Abstract
The myosin superfamily of molecular motors plays essential roles in a wide variety of cellular processes by virtue of their ability to generate force and motion through an ATP-driven cyclic interaction with actin filaments. We provide an overview of the structure, function, and biophysical properties that are common to most characterized myosins and also include examples of how myosins are adapted to perform specific cellular functions. Since many myosins are implicated in disease conditions, a complete understanding of their cellular roles and biophysical properties is critical for developing treatments for these diseases.
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References
Berg JS, Powell BC, Cheney RE (2001) A millennial myosin census. Mol Biol Cell 12:780–794
Richards TA, Cavalier-Smith T (2005) Myosin domain evolution and the primary divergence of eukaryotes. Nature 436:1113–1118
Foth BJ, Goedecke MC, Soldati D (2006) New insights into myosin evolution and classification. Proc Natl Acad Sci U S A 103:3681–3686
Odronitz F, Kollmar M (2007) Drawing the tree of eukaryotic life based on the analysis of 2,269 manually annotated myosins from 328 species. Genome Biol 8:R196
Boger ET, Sellers JR, Friedman TB (2001) Human myosin XVBP is a transcribed pseudogene. J Muscle Res Cell Motil 22:477–483
Desjardins PR, Burkman JM, Shrager JB, Allmond LA, Stedman HH (2002) Evolutionary implications of three novel members of the human sarcomeric myosin heavy chain gene family. Mol Biol Evol 19:375–393
Collucio LM (ed) (2008) Myosins: a superfamily of molecular motors. Springer, Dordrecht
Gillespie PG, Albanesi JP, Bahler M, Bement WM, Berg JS, Burgess DR, Burnside B, Cheney RE, Corey DP, Coudrier E et al (2001) Myosin-I nomenclature. J Cell Biol 155:703–704
Montell C, Rubin GM (1988) The Drosophila ninaC locus encodes two photoreceptor cell specific proteins with domains homologous to protein kinases and the myosin heavy chain head. Cell 52:757–772
Kalhammer G, Bahler M, Schmitz F, Jockel J, Block C (1997) Ras-binding domains: predicting function versus folding. FEBS Lett 414:599–602
Patel KG, Liu C, Cameron PL, Cameron RS (2001) Myr 8, a novel unconventional myosin expressed during brain development associates with the protein phosphatase catalytic subunits 1 alpha and 1 gamma 1. J Neurosci 21:7954–7968
Rayment I, Holden HM, Whittaker M, Yohn CB, Lorenz M, Holmes KC, Milligan RA (1993) Structure of the actin-myosin complex and its implications for muscle contraction. Science 261:58–65
Uyeda TQ, Abramson PD, Spudich JA (1996) The neck region of the myosin motor domain acts as a lever arm to generate movement. Proc Natl Acad Sci U S A 93:4459–4464
Spudich JA (1994) How molecular motors work. Nature 372:515–518
Cheney RE, Mooseker MS (1992) Unconventional myosins. Curr Opin Cell Biol 4:27–35
Houdusse A, Cohen C (1995) Target sequence recognition by the calmodulin superfamily: implications from light chain binding to the regulatory domain of scallop myosin. Proc Natl Acad Sci U S A 92:10644–10647
Espreafico EM, Cheney RE, Matteoli M, Nascimento AA, De Camilli PV, Larson RE, Mooseker MS (1992) Primary structure and cellular localization of chicken brain myosin-V (p190), an unconventional myosin with calmodulin light chains. J Cell Biol 119:1541–1557
Rogers MS, Strehler EE (2001) The tumor-sensitive calmodulin-like protein is a specific light chain of human unconventional myosin X. J Biol Chem 276:12182–12189
Collins JH (1991) Myosin light chains and troponin C: structural and evolutionary relationships revealed by amino acid sequence comparisons. J Muscle Res Cell Motil 12:3–25
Timson DJ (2003) Fine tuning the myosin motor: the role of the essential light chain in striated muscle myosin. Biochimie 85:639–645
Tyska MJ, Mooseker MS (2002) MYO1A (brush border myosin I) dynamics in the brush border of LLC-PK1-CL4 cells. Biophys J 82:1869–1883
Mashanov GI, Tacon D, Peckham M, Molloy JE (2004) The spatial and temporal dynamics of pleckstrin homology domain binding at the plasma membrane measured by imaging single molecules in live mouse myoblasts. J Biol Chem 279:15274–15280
Hokanson DE, Ostap EM (2006) Myo1c binds tightly and specifically to phosphatidylinositol 4,5-bisphosphate and inositol 1,4,5-trisphosphate. Proc Natl Acad Sci U S A 103:3118–3123
Patino-Lopez G, Aravind L, Dong X, Kruhlak MJ, Ostap EM, Shaw S (2010) Myosin 1G is an abundant class I myosin in lymphocytes whose localization at the plasma membrane depends on its ancient divergent pleckstrin homology (PH) domain (Myo1PH). J Biol Chem 285:8675–8686
Tang N, Lin T, Ostap EM (2002) Dynamics of myo1c (myosin-ibeta) lipid binding and dissociation. J Biol Chem 277:42763–42768
Doberstein SK, Pollard TD (1992) Localization and specificity of the phospholipid and actin binding sites on the tail of Acanthamoeba myosin IC. J Cell Biol 117:1241–1249
Weber KL, Sokac AM, Berg JS, Cheney RE, Bement WM (2004) A microtubule-binding myosin required for nuclear anchoring and spindle assembly. Nature 431:325–329
Cao TT, Chang W, Masters SE, Mooseker MS (2004) Myosin-Va binds to and mechanochemically couples microtubules to actin filaments. Mol Biol Cell 15:151–161
Les Erickson F, Corsa AC, Dose AC, Burnside B (2003) Localization of a class III myosin to filopodia tips in transfected HeLa cells requires an actin-binding site in its tail domain. Mol Biol Cell 14:4173–4180
Zhang H, Berg JS, Li Z, Wang Y, Lang P, Sousa AD, Bhaskar A, Cheney RE, Stromblad S (2004) Myosin-X provides a motor-based link between integrins and the cytoskeleton. Nat Cell Biol 6:523–531
Roland JT, Kenworthy AK, Peranen J, Caplan S, Goldenring JR (2007) Myosin Vb interacts with Rab8a on a tubular network containing EHD1 and EHD3. Mol Biol Cell 18:2828–2837
Lapierre LA, Kumar R, Hales CM, Navarre J, Bhartur SG, Burnette JO, Provance DW Jr, Mercer JA, Bahler M, Goldenring JR (2001) Myosin Vb is associated with plasma membrane recycling systems. Mol Biol Cell 12:1843–1857
Huxley HE (1953) Electron microscope studies of the organization of the filaments in striated muscle. Biochim Biophys Acta 12:387–394
Hanson J, Huxley HE (1953) Structural basis of the cross-striations in muscle. Nature 172:530–532
Huxley AF, Niedergerke R (1954a) Structural changes in muscle during contraction; interference microscopy of living muscle fibers. Nature 173:971–973
Huxley AF, Niedergerke R (1954b) Measurement of muscle striations in stretch and contraction. J Physiol 124:46–47P
Huxley AF (1957) Muscle structure and theories of contraction. Prog Biophys Biophys Chem 7:255–318
