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Genetic induction and mechanochemical propagation of a morphogenetic wave


Lecuit, T. & Lenne, P. F. Mechanics of the cell floor and management of cell form, tissue construction and morphogenesis. Nat. Rev. Mol. Cell Biol. eight, 633-644 (2007).


Gilmour, D., Rembold, M. and Leptin, M. From morphogen to morphogenesis and vice versa. Nature 541, 311-320 (2017).


Leptin, M. Gastrulation in Drosophila: logic and mobile mechanisms. EMBO J. 18, 3187-3192 (1999).


Heisenberg, C.P. & Bellaïche, Y. Forces of Morphogenesis and Tissue Structuring. Cell 153, 948-962 (2013).


Martin, C., Kaschube, M. and Wieschaus, E. F. Pulsed contractions of an actin-myosin community lead to apical constriction. Nature 457, 495-499 (2009).


J. Solon, A. Kaya-Copur, J. Colombelli and D. Brunner. Pulsed forces measured by a ratchet-like mechanism trigger directed tissue motion throughout dorsal closure. Cell 137, 1331-1342 (2009).


Roh-Johnson, M. et al. Set off a change of mobile type by exploiting preexisting contractions to actomyosin. Science 335, 1232-1235 (2012).


Martin, A. C. & Goldstein, B. Apical Constriction: Themes and Variations on a Mobile Mechanism Resulting in Morphogenesis. Growth 141, 1987-1998 (2014).


Mason, F.M., Tworoger, M. and Martin, A.C. The polarization of the apical area localizes the exercise of actin and myosin to trigger apical constriction much like a ratchet. Nat. Cell Biol. 15, 926-936 (2013).


Munjal, A., Philippe, J.M., Munro, E. and Lecuit, T. A self-organized biomechanical community results in modifications in form throughout tissue morphogenesis. Nature 524, 351-355 (2015).


Marston, D.J. et al. MRCK-1 causes apical constriction in C. elegans by linking developmental structuring to power technology. Curr. Biol. 26, 2079-2089 (2016).


Michaux, J.B., Robin B.F., McFadden, W.M. & Munro, E.M. The thrilling dynamics of RhoA ends in pulsed contractions of the early C. elegans embryo. J. Cell Biol. 217, 4230-4252 (2018).


Kerridge, S. et al. The modular activation of Rho1 by GPCR signaling confers polarized activation of myosin II throughout morphogenesis. Nat. Cell Biol. 18, 261-270 (2016).


Manning, A.J., Peters, Okay.A., Peifer, M. & Rogers, S.L. Regulation of epithelial morphogenesis by G-protein coupled receptor fog and its ligand fog. Sci. Sign. 6, ra98 (2013).


Costa, M., Wilson, E.T. & Wieschaus, E. A putative cell sign encoded by the folded gastrulation gene coordinates cell form modifications throughout Drosophila gastrulation. Cell 76, 1075-1089 (1994).


Dawes-Hoang, R.E. et al. Folded gastritis, cell form change and localization management of myosin. Growth 132, 4165-4178 (2005).


Rauzi, M., Lenne, P. F. and Lecuit, T. The contractile flux of planar polarized actomyosin controls the reworking of the epithelial junction. Nature 468, 1110-1114 (2010).


Munro, E., Nance, J. & Priess, J. R. Cortical flows fed by uneven contraction transport PAR proteins to determine and keep anteroposterior polarity within the early C. elegans embryo. Dev. Cell 7, 413-424 (2004).


Kim, H.Y. & Davidson, L.A. Actin contractions punctured throughout convergent extension and their permissive regulation by the non-canonical Wnt signaling pathway. J. Cell Sci. 124, 635-646 (2011).


Grasp, J.L., Niwayama, R., Turlier, H., Nedelec, F. & Hiiragi, T. Autonomic contractility of pulsatile cells ends in compaction of the mouse embryo. Nat. Cell Biol. 17, 849-855 (2015).


