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Tandem repeats in extrachromosomal ribosomal DNA of Dictyostelium discoideum, resulting from chromosomal mutations.
Author(s) -
Robert A. Cole,
Keith L. Williams
Publication year - 1992
Publication title -
genetics.
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
ISSN - 3049-7094
DOI - 10.1093/genetics/130.4.757
Subject(s) - extrachromosomal dna , biology , genetics , dictyostelium discoideum , ribosomal dna , tandem repeat , restriction map , microbiology and biotechnology , eukaryote , dna , restriction fragment , centromere , restriction enzyme , gene , chromosome , nucleic acid sequence , phylogenetic tree , genome , plasmid
Extrachromosomal ribosomal DNA in the simple eukaryote Dictyostelium discoideum is readily separated from chromosomal DNA by orthogonal field electrophoresis (OFAGE), forming a prominent band in the 110-kb region of the gel. Here we show that mutations in at least two chromosomal genes give rise to a ladder of rDNA bands increasing in size up to about 300 kb. One of these mutations, the rrcA350 allele, which is recessive to wild type and maps to the centromere-proximal region of linkage group II, has an unstable phenotype; spontaneous revertants, which no longer exhibit the rDNA ladder, have been recovered. Another mutation rrc-351, provisionally mapped to linkage group IV, is dominant to wild type. The rDNA ladder is caused by concatamerization of a 34-kb fragment in the nontranscribed central spacer region of the 88-kb linear rDNA palindrome. Restriction enzyme analysis has revealed that each concatamer is generated by crossovers between two rDNA molecules.

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