1. A gene essential for de novo methylation and development in Ascobolus reveals a novel type of eukaryotic DNA methyltransferase structure.
- Author
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Malagnac F, Wendel B, Goyon C, Faugeron G, Zickler D, Rossignol JL, Noyer-Weidner M, Vollmayr P, Trautner TA, and Walter J
- Subjects
- Amino Acid Sequence, Animals, Arabidopsis, Base Sequence, Cloning, Molecular, DNA (Cytosine-5-)-Methyltransferases chemistry, DNA (Cytosine-5-)-Methyltransferases metabolism, Eukaryotic Cells enzymology, Gene Expression Regulation, Enzymologic genetics, Genetic Complementation Test, Homozygote, Mice, Molecular Sequence Data, Mutation physiology, Reproduction, Asexual physiology, Sequence Homology, Amino Acid, Ascomycota genetics, DNA (Cytosine-5-)-Methyltransferases genetics, DNA Methylation, DNA-Binding Proteins, Fungal Proteins, Methyltransferases genetics
- Abstract
Molecular mechanisms determining methylation patterns in eukaryotic genomes still remain unresolved. We have characterized, in Ascobolus, a gene for de novo methylation. This novel eukaryotic gene, masc1, encodes a protein that has all motifs of the catalytic domain of eukaryotic C5-DNA-methyltransferases but is unique in that it lacks a regulatory N-terminal domain. The disruption of masc1 has no effect on viability or methylation maintenance but prevents the de novo methylation of DNA repeats, which takes place after fertilization, through the methylation induced premeiotically (MIP) process. Crosses between parents harboring the masc1 disruption are arrested at an early stage of sexual reproduction, indicating that the activity of Masc1, the product of the gene, is crucial in this developmental process.
- Published
- 1997
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