Huxley AF, Simmons RM (1971) Proposed mechanism of force generation in striated muscle. Nature 233:533–538
Lymn RW, Taylor EW (1971) Mechanism of adenosine triphosphate hydrolysis by actomyosin. Biochemistry 10:4617–4624
Holmes KC, Geeves MA (2000) The structural basis of muscle contraction. Philos Trans R Soc Lond B Biol Sci 355:419–431
Sweeney HL, Houdusse A (2010) Structural and functional insights into the Myosin motor mechanism. Annu Rev Biophys 39:539–557
Volkmann N, Liu H, Hazelwood L, Krementsova EB, Lowey S, Trybus KM, Hanein D (2005) The structural basis of myosin V processive movement as revealed by electron cryomicroscopy. Mol Cell 19:595–605
Volkmann N, Hanein D, Ouyang G, Trybus KM, DeRosier DJ, Lowey S (2000) Evidence for cleft closure in actomyosin upon ADP release. Nat Struct Biol 7:1147–1155
Dominguez R, Freyzon Y, Trybus KM, Cohen C (1998) Crystal structure of a vertebrate smooth muscle myosin motor domain and its complex with the essential light chain: visualization of the pre-power stroke state. Cell 94:559–571
Menetrey J, Llinas P, Mukherjea M, Sweeney HL, Houdusse A (2007) The structural basis for the large powerstroke of myosin VI. Cell 131:300–308
Menetrey J, Bahloul A, Wells AL, Yengo CM, Morris CA, Sweeney HL, Houdusse A (2005) The structure of the myosin VI motor reveals the mechanism of directionality reversal. Nature 435:779–785
Sweeney HL, Houdusse A (2004) The motor mechanism of myosin V: insights for muscle contraction. Philos Trans R Soc Lond B Biol Sci 359:1829–1841
Holmes KC, Schroder RR, Sweeney HL, Houdusse A (2004) The structure of the rigor complex and its implications for the power stroke. Philos Trans R Soc Lond B Biol Sci 359:1819–1828
Coureux PD, Sweeney HL, Houdusse A (2004) Three myosin V structures delineate essential features of chemo-mechanical transduction. EMBO J 23:4527–4537
Coureux PD, Wells AL, Menetrey J, Yengo CM, Morris CA, Sweeney HL, Houdusse A (2003) A structural state of the myosin V motor without bound nucleotide. Nature 425:419–423
Houdusse A, Szent-Gyorgyi AG, Cohen C (2000) Three conformational states of scallop myosin S1. Proc Natl Acad Sci U S A 97:11238–11243
Houdusse A, Kalabokis VN, Himmel D, Szent-Gyorgyi AG, Cohen C (1999) Atomic structure of scallop myosin subfragment S1 complexed with MgADP: a novel conformation of the myosin head. Cell 97:459–470
Bauer CB, Holden HM, Thoden JB, Smith R, Rayment I (2000) X-ray structures of the apo and MgATP-bound states of Dictyostelium discoideum myosin motor domain. J Biol Chem 275:38494–38499
Gulick AM, Bauer CB, Thoden JB, Pate E, Yount RG, Rayment I (2000) X-ray structures of the Dictyostelium discoideum myosin motor domain with six non-nucleotide analogs. J Biol Chem 275:398–408
Gulick AM, Bauer CB, Thoden JB, Rayment I (1997) X-ray structures of the MgADP, MgATPgammaS, and MgAMPPNP complexes of the Dictyostelium discoideum myosin motor domain. Biochemistry 36:11619–11628
Rayment I (1996) The structural basis of the myosin ATPase activity. J Biol Chem 271:15850–15853
Smith CA, Rayment I (1995) X-ray structure of the magnesium(II)-pyrophosphate complex of the truncated head of Dictyostelium discoideum myosin to 2.7 A resolution. Biochemistry 34:8973–8981
Rayment I, Smith C, Yount RG (1996) The active site of myosin. Annu Rev Physiol 58:671–702
Smith CA, Rayment I (1996) X-ray structure of the magnesium (II).ADP.vanadate complex of the Dictyostelium discoideum myosin motor domain to 1.9 A resolution. Biochemistry 35:5404–5417
Fisher AJ, Smith CA, Thoden JB, Smith R, Sutoh K, Holden HM, Rayment I (1995) X-ray structures of the myosin motor domain of Dictyostelium discoideum complexed with MgADP.BeFx and MgADP.AlF4. Biochemistry 34:8960–8972
Rayment I, Rypniewski WR, Schmidt-Base K, Smith R, Tomchick DR, Benning MM, Winkelmann DA, Wesenberg G, Holden HM (1993) Three-dimensional structure of myosin subfragment-1: a molecular motor. Science 261:50–58
Whittaker M, Wilson-Kubalek EM, Smith JE, Faust L, Milligan RA, Sweeney HL (1995) A 35-A movement of smooth muscle myosin on ADP release. Nature 378:748–751
Milligan RA (1996) Protein-protein interactions in the rigor actomyosin complex. Proc Natl Acad Sci U S A 93:21–26
Vale RD, Milligan RA (2000) The way things move: looking under the hood of molecular motor proteins. Science 288:88–95
Kohler D, Ruff C, Meyhofer E, Bahler M (2003) Different degrees of lever arm rotation control myosin step size. J Cell Biol 161:237–241
Kinoshita K, Sadanami K, Kidera A, Go N (1999) Structural motif of phosphate-binding site common to various protein superfamilies: all-against-all structural comparison of protein-mononucleotide complexes. Protein Eng 12:11–14
Root D (2002) The dance of actin and myosin. Cell Biochemistry and Biophysics 37:111–139
Kull FJ, Vale RD, Fletterick RJ (1998) The case for a common ancestor: kinesin and myosin motor proteins and G proteins. J Muscle Res Cell Motil 19:877–886
Kintses B, Gyimesi M, Pearson DS, Geeves MA, Zeng W, Bagshaw CR, Malnasi-Csizmadia A (2007) Reversible movement of switch 1 loop of myosin determines actin interaction. EMBO J 26:265–274
Fischer S, Windshugel B, Horak D, Holmes KC, Smith JC (2005) Structural mechanism of the recovery stroke in the myosin molecular motor. Proc Natl Acad Sci U S A 102:6873–6878
Sun M, Rose MB, Ananthanarayanan SK, Jacobs DJ, Yengo CM (2008) Characterization of the pre-force-generation state in the actomyosin cross-bridge cycle. Proc Natl Acad Sci U S A 105:8631–8636
Sun M, Oakes JL, Ananthanarayanan SK, Hawley KH, Tsien RY, Adams SR, Yengo CM (2006) Dynamics of the upper 50-kDa domain of myosin V examined with fluorescence resonance energy transfer. J Biol Chem 281:5711–5717
Kelley CA, Takahashi M, Yu JH, Adelstein RS (1993) An insert of seven amino acids confers functional differences between smooth muscle myosins from the intestines and vasculature. J Biol Chem 268:12848–12854
Rovner AS, Freyzon Y, Trybus KM (1997) An insert in the motor domain determines the functional properties of expressed smooth muscle myosin isoforms. J Muscle Res Cell Motil 18:103–110
Lauzon AM, Tyska MJ, Rovner AS, Freyzon Y, Warshaw DM, Trybus KM (1998) A 7-amino-acid insert in the heavy chain nucleotide binding loop alters the kinetics of smooth muscle myosin in the laser trap. J Muscle Res Cell Motil 19:825–837
Baker JE, Brosseau C, Fagnant P, Warshaw DM (2003) The unique properties of tonic smooth muscle emerge from intrinsic as well as intermolecular behaviors of myosin molecules. J Biol Chem 278:28533–28539
