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  HELZ directly interacts with CCR4-NOT and causes decay of bound mRNAs

Hanet, A., Räsch, F., Weber, R., Ruscica, V., Fauser, M., Raisch, T., et al. (2019). HELZ directly interacts with CCR4-NOT and causes decay of bound mRNAs. Life science alliance, 2(5): e201900405. doi:10.26508/lsa.201900405.

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 Creators:
Hanet, A1, Author           
Räsch, F1, Author           
Weber, R1, Author           
Ruscica, V1, Author           
Fauser, M1, Author           
Raisch, T1, Author           
Kuzuoglu-Öztürk, D1, Author           
Chang, C-T1, Author           
Bhandari, D1, Author           
Igreja, C1, 2, Author           
Wohlbold, L1, Author           
Affiliations:
1Department Biochemistry, Max Planck Institute for Developmental Biology, Max Planck Society, ou_3375718              
2Regulation and Post-Translational Modification of Gene Expression in Nematodes Group, Department Integrative Evolutionary Biology, Max Planck Institute for Developmental Biology, Max Planck Society, ou_3507707              

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 Abstract: Eukaryotic superfamily (SF) 1 helicases have been implicated in various aspects of RNA metabolism, including transcription, processing, translation, and degradation. Nevertheless, until now, most human SF1 helicases remain poorly understood. Here, we have functionally and biochemically characterized the role of a putative SF1 helicase termed "helicase with zinc-finger," or HELZ. We discovered that HELZ associates with various mRNA decay factors, including components of the carbon catabolite repressor 4-negative on TATA box (CCR4-NOT) deadenylase complex in human and Drosophila melanogaster cells. The interaction between HELZ and the CCR4-NOT complex is direct and mediated by extended low-complexity regions in the C-terminal part of the protein. We further reveal that HELZ requires the deadenylase complex to mediate translational repression and decapping-dependent mRNA decay. Finally, transcriptome-wide analysis of Helz-null cells suggests that HELZ has a role in the regulation of the expression of genes associated with the development of the nervous system.

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Language(s): eng - English
 Dates: 2019-09
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.26508/lsa.201900405
PMID: 31570513
 Degree: -

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Title: Life science alliance
  Abbreviation : Life Sci Alliance
Source Genre: Journal
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Publ. Info: Heidelberg : EMBO Press
Pages: 16 Volume / Issue: 2 (5) Sequence Number: e201900405 Start / End Page: - Identifier: ISSN: 2575-1077
CoNE: https://pure.mpg.de/cone/journals/resource/2575-1077