Strong dominance of functional alleles over gene deletions in both intensely growing and deeply starved yeast cells

Fission yeast cells divide at a similar cell length with little variation about the mean. This is thought to be the result of a control mechanism that senses size and corrects for any deviations by advancing or delaying onset of mitosis. Gene deletions that advance cells into mitosis at a smaller size or delay cells entering mitosis, have identified genes potentially involved in this mechanism. However, the molecular basis of this control is still not understood. In this work, we have screened for genes, which when deleted, increase the variability in size of dividing cells. The strongest candidate of this screen was mga2. The mga2 deletion shows a greater variation in cell length at division, with a coefficient of variation (CV) of 15-24% while the wild type strain has a CV of 5-8%. Furthermore, unlike wild type cells, the mga2 deletion cells are unable to correct cell size deviations within one cell cycle. We show that the mga2 gene genetically interacts with nem1 and influences the nuclear membrane, and speculate that it may influence the nucleus/cytoplasmic transport of CDK regulators.

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Relief from nitrogen starvation triggers transient destabilization of glycolytic mRNAs inSaccharomyces cerevisiaecells

Molecular Biology of the Cell ◽

10.1091/mbc.e17-01-0061 ◽

2018 ◽

Vol 29 (4) ◽

pp. 490-498 ◽

Cited By ~ 3

Author(s):

Catherine Tesnière ◽

Martine Pradal ◽

Chloé Bessière ◽

Isabelle Sanchez ◽

Bruno Blondin ◽

...

Keyword(s):

Glucose Sensing ◽

Nutrient Sensing ◽

Yeast Cells ◽

Unexpected Result ◽

Tor Signaling ◽

Posttranscriptional Control ◽

Gene Deletions ◽

Glycolytic Gene ◽

Glucose Carbon ◽

Protein Elongation

Nitrogen replenishment of nitrogen-starved yeast cells resulted in substantial transcriptome changes. There was an unexplained rapid, transient down-regulation of glycolytic genes. This unexpected result prompted us to search for the factors controlling these changes, among which is the possible involvement of different nutrient-sensing pathways such as the TORC1 and cAMP/PKA pathways. To that end, the effects of various gene deletions or chemical blocking agents were tested by investigating the expression of PGK1, one of the glycolytic genes most affected after nitrogen replenishment. We report here that several factors affected glycolytic mRNA stability, among which were glucose sensing, protein elongation, nitrogen metabolism, and TOR signaling. Ammonium sensing was not involved in the response, but ammonium metabolism was required. Thus, our results suggest that, in the presence of glucose, carbon/nitrogen cross-talk is likely involved in the response to nitrogen upshift. Our data suggest that posttranscriptional control of glycolytic gene expression may be an important response to nitrogen replenishment.

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Heterogeneity of Size and Distribution of Intramembrane Particles in the Plasma Membrane of Yeast

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100080407 ◽

1977 ◽

Vol 35 ◽

pp. 596-597

Author(s):

E. Keyhani

Keyword(s):

Plasma Membrane ◽

Candida Utilis ◽

Synthetic Medium ◽

Freeze Fracture ◽

Translational Diffusion ◽

Yeast Cells ◽

Distilled Water ◽

Intramembrane Particles ◽

The Matrix ◽

Water Cell

The matrix of biological membranes consists of a lipid bilayer into which proteins or protein aggregates are intercalated. Freeze-fracture techni- ques permit these proteins, perhaps in association with lipids, to be visualized in the hydrophobic regions of the membrane. Thus, numerous intramembrane particles (IMP) have been found on the fracture faces of membranes from a wide variety of cells (1-3). A recognized property of IMP is their tendency to form aggregates in response to changes in experi- mental conditions (4,5), perhaps as a result of translational diffusion through the viscous plane of the membrane. The purpose of this communica- tion is to describe the distribution and size of IMP in the plasma membrane of yeast (Candida utilis).Yeast cells (ATCC 8205) were grown in synthetic medium (6), and then harvested after 16 hours of culture, and washed twice in distilled water. Cell pellets were suspended in growth medium supplemented with 30% glycerol and incubated for 30 minutes at 0°C, centrifuged, and prepared for freeze-fracture, as described earlier (2,3).

