. PMID 17434307. S2CID 54349245.
- ^ Clarke NF, Domazetovska A, Waddell L, Kornberg A, McLean C, North KN (May 2009). "Cap disease due to mutation of the beta-tropomyosin gene (TPM2)". Neuromuscular Disorders. 19 (5): 348–51. doi:10.1016/j.nmd.2009.03.003. PMID 19345583. S2CID 38636941.
- ^ Mokbel N, Ilkovski B, Kreissl M, Memo M, Jeffries CM, Marttila M, Lehtokari VL, Lemola E, Grönholm M, Yang N, Menard D, Marcorelles P, Echaniz-Laguna A, Reimann J, Vainzof M, Monnier N, Ravenscroft G, McNamara E, Nowak KJ, Laing NG, Wallgren-Pettersson C, Trewhella J, Marston S, Ottenheijm C, North KN, Clarke NF (Feb 2013). "K7del is a common TPM2 gene mutation associated with nemaline myopathy and raised myofibre calcium sensitivity". Brain. 136 (Pt 2): 494–507. doi:10.1093/brain/aws348. PMID 23378224.
- ^ Monnier N, Lunardi J, Marty I, Mezin P, Labarre-Vila A, Dieterich K, Jouk PS (Feb 2009). "Absence of beta-tropomyosin is a new cause of Escobar syndrome associated with nemaline myopathy". Neuromuscular Disorders. 19 (2): 118–23. doi:10.1016/j.nmd.2008.11.009. PMID 19155175. S2CID 38985021.
- ^ Donner K, Ollikainen M, Ridanpää M, Christen HJ, Goebel HH, de Visser M, Pelin K, Wallgren-Pettersson C (Feb 2002). "Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy". Neuromuscular Disorders. 12 (2): 151–8. doi:10.1016/s0960-8966(01)00252-8. PMID 11738357. S2CID 54360043.
- ^ Tajsharghi H, Kimber E, Holmgren D, Tulinius M, Oldfors A (Mar 2007). "Distal arthrogryposis and muscle weakness associated with a beta-tropomyosin mutation". Neurology. 68 (10): 772–5. doi:10.1212/01.wnl.0000256339.40667.fb. PMID 17339586. S2CID 41982388.
- ^ Sung SS, Brassington AM, Grannatt K, Rutherford A, Whitby FG, Krakowiak PA, Jorde LB, Carey JC, Bamshad M (Mar 2003). "Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes". American Journal of Human Genetics. 72 (3): 681–90. doi:10.1086/368294. PMC 1180243. PMID 12592607.
- ^ Marttila M, Lehtokari VL, Marston S, Nyman TA, Barnerias C, Beggs AH, Bertini E, Ceyhan-Birsoy O, Cintas P, Gerard M, Gilbert-Dussardier B, Hogue JS, Longman C, Eymard B, Frydman M, Kang PB, Klinge L, Kolski H, Lochmüller H, Magy L, Manel V, Mayer M, Mercuri E, North KN, Peudenier-Robert S, Pihko H, Probst FJ, Reisin R, Stewart W, Taratuto AL, de Visser M, Wilichowski E, Winer J, Nowak K, Laing NG, Winder TL, Monnier N, Clarke NF, Pelin K, Grönholm M, Wallgren-Pettersson C (Jul 2014). "Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies". Human Mutation. 35 (7): 779–90. doi:10.1002/humu.22554. PMC 4200603. PMID 24692096.
- ^ a b Robinson P, Lipscomb S, Preston LC, Altin E, Watkins H, Ashley CC, Redwood CS (Mar 2007). "Mutations in fast skeletal troponin I, troponin T, and beta-tropomyosin that cause distal arthrogryposis all increase contractile function". FASEB Journal. 21 (3): 896–905. doi:10.1096/fj.06-6899com. PMID 17194691. S2CID 25491760.
- ^ Marttila M, Lemola E, Wallefeld W, Memo M, Donner K, Laing NG, Marston S, Grönholm M, Wallgren-Pettersson C (Feb 2012). "Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy". The Biochemical Journal. 442 (1): 231–9. doi:10.1042/BJ20111030. PMID 22084935.
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- ^ Zhu J, Bilan PJ, Moyers JS, Antonetti DA, Kahn CR (Jan 1996). "Rad, a novel Ras-related GTPase, interacts with skeletal muscle beta-tropomyosin". The Journal of Biological Chemistry. 271 (2): 768–73. doi:10.1074/jbc.271.2.768. PMID 8557685.
- ^ Guy PM, Kenny DA, Gill GN (Jun 1999). "The PDZ domain of the LIM protein enigma binds to beta-tropomyosin". Molecular Biology of the Cell. 10 (6): 1973–84. doi:10.1091/mbc.10.6.1973. PMC 25398. PMID 10359609.
- ^ Brown HR, Schachat FH (Apr 1985). "Renaturation of skeletal muscle tropomyosin: implications for in vivo assembly". Proceedings of the National Academy of Sciences of the United States of America. 82 (8): 2359–63. Bibcode:1985PNAS...82.2359B. doi:10.1073/pnas.82.8.2359. PMC 397557. PMID 3857586.