Joel PB, Sweeney HL, Trybus KM (2003) Addition of lysines to the 50/20 kDa junction of myosin strengthens weak binding to actin without affecting the maximum ATPase activity. Biochemistry 42:9160–9166
Onishi H, Mikhailenko SV, Morales MF (2006) Toward understanding actin activation of myosin ATPase: the role of myosin surface loops. Proc Natl Acad Sci U S A 103:6136–6141
Yengo CM, Sweeney HL (2004) Functional role of loop 2 in myosin V. Biochemistry 43:2605–2612
Cecchini M, Houdusse A, Karplus M (2008) Allosteric communication in myosin V: from small conformational changes to large directed movements. PLoS Comput Biol 4:e1000129
Finer JT, Simmons RM, Spudich JA (1994) Single myosin molecule mechanics: piconewton forces and nanometer steps. Nature 368:113–119
Tyska MJ, Dupuis DE, Guilford WH, Patlak JB, Waller GS, Trybus KM, Warshaw DM, Lowey S (1999) Two heads of myosin are better than one for generating force and motion. Proc Natl Acad Sci U S A 96:4402–4407
Howard J (2001) Mechanics of motor proteins and the cytoskeleton. Sinauer Associates Inc, Sunderland
Toyoshima YY, Kron SJ, McNally EM, Niebling KR, Toyoshima C, Spudich JA (1987) Myosin subfragment-1 is sufficient to move actin filaments in vitro. Nature 328:536–539
Cooke R, Franks K, Luciani GB, Pate E (1988) The inhibition of rabbit skeletal muscle contraction by hydrogen ions and phosphate. J Physiol 395:77–97
Pate E, Wilson GJ, Bhimani M, Cooke R (1994) Temperature dependence of the inhibitory effects of orthovanadate on shortening velocity in fast skeletal muscle. Biophys J 66:1554–1562
Barany M (1967) ATPase activity of myosin correlated with speed of muscle shortening. J Gen Physiol 50(Suppl):197–218
Spink BJ, Sivaramakrishnan S, Lipfert J, Doniach S, Spudich JA (2008) Long single alpha-helical tail domains bridge the gap between structure and function of myosin VI. Nat Struct Mol Biol 15:591–597
Pauling L, Corey RB (1953) Compound helical configurations of polypeptide chains: structure of proteins of the alpha-keratin type. Nature 171:59–61
Ikebe M, Komatsu S, Woodhead JL, Mabuchi K, Ikebe R, Saito J, Craig R, Higashihara M (2001) The tip of the coiled-coil rod determines the filament formation of smooth muscle and nonmuscle myosin. J Biol Chem 276:30293–30300
Hostetter D, Rice S, Dean S, Altman D, McMahon PM, Sutton S, Tripathy A, Spudich JA (2004) Dictyostelium myosin bipolar thick filament formation: importance of charge and specific domains of the myosin rod. PLoS Biol 2:e356
Forkey JN, Quinlan ME, Shaw MA, Corrie JE, Goldman YE (2003) Three-dimensional structural dynamics of myosin V by single-molecule fluorescence polarization. Nature 422:399–404
Sun Y, Sato O, Ruhnow F, Arsenault ME, Ikebe M, Goldman YE (2010) Single-molecule stepping and structural dynamics of myosin X. Nat Struct Mol Biol 17:485–491
Yang Y, Kovacs M, Sakamoto T, Zhang F, Kiehart DP, Sellers JR (2006) Dimerized Drosophila myosin VIIa: a processive motor. Proc Natl Acad Sci U S A 103:5746–5751
Yildiz A, Forkey JN, McKinney SA, Ha T, Goldman YE, Selvin PR (2003) Myosin V walks hand-over-hand: single fluorophore imaging with 1.5-nm localization. Science 300:2061–2065
Laakso JM, Lewis JH, Shuman H, Ostap EM (2008) Myosin I can act as a molecular force sensor. Science 321:133–136
Nyitrai M, Geeves MA (2004) Adenosine diphosphate and strain sensitivity in myosin motors. Philos Trans R Soc Lond B Biol Sci 359:1867–1877
Oguchi Y, Mikhailenko SV, Ohki T, Olivares AO, De La Cruz EM, Ishiwata S (2008) Load-dependent ADP binding to myosins V and VI: implications for subunit coordination and function. Proc Natl Acad Sci U S A 105:7714–7719
Purcell TJ, Sweeney HL, Spudich JA (2005) A force-dependent state controls the coordination of processive myosin V. Proc Natl Acad Sci U S A 102:13873–13878
Veigel C, Schmitz S, Wang F, Sellers JR (2005) Load-dependent kinetics of myosin-V can explain its high processivity. Nat Cell Biol 7:861–869
De La Cruz EM, Olivares AO (2009) Watching the walk: observing chemo-mechanical coupling in a processive myosin motor. HFSP J 3:67–70
Dunn AR, Chuan P, Bryant Z, Spudich JA (2010) Contribution of the myosin VI tail domain to processive stepping and intramolecular tension sensing. Proc Natl Acad Sci U S A 107:7746–7750
Brunello E, Reconditi M, Elangovan R, Linari M, Sun YB, Narayanan T, Panine P, Piazzesi G, Irving M, Lombardi, V. (2007) Skeletal muscle resists stretch by rapid binding of the second motor domain of myosin to actin. Proc Natl Acad Sci U S A 104:20114–20119
Hokanson DE, Laakso JM, Lin T, Sept D, Ostap EM (2006) Myo1c binds phosphoinositides through a putative pleckstrin homology domain. Mol Biol Cell 17:4856–4865
Barylko B, Binns DD, Albanesi JP (2000) Regulation of the enzymatic and motor activities of myosin I. Biochim Biophys Acta 1496:23–35
Yonezawa S, Yoshizaki N, Sano M, Hanai A, Masaki S, Takizawa T, Kageyama T, Moriyama A (2003) Possible involvement of myosin-X in intercellular adhesion: importance of serial pleckstrin homology regions for intracellular localization. Dev Growth Differ 45:175–185
Berg JS, Derfler BH, Pennisi CM, Corey DP, Cheney RE (2000) Myosin-X, a novel myosin with pleckstrin homology domains, associates with regions of dynamic actin. J Cell Sci 113(19):3439–3451
Sousa AD, Cheney RE (2005) Myosin-X: a molecular motor at the cell’s fingertips. Trends Cell Biol 15:533–539
Wang F, Thirumurugan K, Stafford WF, Hammer JA, 3rd, Knight PJ, Sellers JR (2004) Regulated conformation of myosin V. J Biol Chem 279:2333–2336
Anderson DW, Probst FJ, Belyantseva IA, Fridell RA, Beyer L, Martin DM, Wu D, Kachar B, Friedman TB, Raphael Y et al (2000) The motor and tail regions of myosin XV are critical for normal structure and function of auditory and vestibular hair cells. Hum Mol Genet 9:1729–1738
Liang Y, Wang A, Belyantseva IA, Anderson DW, Probst FJ, Barber TD, Miller W, Touchman JW, Jin L, Sullivan SL et al (1999) Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2. Genomics 61:243–258
Pashkova N, Jin Y, Ramaswamy S, Weisman LS (2006) Structural basis for myosin V discrimination between distinct cargoes. EMBO J 25:693–700
Mukherjea M, Llinas P, Kim H, Travaglia M, Safer D, Menetrey J, Franzini-Armstrong C, Selvin PR, Houdusse A, Sweeney HL (2009) Myosin VI dimerization triggers an unfolding of a three-helix bundle in order to extend its reach. Mol Cell 35:305–315
Salles FT, Merritt RC Jr, Manor U, Dougherty GW, Sousa AD, Moore JE, Yengo CM, Dose AC, Kachar B (2009) Myosin IIIa boosts elongation of stereocilia by transporting espin 1 to the plus ends of actin filaments. Nat Cell Biol 11:443–450.
