Abstract
The repression of the maternally inherited Igf2 allele has been proposed to depend on a methylation-sensitive chromatin insulator organized by the 11 zinc finger protein CTCF at the H19 imprinting control region (ICR). Here we document that point mutations of the nucleotides in physical contact with CTCF within the endogenous H19 ICR lead to loss of CTCF binding and Igf2 imprinting only when passaged through the female germline. This effect is accompanied by a significant loss of methylation protection of the maternally derived H19 ICR. Because CTCF interacts with other imprinting control regions, it emerges as a central factor responsible for interpreting and propagating gamete-derived epigenetic marks and for organizing epigenetically controlled expression domains.
MeSH Terms
Animals
CCCTC-Binding Factor
DNA Methylation
DNA-Binding Proteins/genetics,metabolism
Female
Gene Expression Regulation
Genomic Imprinting
Insulin-Like Growth Factor II/genetics
Male
Mice
RNA, Long Noncoding
RNA, Untranslated/genetics,metabolism
Repressor Proteins
Transcription Factors/genetics,metabolism
Chemicals
CCCTC-Binding Factor
Ctcf protein, mouse
DNA-Binding Proteins
H19 long non-coding RNA
RNA, Long Noncoding
RNA, Untranslated
Repressor Proteins
Transcription Factors
Insulin-Like Growth Factor II
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Pant Vinod
Department of Development & Genetics, Evolution Biology Centre, Uppsala University, S-752 36 Uppsala, Sweden.
Mariano Piero
Kanduri Chandrasekhar
Mattsson Anita
Lobanenkov Victor
Heuchel Rainer
Ohlsson Rolf
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