Complementation between inactive fragments of SssI DNA methyltransferase
نویسندگان
چکیده
منابع مشابه
Cytosine-to-Uracil Deamination by SssI DNA Methyltransferase
The prokaryotic DNA(cytosine-5)methyltransferase M.SssI shares the specificity of eukaryotic DNA methyltransferases (CG) and is an important model and experimental tool in the study of eukaryotic DNA methylation. Previously, M.SssI was shown to be able to catalyze deamination of the target cytosine to uracil if the methyl donor S-adenosyl-methionine (SAM) was missing from the reaction. To test ...
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The 5mC DNA methyltransferase M.HhaI can be split into two individually inactive N- and C-terminal fragments that together can form an active enzyme in vivo capable of efficiently methylating DNA. This active fragment pair was identified by creating libraries of M.HhaI gene fragment pairs and then selecting for the pairs that code for an active 5mC methyltransferase. The site of bisection for s...
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ژورنال
عنوان ژورنال: BMC Molecular Biology
سال: 2012
ISSN: 1471-2199
DOI: 10.1186/1471-2199-13-17