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SMG5-SMG7 authorize nonsense-mediated mRNA decay by enabling SMG6 endonucleolytic activity
by
Kueckelmann, Sabrina
, Krüger, Marcus
, Britto-Borges, Thiago
, Boehm, Volker
, Gerbracht, Jennifer V.
, Dieterich, Christoph
, Gehring, Niels H.
, Kallabis, Sebastian
, Altmüller, Janine
in
13/106
/ 13/44
/ 38/1
/ 42/89
/ 45/41
/ 45/77
/ 49/109
/ 49/88
/ 49/90
/ 49/91
/ 631/337/1645
/ 631/337/1645/1769
/ 631/337/1645/2020
/ 82/29
/ 82/58
/ Carrier Proteins - chemistry
/ Carrier Proteins - genetics
/ Carrier Proteins - metabolism
/ Cell Line
/ Decay
/ Degradation
/ Female
/ Gene expression
/ Gene Knockout Techniques
/ Humanities and Social Sciences
/ Humans
/ mRNA turnover
/ multidisciplinary
/ Nonsense Mediated mRNA Decay - physiology
/ Nonsense-mediated mRNA decay
/ Phosphorylation
/ RNA Helicases - genetics
/ RNA Helicases - metabolism
/ Science
/ Science (multidisciplinary)
/ Substrates
/ Telomerase - metabolism
/ Trans-Activators - genetics
/ Trans-Activators - metabolism
/ Transcriptomes
/ Translation
/ Translation termination
2021
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SMG5-SMG7 authorize nonsense-mediated mRNA decay by enabling SMG6 endonucleolytic activity
by
Kueckelmann, Sabrina
, Krüger, Marcus
, Britto-Borges, Thiago
, Boehm, Volker
, Gerbracht, Jennifer V.
, Dieterich, Christoph
, Gehring, Niels H.
, Kallabis, Sebastian
, Altmüller, Janine
in
13/106
/ 13/44
/ 38/1
/ 42/89
/ 45/41
/ 45/77
/ 49/109
/ 49/88
/ 49/90
/ 49/91
/ 631/337/1645
/ 631/337/1645/1769
/ 631/337/1645/2020
/ 82/29
/ 82/58
/ Carrier Proteins - chemistry
/ Carrier Proteins - genetics
/ Carrier Proteins - metabolism
/ Cell Line
/ Decay
/ Degradation
/ Female
/ Gene expression
/ Gene Knockout Techniques
/ Humanities and Social Sciences
/ Humans
/ mRNA turnover
/ multidisciplinary
/ Nonsense Mediated mRNA Decay - physiology
/ Nonsense-mediated mRNA decay
/ Phosphorylation
/ RNA Helicases - genetics
/ RNA Helicases - metabolism
/ Science
/ Science (multidisciplinary)
/ Substrates
/ Telomerase - metabolism
/ Trans-Activators - genetics
/ Trans-Activators - metabolism
/ Transcriptomes
/ Translation
/ Translation termination
2021
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SMG5-SMG7 authorize nonsense-mediated mRNA decay by enabling SMG6 endonucleolytic activity
by
Kueckelmann, Sabrina
, Krüger, Marcus
, Britto-Borges, Thiago
, Boehm, Volker
, Gerbracht, Jennifer V.
, Dieterich, Christoph
, Gehring, Niels H.
, Kallabis, Sebastian
, Altmüller, Janine
in
13/106
/ 13/44
/ 38/1
/ 42/89
/ 45/41
/ 45/77
/ 49/109
/ 49/88
/ 49/90
/ 49/91
/ 631/337/1645
/ 631/337/1645/1769
/ 631/337/1645/2020
/ 82/29
/ 82/58
/ Carrier Proteins - chemistry
/ Carrier Proteins - genetics
/ Carrier Proteins - metabolism
/ Cell Line
/ Decay
/ Degradation
/ Female
/ Gene expression
/ Gene Knockout Techniques
/ Humanities and Social Sciences
/ Humans
/ mRNA turnover
/ multidisciplinary
/ Nonsense Mediated mRNA Decay - physiology
/ Nonsense-mediated mRNA decay
/ Phosphorylation
/ RNA Helicases - genetics
/ RNA Helicases - metabolism
/ Science
/ Science (multidisciplinary)
/ Substrates
/ Telomerase - metabolism
/ Trans-Activators - genetics
/ Trans-Activators - metabolism
/ Transcriptomes
/ Translation
/ Translation termination
2021
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SMG5-SMG7 authorize nonsense-mediated mRNA decay by enabling SMG6 endonucleolytic activity
Journal Article
SMG5-SMG7 authorize nonsense-mediated mRNA decay by enabling SMG6 endonucleolytic activity
2021
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Overview
Eukaryotic gene expression is constantly controlled by the translation-coupled nonsense-mediated mRNA decay (NMD) pathway. Aberrant translation termination leads to NMD activation, resulting in phosphorylation of the central NMD factor UPF1 and robust clearance of NMD targets via two seemingly independent and redundant mRNA degradation branches. Here, we uncover that the loss of the first SMG5-SMG7-dependent pathway also inactivates the second SMG6-dependent branch, indicating an unexpected functional connection between the final NMD steps. Transcriptome-wide analyses of SMG5-SMG7-depleted cells confirm exhaustive NMD inhibition resulting in massive transcriptomic alterations. Intriguingly, we find that the functionally underestimated SMG5 can substitute the role of SMG7 and individually activate NMD. Furthermore, the presence of either SMG5 or SMG7 is sufficient to support SMG6-mediated endonucleolysis of NMD targets. Our data support an improved model for NMD execution that features two-factor authentication involving UPF1 phosphorylation and SMG5-SMG7 recruitment to access SMG6 activity.
Degradation of nonsense mediated mRNA decay (NMD) substrates is carried out by two seemingly independent pathways, SMG6-mediated endonucleolytic cleavage and/or SMG5-SMG7-induced accelerated deadenylation. Here the authors show that SMG5-SMG7 maintain NMD activity by permitting SMG6 activation.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ 13/44
/ 38/1
/ 42/89
/ 45/41
/ 45/77
/ 49/109
/ 49/88
/ 49/90
/ 49/91
/ 82/29
/ 82/58
/ Carrier Proteins - chemistry
/ Carrier Proteins - metabolism
/ Decay
/ Female
/ Humanities and Social Sciences
/ Humans
/ Nonsense Mediated mRNA Decay - physiology
/ Nonsense-mediated mRNA decay
/ Science
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