Two-Dimensional DNA Gel Electrophoresis as a Method for Analysis of Eukaryotic Genome Structure: Evaluation Using Tetrahymena thermophila DNA
Document Type
Article
Language
eng
Format of Original
9 p.
Publication Date
3-31-1988
Publisher
Elsevier
Source Publication
Biochimica et Biophysica Acta: Gene Structure and Expression
Source ISSN
0167-4781
Abstract
There is growing interest in mapping and analyzing complete eukaryotic genomes. Yee and Inouye (in Experimental Manipulation of Gene Expression, pp. 279–290, Academic Press, New York) demonstrated that bacterial chromosomes can be resolved into interpretable patterns of DNA fragments by means of restriction enzyme digestion and electrophoresis in two dimensions. We have begun to explore applications of this procedure to analysis of eukaryotic genomes, which are far more complex. Tetrahymena thermophila was selected as a model organism because its genome is small, roughly equivalent to that of a single human chromosome. In addition, each Tetrahymena cell contains two nuclei which differ in sequence composition and methylation. Our results demonstrate that the Tetrahymena genome can be resolved into complex patterns of fragments in two dimensions. Hybridization to Southern blots of these gels with a multiply repeated sequence probe yielded analyzable patterns of a subset of the genome. The blots reveal alterations in genome structure due to methylation and rearrangement. Future extensions of the method are discussed.
Recommended Citation
Hüvös, Piroska E.; Sanchez, J. Aquiles; Kramer, Kate M.; Karrer, Kathleen M.; and Wangh, Lawrence J., "Two-Dimensional DNA Gel Electrophoresis as a Method for Analysis of Eukaryotic Genome Structure: Evaluation Using Tetrahymena thermophila DNA" (1988). Biological Sciences Faculty Research and Publications. 240.
https://epublications.marquette.edu/bio_fac/240
Comments
Biochimica et Biophysica Acta: Gene Structure and Expression, Vol. 949, No. 3 (March 31, 1988): 325-333. DOI.
Kathleen Karrer was affiliated with Brandeis University at the time of publication.