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Acute kidney injury induces somatic mitochondrial DNA mutations that impair energy metabolism and the resilience of kidney tissue to following injuries.
Independently of its nuclear DNA-binding activity, the transcription factor PXR has a cytoplasmic function: it binds to mRNAs and promotes their stability.
Paul et al. demonstrate that entry into the cell cycle from quiescence involves a transient, partial inactivation of the APC/C ubiquitin ligase, which halts the degradation of glycolysis enzymes and ensures sufficient ATP production for cell division.
H3.14, a histone variant of unknown role, has a dual transcriptional function in the abiotic stress response in plants: activation of stress response genes and inhibition of growth genes.
Reactive oxygen species (ROS) induce the multimerization of Aux/IAA transcriptional repressors, and this ROS–auxin signalling connection functions as a rapid adaptive response to water deficit, inducing a temporary stop in root growth.
Adequate levels of nucleotides are essential to ensure genetic stability of proliferating cells. A study finds gap-junction-mediated transport of nucleotides in specific tissues of Drosophila.
Repair of DNA double-strand breaks requires chromatin opening; however, the mechanisms involved were unclear. This work shows that sequential histone deamidation and acetylation modifications induce chromatin decompaction by reducing positive charge at the DNA–nucleosome interface.
The authors of a new study characterize blebbisomes, large extracellular vesicles that contain functional mitochondria and other organelles and have significant roles in inter-cellular communication and the tumour microenvironment.
This study shows that zotatifin selectively inhibits the translation of prostate cancer oncogene transcripts by restructuring their 5′ untranslated regions. In mice, this agent reversed treatment resistance, which led to improved survival.
Subunits of mitochondrial and cytosolic ribosomes need to be targeted to their correction cellular location. A study identified a mitochondrial avoidance segment in a eukaryotic cytosolic ribosome subunit that prevents its mislocalization to mitochondria.