Results 31 to 40 of about 24,702 (192)

The CCR4-NOT complex suppresses untimely translational activation of maternal mRNAs.

open access: yesDevelopment, 2023
ABSTRACT Control of mRNA poly(A) tails is essential for regulation of mRNA metabolism, specifically translation efficiency and mRNA stability. Gene expression in maturing oocytes relies largely on post-transcriptional regulation, as genes are transcriptionally silent during oocyte maturation.
Soeda S   +3 more
europepmc   +3 more sources

Stoichiometry and Change of the mRNA Closed-Loop Factors as Translating Ribosomes Transit from Initiation to Elongation [PDF]

open access: yes, 2016
Protein synthesis is a highly efficient process and is under exacting control. Yet, the actual abundance of translation factors present in translating complexes and how these abundances change during the transit of a ribosome across an mRNA remains ...
Chiang, Yueh-Chin   +6 more
core   +15 more sources

Human Ccr4–Not complexes contain variable deadenylase subunits [PDF]

open access: yesBiochemical Journal, 2009
The Ccr4–Not complex is evolutionarily conserved and important for regulation of mRNA synthesis and decay. The composition of the yeast complex has been well described. Orthologues of the yeast Ccr4–Not components have been identified in human cells including multiple subunits with mRNA deadenylase activity.
Lau, N.C.   +6 more
openaire   +3 more sources

The CCR4-NOT complex physically and functionally interacts with TRAMP and the nuclear exosome. [PDF]

open access: yesPLoS ONE, 2009
BACKGROUND:Ccr4-Not is a highly conserved multi-protein complex consisting in yeast of 9 subunits, including Not5 and the major yeast deadenylase Ccr4.
Nowel Azzouz   +3 more
doaj   +1 more source

The CCR4–NOT Deadenylase Complex Maintains Adipocyte Identity [PDF]

open access: yesInternational Journal of Molecular Sciences, 2019
Shortening of poly(A) tails triggers mRNA degradation; hence, mRNA deadenylation regulates many biological events. In the present study, we generated mice lacking the Cnot1 gene, which encodes an essential scaffold subunit of the CCR4–NOT deadenylase complex in adipose tissues (Cnot1-AKO mice) and we examined the role of CCR4–NOT in adipocyte function.
Akinori Takahashi   +7 more
openaire   +2 more sources

The Ccr4-Not Complex Regulates Skn7 through Srb10 Kinase [PDF]

open access: yesEukaryotic Cell, 2007
ABSTRACT The Ccr4-Not complex is a multifunctional regulatory platform composed of nine subunits that controls diverse cellular events including mRNA degradation, protein ubiquitination, and transcription. In this study, we identified the yeast Saccharomyces cerevisiae osmotic and oxidative stress ...
Lenssen, Eve   +4 more
openaire   +3 more sources

RNF219 regulates CCR4-NOT function in mRNA translation and deadenylation

open access: yesScientific Reports, 2022
Post-transcriptional regulatory mechanisms play a role in many biological contexts through the control of mRNA degradation, translation and localization.
Aude Guénolé   +7 more
doaj   +1 more source

The multifunctional Ccr4–Not complex directly promotes transcription elongation [PDF]

open access: yesGenes & Development, 2011
The Ccr4–Not complex has been implicated in the control of multiple steps of mRNA metabolism; however, its functions in transcription remain ambiguous. The discovery that Ccr4/Pop2 is the major cytoplasmic mRNA deadenylase and the detection of Not proteins within mRNA processing bodies have raised questions about the roles of the Ccr4–Not complex in ...
Jennifer A, Kruk   +4 more
openaire   +2 more sources

The Ccr4-Not Complex: Architecture and Structural Insights

open access: yesSubcellular Biochemistry, 2017
The Ccr4-Not complex is an essential multi-subunit protein complex that plays a fundamental role in eukaryotic mRNA metabolism and has a multitude of different roles that impact eukaryotic gene expression . It has a conserved core of three Not proteins, the Ccr4 protein, and two Ccr4 associated factors, Caf1 and Caf40.
Collart, Martine, Panasenko, Olesya
openaire   +4 more sources

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