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Ultrathin frozen sections of yeast without aldehyde prefixation

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100081152 ◽

1978 ◽

Vol 36 (2) ◽

pp. 58-59

Author(s):

K. J. Böhm ◽

a. E. Unger

Keyword(s):

Aqueous Solutions ◽

Biological Material ◽

Yeast Cells ◽

Frozen Sections ◽

Good Preservation ◽

Ultrathin Frozen Sections

During the last years it was shown that also by means of cryo-ultra-microtomy a good preservation of substructural details of biological material was possible. However the specimen generally was prefixed in these cases with aldehydes.Preparing ultrathin frozen sections of chemically non-prefixed material commonly was linked up to considerable technical and manual expense and the results were not always satisfying. Furthermore, it seems to be impossible to carry out cytochemical investigations by means of treating sections of unfixed biological material with aqueous solutions.We therefore tried to overcome these difficulties by preparing yeast cells (S. cerevisiae) in the following manner:

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Deformation of Yeast Plasma Membrane by Ethidium Bromide

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100103334 ◽

1988 ◽

Vol 46 ◽

pp. 254-255

Author(s):

E. Keyhani

Keyword(s):

Plasma Membrane ◽

Thin Section ◽

Ethidium Bromide ◽

Freeze Fracture ◽

Mutagenic Effect ◽

Yeast Cells ◽

Hydrophobic Region ◽

Thin Section Electron Microscopy ◽

Section Electron ◽

Deep Pits

The mutagenic effect of ethidium bromide on the mitochondrial DNA is well established. Using thin section electron microscopy, it was shown that when yeast cells were grown in the presence of ethidium bromide, besides alterations in the mitochondria, the plasma membrane also showed alterations consisting of 75 to 110 nm-deep pits. Furthermore, ethidium bromide induced an increase in the length and number of endoplasmic reticulum and in the number of intracytoplasmic vesicles.Freeze-fracture, by splitting the hydrophobic region of the membrane, allows the visualization of the surface view of the membrane, and consequently, any alteration induced by ethidium bromide on the membrane can be better examined by this method than by the thin section method.Yeast cells, Candida utilis. were grown in the presence of 35 μM ethidium bromide. Cells were harvested and freeze-fractured according to the procedure previously described.

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Three-Dimensional Immunoelectron Microscopy of Yeast Cells by a New High-Resolution Replica Method

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100119594 ◽

1985 ◽

Vol 43 ◽

pp. 562-563

Author(s):

Hirano T. ◽

M. Yamaguchi ◽

M. Hayashi ◽

Y. Sekiguchi ◽

A. Tanaka

Keyword(s):

High Resolution ◽

Plasma Polymerization ◽

Three Dimensional ◽

Freeze Fracture ◽

Replica Method ◽

Yeast Cells ◽

Dynamic Aspect ◽

Replica Technique ◽

Gaseous Hydrocarbon ◽

Transmission Electron

A plasma polymerization film replica method is a new high resolution replica technique devised by Tanaka et al. in 1978. It has been developed for investigation of the three dimensional ultrastructure in biological or nonbiological specimens with the transmission electron microscope. This method is based on direct observation of the single-stage replica film, which was obtained by directly coating on the specimen surface. A plasma polymerization film was deposited by gaseous hydrocarbon monomer in a glow discharge.The present study further developed the freeze fracture method by means of a plasma polymerization film produces a three dimensional replica of chemically untreated cells and provides a clear evidence of fine structure of the yeast plasma membrane, especially the dynamic aspect of the structure of invagination (Figure 1).

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