Mitochondrial PARP1 regulates NAD+-dependent poly ADP-ribosylation of mitochondrial nucleoids
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PARPs play fundamental roles in multiple DNA damage recognition and repair pathways. Persistent nuclear PARP activation causes cellular NAD(+) depletion and exacerbates cellular aging. However, very little is known about mitochondrial PARP (mtPARP) and poly ADP-ribosylation (PARylation). The existence of mtPARP is controversial, and the biological roles of mtPARP-induced mitochondrial PARylation are unclear. Here, we demonstrate the presence of PARP1 and PARylation in purified mitochondria. The addition of the PARP1 substrate NAD(+) to isolated mitochondria induced PARylation, which was suppressed by treatment with the inhibitor olaparib. Mitochondrial PARylation was also evaluated by enzymatic labeling of terminal ADP-ribose (ELTA). To further confirm the presence of mtPARP1, we evaluated mitochondrial nucleoid PARylation by ADP ribose-chromatin affinity purification (ADPr-ChAP) and PARP1 chromatin immunoprecipitation (ChIP). We observed that NAD(+) stimulated PARylation and TFAM occupancy on the mtDNA regulatory region D-loop, inducing mtDNA transcription. These findings suggest that PARP1 is integrally involved in mitochondrial PARylation and that NAD(+)-dependent mtPARP1 activity contributes to mtDNA transcriptional regulation.
Original language | English |
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Journal | Experimental and Molecular Medicine |
Volume | 54 |
Pages (from-to) | 2135–2147 |
Number of pages | 13 |
ISSN | 1226-3613 |
DOIs | |
Publication status | Published - 2022 |
- TRANSCRIPTION FACTOR-A, DNA-DAMAGE, GENOME-WIDE, CELL-DEATH, HUMAN TFAM, NAD(+), BINDING, IDENTIFICATION, ACTIVATION, PHOSPHORYLATION
Research areas
ID: 330738874