Abstract
Methylation patterns of the mammalian genome are thought to be crucial for development. The precise mechanisms designating specific genomic loci for methylation are not known. Targeted deletion of Lsh results in perinatal lethality with a rather normal development. We report here, however, that Lsh(-/-) mice show substantial loss of methylation throughout the genome. The hypomethylated loci comprise repetitive elements and single copy genes. This suggests that global genomic methylation is not absolutely required for normal embryogenesis. Based on the similarity of Lsh to other SNF2 chromatin remodeling proteins, it suggests that alteration of chromatin affects global methylation patterns in mice.
Publication types
-
Research Support, U.S. Gov't, P.H.S.
MeSH terms
-
Animals
-
Blotting, Southern
-
Chromatin / metabolism
-
DNA Helicases
-
DNA Methylation
-
DNA-Binding Proteins / genetics
-
DNA-Binding Proteins / physiology*
-
Genome
-
Genomic Imprinting
-
Genotype
-
Globins / metabolism
-
Isoenzymes / metabolism
-
Mice
-
Multigene Family
-
Nuclear Proteins*
-
Phosphoglycerate Kinase / metabolism
-
Protein Structure, Tertiary
-
Reverse Transcriptase Polymerase Chain Reaction
-
Tissue Distribution
-
Transcription Factors / genetics
-
Transcription Factors / physiology*
Substances
-
Chromatin
-
DNA-Binding Proteins
-
Isoenzymes
-
Nuclear Proteins
-
Smarca2 protein, mouse
-
Transcription Factors
-
Globins
-
Phosphoglycerate Kinase
-
phosphoglycerate kinase, testis specific
-
Smarca4 protein, mouse
-
DNA Helicases