Further reading
[edit]- Gunning P, Weinberger R, Jeffrey P (Apr 1997). "Actin and tropomyosin isoforms in morphogenesis". Anatomy and Embryology. 195 (4): 311–5. doi:10.1007/s004290050050. PMID 9108196. S2CID 9692297.
- Holtzer ME, Kidd SG, Crimmins DL, Holtzer A (Mar 1992). "Beta beta homodimers exist in native rabbit skeletal muscle tropomyosin and increase after denaturation-renaturation". Protein Science. 1 (3): 335–41. doi:10.1002/pro.5560010305. PMC 2142203. PMID 1304342.
- Höner B, Shoeman RL, Traub P (Jul 1992). "Degradation of cytoskeletal proteins by the human immunodeficiency virus type 1 protease". Cell Biology International Reports. 16 (7): 603–12. doi:10.1016/S0309-1651(06)80002-0 (inactive 2024-03-27). PMID 1516138.
{{cite journal}}: CS1 maint: DOI inactive as of March 2024 (link) - Chevray PM, Nathans D (Jul 1992). "Protein interaction cloning in yeast: identification of mammalian proteins that react with the leucine zipper of Jun". Proceedings of the National Academy of Sciences of the United States of America. 89 (13): 5789–93. Bibcode:1992PNAS...89.5789C. doi:10.1073/pnas.89.13.5789. PMC 402103. PMID 1631061.
- Prasad GL, Meissner S, Sheer DG, Cooper HL (Jun 1991). "A cDNA encoding a muscle-type tropomyosin cloned from a human epithelial cell line: identity with human fibroblast tropomyosin TM1". Biochemical and Biophysical Research Communications. 177 (3): 1068–75. doi:10.1016/0006-291X(91)90647-P. PMID 2059197.
- Libri D, Mouly V, Lemonnier M, Fiszman MY (Feb 1990). "A nonmuscle tropomyosin is encoded by the smooth/skeletal beta-tropomyosin gene and its RNA is transcribed from an internal promoter". The Journal of Biological Chemistry. 265 (6): 3471–3. doi:10.1016/S0021-9258(19)39791-1. PMID 2303454.
- Widada JS, Ferraz C, Capony JP, Liautard JP (Apr 1988). "Complete nucleotide sequence of the adult skeletal isoform of human skeletal muscle beta-tropomyosin". Nucleic Acids Research. 16 (7): 3109. doi:10.1093/nar/16.7.3109. PMC 336462. PMID 3368322.
- MacLeod AR, Houlker C, Reinach FC, Smillie LB, Talbot K, Modi G, Walsh FS (Dec 1985). "A muscle-type tropomyosin in human fibroblasts: evidence for expression by an alternative RNA splicing mechanism". Proceedings of the National Academy of Sciences of the United States of America. 82 (23): 7835–9. Bibcode:1985PNAS...82.7835M. doi:10.1073/pnas.82.23.7835. PMC 390864. PMID 3865200.
- Gimona M, Watakabe A, Helfman DM (Oct 1995). "Specificity of dimer formation in tropomyosins: influence of alternatively spliced exons on homodimer and heterodimer assembly". Proceedings of the National Academy of Sciences of the United States of America. 92 (21): 9776–80. Bibcode:1995PNAS...92.9776G. doi:10.1073/pnas.92.21.9776. PMC 40885. PMID 7568216.
- Bamshad M, Watkins WS, Zenger RK, Bohnsack JF, Carey JC, Otterud B, Krakowiak PA, Robertson M, Jorde LB (Dec 1994). "A gene for distal arthrogryposis type I maps to the pericentromeric region of chromosome 9". American Journal of Human Genetics. 55 (6): 1153–8. PMC 1918435. PMID 7977374.
- Takenaga K, Nakamura Y, Sakiyama S, Hasegawa Y, Sato K, Endo H (Mar 1994). "Binding of pEL98 protein, an S100-related calcium-binding protein, to nonmuscle tropomyosin". The Journal of Cell Biology. 124 (5): 757–68. doi:10.1083/jcb.124.5.757. PMC 2119958. PMID 8120097.
- Maruyama K, Sugano S (Jan 1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
- Shoeman RL, Sachse C, Höner B, Mothes E, Kaufmann M, Traub P (Jan 1993). "Cleavage of human and mouse cytoskeletal and sarcomeric proteins by human immunodeficiency virus type 1 protease. Actin, desmin, myosin, and tropomyosin". The American Journal of Pathology. 142 (1): 221–30. PMC 1886840. PMID 8424456.
- Tiso N, Rampoldi L, Pallavicini A, Zimbello R, Pandolfo D, Valle G, Lanfranchi G, Danieli GA (Jan 1997). "Fine mapping of five human skeletal muscle genes: alpha-tropomyosin, beta-tropomyosin, troponin-I slow-twitch, troponin-I fast-twitch, and troponin-C fast". Biochemical and Biophysical Research Communications. 230 (2): 347–50. doi:10.1006/bbrc.1996.5958. PMID 9016781.
- Gimona M, Lando Z, Dolginov Y, Vandekerckhove J, Kobayashi R, Sobieszek A, Helfman DM (Mar 1997). "Ca2+-dependent interaction of S100A2 with muscle and nonmuscle tropomyosins". Journal of Cell Science. 110 (5): 611–21. doi:10.1242/jcs.110.5.611. PMID 9092943.
- Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (Oct 1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.