Dose AC, Ananthanarayanan S, Moore JE, Burnside B, Yengo CM (2007) Kinetic mechanism of human myosin IIIA. J Biol Chem 282:216–231
Huxley HE (1971) Structural changes during muscle contraction. Biochem J 125:85P
Vibert P, Craig R, Lehman W (1997) Steric-model for activation of muscle thin filaments. J Mol Biol 266:8–14
Trybus KM, Waller GS, Chatman TA (1994) Coupling of ATPase activity and motility in smooth muscle myosin is mediated by the regulatory light chain. J Cell Biol 124:963–969
Lu H, Krementsova EB, Trybus KM (2006) Regulation of myosin V processivity by calcium at the single molecule level. J Biol Chem 281:31987–31994
Olivares AO, Chang W, Mooseker MS, Hackney DD, De La Cruz EM (2006) The tail domain of myosin Va modulates actin binding to one head. J Biol Chem 281:31326–31336
Krementsov DN, Krementsova EB, Trybus KM (2004) Myosin V: regulation by calcium, calmodulin, and the tail domain. J Cell Biol 164:877–886
Li JF, Nebenfuhr A (2008) The tail that wags the dog: the globular tail domain defines the function of myosin V/XI. Traffic 9:290–298
Umeki N, Jung HS, Watanabe S, Sakai T, Li XD, Ikebe R, Craig R, Ikebe M (2009) The tail binds to the head-neck domain, inhibiting ATPase activity of myosin VIIA. Proc Natl Acad Sci U S A 106:8483–8488
Yu C, Feng W, Wei Z, Miyanoiri Y, Wen W, Zhao Y, Zhang M (2009) Myosin VI undergoes cargo-mediated dimerization. Cell 138:537–548
Bement WM, Mooseker MS (1995) TEDS rule: a molecular rationale for differential regulation of myosins by phosphorylation of the heavy chain head. Cell Motil Cytoskeleton 31:87–92
Brzeska H, Korn ED (1996) Regulation of class I and class II myosins by heavy chain phosphorylation. J Biol Chem 271:16983–16986
Redowicz MJ (2001) Regulation of nonmuscle myosins by heavy chain phosphorylation. J Muscle Res Cell Motil 22:163–173
De La Cruz EM, Ostap EM, Sweeney HL (2001) Kinetic mechanism and regulation of myosin VI. J Biol Chem 276:32373–32381
Morris CA, Wells AL, Yang Z, Chen LQ, Baldacchino CV, Sweeney HL (2003) Calcium functionally uncouples the heads of myosin VI. J Biol Chem 278:23324–23330
Buss F, Kendrick-Jones J (2008) How are the cellular functions of myosin VI regulated within the cell? Biochem Biophys Res Commun 369:165–175
Quintero OA, Moore JE, Unrath WC, Manor U, Salles FT, Grati M, Kachar B, Yengo CM (2010) Intermolecular autophosphorylation regulates myosin IIIA activity and localization in parallel actin bundles. J Biol Chem 285:35770–35782
Komaba S, Inoue A, Maruta S, Hosoya H, Ikebe M (2003) Determination of human myosin III as a motor protein having a protein kinase activity. J Biol Chem 278:21352–21360
Altman D, Sweeney HL, Spudich JA (2004) The mechanism of myosin VI translocation and its load-induced anchoring. Cell 116:737–749
Park H, Ramamurthy B, Travaglia M, Safer D, Chen LQ, Franzini-Armstrong C, Selvin PR, Sweeney HL (2006) Full-length myosin VI dimerizes and moves processively along actin filaments upon monomer clustering. Mol Cell 21:331–336
Buss F, Spudich G, Kendrick-Jones J (2004) Myosin VI: cellular functions and motor properties. Annu Rev Cell Dev Biol 20:649–676
Knight PJ, Thirumurugan K, Xu Y, Wang F, Kalverda AP, Stafford WF 3rd, Sellers JR, Peckham M (2005) The predicted coiled-coil domain of myosin 10 forms a novel elongated domain that lengthens the head. J Biol Chem 280:34702–34708
Nagy S, Ricca BL, Norstrom MF, Courson DS, Brawley CM, Smithback PA, Rock RS (2008) A myosin motor that selects bundled actin for motility. Proc Natl Acad Sci U S A 105:9616–9620
Trybus KM, Freyzon Y, Faust LZ, Sweeney HL (1997) Spare the rod, spoil the regulation: necessity for a myosin rod. Proc Natl Acad Sci U S A 94:48–52
Periasamy M, Strehler EE, Garfinkel LI, Gubits RM, Ruiz-Opazo N, Nadal-Ginard B (1984) Fast skeletal muscle myosin light chains 1 and 3 are produced from a single gene by a combined process of differential RNA transcription and splicing. J Biol Chem 259:13595–13604
Schiaffino S, Reggiani C (1996) Molecular diversity of myofibrillar proteins: gene regulation and functional significance. Physiol Rev 76:371–423
Reggiani C, Bottinelli R, Stienen GJ (2000) Sarcomeric myosin isoforms: fine tuning of a molecular motor. News Physiol Sci 15:26–33
Rossi AC, Mammucari C, Argentini C, Reggiani C, Schiaffino S (2010) Two novel/ancient myosins in mammalian skeletal muscles: MYH14/7b and MYH15 are expressed in extraocular muscles and muscle spindles. J Physiol 588:353–364
Winters LM, Briggs MM, Schachat F (1998) The human extraocular muscle myosin heavy chain gene (MYH13) maps to the cluster of fast and developmental myosin genes on chromosome 17. Genomics 54:188–189
Stephenson GM (2001) Hybrid skeletal muscle fibers: a rare or common phenomenon? Clin Exp Pharmacol Physiol 28:692–702
Oukhai K, Maricic N, Schneider M, Harzer W, Tausche E (2010) Developmental myosin heavy chain mRNA in masseter after orthognathic surgery: a preliminary study. J Craniomaxillofac Surg 39:401–406
Reggiani C, Bottinelli R (2008) Myosin II: Sarcomeric myosins, the motors or contraction in cardiac and skeletal muscles. In: Coluccio LM (ed) Myosins: a superfamily of molecular motors. Springer: Dordrecht, pp 125–169
Miyata S, Minobe W, Bristow MR, Leinwand LA (2000) Myosin heavy chain isoform expression in the failing and nonfailing human heart. Circ Res 86:386–390
Nakao K, Minobe W, Roden R, Bristow MR, Leinwand LA (1997) Myosin heavy chain gene expression in human heart failure. J Clin Invest 100:2362–2370
Geisterfer-Lowrance AA, Kass S, Tanigawa G, Vosberg HP, McKenna W, Seidman CE, Seidman JG (1990) A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation. Cell 62:999–1006
Hamada Y, Yanagisawa M, Katsuragawa Y, Coleman JR, Nagata S, Matsuda G, Masaki T (1990) Distinct vascular and intestinal smooth muscle myosin heavy chain mRNAs are encoded by a single-copy gene in the chicken. Biochem Biophys Res Commun 170:53–58
White S, Martin AF, Periasamy M (1993) Identification of a novel smooth muscle myosin heavy chain cDNA: isoform diversity in the S1 head region. Am J Physiol 264:C1252–1258
Rovner AS, Thompson MM, Murphy RA (1986) Two different heavy chains are found in smooth muscle myosin. Am J Physiol 250:C861–870
