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   <subfield code="a">O -GlcNAc modification is essential for the regulation of autophagy in Drosophila melanogaster</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Sujin Park, Yangsin Lee, Jin Pak, Hanbyeol Kim, Hyeonjin Choi, Jae-woo Kim, Jürgen Roth, Jin Cho]</subfield>
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   <subfield code="a">O-GlcNAcylation is a dynamic post-translational modification that takes place on ser/thr residues of nucleocytoplasmic proteins. O-GlcNAcylation regulates almost all cellular events as a nutrient sensor, a transcriptional and translational regulator, and a disease-related factor. Although the role of O-GlcNAcylation in insulin signaling and metabolism are well established, the relationship between O-GlcNAcylation and autophagy is largely unknown. Here, we manipulated O-GlcNAcylation in Drosophila and found that it regulates autophagy through Akt/dFOXO signaling. We demonstrate that O-GlcNAcylation and the levels of O-GlcNAc transferase (OGT) are increased during starvation. Furthermore, Atg proteins and autolysosomes are increased in OGT-reduced flies without fasting. Atg proteins and autophagosomes are reduced in OGT-overexpressing flies. Our results suggest that not only autophagy gene expression but also autophagic structures are regulated by OGT through Akt and dFOXO. These data imply that O-GlcNAcylation is important in modulating autophagy as well as insulin signaling in Drosophila.</subfield>
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   <subfield code="a">Springer Basel, 2015</subfield>
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   <subfield code="a">O -GlcNAc modification</subfield>
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   <subfield code="a">Park</subfield>
   <subfield code="D">Sujin</subfield>
   <subfield code="u">Department of Integrated OMICS for Biomedical Science, Graduate School, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, 120-749, Seoul, South Korea</subfield>
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   <subfield code="a">Lee</subfield>
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   <subfield code="u">Department of Integrated OMICS for Biomedical Science, Graduate School, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, 120-749, Seoul, South Korea</subfield>
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   <subfield code="a">Pak</subfield>
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   <subfield code="u">Department of Integrated OMICS for Biomedical Science, Graduate School, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, 120-749, Seoul, South Korea</subfield>
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   <subfield code="a">Kim</subfield>
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   <subfield code="u">Department of Integrated OMICS for Biomedical Science, Graduate School, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, 120-749, Seoul, South Korea</subfield>
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   <subfield code="a">Choi</subfield>
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   <subfield code="u">Department of Biochemistry and Molecular Biology, Integrated Genomic Research Center for Metabolic Regulation, Institute of Genetic Science, Yonsei University College of Medicine, Seoul, Korea</subfield>
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   <subfield code="u">Department of Biochemistry and Molecular Biology, Integrated Genomic Research Center for Metabolic Regulation, Institute of Genetic Science, Yonsei University College of Medicine, Seoul, Korea</subfield>
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   <subfield code="a">Roth</subfield>
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   <subfield code="u">Department of Integrated OMICS for Biomedical Science, Graduate School, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, 120-749, Seoul, South Korea</subfield>
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   <subfield code="u">Department of Integrated OMICS for Biomedical Science, Graduate School, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, 120-749, Seoul, South Korea</subfield>
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   <subfield code="t">Cellular and Molecular Life Sciences</subfield>
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   <subfield code="g">72/16(2015-08-01), 3173-3183</subfield>
   <subfield code="x">1420-682X</subfield>
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   <subfield code="a">BK010053</subfield>
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   <subfield code="c">XK010000</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
   <subfield code="2">nationallicence</subfield>
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