Mayer, M., Depken, M., Wooden, J.S., Jülicher, F. and Grill, S.W. Anisotropies in cortical stress reveal the bodily foundation of polarizing cortical flows. Nature 467, 617-621 (2010).


Behrndt, M. et al. Forces resulting in epithelial propagation in zebrafish gastrulation. Science 338, 257-260 (2012).


Bement, W.M. et al. Activator-inhibitor coupling between Rho signaling and actin meeting makes the mobile cortex an excitable medium. Nat. Cell Biol. 17, 1471-1483 (2015).


Nishikawa, M., Naganathan, S.R., Jülicher, F. & Grill, S.W. Management of contractile instabilities within the cortex of actomyosin. eLife 6, 195595 (2017).


Fernandez-Gonzalez, R., Simoes, Sde. M., Röper, J.C., Eaton, S. and Zallen, J. A. The dynamics of myosin II is regulated by the voltage within the intercalating cells. Dev. Cell 17, 736-743 (2009).


Chanet, S. et al. The mechanosensitivity to the mesh of actomyosin permits the form of the tissue to orient the mobile power. Nat. Frequent. eight, 15014 (2017).


Mitrossilis, D. et al. Mechanotransductive cascade of mesoderm invaginations and Myo-II dependent endoderm in embryo gastrulation. Nat. Frequent. eight, 13883 (2017).


Tan, P. Y. and Zaidel-Bar, R. The transient location of the SPV-1 membrane ends in cyclic contractions of actomyosin within the spermatheca of C. elegans. Curr. Biol. 25, 141-151 (2015).


Collinet, C., M. Rauzi, Lenne, P. F. & Lecuit, T. The native and scale forces of the tissue outcome within the development of oriented junctions in the course of the extension of the tissue. Nat. Cell Biol. 17, 1247-1258 (2015).


Lye, C.M. et al. Mechanical coupling between invagination of the endoderm and axis extension in Drosophila. PLoS Biol. 13, e1002292 (2015).


Younger, P.E., Pesacreta, T.C. & Kiehart, D.P. Dynamic modifications within the distribution of cytoplasmic myosin throughout embryogenesis of Drosophila. Growth 111, 1-14 (1991).


Sweeton, D., Parks, S., Costa, M. & Wieschaus, E. Gastrulation in Drosophila: formation of invaginations of ventral sulcus and posterior midgut. Growth 112, 775-789 (1991).


Casanova, J. & Struhl, G. The localized floor exercise of the torso, a receptor tyrosine kinase, specifies the terminal physique sample in Drosophila. Genes Dev. three (12B), 2025-2038 (1989).


Weigel, D., Jürgens, G., Klingler, M. and Jäckle, H. Two spacing genes play the position of mediator within the info of the maternal terminal sample in Drosophila. Science 248, 495-498 (1990).


Garcia, H.G., Tikhonov, M., Lin, A. and Gregor, T. The quantitative imaging of transcription in reside Drosophila embryos relates the exercise of polymerase to sample formation. Curr. Biol. 23, 2140-2145 (2013).


Edgar, B.A., Lehman, D.A. and O'Farrell, P.H.Transcriptional regulation of the chain (cdc25): hyperlink between growth programming and the cell cycle. Growth 120, 3131-3143 (1994).


Paré, C.C. et al. A positional toll receiver code directs convergent extension in Drosophila. Nature 515, 523-527 (2014).


Kerszberg, M. & Wolpert, L. Morphogen transport place signaling mechanisms: theoretical research. J. Theor. Biol. 191, 103-114 (1998).


Lander, A.D., Nie, Q. and Wan, F. Y. Do morphogen gradients seem by diffusion? Dev. Cell 2, 785-796 (2002).


Seher, T.C., Narasimha, M., Vogelsang, E. & Leptin, M .. Evaluation and reconstitution of the genetic cascade controlling early morphogenesis of mesoderm within the Drosophila embryo. Mech. Dev. 124, 167-179 (2007).


Heissler, S.M. & Sellers, J.R. Kinetic diversifications of myosins to their numerous mobile features. Site visitors 17, 839-859 (2016).


