Author
Listed:
- Eric U. Selker
(University of Oregon)
- Nikolaos A. Tountas
(University of Edinburgh
University of Virginia School of Medicine)
- Sally H. Cross
(University of Edinburgh
Western General Hospital)
- Brian S. Margolin
(University of Oregon
University of California San Francisco)
- Jonathan G. Murphy
(University of Oregon)
- Adrian P. Bird
(University of Edinburgh)
- Michael Freitag
(University of Oregon)
Abstract
Cytosine methylation is common, but not ubiquitous, in eukaryotes. Mammals1 and the fungus Neurospora crassa2,3 have about 2–3% of cytosines methylated. In mammals, methylation is almost exclusively in the under-represented CpG dinucleotides, and most CpGs are methylated1 whereas in Neurospora, methylation is not preferentially in CpG dinucleotides and the bulk of the genome is unmethylated4. DNA methylation is essential in mammals5 but is dispensable in Neurospora3,6, making this simple eukaryote a favoured organism in which to study methylation. Recent studies indicate that DNA methylation in Neurospora depends on one DNA methyltransferase, DIM-2 (ref. 6), directed by a histone H3 methyltransferase, DIM-5 (ref. 7), but little is known about its cellular and evolutionary functions. As only four methylated sequences have been reported previously in N. crassa, we used methyl-binding-domain agarose chromatography8 to isolate the methylated component of the genome. DNA sequence analysis shows that the methylated component of the genome consists almost exclusively of relics of transposons that were subject to repeat-induced point mutation—a genome defence system that mutates duplicated sequences9.
Suggested Citation
Eric U. Selker & Nikolaos A. Tountas & Sally H. Cross & Brian S. Margolin & Jonathan G. Murphy & Adrian P. Bird & Michael Freitag, 2003.
"The methylated component of the Neurospora crassa genome,"
Nature, Nature, vol. 422(6934), pages 893-897, April.
Handle:
RePEc:nat:nature:v:422:y:2003:i:6934:d:10.1038_nature01564
DOI: 10.1038/nature01564
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