Drosophila Low Temperature Viability Protein 1 (LTV1) Is Required for Ribosome Biogenesis and Cell Growth Downstream of Drosophila Myc (dMyc)
Drosophila Low Temperature Viability Protein 1 (LTV1) Is Required for Ribosome Biogenesis and Cell Growth Downstream of Drosophila Myc (dMyc)
During animal development, various signaling pathways converge to regulate cell growth. In this study, we identified LTV1 as a novel cell growth regulator in Drosophila. LTV1 mutant larvae exhibited developmental delays and lethality at the second larval stage. Using biochemical studies, we discovered that LTV1 interacted with ribosomal protein S3 and co-purified with free 40S ribosome subunits. We further demonstrated that LTV1 is crucial for ribosome biogenesis through 40S ribosome subunit synthesis and preribosomal RNA processing, suggesting that LTV1 is required for cell growth by regulating protein synthesis. We also demonstrated that Drosophila Myc (dMyc) directly regulates LTV1 transcription and requires LTV1 to stimulate ribosome biogenesis. Importantly, the loss of LTV1 blocked the cell growth and endoreplication induced by dMyc. Combined, these results suggest that LTV1 is a key downstream factor of dMyc-induced cell growth by properly maintaining ribosome biogenesis.
- Seoul National University Korea (Republic of)
- Korean Association Of Science and Technology Studies Korea (Republic of)
- Korea Advanced Institute of Science and Technology Korea (Republic of)
- Korea University Korea (Republic of)
Chromatin Immunoprecipitation, Reverse Transcriptase Polymerase Chain Reaction, Temperature, Blotting, Northern, Real-Time Polymerase Chain Reaction, Animals, Genetically Modified, Immunoenzyme Techniques, Proto-Oncogene Proteins c-myc, Microscopy, Electron, Drosophila melanogaster, Protein Biosynthesis, Animals, Drosophila Proteins, RNA, Messenger, Ribosomes, Cells, Cultured, Cell Proliferation
Chromatin Immunoprecipitation, Reverse Transcriptase Polymerase Chain Reaction, Temperature, Blotting, Northern, Real-Time Polymerase Chain Reaction, Animals, Genetically Modified, Immunoenzyme Techniques, Proto-Oncogene Proteins c-myc, Microscopy, Electron, Drosophila melanogaster, Protein Biosynthesis, Animals, Drosophila Proteins, RNA, Messenger, Ribosomes, Cells, Cultured, Cell Proliferation
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