
Melody Di Bona
Articles
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Sep 4, 2024 |
nature.com | Manisha Jalan |Aman Sharma |Xin Pei |Yingjie Zhu |Melody Di Bona |Nadeem Riaz
AbstractCollisions of the transcription and replication machineries on the same DNA strand can pose a significant threat to genomic stability. These collisions occur in part due to the formation of RNA-DNA hybrids termed R-loops, in which a newly transcribed RNA molecule hybridizes with the DNA template strand. This study investigated the role of RAD52, a known DNA repair factor, in preventing collisions by directing R-loop formation and resolution.
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Aug 29, 2024 |
science.org | Sara Martin |Melody Di Bona |Michael P. Fatt |Richard J. Conk
AbstractThe selective conversion of polyethylene, polypropylene, and mixtures of the two polymers to form products with high volume demand is urgently needed because current methods suffer from low selectivity, produce large quantities of greenhouse gases, or rely on expensive, single-use catalysts.
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Aug 29, 2024 |
science.org | Sara Martin |Melody Di Bona |Michael P. Fatt |Konstantina Agiadi
Editor’s summaryThe disconnection of the Mediterranean Sea from the Atlantic in the late Miocene 5 to 6 million years ago led to the sea’s nearly complete desiccation, leaving only a few hypersaline lakes similar to the present-day Dead Sea. There is a mass of data from both the geological and modern biological records that tracks this crisis and its legacy. Agiadi et al.
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Aug 29, 2024 |
science.org | Sara Martin |Melody Di Bona |Michael P. Fatt |Jonathan Benn
Editor’s summaryProtein aggregates are the major cause of neuronal death in many neurodegenerative disorders. However, in the nonaggregate form, the same proteins play important physiological roles. Benn et al. developed a strategy to target intracellular protein aggregates while sparing the monomeric form. Exploiting the clustering-dependent activation of TRIM21, the authors generated degraders combining the RING domain of TRIM21 with a target-specific nanobody.
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Aug 29, 2024 |
science.org | Sara Martin |Melody Di Bona |Michael P. Fatt |Yuanyuan Wang
AbstractDespite continuous expansion of the RNA-binding protein (RBP) world, there is a lack of systematic understanding of RBPs in mammalian testis, which harbors one of the most complex tissue transcriptomes. We adapted RNA interactome capture to mouse male germ cells, building an RBP atlas characterized by multiple layers of dynamics along spermatogenesis.
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