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E2F1 controls alternative splicing pattern of genes involved in apoptosis through upregulation of the splicing factor SC35

Authors :
S. De Seranno
Beatrice Eymin
Elizabeth Brambilla
Valérie Edmond
Sylvie Gazzeri
G. Merdzhanova
Laurent Corcos
Christian Brambilla
A. Van Den Broeck
Equipe 2 - Bases Moléculaires de la Progression des Cancers du Poumon, Inserm U823
Institut d'oncologie/développement Albert Bonniot de Grenoble (INSERM U823)
Université Joseph Fourier - Grenoble 1 (UJF)-CHU Grenoble-EFS-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Joseph Fourier - Grenoble 1 (UJF)-CHU Grenoble-EFS-Institut National de la Santé et de la Recherche Médicale (INSERM)
Eq 2 - Bases Moléculaires de la Progression des Cancers du Poumon [La Tronche] (Inserm U823/UJF/Institut Albert Bonniot)
Institut National de la Santé et de la Recherche Médicale (INSERM)-EFS-CHU Grenoble-Université Joseph Fourier - Grenoble 1 (UJF)-Institut National de la Santé et de la Recherche Médicale (INSERM)-EFS-CHU Grenoble-Université Joseph Fourier - Grenoble 1 (UJF)
Génétique moléculaire et génétique épidémiologique
Université de Brest (UBO)-Institut National de la Santé et de la Recherche Médicale (INSERM)
This work was supported by grants from the region Rhône Alpes (Thématique Prioritaire Cancer and Canceropole 2003: Oncocell, Epimed and INACancer), by the Ligue contre le Cancer (Comité de Savoie), by the Ligue Nationale contre le Cancer (Equipe Labellisée), by INCa (PNES, Programme National d’Excellence Spécialisé 2005) and by the Conseil Scientifique National d’AGIR à dom. Arnaud van den Broeck was supported by a fellowship from the French Research Ministery. GalinaMerdzhanova was supported by fellowships from the French Research Ministery and the Fondation pour la Recherche Medicale (FRM). Valerie Edmond was supported by a grant from the Conseil Scientifique National d’AGIR à dom. Sandrine De Seranno was supported by a grant from INCa.
Brambilla, Christian
Université Joseph Fourier - Grenoble 1 (UJF)-CHU Grenoble-EFS-Institut National de la Santé et de la Recherche Médicale (INSERM)
INSERM U823, équipe 2 (Bases Moléculaires de la Progression des Cancers du Poumon)
Eymin, Beatrice
Département d'anatomie et cythologie pathologique
CHU Grenoble-Hôpital Michallon
Institut National de la Santé et de la Recherche Médicale (INSERM)-EFS-CHU Grenoble-Université Joseph Fourier - Grenoble 1 (UJF)
Source :
Cell Death and Differentiation, Cell Death and Differentiation, Nature Publishing Group, 2008, 15 (12), pp.1815-1823, Cell Death and Differentiation, Nature Publishing Group, 2008, 15 (12), pp.1815-23. ⟨10.1038/cdd.2008.135⟩, Cell Death and Differentiation, Nature Publishing Group, 2008, 15 (12), pp.1815-1823. ⟨10.1038/cdd.2008.135⟩, Cell Death and Differentiation, 2008, 15 (12), pp.1815-23. ⟨10.1038/cdd.2008.135⟩
Publication Year :
2008
Publisher :
HAL CCSD, 2008.

Abstract

Comment in Many pathways to apoptosis: E2F1 regulates splicing of apoptotic genes. [Cell Death Differ. 2008]; International audience; The transcription factor E2F1 has a key function during S phase progression and apoptosis. It has been well-demonstrated that the apoptotic function of E2F1 involves its ability to transactivate pro-apoptotic target genes. Alternative splicing of pre-mRNAs also has an important function in the regulation of apoptosis. In this study, we identify the splicing factor SC35, a member of the Ser-Rich Arg (SR) proteins family, as a new transcriptional target of E2F1. We demonstrate that E2F1 requires SC35 to switch the alternative splicing profile of various apoptotic genes such as c-flip, caspases-8 and -9 and Bcl-x, towards the expression of pro-apoptotic splice variants. Finally, we provide evidence that E2F1 upregulates SC35 in response to DNA-damaging agents and show that SC35 is required for apoptosis in response to these drugs. Taken together, these results demonstrate that E2F1 controls pre-mRNA processing events to induce apoptosis and identify the SC35 SR protein as a key direct E2F1-target in this setting.

Subjects

Subjects :
MESH: CASP8 and FADD-Like Apoptosis Regulating Protein
SC35
Transcription, Genetic
[SDV]Life Sciences [q-bio]
CASP8 and FADD-Like Apoptosis Regulating Protein
Apoptosis
MESH: Caspase 9
MESH: Caspase 8
Mice
0302 clinical medicine
MESH: Up-Regulation
RNA Precursors
E2F1
MESH: Animals
0303 health sciences
Caspase 8
Serine-Arginine Splicing Factors
MESH: Alternative Splicing
Nuclear Proteins
MESH: Gene Expression Regulation
Caspase 9
Up-Regulation
[SDV] Life Sciences [q-bio]
MESH: E2F1 Transcription Factor
Ribonucleoproteins
030220 oncology & carcinogenesis
biological phenomena, cell phenomena, and immunity
Protein Binding
endocrine system
MESH: Cell Line, Tumor
bcl-X Protein
MESH: RNA Precursors
[SDV.BC]Life Sciences [q-bio]/Cellular Biology
Biology
MESH: bcl-X Protein
03 medical and health sciences
SR protein
Downregulation and upregulation
Cell Line, Tumor
[SDV.BBM] Life Sciences [q-bio]/Biochemistry, Molecular Biology
MESH: Protein Binding
Animals
Humans
splice
[SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology
Molecular Biology
Gene
[SDV.BC] Life Sciences [q-bio]/Cellular Biology
MESH: Mice
Cyclophosphamide
030304 developmental biology
MESH: DNA Damage
MESH: Humans
MESH: Transcription, Genetic
MESH: Apoptosis
Alternative splicing
MESH: Cyclophosphamide
Cell Biology
MESH: Ribonucleoproteins
Alternative Splicing
Gene Expression Regulation
Cancer research
Many pathways to apoptosis: E2F1 regulates splicing of apoptotic genes
MESH: Nuclear Proteins
Function (biology)
SR proteins
E2F1 Transcription Factor
DNA Damage

Details

Language :
English
ISSN :
13509047 and 14765403
Database :
OpenAIRE
Journal :
Cell Death and Differentiation, Cell Death and Differentiation, Nature Publishing Group, 2008, 15 (12), pp.1815-1823, Cell Death and Differentiation, Nature Publishing Group, 2008, 15 (12), pp.1815-23. ⟨10.1038/cdd.2008.135⟩, Cell Death and Differentiation, Nature Publishing Group, 2008, 15 (12), pp.1815-1823. ⟨10.1038/cdd.2008.135⟩, Cell Death and Differentiation, 2008, 15 (12), pp.1815-23. ⟨10.1038/cdd.2008.135⟩
Accession number :
edsair.doi.dedup.....e48cb328657aab09b3766e7e1d46e311
Full Text :
https://doi.org/10.1038/cdd.2008.135⟩