TY - JOUR
T1 - Isolation of uracil auxotroph mutants of coral symbiont alga for symbiosis studies
AU - Ishii, Yuu
AU - Maruyama, Shinichiro
AU - Fujimura-Kamada, Konomi
AU - Kutsuna, Natsumaro
AU - Takahashi, Shunichi
AU - Kawata, Masakado
AU - Minagawa, Jun
N1 - Funding Information:
Prof. Yusuke Matsuda, Drs. Yoshinori Tsuji and Chuya Shinzato are acknowledged for their initial contributions to this research. We thank Profs. John R. Pringle and Arthur R. Grossman for providing algal cultures, Prof. Koji Tamura and Drs. Gembu Abe and Daisuke Saito for their help in microscopy, Dr. Takuro Nakayama for his assistance in sequence analysis, and Dr. Eunsoo Kim for her critical reading and comments on the manuscript. This work was supported by NIBB Collaborative Research Program (15-362, 16-334, 17-310), research grants from the Frontier Research Institute for Interdisciplinary Sciences, Tohoku University, and Institute for Fermentation, Osaka, and JSPS KAKENHI Grant Number JP17K15163 and JP17H05713 (to S.M.); JP16H06280 and JP16K18562 (to N.K.); the Gordon and Betty Moore Foundation through Grant GBMF4985 (to J.M.). Computational resources were provided by the Data Integration and Analysis Facility at the National Institute for Basic Biology.
Publisher Copyright:
© 2018 The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Coral reef ecosystems rely on stable symbiotic relationship between the dinoflagellate Symbiodinium spp. and host cnidarian animals. The collapse of such symbiosis could cause coral 'bleaching' and subsequent host death. Despite huge interest on Symbiodinium, lack of mutant strains and readily available genetic tools have hampered molecular research. A major issue was the tolerance to marker antibiotics. Here, we isolated Symbiodinium mutants requiring uracil for growth, and hence, useful in transformation screening. We cultured Symbiodinium spp. cells in the presence of 5-fluoroorotic acid (5FOA), which inhibits the growth of cells expressing URA3 encoding orotidine-5′-monophosphate decarboxylase, and isolated cells that require uracil for growth. Sequence analyses and genetic complementation tests using yeast demonstrated that one of the mutant cell lines had a point mutation in URA3, resulting in a splicing error at an unusual exon-intron junction, and consequently, loss of enzyme activity. This mutant could maintain a symbiotic relationship with the model sea anemone Exaiptasia pallida only in sea water containing uracil. Results show that the URA3 mutant will be a useful tool for screening Symbiodinium transformants, both ex and in hospite, as survival in the absence of uracil is possible only upon successful introduction of URA3.
AB - Coral reef ecosystems rely on stable symbiotic relationship between the dinoflagellate Symbiodinium spp. and host cnidarian animals. The collapse of such symbiosis could cause coral 'bleaching' and subsequent host death. Despite huge interest on Symbiodinium, lack of mutant strains and readily available genetic tools have hampered molecular research. A major issue was the tolerance to marker antibiotics. Here, we isolated Symbiodinium mutants requiring uracil for growth, and hence, useful in transformation screening. We cultured Symbiodinium spp. cells in the presence of 5-fluoroorotic acid (5FOA), which inhibits the growth of cells expressing URA3 encoding orotidine-5′-monophosphate decarboxylase, and isolated cells that require uracil for growth. Sequence analyses and genetic complementation tests using yeast demonstrated that one of the mutant cell lines had a point mutation in URA3, resulting in a splicing error at an unusual exon-intron junction, and consequently, loss of enzyme activity. This mutant could maintain a symbiotic relationship with the model sea anemone Exaiptasia pallida only in sea water containing uracil. Results show that the URA3 mutant will be a useful tool for screening Symbiodinium transformants, both ex and in hospite, as survival in the absence of uracil is possible only upon successful introduction of URA3.
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U2 - 10.1038/s41598-018-21499-3
DO - 10.1038/s41598-018-21499-3
M3 - Article
C2 - 29459692
AN - SCOPUS:85042232932
SN - 2045-2322
VL - 8
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 3237
ER -