Eddinger TJ, Murphy RA (1988) Two smooth muscle myosin heavy chains differ in their light meromyosin fragment. Biochemistry 27:3807–3811
Nagai R, Kuro-o M, Babij P, Periasamy M (1989) Identification of two types of smooth muscle myosin heavy chain isoforms by cDNA cloning and immunoblot analysis. J Biol Chem 264:9734–9737
Cavaille F, Janmot C, Ropert S, d’Albis A (1986) Isoforms of myosin and actin in human, monkey and rat myometrium. Comparison of pregnant and non-pregnant uterus proteins. Eur J Biochem 160:507–513
Totsukawa G, Wu Y, Sasaki Y, Hartshorne DJ, Yamakita Y, Yamashiro S, Matsumura F (2004) Distinct roles of MLCK and ROCK in the regulation of membrane protrusions and focal adhesion dynamics during cell migration of fibroblasts. J Cell Biol 164:427–439
Gupton SL, Waterman-Storer CM (2006) Spatiotemporal feedback between actomyosin and focal-adhesion systems optimizes rapid cell migration. Cell 125:1361–1374
Brahmbhatt AA, Klemke RL (2003) ERK and RhoA differentially regulate pseudopodia growth and retraction during chemotaxis. J Biol Chem 278:13016–13025
Fishkind DJ, Wang YL (1993) Orientation and three-dimensional organization of actin filaments in dividing cultured cells. J Cell Biol 123:837–848
Pollard TD (2010) Mechanics of cytokinesis in eukaryotes. Curr Opin Cell Biol 22:50–56
Fujiwara K, Pollard TD (1976) Fluorescent antibody localization of myosin in the cytoplasm, cleavage furrow, and mitotic spindle of human cells. J Cell Biol 71:848–875
Shewan AM, Maddugoda M, Kraemer A, Stehbens SJ, Verma S, Kovacs EM, Yap AS (2005) Myosin 2 is a key Rho kinase target necessary for the local concentration of E-cadherin at cell-cell contacts. Mol Biol Cell 16:4531–4542
Ivanov AI, Hunt D, Utech M, Nusrat A, Parkos CA (2005) Differential roles for actin polymerization and a myosin II motor in assembly of the epithelial apical junctional complex. Mol Biol Cell 16:2636–2650
Miyake Y, Inoue N, Nishimura K, Kinoshita N, Hosoya H, Yonemura, S (2006) Actomyosin tension is required for correct recruitment of adherens junction components and zonula occludens formation. Exp Cell Res 312:1637–1650
Betapudi V, Licate LS, Egelhoff TT (2006) Distinct roles of nonmuscle myosin II isoforms in the regulation of MDA-MB-231 breast cancer cell spreading and migration. Cancer Res 66:4725–4733
Lo CM, Buxton DB, Chua GC, Dembo M, Adelstein RS, Wang YL (2004) Nonmuscle myosin IIb is involved in the guidance of fibroblast migration. Mol Biol Cell 15:982–989
Engler AJ, Sen S, Sweeney HL, Discher DE (2006) Matrix elasticity directs stem cell lineage specification. Cell 126:677–689
Forscher P, Smith SJ (1988) Actions of cytochalasins on the organization of actin filaments and microtubules in a neuronal growth cone. J Cell Biol 107:1505–1516
Medeiros NA, Burnette DT, Forscher P (2006) Myosin II functions in actin-bundle turnover in neuronal growth cones. Nat Cell Biol 8:215–226
Diefenbach TJ, Latham VM, Yimlamai D, Liu CA, Herman IM, Jay DG (2002) Myosin 1c and myosin IIB serve opposing roles in lamellipodial dynamics of the neuronal growth cone. J Cell Biol 158:1207–1217
Belyantseva IA, Boger ET, Friedman TB (2003) Myosin XVa localizes to the tips of inner ear sensory cell stereocilia and is essential for staircase formation of the hair bundle. Proc Natl Acad Sci U S A 100:13958–13963
Belyantseva IA, Boger ET, Naz S, Frolenkov GI, Sellers JR, Ahmed ZM, Griffith AJ, Friedman TB (2005) Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia. Nat Cell Biol 7:148–156
Self T, Mahony M, Fleming J, Walsh J, Brown SD, Steel KP (1998) Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells. Development 125:557–566
Self T, Sobe T, Copeland NG, Jenkins NA, Avraham KB, Steel KP (1999) Role of myosin VI in the differentiation of cochlear hair cells. Dev Biol 214:331–341
Kerber ML, Jacobs DT, Campagnola L, Dunn BD, Yin T, Sousa AD, Quintero OA, Cheney RE (2009) A novel form of motility in filopodia revealed by imaging myosin-X at the single-molecule level. Curr Biol 19:967–973
Berg JS, Cheney RE (2002) Myosin-X is an unconventional myosin that undergoes intrafilopodial motility. Nat Cell Biol 4:246–250
Quintero OA, Svitkina TM, Chaga OY, Bhaskar A, Borisy GG, Cheney RE (2003) Dynamics of myosin-X (Myo10) and VASP at the filopodial tip. Mol Biol Cell 14:1010
Tokuo H, Ikebe M (2004) Myosin X transports Mena/VASP to the tip of filopodia. Biochem Biophys Res Commun 319:214–220
Bohil AB, Robertson BW, Cheney RE (2006) Myosin-X is a molecular motor that functions in filopodia formation. Proc Natl Acad Sci U S A 103:12411–12416
Jaffe AB, Hall A (2005) Rho GTPases: biochemistry and biology. Annu Rev Cell Dev Biol 21:247–269
Reinhard J, Scheel AA, Diekmann D, Hall A, Ruppert C, Bahler M (1995) A novel type of myosin implicated in signalling by rho family GTPases. EMBO J 14:697–704
Muller RT, Honnert U, Reinhard J, Bahler M (1997) The rat myosin myr 5 is a GTPase-activating protein for Rho in vivo: essential role of arginine 1695. Mol Biol Cell 8:2039–2053
Graf B, Bahler M, Hilpela P, Bowe C, Adam T (2000) Functional role for the class IX myosin myr5 in epithelial cell infection by Shigella flexneri. Cell Microbiol 2:601–616
Rao MV, Engle LJ, Mohan PS, Yuan A, Qiu D, Cataldo A, Hassinger L, Jacobsen S, Lee VM, Andreadis A et al (2002) Myosin Va binding to neurofilaments is essential for correct myosin Va distribution and transport and neurofilament density. J Cell Biol 159:279–290
Wehrle-Haller B, Imhof BA (2003) Actin, microtubules and focal adhesion dynamics during cell migration. Int J Biochem Cell Biol 35:39–50
Wu XS, Tsan GL, Hammer JA 3rd (2005) Melanophilin and myosin Va track the microtubule plus end on EB1. J Cell Biol 171:201–207
McMichael BK, Cheney RE, Lee BS (2010) Myosin X regulates sealing zone patterning in osteoclasts through linkage of podosomes and microtubules. J Biol Chem 285:9506–9515
Woolner S, O’Brien LL, Wiese C, Bement WM (2008) Myosin-10 and actin filaments are essential for mitotic spindle function. J Cell Biol 182:77–88
Toyoshima F, Nishida E (2007) Integrin-mediated adhesion orients the spindle parallel to the substratum in an EB1- and myosin X-dependent manner. EMBO J 26:1487–1498
