Post-transcriptional regulation by the exosome complex is required for cell survival and forebrain development via repression of P53 signaling

Autor: Linh Pham, Godwin Sokpor, Uttiya Basu, Orr Shomroni, Yuanbin Xie, Tea Berulava, Jochen F. Staiger, Joachim Rosenbusch, Tran Tuoc, Huu Phuc Nguyen, Pauline Antonie Ulmke, Andre Fischer
Rok vydání: 2021
Předmět:
Exosome complex
RNA Stability
genetics [Tumor Suppressor Protein p53]
Apoptosis
Exosomes
RNA decay
Mice
0302 clinical medicine
pathology [Prosencephalon]
metabolism [Exosomes]
Gene expression
growth & development [Prosencephalon]
PUMA protein
mouse

0303 health sciences
Exosome Multienzyme Ribonuclease Complex
Gene Expression Regulation
Developmental

Stem Cells and Regeneration
Cell biology
metabolism [RNA]
Signal Transduction
Cell Survival
physiology [Cell Survival]
Mice
Transgenic

Biology
genetics [Signal Transduction]
genetics [Exosomes]
03 medical and health sciences
Prosencephalon
ddc:570
Animals
Humans
Molecular Biology
Gene
Post-transcriptional regulation
030304 developmental biology
genetics [Exosome Multienzyme Ribonuclease Complex]
Cortical development
Tumor Suppressor Proteins
Computational Biology
RNA
Mice
Inbred C57BL

metabolism [Exosome Multienzyme Ribonuclease Complex]
genetics [Exoribonucleases]
P53 pathway
Aen and Bbc3
Exosc10
Exoribonucleases
Forebrain
metabolism [Tumor Suppressor Protein p53]
Tumor Suppressor Protein p53
Apoptosis Regulatory Proteins
030217 neurology & neurosurgery
Developmental Biology
Zdroj: Development 148(3), dev188276 (2021). doi:10.1242/dev.188276
Development
ISSN: 1477-9129
0950-1991
Popis: Fine-tuned gene expression is crucial for neurodevelopment. The gene expression program is tightly controlled at different levels, including RNA decay. N6-methyladenosine (m6A) methylation-mediated degradation of RNA is essential for brain development. However, m6A methylation impacts not only RNA stability, but also other RNA metabolism processes. How RNA decay contributes to brain development is largely unknown. Here, we show that Exosc10, a RNA exonuclease subunit of the RNA exosome complex, is indispensable for forebrain development. We report that cortical cells undergo overt apoptosis, culminating in cortical agenesis upon conditional deletion of Exosc10 in mouse cortex. Mechanistically, Exosc10 directly binds and degrades transcripts of the P53 signaling-related genes, such as Aen and Bbc3. Overall, our findings suggest a crucial role for Exosc10 in suppressing the P53 pathway, in which the rapid turnover of the apoptosis effectors Aen and Bbc3 mRNAs is essential for cell survival and normal cortical histogenesis.
Databáze: OpenAIRE