» Articles » PMID: 17596521

The Size of the Nucleus Increases As Yeast Cells Grow

Overview
Journal Mol Biol Cell
Date 2007 Jun 29
PMID 17596521
Citations 197
Authors
Affiliations
Soon will be listed here.
Abstract

It is not known how the volume of the cell nucleus is set, nor how the ratio of nuclear volume to cell volume (N/C) is determined. Here, we have measured the size of the nucleus in growing cells of the budding yeast Saccharomyces cerevisiae. Analysis of mutant yeast strains spanning a range of cell sizes revealed that the ratio of average nuclear volume to average cell volume was quite consistent, with nuclear volume being approximately 7% that of cell volume. At the single cell level, nuclear and cell size were strongly correlated in growing wild-type cells, as determined by three different microscopic approaches. Even in G1-phase, nuclear volume grew, although it did not grow quite as fast as overall cell volume. DNA content did not appear to have any immediate, direct influence on nuclear size, in that nuclear size did not increase sharply during S-phase. The maintenance of nuclear size did not require continuous growth or ribosome biogenesis, as starvation and rapamycin treatment had little immediate impact on nuclear size. Blocking the nuclear export of new ribosomal subunits, among other proteins and RNAs, with leptomycin B also had no obvious effect on nuclear size. Nuclear expansion must now be factored into conceptual and mathematical models of budding yeast growth and division. These results raise questions as to the unknown force(s) that expand the nucleus as yeast cells grow.

Citing Articles

Advancing yeast cell analysis: A cryomethod for serial block-face scanning electron microscopy imaging in mitochondrial morphology studies.

Blancard C, Decoeur F, Duvezin-Caubet S, Giraud M, Salin B Biol Cell. 2024; 117(1):e2400038.

PMID: 39648486 PMC: 11758470. DOI: 10.1111/boc.202400038.


Homeostasis of mRNA concentrations through coupling transcription, export, and degradation.

Wang Q, Lin J iScience. 2024; 27(8):110531.

PMID: 39175768 PMC: 11338957. DOI: 10.1016/j.isci.2024.110531.


Modeling the START transition in the budding yeast cell cycle.

Ravi J, Samart K, Zwolak J PLoS Comput Biol. 2024; 20(8):e1012048.

PMID: 39093881 PMC: 11324117. DOI: 10.1371/journal.pcbi.1012048.


Plasma membrane folding enables constant surface area-to-volume ratio in growing mammalian cells.

Wu W, Lam A, Suarez K, Smith G, Duquette S, Yu J bioRxiv. 2024; .

PMID: 39005340 PMC: 11244959. DOI: 10.1101/2024.07.02.601447.


Chemical transformation of the multibudding yeast, Aureobasidium pullulans.

Wirshing A, Petrucco C, Lew D J Cell Biol. 2024; 223(10).

PMID: 38935076 PMC: 11211067. DOI: 10.1083/jcb.202402114.


References
1.
Johnston G, Ehrhardt C, Lorincz A, Carter B . Regulation of cell size in the yeast Saccharomyces cerevisiae. J Bacteriol. 1979; 137(1):1-5. PMC: 218410. DOI: 10.1128/jb.137.1.1-5.1979. View

2.
Cullen B . Nuclear RNA export. J Cell Sci. 2003; 116(Pt 4):587-97. DOI: 10.1242/jcs.00268. View

3.
Maul G, Maul H, Scogna J, Lieberman M, Stein G, Hsu B . Time sequence of nuclear pore formation in phytohemagglutinin-stimulated lymphocytes and in HeLa cells during the cell cycle. J Cell Biol. 1972; 55(2):433-47. PMC: 2108790. DOI: 10.1083/jcb.55.2.433. View

4.
Csikasz-Nagy A, Battogtokh D, Chen K, Novak B, Tyson J . Analysis of a generic model of eukaryotic cell-cycle regulation. Biophys J. 2006; 90(12):4361-79. PMC: 1471857. DOI: 10.1529/biophysj.106.081240. View

5.
Sulston J, Schierenberg E, White J, Thomson J . The embryonic cell lineage of the nematode Caenorhabditis elegans. Dev Biol. 1983; 100(1):64-119. DOI: 10.1016/0012-1606(83)90201-4. View