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Part 1: Document Description
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Citation |
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Title: |
CDK1 couples proliferation with protein synthesis [Repository Tables R1-R4] |
Identification Number: |
doi:10.11588/data/EFHOBZ |
Distributor: |
heiDATA |
Date of Distribution: |
2020-02-06 |
Version: |
1 |
Bibliographic Citation: |
Haneke, Katharina; Stoecklin, Georg, 2020, "CDK1 couples proliferation with protein synthesis [Repository Tables R1-R4]", https://doi.org/10.11588/data/EFHOBZ, heiDATA, V1, UNF:6:+D39RBZQyWVzfn6Sv1nj+w== [fileUNF] |
Citation |
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Title: |
CDK1 couples proliferation with protein synthesis [Repository Tables R1-R4] |
Identification Number: |
doi:10.11588/data/EFHOBZ |
Authoring Entity: |
Haneke, Katharina (Division of Biochemistry, Mannheim Institute for Innate Immunoscience (MI3), Medical Faculty Mannheim, Heidelberg University, Germany) |
Stoecklin, Georg (Division of Biochemistry, Mannheim Institute for Innate Immunoscience (MI3), Medical Faculty Mannheim, Heidelberg University, Germany) |
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Other identifications and acknowledgements: |
Stoecklin, Georg |
Producer: |
Division of Biochemistry, Medical Faculty Mannheim |
Grant Number: |
SFB1036, 201348542 |
Grant Number: |
TRR186, 278001972 |
Distributor: |
heiDATA |
Access Authority: |
Haneke, Katharina |
Depositor: |
Stoecklin, Georg |
Date of Deposit: |
2019-11-20 |
Holdings Information: |
https://doi.org/10.11588/data/EFHOBZ |
Study Scope |
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Keywords: |
Medicine, Health and Life Sciences |
Abstract: |
Cell proliferation exerts a high demand on protein synthesis, yet the mechanisms coupling the two processes are not fully understood. A kinase and phosphatase screen for activators of translation, based on the formation of stress granules in human cells, revealed cell cycle-associated kinases as major candidates. CDK1 was identified as a positive regulator of global translation, and cell synchronization experiments showed that this is an extra-mitotic function of CDK1. Different pathways including eIF2α, 4EBP1 and S6K1 signaling contribute to controlling global translation downstream of CDK1. Moreover, Ribo-Seq analysis uncovered that CDK1 exerts a particularly strong effect on the translation of 5’TOP mRNAs, which includes mRNAs encoding for ribosomal proteins and several translation factors. This effect requires the 5’TOP mRNA-binding protein LARP1, concurrent to our finding that LARP1 phosphorylation is strongly dependent on CDK1. Thus, CDK1 provides a direct means to couple cell proliferation with biosynthesis of the translation machinery and the rate of protein synthesis. |
Methodology and Processing |
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Data Access |
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Other Study Description Materials |
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Related Publications |
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Citation |
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Title: |
Katharina Haneke, Johanna Schott, Doris Lindner, Anne Kruse Hollensen, Christian Kroun Damgaard, Cyril Mongis, Michael Knop, Wilhelm Palm, Alessia Ruggieri, Georg Stoecklin; CDK1 couples proliferation with protein synthesis. J Cell Biol 2 March 2020; 219 (3): e201906147. |
Identification Number: |
https://doi.org/10.1083/jcb.201906147 |
Bibliographic Citation: |
Katharina Haneke, Johanna Schott, Doris Lindner, Anne Kruse Hollensen, Christian Kroun Damgaard, Cyril Mongis, Michael Knop, Wilhelm Palm, Alessia Ruggieri, Georg Stoecklin; CDK1 couples proliferation with protein synthesis. J Cell Biol 2 March 2020; 219 (3): e201906147. |
File Description--f3297 |
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File: Repository Table R1 SG Screen.tab.tab |
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Notes: |
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Notes: |
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Notes: |
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