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Biology subjects

MARI, P.-O.

Publications and source records attributed to MARI, P.-O..

3 recordsLinked to original sources

Stress-Induced Nuclear Import Governs Transcription Recovery after DNA Damage

Genotoxic stress inhibits transcription, generating RNA-DNA hybrid intermediates that promote toxic transcription-replication conflicts (TRCs). Here, we show that genotoxic stress triggers transient Importin-/{beta}1-dependent nuclear import of the mitochondrial exonuclease EXD2 to resolve these conflicts and maintain genome stability. Mechanistically, once imported into the nucleus, EXD2 is recruited to elongation-arrested RNA polymerase II (RNAPII) associated with RNA-DNA hybrids, and its exonuclease activity limits their accumulation, thereby suppressing TRCs. Mutation of a putative EXD2 nuclear localization signal phenocopies disruption of nuclear import, whereas forced nuclear targeting of EXD2 bypasses it. However, sustained nuclear localization of EXD2 leads to mitotic defects, underscoring the importance of its tight spatial regulation. Consistent with a direct role for EXD2 in RNA-DNA hybrid resolution, overexpression of the ribonuclease RNaseH1 compensates for its depletion following DNA damage. Together, our findings introduce the concept of a trafficking-dependent checkpoint that transiently licenses EXD2 nuclease activity in the nucleus in response to genotoxic stress to resolve RNA-DNA hybrid intermediates at stalled RNAPII complexes TeaserStress-triggered nuclear import of EXD2 resolves harmful RNA-DNA hybrids to protect genome stability after DNA damage.

molecular biology↗

Decline of DNA damage response along with myogenic differentiation

DNA integrity is incessantly confronted to endogenous and exogenous agents inducing DNA lesions, which are harmful for cellular homeostasis. Luckily all organisms are equipped with a network of DNA damage response (DDR) mechanisms that will repair DNA lesions and restore the proper cellular activities. Despite DNA repair mechanisms have been revealed in vitro and in replicating cells, still little is known on how DNA lesions are repaired and consequently how cellular homeostasis is maintained in post-mitotic cells. Muscle fibers are highly specialised post-mitotic cells organized in syncytia and, they are vulnerable to age-related degeneration and atrophy following radiotherapy treatment. We have here studied in detail the DNA repair capacity of muscle fibers nuclei and compared it with the one measured in proliferative myoblasts. We focused on the DNA repair mechanisms that correct ionizing radiation (IR)-induced lesions, namely the base excision repair (BER), the non-homologous end joining (NHEJ) and the homologous recombination (HR). We found that in the most differentiated myogenic cells, myotubes, all of these DNA repair mechanisms present weakened kinetics of recruitment of DNA repair proteins to IR-damaged DNA. For BER and HR, this decline can be linked to reduced steady state levels of key proteins involved in these processes, probably since nuclei within muscle fibers no longer replicate their DNA. SIGNIFICANCEAlthough skeletal muscle tissue has been considered as resistant to injury caused by ionizing radiations (IR), in the long term, muscle surrounding irradiated regions of the body following radiotherapy has physiological consequences such as atrophy and muscle wasting. To prevent and/or counteract the harmful effects of IR in muscle fibers, it is essential, to evaluate the DNA repair capacity of post-mitotic myonuclei. By using fluorescently tagged DNA repair proteins expressed in myoblasts and myotubes, we were able to assess the kinetics of the DNA damage response in these cells and determine that DNA damage response is weakened during the process of myofibrillogenesis.

cell biology↗

CSB-dependent CDK9 degradation and RNA Polymerase II phosphorylation during Transcription Coupled Repair

AUTHOR SUMMARYDNA lesions block cellular processes such as transcription, inducing apoptosis, tissue failures and premature ageing. To counteract the deleterious effects of DNA damage, cells are equipped with various DNA repair pathways. Transcription Coupled Repair specifically removes helix-distorting DNA adducts in a coordinated multi-step process. This process has been extensively studied, however once the repair reaction is accomplished, little is known about how transcription restarts. In this study, we show that, after UV irradiation, the CDK9/CyclinT1 kinase unit is specifically released from the HEXIM1 complex and that this released fraction is degraded in the absence of CSB. We determine that UV-irradiation induces a specific Ser2 phosphorylation of the RNA polymerase II and that this phosphorylation is CSB dependent. Surprisingly CDK9 is not responsible for this phosphorylation but instead plays a non-enzymatic role in transcription restart after DNA repair.

cell biology↗