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Abnormal nuclear morphology is suggested to be a hallmark of aging and one such abnormality is nuclear blebbing. However, little is known about whether and how nuclear blebbing participates in animal aging, and what regulates it. In this study, we show that the frequency of nuclear blebbing in the hypodermis increases during aging in wild-type C. elegans. These nuclear blebs are enveloped by the nuclear lamina, the inner and the outer nuclear membrane, and 42% of them contain chromatin. Although nuclear blebbing could lead to DNA loss if chromatin-containing blebs detach and fuse with lysosomes, we find by time-lapse imaging that nuclear blebs rarely detach, and the estimated lifetime of a nuclear bleb is 772 h or 32 days. The amount of DNA lost through nuclear blebbing is estimated to be about 0.1% of the total DNA loss by adult Day 11. Furthermore, the frequency of nuclear blebbing does not correlate with the rate of aging in C. elegans. Old age does not necessarily induce nuclear blebbing, neither does starvation, heat stress, or oxidative stress. Intriguingly, we find that proliferation of germ cells promotes nuclear blebbing.
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http://dx.doi.org/10.1093/g3journal/jkad029 | DOI Listing |
Int J Biol Macromol
September 2025
Liaoning Key Laboratory of Marine Animal Immunology and Disease Control, Dalian Ocean University, Dalian 116023, China; Dalian Key Laboratory of Aquatic Animal Disease Prevention and Control, Dalian Ocean University, Dalian 116023, China.
Vitellogenin-binding protein (VBP), a PAR bZIP transcription factor with homology to the cell death specification gene 2 (Ces-2) in Caenorhabditis elegans, is recognized for its role in cell apoptosis. In the present study, a VBP homolog CgVBP (also annotated as CgCes-2) containing a typical bZIP domain was identified from the Pacific oyster Crassostrea gigas. The transcript of CgVBP was predominantly expressed in haemocytes, specifically enriched within the granulocyte subpopulation.
View Article and Find Full Text PDFNucleus
December 2025
Biology Department, University of Massachusetts Amherst, Amherst, MA, USA.
Aberrant nuclear morphology is a hallmark of human disease and causes nuclear dysfunction. Perturbed nuclear mechanics via reduced heterochromatin weakens the nucleus resulting in nuclear blebbing and rupture. While the role of heterochromatin is known, the separate roles of constitutive heterochromatin methylation states remains elusive.
View Article and Find Full Text PDFMol Biol Cell
September 2025
Cardiovascular Research Institute, University of California, San Francisco, CA 94158.
The nuclear lamins are extremely long-lived proteins in most cell types. As a consequence, lamin function cannot be effectively dissected with temporal precision using standard knockdown approaches. Here, we apply the auxin-inducible degron system to rapidly deplete each lamin isoform within one cell cycle and reveal the immediate impacts of lamin loss on the nucleus.
View Article and Find Full Text PDFSci Total Environ
September 2025
Department of Zoology, Visva-Bharati, Santiniketan 731235, West Bengal, India. Electronic address:
Lead (Pb) and chromium (Cr) are among the most extensively studied heavy metals due to their widespread presence and hazardous impacts on aquatic life. Pb and Cr exhibit strong genotoxic potential in aquatic environments by inducing DNA damage through overproduction of reactive oxygen species, resulting in oxidative stress, DNA strand breaks, and chromosomal aberrations. Disruption of nuclear integrity, impaired DNA repair pathways, and apoptosis activation further exacerbate their toxicity.
View Article and Find Full Text PDFJ Cell Biol
August 2025
Department of Molecular, Cell and Cancer Biology, University of Massachusetts Chan Medical School, Worcester, MA, USA.
Lipid synthesis must be precisely regulated to support membrane growth and organelle biogenesis during cell division, yet little is known about how this process is coordinated with other cell cycle events. Here, we show that de novo synthesis of sphingolipids during the S and G2 phases of the cell cycle is essential to increasing nuclear membranes. Indeed, the products of serine palmitoyltransferase (SPT), long-chain bases, localize to the nucleus and are integral components of nuclear membranes in yeast and human cells.
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