FN Archimer Export Format PT J TI A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment BT AF Bernard, Clément Locard-Paulet, Marie Noël, Cyril Duchateau, Magalie Giai Gianetto, Quentin Moumen, Bouziane Rattei, Thomas Hechard, Yann Jensen, Lars Juhl Matondo, Mariette Samba-Louaka, Ascel AS 1:1;2:2;3:3;4:4;5:4,5;6:1;7:6;8:1;9:2;10:4;11:1; FF 1:;2:;3:PDG-IRSI-SEBIMER;4:;5:;6:;7:;8:;9:;10:;11:; C1 Laboratoire Ecologie et Biologie des Interactions, Université de Poitiers, UMR CNRS, 7267, Poitiers, France Novo Nordisk Foundation Center for Protein Research, University of Copenhagen, Copenhagen, Denmark IFREMER-IRSI-Service de Bioinformatique (SeBiMER), Centre Bretagne, Plouzane, France Institut Pasteur, Université de Paris, Proteomics Platform, Mass Spectrometry for Biology Unit, UAR2024, CNRS 2000, Paris, France Institut Pasteur, Université de Paris, Department of Computation Biology, Bioinformatics and Biostatistics Hub, Paris, France Centre for Microbiology and Environmental Systems Science; Doctoral School Microbiology and Environmental Science, University of Vienna, Vienna, Austria C2 UNIV POITIERS, FRANCE UNIV COPENHAGEN, DENMARK IFREMER, FRANCE INST PASTEUR, FRANCE INST PASTEUR, FRANCE UNIV VIENNA, AUSTRIA SI BREST SE PDG-IRSI-SEBIMER IN WOS Ifremer UPR DOAJ copubli-france copubli-europe copubli-univ-france IF 16.6 TC 12 UR https://archimer.ifremer.fr/doc/00785/89743/95237.pdf https://archimer.ifremer.fr/doc/00785/89743/95238.pdf https://archimer.ifremer.fr/doc/00785/89743/95239.pdf https://archimer.ifremer.fr/doc/00785/89743/95240.docx https://archimer.ifremer.fr/doc/00785/89743/95241.xlsx https://archimer.ifremer.fr/doc/00785/89743/95242.xlsx https://archimer.ifremer.fr/doc/00785/89743/95243.xlsx https://archimer.ifremer.fr/doc/00785/89743/95244.xlsx https://archimer.ifremer.fr/doc/00785/89743/95245.xlsx https://archimer.ifremer.fr/doc/00785/89743/95246.xlsx https://archimer.ifremer.fr/doc/00785/89743/95247.xlsx https://archimer.ifremer.fr/doc/00785/89743/95248.pdf https://archimer.ifremer.fr/doc/00785/89743/95249.xlsx LA English DT Article AB Encystment is a common stress response of most protists, including free-living amoebae. Cyst formation protects the amoebae from eradication and can increase virulence of the bacteria they harbor. Here, we mapped the global molecular changes that occur in the facultatively pathogenic amoeba Acanthamoeba castellanii during the early steps of the poorly understood process of encystment. By performing transcriptomic, proteomic, and phosphoproteomic experiments during encystment, we identified more than 150,000 previously undescribed transcripts and thousands of protein sequences absent from the reference genome. These results provide molecular details to the regulation of expected biological processes, such as cell proliferation shutdown, and reveal new insights such as a rapid phospho-regulation of sites involved in cytoskeleton remodeling and translation regulation. This work constitutes the first time-resolved molecular atlas of an encysting organism and a useful resource for further investigation of amoebae encystment to allow for a better control of pathogenic amoebae. PY 2022 PD JUN SO Nature Communications SN 2041-1723 PU Springer Science and Business Media LLC VL 13 IS 1 UT 000825733500004 DI 10.1038/s41467-022-31832-0 ID 89743 ER EF