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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Inhibition of mRNA deadenylation by the nuclear cap binding complex (CBC)

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Συγγραφέας
Balatsos, N. A. A.; Nilsson, P.; Mazza, C.; Cusack, S.; Virtanen, A.
Ημερομηνία
2006
DOI
10.1074/jbc.M508590200
Λέξη-κλειδί
Binding energy
Biomedical engineering
Data acquisition
Enzyme inhibition
Cap binding complex (CBC)
Deadenylation
Poly(A)-specific ribonuclease (PARN)
RNA
initiation factor 4E
messenger RNA
nuclear cap binding protein
polyadenylate specific ribonuclease
protein subunit
ribonuclease
unclassified drug
capped RNA
exoribonuclease
poly(A)-specific ribonuclease
adenylation
article
enzyme activity
in vitro study
priority journal
protein function
protein protein interaction
RNA degradation
RNA translation
translation regulation
drug antagonism
human
metabolism
physiology
polyadenylation
Exoribonucleases
Humans
Nuclear Cap-Binding Protein Complex
Protein Subunits
RNA Caps
RNA, Messenger
Εμφάνιση Μεταδεδομένων
Επιτομή
Poly(A)-specific ribonuclease (PARN) is a cap-interacting and poly(A)-specific 3′-exoribonuclease. Here we have investigated how the cap binding complex (CBC) affects human PARN activity. We showed that CBC, via its 80-kDa subunit (CBP80), inhibited PARN, suggesting that CBC can regulate mRNA deadenylation. The CBC-mediated inhibition of PARN was cap-independent, and in keeping with this, the CBP80 subunit alone inhibited PARN. Our data suggested a new function for CBC, identified CBC as a potential regulator of PARN, and emphasized the importance of communication between the two extreme ends of the mRNA as a key strategy to regulate mRNA degradation. Based on our data, we have proposed a model for CBC-mediated regulation of PARN, which relies on an interaction between CBP80 and PARN. Association of CBC with PARN might have importance in the regulated recruitment of PARN to the nonsense-mediated decay pathway during the pioneer round of translation. © 2006 by The American Society for Biochemistry and Molecular Biology, Inc.
URI
http://hdl.handle.net/11615/26128
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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