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Reporter Gene Silencing in Targeted Mouse Mutants Is Associated with Promoter CpG Island Methylation
- Source :
- PloS one, vol 10, iss 8, PLoS ONE, Vol 10, Iss 8, p e0134155 (2015), PLoS ONE
- Publication Year :
- 2015
- Publisher :
- eScholarship, University of California, 2015.
-
Abstract
- Targeted mutations in mouse disrupt local chromatin structure and may lead to unanticipated local effects. We evaluated targeted gene promoter silencing in a group of six mutants carrying the tm1a Knockout Mouse Project allele containing both a LacZ reporter gene driven by the native promoter and a neo selection cassette. Messenger RNA levels of the reporter gene and targeted gene were assessed by qRT-PCR, and methylation of the promoter CpG islands and LacZ coding sequence were evaluated by sequencing of bisulfite-treated DNA. Mutants were stratified by LacZ staining into presumed Silenced and Expressed reporter genes. Silenced mutants had reduced relative quantities LacZ mRNA and greater CpG Island methylation compared with the Expressed mutant group. Within the silenced group, LacZ coding sequence methylation was significantly and positively correlated with CpG Island methylation, while promoter CpG methylation was only weakly correlated with LacZ gene mRNA. The results support the conclusion that there is promoter silencing in a subset of mutants carrying the tm1a allele. The features of targeted genes which promote local silencing when targeted remain unknown.
- Subjects :
- General Science & Technology
Knockout
Messenger
lcsh:Medicine
Biology
Promoter Regions
Mice
Epigenetics of physical exercise
Genetic
Genes, Reporter
Genetics
Gene silencing
Animals
RNA, Messenger
Gene Silencing
Promoter Regions, Genetic
lcsh:Science
Gene
Reporter
Mice, Knockout
Reporter gene
Multidisciplinary
Gene Expression Profiling
lcsh:R
Promoter
Methylation
DNA Methylation
Molecular biology
CpG site
Lac Operon
Genes
DNA methylation
Mutation
RNA
lcsh:Q
CpG Islands
Research Article
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- PloS one, vol 10, iss 8, PLoS ONE, Vol 10, Iss 8, p e0134155 (2015), PLoS ONE
- Accession number :
- edsair.doi.dedup.....ceb96dedf2de4b8c358716ba0769b3da