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The Caenorhabditis elegans (C. elegans) germline is used to study several biologically important processes including stem cell development, apoptosis, and chromosome dynamics. While the germline is an excellent model, the analysis is often two dimensional due to the time and labor required for three-dimensional analysis. Major readouts in such studies are the number/position of nuclei and protein distribution within the germline. Here, we present a method to perform automated analysis of the germline using confocal microscopy and computational approaches to determine the number and position of nuclei in each region of the germline. Our method also analyzes germline protein distribution that enables the three-dimensional examination of protein expression in different genetic backgrounds. Further, our study shows variations in cytoskeletal architecture in distinct regions of the germline that may accommodate specific spatial developmental requirements. Finally, our method enables automated counting of the sperm in the spermatheca of each germline. Taken together, our method enables rapid and reproducible phenotypic analysis of the C. elegans germline.
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http://dx.doi.org/10.3791/57702 | DOI Listing |
PNAS Nexus
August 2025
Department of Developmental Biology, Washington University School of Medicine, 660 S. Euclid Ave, St. Louis, MO 63108, USA.
Adult stem cells maintain and rejuvenate a wide range of tissues, and the progressive, age-related decline of adult stem cells is a hallmark of aging. We propose that the germline is an experimentally tractable model of adult stem cell aging and that stem cell exhaustion is a cause of reproductive senescence. Because these are the only stem cells in adult worms, this system provides a unique opportunity to exploit the power of to address stem cell exhaustion during aging.
View Article and Find Full Text PDFSemin Cell Dev Biol
August 2025
Institute for Genetic Medicine, Hokkaido University, Japan. Electronic address:
Germ cells are organized into a syncytial architecture, wherein individual cells remain connected via intercellular bridges. Within this structural framework, known as germline cysts, a subset of germ cells enlarges and develops into oocytes, while others shrink and are eliminated through cell death. Recent studies with Caenorhabditis elegans have revealed that both apoptosis-mediated germ cell death and enlargement of surviving germ cells are regulated by mechanical forces.
View Article and Find Full Text PDFMicroPubl Biol
July 2025
Veterinary Biomedical Sciences, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
The CSR-1 encodes an essential Argonaute protein that binds to 22 nucleotide small guide RNA to regulate germline gene expression. Recent characterization of the two CSR-1 isoforms (a and b) have demonstrated tissue-specific expression and functions. Here, we found that loss of function to the isoform has minimal effect on lifespan while a mutant with deletion to both and isoforms shows a significant decrease in lifespan.
View Article and Find Full Text PDFGenetics
August 2025
Kenyon College, Gambier, OH 43033, USA.
Fatty acids function not only as signaling molecules and for energy storage, but also as essential cofactors for mitochondrial enzymes. These fatty acid cofactors are produced by the mitochondrial fatty acid synthesis pathway (mtFAS), the terminal enzyme of which is mitochondrial trans-2-enoyl-coA reductase (MECR). Dysfunction of MECR prevents the synthesis of fatty acids and is the monogenic cause of MEPAN syndrome, a rare mitochondrial disease characterized by dystonia, basal ganglia degeneration, and optic nerve atrophy.
View Article and Find Full Text PDFbioRxiv
July 2025
Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY, USA.
The nuclear hormone receptor NHR-49, a homolog of mammalian PPARα and HNF4α, is a key transcriptional regulator of nutrition sensing and fatty acid metabolism in . Here we uncovered a new function of NHR-49 in reproduction - controlling oocyte activation and ovulation. Loss of NHR-49 causes inappropriate oocyte activation and laying of unfertilized oocytes in the absence of sperm, resulting in rapid loss of yolk and stored fat, and drastically shortening of lifespan.
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