M. Aliee, J. Röper, K. P. Landsberg, C. Pentzold, T. J. Widmann et al., Physical mechanisms shaping the Drosophila dorsoventral compartment boundary, Curr Biol, vol.22, pp.967-976, 2012.

D. Allen and J. Seo, ER stress activates the TOR pathway through Atf6, J Mol Signal, vol.13, 2018.

D. S. Andersen, J. Colombani, V. Palmerini, K. Chakrabandhu, E. Boone et al., The Drosophila TNF receptor Grindelwald couples loss of cell polarity and neoplastic growth, Nature, vol.522, pp.482-486, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01255294

T. J. Bergmann, I. Fregno, F. Fumagalli, A. Rinaldi, F. Bertoni et al., Chemical stresses fail to mimic the unfolded protein response resulting from luminal load with unfolded polypeptides, J Biol Chem, vol.293, pp.5600-5612, 2018.

R. Bravo, V. Parra, and D. Gatica, Endoplasmic reticulum and the unfolded protein response: dynamics and metabolic integration, Int Rev Cell Mol Biol, vol.301, pp.215-290, 2013.

N. Chatterjee and D. Bohmann, A versatile PhiC31 based reporter system for measuring AP-1 and Nrf2 signaling in Drosophila and in tissue culture, PLoS One, vol.7, 2012.

K. Cheung, D. Shineman, M. Müller, C. Cárdenas, L. Mei et al., Mechanism of Ca2+ disruption in Alzheimer's disease by presenilin regulation of InsP3 receptor channel gating, Neuron, vol.58, pp.871-883, 2008.

N. J. Colley, J. A. Cassill, E. K. Baker, and C. S. Zuker, Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degeneration, Proc Natl Acad Sci U S A, vol.92, pp.3070-3074, 1995.

J. Colombani, D. S. Andersen, and P. Léopold, Secreted peptide Dilp8 coordinates Drosophila tissue growth with developmental timing, Science, vol.336, pp.582-585, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00766336

Y. Demay, J. Perochon, S. Szuplewski, B. Mignotte, and S. Gaumer, The PERK pathway independently triggers apoptosis and a Rac1/Slpr/ JNK/Dilp8 signaling favoring tissue homeostasis in a chronic ER stress Drosophila model, Cell Death Dis, vol.5, 2014.

S. Eaton, P. Auvinen, L. Luo, and Y. N. Jan, Simons K (1995) CDC42 and Rac1 control different actin-dependent processes in the Drosophila wing disc epithelium, J Cell Biol, vol.131, pp.151-164

A. Garelli, A. M. Gontijo, V. Miguela, E. Caparros, and M. Dominguez, Imaginal discs secrete insulin-like peptide 8 to mediate plasticity of growth and maturation, Science, vol.336, pp.579-582, 2012.

H. P. Harding, Y. Zhang, A. Bertolotti, H. Zeng, and D. Ron, Perk is essential for translational regulation and cell survival during the unfolded protein response, Molecular Cell, vol.5, issue.5, pp.897-904, 2000.

V. Hayrapetyan, V. Rybalchenko, N. Rybalchenko, and P. Koulen, The Nterminus of presenilin-2 increases single channel activity of brain ryanodine receptors through direct protein-protein interaction, Cell Calcium, vol.44, pp.507-518, 2008.

M. Kang, J. Chung, and H. D. Ryoo, CDK5 and MEKK1 mediate proapoptotic signalling following endoplasmic reticulum stress in an autosomal dominant retinitis pigmentosa model, Nat Cell Biol, vol.14, pp.409-415, 2012.

K. Kang, H. D. Ryoo, J. E. Park, J. H. Yoon, and M. J. Kang, ) A drosophila reporter for the translational activation of ATF4 marks stressed cells during development, PLOS ONE, vol.10, issue.5, p.126795, 2015.

A. Kim, J. B. Seo, W. Kim, H. J. Choi, S. Y. Kim et al., The pathogenic human Torsin A in Drosophila activates the unfolded protein response and increases susceptibility to oxidative stress, BMC Genomics, vol.16, p.338, 2015.

M. Michel, M. Aliee, R. K. Bialas, L. Jülicher, F. Dahmann et al., The selector gene apterous and notch are required to locally increase mechanical cell bond tension at the Drosophila dorsoventral compartment boundary, PLoS One, vol.11, 2016.

K. Michno, D. Knight, and J. M. Campusano, Intracellular calcium deficits in Drosophila cholinergic neurons expressing wild type or FAD-mutant presenilin, PLoS One, vol.4, 2009.

V. Rybalchenko, S. Hwang, N. Rybalchenko, and P. Koulen, The cytosolic N-terminus of presenilin-1 potentiates mouse ryanodine receptor single channel activity, Int J Biochem Cell Biol, vol.40, pp.84-97, 2008.

H. D. Ryoo, Drosophila as a model for unfolded protein response research, BMB Rep, vol.48, pp.445-453, 2015.

H. D. Ryoo, P. M. Domingos, M. Kang, and H. Steller, Unfolded protein response in a Drosophila model for retinal degeneration, EMBO J, vol.26, pp.242-252, 2007.

S. Souid, J. Lepesant, and C. Yanicostas, The xbp-1 gene is essential for development in Drosophila, Dev Genes Evol, vol.217, pp.159-167, 2007.
URL : https://hal.archives-ouvertes.fr/hal-00125444

G. E. Stutzmann, I. Smith, and A. Caccamo, Enhanced ryanodinemediated calcium release in mutant PS1-expressing Alzheimer's mouse models, Ann N Y Acad Sci, vol.1097, pp.265-277, 2007.

K. M. Vattem and R. C. Wek, Reinitiation involving upstream ORFs regulates ATF4 mRNA translation in mammalian cells, Proc Natl Acad Sci, vol.101, issue.31, pp.11269-11274, 2004.

S. Wang and R. J. Kaufman, The impact of the unfolded protein response on human disease, J Cell Biol, vol.197, pp.857-867, 2012.

Y. Zhang, C. Cui, and Z. Lai, The defender against apoptotic cell death 1 gene is required for tissue growth and efficient N-glycosylation in Drosophila melanogaster, Dev Biol, vol.420, pp.186-195, 2016.

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