Cellular bases of the RNA metabolism dysfunction in motor neurons of a murine model of spinal muscular atrophy: Role of Cajal bodies and the nucleolus

Author

Tapia, Olga

Narcís, Oriol J.

Riancho, Javier

Tarabal Mostazo, Olga

Piedrafita Llorens, Lídia

Calderó i Pardo, Jordi

Berciano, Maria T.

Lafarga, Miguel

Publication date

2020-01-14T13:01:54Z

2020-01-14T13:01:54Z

2017



Abstract

Spinal muscular atrophy (SMA) is caused by a homozygous deletion or mutation in the survival motor neuron 1 (SMN1) gene that leads to reduced levels of SMN protein resulting in degeneration of motor neurons (MNs). The best known functions of SMN is the biogenesis of spliceosomal snRNPs. Linked to this function, Cajal bodies (CBs) are involved in the assembly of spliceosomal (snRNPs) and nucleolar (snoRNPs) ribonucleoproteins required for pre-mRNA and pre-rRNA processing. Recent studies support that the interaction between CBs and nucleoli, which are especially prominent in neurons, is essential for the nucleolar rRNA homeostasis. We use the SMN∆7 murine model of type I SMA to investigate the cellular basis of the dysfunction of RNA metabolism in MNs. SMN deficiency in postnatal MNs produces a depletion of functional CBs and relocalization of coilin, which is a scaffold protein of CBs, in snRNP-free perinucleolar caps or within the nucleolus. Disruption of CBs is the earliest nuclear sign of MN degeneration. We demonstrate that depletion of CBs, with loss of CB-nucleolus interactions, induces a progressive nucleolar dysfunction in ribosome biogenesis. It includes reorganization and loss of nucleolar transcription units, segregation of dense fibrillar and granular components, retention of SUMO-conjugated proteins in intranucleolar bodies and a reactive, compensatory, up-regulation of mature 18S rRNA and genes encoding key nucleolar proteins, such as upstream binding factor, fibrillarin, nucleolin and nucleophosmin. We propose that CB depletion and nucleolar alterations are essential components of the dysfunction of RNA metabolism in SMA.


This work was supported by the following grants: “Dirección General de Investigación” of Spain (BFU2014-54754-P), “Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED; CB06/05/0037)” from Spain, and “Ministerio de Economía y Competitividad” of Spain cofinanced by FEDER (SAF2015-70801-R). Dr. Tapia is a recipient of a grant from SMA Europe cofinanced by FundAME (Spain) and "Instituto de Investigación Valdecilla" (IDIVAL; Next-Val) from Santander, Spain.

Document Type

Article
Submitted version

Language

English

Subjects and keywords

Spinal muscular atrophy; Motor neurons; Cajal bodies; Nucleolar dysfunction; Protein synthesis machinery

Publisher

Elsevier

Related items

info:eu-repo/grantAgreement/MINECO//BFU2014-54754-P/ES/REGULACION POR ACETILACION DEL FACTOR DE SUPERVIVENCIA DE LAS NEURONAS MOTORAS: SU IMPORTANCIA EN LA BIOGENESIS DE SNRNPS Y EN EL ENSAMBLAJE DE CUERPOS NUCLEARES DE CAJAL/

info:eu-repo/grantAgreement/MINECO//SAF2015-70801-R/ES/LOS AFERENTES SINAPTICOS DE TIPO C EN LAS MOTONEURONAS: IMPLICACIONES EN LA FISIOPATOLOGIA Y TERAPIA DE LA ESCLEROSIS LATERAL AMIOTROFICA Y DE LA ATROFIA MUSCULAR ESPINAL/

Reproducció del document publicat a https://doi.org/10.1016/j.nbd.2017.08.004

Neurobiology of Disease, 2017, vol. 108, p. 83-99

Rights

(c) Elsevier, 2017

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