Geiger, B., Spatz, J.P. & Bershadsky, A.D. Environmental detection by focal adhesion. Nat. Rev. Mol. Cell Biol. 10, 21-33 (2009).


Iskratsch, T., Wolfenson, H. & Sheetz, M. P. Evaluation of power and type: the rise of mechanotransduction in cell biology. Nat. Rev. Mol. Cell Biol. 15, 825-833 (2014).


Rauzi, M. et al. Tissue mechanics on the embryonic scale throughout Drosophila gastrulation actions. Nat. Frequent. 6, 8677 (2015).


Odell, G.M., Oster, G., Alberch, P. and Burnside, B. The Mechanical Foundation of Morphogenesis. I. Epithelial folding and intussusception. Dev. Biol. 85, 446-462 (1981).


He, B., Doubrovinski Okay., Polyakov, O. & Wieschaus, E. Apical constriction causes the tissue-scale hydrodynamic stream to control cell elongation. Nature 508, 392-396 (2014).


Stark, Okay.A. et al. A brand new α-integrin subunit associates βPS and performs a job in tissue morphogenesis and motion throughout Drosophila growth. Growth 124, 4583-4594 (1997).


Münster, S. et al. The attachment of the blastoderm to the vitelline envelope impacts the gastrulation of bugs. Nature 568, 395-399 (2019).


Gelens, L., Anderson, G.A. and Ferrell, J.E. Jr. Spatial space-triggered waves: Constructive suggestions lets you go a great distance. Mol. Biol. Cell 25, 3486-3493 (2014).


Allard, J. & Mogilner, A. Progressive waves in actin dynamics and cell motility. Curr. Opin. Cell Biol. 25, 107-115 (2013).


Diz-Munoz, A., Fletcher, D.A. and Weiner, O. D. Use power: membrane stress because the organizer of cell form and motility. Developments Cell Biol. 23, 47-53 (2013).


Hashimoto, H., Robin, F.B., Sherrard, Okay.M. & Munro, E.M. Sequential contraction and apical junction trade lead to zipper closure of the neural tube in a easy settlement. Dev. Cell 32, 241-255 (2015).


Morize, P., Christiansen, A.E, Costa, M., Parks, S. & Wieschaus, E. The hyperactivation of the folded gastrulation pathway induces particular modifications in cell form. Growth 125, 589-597 (1998).


Huang, J., W. Zhou, W. Dong, Watson, A.M. and Hong, Y. From the duvet: Directed, efficient and versatile modifications of the Drosophila genome by genomic engineering. Proc. Natl Acad. Sci. USA 106, 8284-8289 (2009).


Venken, Okay.J. et al. P versatile[acman] BAC libraries for transgenesis research in Drosophila melanogaster. Nat. Strategies 6, 431-434 (2009).


Bertet, C., Sulak, L. & Lecuit, T. The transforming of the junction-dependent myosin controls planar cell intercalation and axis elongation. Nature 429, 667-671 (2004).


Cavey, M. & Lecuit, T. Imaging mobile and molecular dynamics of reside embryos utilizing fluorescent proteins. Mol. Biol. 420, 219-238 (2008).


Müller, H. A. Immunolabeling of embryos. Mol. Biol. 420, 207-218 (2008).


Fuse, N., Yu, F. and Hirose, S. Gprk2 modify fog signaling to prepare cell motions in Drosophila gastrulation. Growth 140, 4246-4255 (2013).


Kosman, D., Small, S. and Reinitz, J. Speedy preparation of a panel of polyclonal antibodies directed in opposition to Drosophila segmentation proteins. Dev. Evol genes. 208, 290-294 (1998).


Aigouy, B. et al. The mobile stream reorients the flat polarity axis within the Drosophila wing epithelium. Cell 142, 773-786 (2010).


Butler, L.C. et al. Modifications in cell form point out that extrinsic tensile forces play a job within the extension of the Drosophila germline. Nat. Cell Biol. 11, 859-864 (2009).

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