Kelley CA, Sellers JR, Gard DL, Bui D, Adelstein RS, Baines IC (1996) Xenopus nonmuscle myosin heavy chain isoforms have different subcellular localizations and enzymatic activities. J Cell Biol 134:675–687
Matsumura F, Ono S, Yamakita Y, Totsukawa G, Yamashiro S (1998) Specific localization of serine 19 phosphorylated myosin II during cell locomotion and mitosis of cultured cells. J Cell Biol 140:119–129
Matson S, Markoulaki S, Ducibella T (2006) Antagonists of myosin light chain kinase and of myosin II inhibit specific events of egg activation in fertilized mouse eggs. Biol Reprod 74:169–176
Mooseker MS, Foth BJ (2008) The structural and functional diversity of the myosin family of actin-based molecular motors. In: Coluccio LM (ed) Myosins, Vol. 7, pp. 1–34. The Netherlands, Springer
Titus MA (2000) The role of unconventional myosins in Dictyostelium endocytosis. J Eukaryot Microbiol 47:191–196
Gibbs D, Kitamoto J, Williams DS (2003) Abnormal phagocytosis by retinal pigmented epithelium that lacks myosin VIIa, the Usher syndrome 1B protein. Proc Natl Acad Sci U S A 100:6481–6486
Araki N (2006) Role of microtubules and myosins in Fc gamma receptor-mediated phagocytosis. Front Biosci 11:1479–1490
Ungewickell EJ, Hinrichsen L (2007) Endocytosis: clathrin-mediated membrane budding. Curr Opin Cell Biol 19:417–425
Holt JP, Bottomly K, Mooseker MS (2007) Assessment of myosin II, Va, VI and VIIa loss of function on endocytosis and endocytic vesicle motility in bone marrow-derived dendritic cells. Cell Motil Cytoskeleton 64:756–766
Araki N, Hatae T, Furukawa A, Swanson JA (2003) Phosphoinositide-3-kinase-independent contractile activities associated with Fcgamma-receptor-mediated phagocytosis and macropinocytosis in macrophages. J Cell Sci 116:247–257
Kolpak AL, Jiang J, Guo D, Standley C, Bellve K, Fogarty K, Bao ZZ (2009) Negative guidance factor-induced macropinocytosis in the growth cone plays a critical role in repulsive axon turning. J Neurosci 29:10488–10498
Jiang J, Kolpak AL, Bao ZZ (2010) Myosin IIB isoform plays an essential role in the formation of two distinct types of macropinosomes. Cytoskeleton (Hoboken) 67:32–42
Cox D, Berg JS, Cammer M, Chinegwundoh JO, Dale BM, Cheney RE, Greenberg S (2002) Myosin X is a downstream effector of PI(3)K during phagocytosis. Nat Cell Biol 4:469–477
Swanson JA, Johnson MT, Beningo K, Post P, Mooseker M, Araki N (1999) A contractile activity that closes phagosomes in macrophages. J Cell Sci 112(3):307–316
Rey M, Valenzuela-Fernandez A, Urzainqui A, Yanez-Mo M, Perez-Martinez M, Penela P, Mayor F Jr, Sanchez-Madrid F (2007) Myosin IIA is involved in the endocytosis of CXCR4 induced by SDF-1alpha. J Cell Sci 120:1126–1133
Osterweil E, Wells DG, Mooseker MS (2005) A role for myosin VI in postsynaptic structure and glutamate receptor endocytosis. J Cell Biol 168:329–338
Gotoh N, Yan Q, Du Z, Biemesderfer D, Kashgarian M, Mooseker MS, Wang T (2010) Altered renal proximal tubular endocytosis and histology in mice lacking myosin-VI. Cytoskeleton 67:178–192
Hasson T (2003) Myosin VI: two distinct roles in endocytosis. J Cell Sci 116:3453–3461
Dance AL, Miller M, Seragaki S, Aryal P, White B, Aschenbrenner, L, Hasson T (2004) Regulation of myosin-VI targeting to endocytic compartments. Traffic 5:798–813
Buss F, Kendrick-Jones J, Lionne C, Knight AE, Cote GP, Luzio JP (1998) The localization of myosin VI at the golgi complex and leading edge of fibroblasts and its phosphorylation and recruitment into membrane ruffles of A431 cells after growth factor stimulation. J Cell Biol 143:1535–1545
Warner CL, Stewart A, Luzio JP, Steel KP, Libby RT, Kendrick-Jones J, Buss F (2003) Loss of myosin VI reduces secretion and the size of the Golgi in fibroblasts from Snell’s waltzer mice. EMBO J 22:569–579
Provance DW, Mercer JA (1999) Myosin-V: head to tail. Cell Mol Life Sci 56:233–242
Reck-Peterson SL, Provance DW Jr, Mooseker MS, Mercer JA (2000) Class V myosins. Biochim Biophys Acta 1496:36–51
Dekker-Ohno K, Hayasaka S, Takagishi Y, Oda S, Wakasugi N, Mikoshiba K, Inouye M, Yamamura H (1996) Endoplasmic reticulum is missing in dendritic spines of Purkinje cells of the ataxic mutant rat. Brain Res 714:226–230
Takagishi Y, Oda S, Hayasaka S, Dekker-Ohno K, Shikata T, Inouye M, Yamamura H (1996) The dilute-lethal (dl) gene attacks a Ca2 + store in the dendritic spine of Purkinje cells in mice. Neurosci Lett 215:169–172
Prekeris R, Terrian DM (1997) Brain myosin V is a synaptic vesicle-associated motor protein: evidence for a Ca2 +- dependent interaction with the synaptobrevin–synaptophysin complex. J Cell Biol 137:1589–1601
Rudolf R, Kogel T, Kuznetsov SA, Salm T, Schlicker O, Hellwig A, Hammer JA 3rd, Gerdes HH (2003) Myosin Va facilitates the distribution of secretory granules in the F-actin rich cortex of PC12 cells. J Cell Sci 116:1339–1348
Evans LL, Lee AJ, Bridgman PC, Mooseker MS (1998) Vesicle-associated brain myosin-V can be activated to catalyze actin-based transport. J Cell Sci 111(14):2055–2066
Lapierre LA, Goldenring JR (2005) Interactions of myosin vb with rab11 family members and cargoes traversing the plasma membrane recycling system. Methods Enzymol 403:715–723
Provance DW Jr, Gourley CR, Silan CM, Cameron LC, Shokat KM, Goldenring JR, Shah K, Gillespie PG, Mercer JA (2004) Chemical-genetic inhibition of a sensitized mutant myosin Vb demonstrates a role in peripheral-pericentriolar membrane traffic. Proc Natl Acad Sci U S A 101:1868–1873
Nedvetsky PI, Stefan E, Frische S, Santamaria K, Wiesner B, Valenti G, Hammer JA 3rd, Nielsen S, Goldenring JR, Rosenthal W et al (2007) A Role of myosin Vb and Rab11-FIP2 in the aquaporin-2 shuttle. Traffic 8:110–123
Tzaban S, Massol RH, Yen E, Hamman W, Frank SR, Lapierre LA, Hansen SH, Goldenring JR, Blumberg RS, Lencer WI (2009) The recycling and transcytotic pathways for IgG transport by FcRn are distinct and display an inherent polarity. J Cell Biol 185:673–684
Gardner LA, Hajjhussein H, Frederick-Dyer KC, Bahouth SW (2010) Rab11a and its binding partners regulate the recycling of the β1-adrenergic receptor. Cellular Signalling 23:46–57
