Catia Andreassi
University College London
11 Papers
35 Citations
Catia Andreassi is an academic researcher from University College London. The author has contributed to research in topics: Messenger RNA & Untranslated region. The author has an hindex of 9, co-authored 11 publications. Previous affiliations of Catia Andreassi include Medical Research Council.
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Papers
Cytoplasmic cleavage of IMPA1 3′ UTR is necessary for maintaining axon integrity
Catia Andreassi,Raphaëlle Luisier,Hamish Crerar,Marousa Darsinou,Sasja Blokzijl-Franke,Tchern Lenn,Nicholas M. Luscombe,Giovanni Cuda,Marco Gaspari,Adolfo Saiardi,Antonella Riccio +10 more
TL;DR: In this paper, the 3' untranslated regions (3' UTRs) of many transcripts undergo cleavage, generating isoforms that express the coding sequence with a short 3'UTR and stable 3" UTR-derived fragments of unknown function.
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RETRACTED: Mitochondrial Dynamics, Biogenesis, and Function Are Coordinated with the Cell Cycle by APC/CCDH1
TL;DR: In this article, it was shown that cell proliferation is associated with an increase in both glycolysis and respiration, in conjunction with mitochondrial fusion and biogenesis, and that changes in mitochondrial morphology and mass are due to accumulation of OPA1, MFN1, and TFAM, silencing any of which hinders cell proliferation.
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Proteomic analysis of S-nitrosylated nuclear proteins in rat cortical neurons
TL;DR: The findings characterize S-nitrosylated nuclear proteins in neurons and identify S- Nitrosylation motifs that may be shared with other targets of NO signaling, which provide a resource from which to explore the role of S-Nitrosylations in neuronal development.
3’UTR cleavage of transcripts localized in axons of sympathetic neurons
Catia Andreassi,Raphaëlle Luisier,Hamish Crerar,Blokzijl-Franke S,Nicholas M. Luscombe,Nicholas M. Luscombe,Giovanni Cuda,Marco Gaspari,Antonella Riccio +8 more
TL;DR: Analysis of the Inositol monophosphatase 1 (Impa1) mRNA revealed that a stem loop structure within the 3’UTR is necessary for Ago2 cleavage, which provides an alternative mechanism that simultaneously regulates local protein synthesis and generates a new class of 3'UTR RNAs with yet unknown functions.
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Corrigendum: An NGF-responsive element targets myo-inositol monophosphatase-1 mRNA to sympathetic neuron axons
Catia Andreassi,Carola Zimmermann,Richard Mitter,Salvatore Fusco,Serena Devita,Adolfo Saiardi,Antonella Riccio +6 more
TL;DR: It is shown that an NGF-responsive element targets myo-inositol monophosphatase-1 mRNA to sympathetic neuron axons in a manner similar to that of NGFs responding to EMTs.