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  To be (in a transcriptional complex) or not to be (promoting UBR5 ubiquitylation): That is an answer to how degradation controls gene expression

Hehl, L. A., & Schulman, B. A. (2023). To be (in a transcriptional complex) or not to be (promoting UBR5 ubiquitylation): That is an answer to how degradation controls gene expression. Molecular Cell, 83(15), 2616-2618. doi:10.1016/j.molcel.2023.07.010.

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Item Permalink: https://hdl.handle.net/21.11116/0000-000D-C13F-3 Version Permalink: https://hdl.handle.net/21.11116/0000-000D-C140-0
Genre: Journal Article

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 Creators:
Hehl, Laura A.1, Author           
Schulman, Brenda A.1, Author           
Affiliations:
1Schulman, Brenda / Molecular Machines and Signaling, Max Planck Institute of Biochemistry, Max Planck Society, ou_2466699              

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Free keywords: UBIQUITIN LIGASEBiochemistry & Molecular Biology; Cell Biology;
 Abstract: Tsai et al.1 in this issue and Mark et al.2 in Cell reveal how the E3 ligase UBR5 mediates broad regulation by selectively targeting agonist-bound nuclear hormone receptors, MYC, and other transcriptional regulators not incorporated into active gene expression complexes.

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Language(s): eng - English
 Dates: 2023-08-032023-08-03
 Publication Status: Issued
 Pages: 3
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: ISI: 001052967700001
DOI: 10.1016/j.molcel.2023.07.010
 Degree: -

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Title: Molecular Cell
Source Genre: Journal
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Publ. Info: Cambridge, Mass. : Cell Press
Pages: - Volume / Issue: 83 (15) Sequence Number: - Start / End Page: 2616 - 2618 Identifier: ISSN: 1097-2765
CoNE: https://pure.mpg.de/cone/journals/resource/954925610929