Jacobs DT, Weigert R, Grode KD, Donaldson JG, Cheney RE (2009) Myosin Vc is a molecular motor that functions in secretary granule trafficking. Mol Biol Cell 20:4471–4488
Marchelletta RR, Jacobs DT, Schechter JE, Cheney RE, Hamm-Alvarez SF (2008) The class V myosin motor, myosin 5c, localizes to mature secretary vesicles and facilitates exocytosis in lacrimal acini. Am J Physiol Cell Physiol 295:C13–28
Wang Z, Edwards JG, Riley N, Provance Jr DW, Karcher R, Li X-d, Davison IG, Ikebe M, Mercer JA, Kauer JA et al (2008) Myosin Vb mobilizes recycling endosomes and AMPA receptors for postsynaptic plasticity. Cell 135:535–548
Lisé MF, Wong TP, Trinh A, Hines RM, Liu L, Kang R, Hines DJ, Lu J, Goldenring JR, Wang YT et al (2006) Involvement of myosin Vb in glutamate receptor trafficking. J Biol Chem 281:3669–3678
Miyata M, Finch EA, Khiroug L, Hashimoto K, Hayasaka S, Oda S-I, Inouye M, Takagishi Y, Augustine GJ, Kano M (2000) Local calcium release in dendritic spines required for long-term synaptic depression. Neuron 28:233–244
Quintero OA, DiVito MM, Adikes RC, Kortan MB, Case LB, Lier AJ, Panaretos NS, Slater SQ, Rengarajan M, Feliu M et al (2009) Human Myo19 is a novel myosin that associates with mitochondria. Curr Biol 19:2008–2013
Nambiar R, McConnell RE, Tyska MJ (2010) Myosin motor function: the ins and outs of actin-based membrane protrusions. Cell Mol Life Sci 67:1239–1254
Nambiar R, McConnell RE, Tyska MJ (2009) Control of cell membrane tension by myosin-I. Proc Natl Acad Sci U S A 106:11972–11977
Tyska MJ, Mackey AT, Huang JD, Copeland NG, Jenkins NA, Mooseker MS (2005) Myosin-1a is critical for normal brush border structure and composition. Mol Biol Cell 16:2443–2457
McConnell RE, Higginbotham JN, Shifrin DA Jr, Tabb DL, Coffey RJ, Tyska MJ (2009) The enterocyte microvillus is a vesicle-generating organelle. J Cell Biol 185:1285–1298
McConnell RE, Tyska MJ (2007) Myosin-1a powers the sliding of apical membrane along microvillar actin bundles. J Cell Biol 177:671–681
Bobola N, Jansen RP, Shin TH, Nasmyth K (1996) Asymmetric accumulation of Ash1p in postanaphase nuclei depends on a myosin and restricts yeast mating-type switching to mother cells. Cell 84:699–709
Jansen RP, Dowzer C, Michaelis C, Galova M, Nasmyth K (1996) Mother cell-specific HO expression in budding yeast depends on the unconventional myosin myo4p and other cytoplasmic proteins. Cell 84:687–697
Krauss J, Lopez de Quinto S, Nusslein-Volhard C, Ephrussi A (2009) Myosin-V regulates oskar mRNA localization in the Drosophila oocyte. Curr Biol 19:1058–1063
Sotelo-Silveira JR, Calliari A, Cardenas M, Koenig E, Sotelo JR (2004) Myosin Va and kinesin II motor proteins are concentrated in ribosomal domains (periaxoplasmic ribosomal plaques) of myelinated axons. J Neurobiol 60:187–196
Sotelo-Silveira J, Crispino M, Puppo A, Sotelo JR, Koenig E (2008) Myelinated axons contain beta-actin mRNA and ZBP-1 in periaxoplasmic ribosomal plaques and depend on cyclic AMP and F-actin integrity for in vitro translation. J Neurochem 104:545–557
Ohashi S, Koike K, Omori A, Ichinose S, Ohara S, Kobayashi S, Sato TA, Anzai K (2002) Identification of mRNA/protein (mRNP) complexes containing Puralpha, mStaufen, fragile X protein, and myosin Va and their association with rough endoplasmic reticulum equipped with a kinesin motor. J Biol Chem 277:37804–37810
Yoshimura A, Fujii R, Watanabe Y, Okabe S, Fukui K, Takumi T (2006) Myosin-Va facilitates the accumulation of mRNA/protein complex in dendritic spines. Curr Biol 16:2345–2351
Salerno VP, Calliari A, Provance DW Jr, Sotelo-Silveira JR, Sotelo JR, Mercer JA (2008) Myosin-Va mediates RNA distribution in primary fibroblasts from multiple organs. Cell Motil Cytoskeleton 65:422–433
Nowak G, Pestic-Dragovich L, Hozak P, Philimonenko A, Simerly C, Schatten G, de Lanerolle P (1997) Evidence for the presence of myosin I in the nucleus. J Biol Chem 272:17176–17181
Pestic-Dragovich L, Stojiljkovic L, Philimonenko AA, Nowak G, Ke Y, Settlage RE, Shabanowitz J, Hunt DF, Hozak P, de Lanerolle P (2000) A myosin I isoform in the nucleus. Science 290:337–341
Li Q, Sarna SK (2009) Nuclear myosin II regulates the assembly of preinitiation complex for ICAM-1 gene transcription. Gastroenterology 137:1051–1060
Pranchevicius MC, Baqui MM, Ishikawa-Ankerhold HC, Lourenco EV, Leao RM, Banzi SR, dos Santos CT, Roque-Barreira MC, Espreafico EM, Larson RE (2008) Myosin Va phosphorylated on Ser1650 is found in nuclear speckles and redistributes to nucleoli upon inhibition of transcription. Cell Motil Cytoskeleton 65:441–456
Jung EJ, Liu G, Zhou W, Chen X (2006) Myosin VI is a mediator of the p53-dependent cell survival pathway. Mol Cell Biol 26:2175–2186
Salamon M, Millino C, Raffaello A, Mongillo M, Sandri C, Bean C, Negrisolo E, Pallavicini A, Valle G, Zaccolo M et al (2003) Human MYO18B, a novel unconventional myosin heavy chain expressed in striated muscles moves into the myonuclei upon differentiation. J Mol Biol 326:137–149
Cameron RS, Liu C, Mixon AS, Pihkala JP, Rahn RJ, Cameron PL (2007) Myosin16b: The COOH-tail region directs localization to the nucleus and overexpression delays S-phase progression. Cell Motil Cytoskeleton 64:19–48
Philimonenko VV, Zhao J, Iben S, Dingova H, Kysela K, Kahle M, Zentgraf H, Hofmann WA, de Lanerolle P, Hozak P et al (2004) Nuclear actin and myosin I are required for RNA polymerase I transcription. Nat Cell Biol 6:1165–1172
Percipalle P, Fomproix N, Cavellan E, Voit R, Reimer G, Kruger T, Thyberg J, Scheer U, Grummt I, Farrants AK (2006) The chromatin remodelling complex WSTF-SNF2 h interacts with nuclear myosin 1 and has a role in RNA polymerase I transcription. EMBO Rep 7:525–530
Cavellan E, Asp P, Percipalle P, Farrants AK (2006) The WSTF-SNF2 h chromatin remodeling complex interacts with several nuclear proteins in transcription. J Biol Chem 281:16264–16271
Ye J, Zhao J, Hoffmann-Rohrer U, Grummt I (2008) Nuclear myosin I acts in concert with polymeric actin to drive RNA polymerase I transcription. Genes Dev 22:322–330
