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Dissection of Saccharomyces Cerevisiae Asci
Published on: May 19, 2009
Meiotic cytology of Saccharomyces cerevisiae in protoplast lysates
Abstract:
This report describes cytological features of meiosis in Saccharomyces cerevisiae prepared for electron microscopy by lysis of protoplasts or nuclei on an aqueous surface. Whereas the chromatin of cells lysed before or after meiotic prophase was widely dispersed, pachytene bivalents appeared as discrete, elongate masses of compact chromatin. These bivalents were of nearly uniform thickness; they ranged in length from about 0.6 micrograms to 4.0 micrograms, with a median of 1.6-1.8 micrograms. Enzymatic digestion of chromosomal DNA removed the chromatin to reveal the underlying synaptonemal complex. The lysis of partially purified nuclei was less disruptive and thereby revealed the regular association of the telomeres with fragments of the nuclear envelope. In tetraploid cells, pachytene lysates contained quadrivalents characterized by the close apposition of chromatin masses of similar length. One or more points of intimate association appear to represent sites of exchange between pairing partners. The departure of the diploid cells from pachytene was accompanied by the renewed association of spindle microtubules with the chromosomes shortly before the diplotene chromosomes decondensed. Later, the successive meiotic divisions were identified by the appearance of a single spindle for meiosis I and of two spindles for meiosis II.
Insights
This study visualizes meiosis in yeast using electron microscopy. Pachytene bivalents appear as distinct chromatin masses, revealing the synaptonemal complex and telomere-nuclear envelope associations.
Area of Science:
- Cell Biology
- Genetics
- Microscopy
Background:
- Meiosis is a fundamental process for sexual reproduction.
- Visualizing meiotic chromosomes requires advanced preparation techniques.
Purpose of the Study:
- To describe the cytological features of meiosis in Saccharomyces cerevisiae.
- To utilize electron microscopy for detailed chromosome structure analysis.
Main Methods:
- Preparation of yeast cells for electron microscopy via protoplast or nuclear lysis on an aqueous surface.
- Enzymatic digestion of chromosomal DNA to reveal the synaptonemal complex.
- Observation of both diploid and tetraploid yeast cells.
Main Results:
- Pachytene bivalents observed as discrete, compact chromatin masses (0.6-4.0 µm).
- Synaptonemal complex visualized after DNA digestion, showing telomere association with nuclear envelope fragments.
- Tetraploid cells displayed quadrivalents with potential exchange sites.
- Spindle microtubule association with chromosomes and distinct spindles for meiosis I and II identified.
Conclusions:
- The described lysis method effectively visualizes meiotic chromosome structures in yeast.
- Detailed cytological features of meiotic prophase, including bivalent structure and telomere associations, were elucidated.
- The study provides insights into chromosome dynamics during meiosis I and II in Saccharomyces cerevisiae.

