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Molecular Maps in Yeast and Other Fungi - Since, E. coli can not serve the purpose of understanding eukaryotic genomes, yeast has been selected as the simplest eukaryote to understand the eukaryotic genome.
Following are the reasons for the choice:
(i) yeast has haploid DNA (14 X 103 kilobasepairs), which is only 3.5 times that in E. coli (4.0 X 103 kbp) ; Drosophila contains 25 times the DNA of E. coli, and higher vertebrates have 1000 times this DNA
(ii) work with yeast is not as expensive as with higher vertebrate cells, due to high cost of media required to grow them in future;
(iii) yeast cells grow and divide like bacteria, doubling their mass every 90 minutes;

(iv) yeast genetic system has been very thoroughly understood where about 600 genes are already mapped, although they may still represent a fraction of the whole genome;
(v) DNA molecules as long as 100kb can be routinely handled through PFGE. These can be produced by enzymes like Dpn I or Not I, which recognize rare sites.
 Yeast cell has 16 chromosomes, each with a single DNA molecule. Until recently, even the smallest of these DNA molecules was too large to be isolated in pure form, but due to the recent availability of pulsed field gel electrophoresis (PFGE), where short pulses of electricity are used in two different directions, separation of DNA belonging lo each of the 16 individual chromosomes has become possible.

Centromere sequence (CEM), about 130 bp and telomere sequence (TEL), about 100bp with repeat sequence, (CCCACACA)n have also been isolated. These sequences, when used as probes, can help in positioning the centromere and the telomeric ends on the chromosome map.
Using the technique of PFGE and its refinement known as contour ­clamped homogeneous electric field (CHEF) gel electrophoresis, genomes of several fungi could be resolved in chromosome bands, popularly described as electrophoretic karyotypes.
These included Saccharomyces cerevisae (14 Mbp), Schizosaccharomyces pombe (15 Mbp), Neurospora crassa (47 Mbp), Aspergillus nidulans (31 Mbp) and Dictyostelium discoideum (52c56 Mbp). For electrophoretic karyotypes, intact chromosomal DNA has to be prepared in agarose plugs, which can also be purchased from commercial firms for organisms like yeast.

These agarose plugs are subjected to PFGE or CHEF gel electrophoresis, which yields 15 bands for 16 chromosomes in case of yeast, 6 bands for 8 chromosomes in Aspergillus nidulans, and 7 bands for 7 chromosomes in D. discoideum. In case of yeast, initally chromosome 12 did not clearly separate.
Another strain of yeast (YPH 149) allowed identification of each of the 16 chromosomes as 17 distinct bands using alternating CHEF gel electrophoresis (chromosome VII split into two). In Aspergillus, 2 of the 6 bands are doublets with 3.8 Mbp and 3.5 Mbp respectively. Thus these bands are in agreement with genetic and cytological information available in these cases.
The details of different DNA bands in yeast and Aspergillus nidulans along with the linkage groups to which these bands belong. The sizes of bands are measured by comparing with bands of known sizes obtained from agarose plugs having yeast intact chromosomes, The bands are assigned to specific linkage groups by using one of the several possible methods.

For instance, in Aspergillus, this was achieved by combination of two methods:
(i) hybridization with labelled DNA probes containing genes that are already mapped to their respective linkage groups;
(ii) examination of CHEF gel band patterns of genomic DNAs from strains carrying known translocations.
Utilizing these approaches, eight different linkage groups (LGs) in Aspergillus could be assigned to six electrophoretic DNA bands. The CHEF and genetic linkage data agreed that LGs VIII (5.0 Mh), VII' (4.5 Mb) and II (4.2 Mb) are the largest, with LGs I (3.8 Mb) and III (3.5 Mb) of intermediate size and LG IV (2.0 Mb) as the smallest.