Yeast cells contain a heterogeneous population of peroxisomes that segregate asymmetrically during cell division.
Sanjeev K ChoudhryRinse de BoerIda J van der KleiPublished in: Journal of cell science (2018)
Here, we used fluorescence microscopy and a peroxisome-targeted tandem fluorescent protein timer to determine the relative age of peroxisomes in yeast. Our data indicate that yeast cells contain a heterogeneous population of relatively old and young peroxisomes. During budding, the peroxisome retention factor inheritance of peroxisomes protein 1 (Inp1) selectively associates to the older organelles, which are retained in the mother cells. Inp2, a protein required for transport of peroxisomes to the bud, preferentially associates to younger organelles. Using a microfluidics device, we demonstrate that the selective segregation of younger peroxisomes to the buds is carefully maintained during multiple budding events. The replicative lifespan of mother cells increased upon deletion of INP2, which resulted in the retention of all organelles in mother cells. These data suggest that, in wild-type yeast, transport of aged and deteriorated peroxisomes to the bud is prevented, whereas the young and vital organelles are preferably transported to the newly forming buds.
Keyphrases
- induced apoptosis
- cell cycle arrest
- endoplasmic reticulum stress
- cell death
- signaling pathway
- physical activity
- stem cells
- oxidative stress
- single molecule
- cell therapy
- machine learning
- gene expression
- single cell
- big data
- mesenchymal stem cells
- cell proliferation
- amino acid
- high resolution
- mass spectrometry
- cell wall
- artificial intelligence
- protein protein
- living cells
- community dwelling
- high speed