Lindsay AJ, McCaffrey MW (2009) Myosin Vb localises to nucleoli and associates with the RNA polymerase I transcription complex. Cell Motil Cytoskeleton 66:1057–1072
Hofmann WA, Vargas GM, Ramchandran R, Stojiljkovic L, Goodrich JA, de Lanerolle P (2006) Nuclear myosin I is necessary for the formation of the first phosphodiester bond during transcription initiation by RNA polymerase II. J Cell Biochem 99:1001–1009
Vreugde S, Ferrai C, Miluzio A, Hauben E, Marchisio PC, Crippa MP, Bussi M, Biffo S (2006) Nuclear myosin VI enhances RNA polymerase II-dependent transcription. Mol Cell 23:749–755
Philimonenko VV, Janacek J, Harata M, Hozak P (2010) Transcription-dependent rearrangements of actin and nuclear myosin I in the nucleolus. Histochem Cell Biol 134:243–249
Obrdlik A, Louvet E, Kukalev A, Naschekin D, Kiseleva E, Fahrenkrog B, Percipalle P (2010) Nuclear myosin 1 is in complex with mature rRNA transcripts and associates with the nuclear pore basket. FASEB J 24:146–157
Cisterna B, Malatesta M, Dieker J, Muller S, Prosperi E, Biggiogera M (2009) An active mechanism flanks and modulates the export of the small ribosomal subunits. Histochem Cell Biol 131:743–753
Hu Q, Kwon YS, Nunez E, Cardamone MD, Hutt KR, Ohgi KA, Garcia-Bassets I, Rose DW, Glass CK, Rosenfeld MG et al (2008) Enhancing nuclear receptor-induced transcription requires nuclear motor and LSD1-dependent gene networking in interchromatin granules. Proc Natl Acad Sci U S A 105:19199–19204
Mehta IS, Amira M, Harvey AJ, Bridger JM (2010) Rapid chromosome territory relocation by nuclear motor activity in response to serum removal in primary human fibroblasts. Genome Biol 11:R5
Chuang CH, Carpenter AE, Fuchsova B, Johnson T, de Lanerolle P, Belmont AS (2006) Long-range directional movement of an interphase chromosome site. Curr Biol 16:825–831
Althaus K, Greinacher A (2009) MYH9-related platelet disorders. Semin Thromb Hemost 35:189–203
Chroneos ZC, Abdolrasulnia R, Whitsett JA, Rice WR, Shepherd VL (1996) Purification of a cell-surface receptor for surfactant protein A. J Biol Chem 271:16375–16383
Yang CH, Szeliga J, Jordan J, Faske S, Sever-Chroneos Z, Dorsett B, Christian RE, Settlage RE, Shabanowitz J, Hunt DF et al (2005) Identification of the surfactant protein A receptor 210 as the unconventional myosin 18 A. J Biol Chem 280:34447–34457
Weikert LF, Lopez JP, Abdolrasulnia R, Chroneos ZC, Shepherd VL (2000) Surfactant protein A enhances mycobacterial killing by rat macrophages through a nitric oxide-dependent pathway. Am J Physiol Lung Cell Mol Physiol 279:L216–223
Weikert LF, Edwards K, Chroneos ZC, Hager C, Hoffman L, Shepherd VL (1997) SP-A enhances uptake of bacillus Calmette-Guerin by macrophages through a specific SP-A receptor. Am J Physiol 272:L989–995
Borron P, McCormack FX, Elhalwagi BM, Chroneos ZC, Lewis JF, Zhu S, Wright JR, Shepherd VL, Possmayer F, Inchley K et al (1998) Surfactant protein A inhibits T cell proliferation via its collagen-like tail and a 210-kDa receptor. Am J Physiol 275:L679–686
Gruenheid S, Finlay BB (2003) Microbial pathogenesis and cytoskeletal function. Nature 422:775–781
Henry T, Gorvel JP, Méresse S (2006) Molecular motors hijacking by intracellular pathogens. Cellular Microbiology 8:23–32
Kolesnikova L, Bohil AB, Cheney RE, Becker S (2007) Budding of Marburg virus is associated with filopodia. Cell Microbiol 9:939–951
Roberts KL, Baines JD (2010) Myosin va enhances secretion of herpes simplex virus 1 virions and cell surface expression of viral glycoproteins. J Virol 84:9889–9896
Nakano T, Tani M, Nishioka M, Kohno T, Otsuka A, Ohwada S, Yokota J (2005) Genetic and epigenetic alterations of the candidate tumor-suppressor gene MYO18B, on chromosome arm 22q, in colorectal cancer. Genes Chromosomes Cancer 43:162–171
Nishioka M, Kohno T, Tani M, Yanaihara N, Tomizawa Y, Otsuka A, Sasaki S, Kobayashi K, Niki T, Maeshima A et al (2002) MYO18B, a candidate tumor suppressor gene at chromosome 22q12.1, deleted, mutated, and methylated in human lung cancer. Proc Natl Acad Sci U S A 99:12269–12274
Tani M, Ito J, Nishioka M, Kohno T, Tachibana K, Shiraishi M, Takenoshita S, Yokota J (2004) Correlation between histone acetylation and expression of the MYO18B gene in human lung cancer cells. Genes Chromosomes Cancer 40:146–151
Yanaihara N, Nishioka M, Kohno T, Otsuka A, Okamoto A, Ochiai K, Tanaka T, Yokota J (2004) Reduced expression of MYO18B, a candidate tumor-suppressor gene on chromosome arm 22q, in ovarian cancer. Int J Cancer 112:150–154
Dunn TA, Chen S, Faith DA, Hicks JL, Platz EA, Chen Y, Ewing CM, Sauvageot J, Isaacs WB, De Marzo AM et al (2006) A novel role of myosin VI in human prostate cancer. Am J Pathol 169:1843–1854
Yoshida H, Cheng W, Hung J, Montell D, Geisbrecht E, Rosen D, Liu J, Naora H (2004) Lessons from border cell migration in the Drosophila ovary: A role for myosin VI in dissemination of human ovarian cancer. Proc Natl Acad Sci U S A 101:8144–8149
Shigesada K, van de Sluis B, Liu PP (2004) Mechanism of leukemogenesis by the inv(16) chimeric gene CBFB/PEBP2B-MHY11. Oncogene 23:4297–4307
Woolner S, Bement WM (2009) Unconventional myosins acting unconventionally. Trends Cell Biol 19:245–252
Chantler P, Wylie S, Wheeler-Jones C, McGonnell I (2010) Conventional myosins—unconventional functions. Biophysical Reviews 2:67–82
Finn RD, Mistry J, Tate J, Coggill P, Heger A, Pollington JE, Gavin OL, Gunasekaran P, Ceric G, Forslund K et al (2010) The Pfam protein families database. Nucleic Acids Res 38:D211–222
Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA, McWilliam H, Valentin F, Wallace IM, Wilm A, Lopez R et al (2007) Clustal W and Clustal X version 2.0. Bioinformatics 23:2947–2948
Lorenz M, Holmes KC (2010) The actin-myosin interface. Proc Natl Acad Sci U S A 107:12529–12534
Houdusse A, Sweeney HL (2001) Myosin motors: missing structures and hidden springs. Curr Opin Struct Biol 11:182–194
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Quintero, O.A., Moore, J.E., Yengo, C.M. (2012). Basics of the Cytoskeleton: Myosins. In: Kavallaris, M. (eds) Cytoskeleton and Human Disease. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-61779-788-0_4
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