A DDX6-CNOT1 complex and W-binding pockets in CNOT9 reveal direct links between miRNA target recognition and silencing (Q24295604)

DEAD-box helicase 6

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CCR4-NOT transcription complex subunit 1

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protein homodimerization activity

1 reference

1 reference

8

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Oliver Weichenrieder

7

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Duygu Kuzuoğlu-Öztürk

3

object named as

Duygu Kuzuoğlu-Öztürk

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Belinda Loh

object named as

Belinda Loh

5

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author name string

Ying Chen

1

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Andreas Boland

2

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Praveen Bawankar

4

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Chung-Te Chang

The role of GW182 proteins in miRNA-mediated gene silencing

6

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language of work or name

English

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publication date

5 June 2014

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published in

Molecular Cell

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volume

54

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page(s)

737-50

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issue

5

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cites work

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Drosophila argonaute1 and argonaute2 employ distinct mechanisms for translational repression.

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Structural basis for the mutually exclusive anchoring of P body components EDC3 and Tral to the DEAD box protein DDX6/Me31B

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GW182 proteins directly recruit cytoplasmic deadenylase complexes to miRNA targets

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Structure of the PAN3 pseudokinase reveals the basis for interactions with the PAN2 deadenylase and the GW182 proteins

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Structural and biochemical insights to the role of the CCR4-NOT complex and DDX6 ATPase in microRNA repression

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The DEAD box helicase, Dhh1p, functions in mRNA decapping and interacts with both the decapping and deadenylase complexes.

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GW182 proteins cause PABP dissociation from silenced miRNA targets in the absence of deadenylation

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Gene silencing by microRNAs: contributions of translational repression and mRNA decay

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Diversifying microRNA sequence and function

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miRNA-mediated deadenylation is orchestrated by GW182 through two conserved motifs that interact with CCR4-NOT

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miRNA repression involves GW182-mediated recruitment of CCR4-NOT through conserved W-containing motifs

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The mechanics of miRNA-mediated gene silencing: a look under the hood of miRISC.

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Crystal structure of the yeast eIF4A-eIF4G complex: an RNA-helicase controlled by protein-protein interactions

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Structural features of Argonaute-GW182 protein interactions

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Crystal structure of the human eIF4AIII-CWC22 complex shows how a DEAD-box protein is inhibited by a MIF4G domain

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Interaction between Not1p, a component of the Ccr4-not complex, a global regulator of transcription, and Dhh1p, a putative RNA helicase

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Mammalian Rcd1 is a novel transcriptional cofactor that mediates retinoic acid-induced cell differentiation

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The interactions of GW182 proteins with PABP and deadenylases are required for both translational repression and degradation of miRNA targets

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The structural basis for the interaction between the CAF1 nuclease and the NOT1 scaffold of the human CCR4-NOT deadenylase complex

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miRISC recruits decapping factors to miRNA targets to enhance their degradation

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The role of disordered protein regions in the assembly of decapping complexes and RNP granules

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Target-specific requirements for enhancers of decapping in miRNA-mediated gene silencing

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The Crystal Structure of Human Argonaute2

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Translational repression and eIF4A2 activity are critical for microRNA-mediated gene regulation

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Translation repression in human cells by microRNA-induced gene silencing requires RCK/p54

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NOT10 and C2orf29/NOT11 form a conserved module of the CCR4-NOT complex that docks onto the NOT1 N-terminal domain

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