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Malagise, E. M.

Publications and source records attributed to Malagise, E. M..

2 recordsLinked to original sources

Nup98 regulates the G1/S transition

Nuclear pore complexes (NPCs) are embedded throughout the nuclear envelope of all eukaryotic cells and are composed of 30 unique proteins called nucleoporins (Nups). While Nups primarily function at NPCs, multiple Nups function in the nucleoplasm independent of the NPC. We previously found that Nup98-96 is necessary for entry into S phase in Drosophila cells, however, the mechanism is unknown. Here, we demonstrate that Nup98-96 is one of only a subset of Nup genes that can promote entry into S phase. We identify that transcripts dependent on Nup98-96 in Drosophila cells are enriched in cell cycle processes and that many of these transcripts are also dependent on the cell cycle regulator, E2f1. Importantly, we find that entry into S phase can be rescued by co-depleting the CycE/CDK2 inhibitor, dacapo, in Nup98-96-depleted cells. Furthermore, Nup96-98 promotes S phase entry across multiple cell and tissue types and cell cycle contexts. Critically, overexpression of Nup98 has a dominant-negative effect on entry into S phase in larval salivary glands, suggesting that Nup98, not Nup96, promotes entry into S phase. Our work identifies Nup98 as a key regulator of the G1/S transition in metazoans.

molecular biology↗

A role for N6-methyldeoxyadenosine in C. elegans mitochondrial genome regulation

Epigenetic modifications provide powerful means for transmitting information from parent to progeny. As a maternally inherited genome that encodes essential components of the electron transport chain, the mitochondrial genome (mtDNA) is ideally positioned to serve as a conduit for the transgenerational transmission of metabolic information. Here, we provide evidence that mtDNA of C. elegans contains the epigenetic mark N6-methyldeoxyadenosine (6mA). Bioinformatic analysis of SMRT sequencing data and methylated DNA IP sequencing data reveal that C. elegans mtDNA is methylated at high levels in a site-specific manner. We further confirmed that mtDNA contains 6mA by leveraging highly specific anti-6mA antibodies. Additionally, we find that mtDNA methylation is dynamically regulated in response to antimycin, a mitochondrial stressor. Further, 6mA is increased in nmad-1 mutants and is accompanied by a significant decrease in mtDNA copy number. Our discovery paves the way for future studies to investigate the regulation and inheritance of mitochondrial epigenetics.

genetics↗