Analysis of sequence upstream of the endogenous H19 gene reveals elements both essential and dispensable for imprinting

Molecular and Cellular Biology

Volumn 22, Issue 8, 2002, Pages 2450-2462

  Thorvaldsen, Joanne L ^a   Mann, Mellissa R W ^a   Nwoko, Okechukwu ^a   Duran, Kristen L ^a   Bartolomei, Marisa S ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING PROTEIN; GENE PRODUCT; PROTEIN CTCF; PROTEIN H19; UNCLASSIFIED DRUG;

ALLELE; ANIMAL CELL; ARTICLE; BINDING SITE; CONTROLLED STUDY; DNA FLANKING REGION; EMBRYO; GENE ACTIVITY; GENE DELETION; GENE EXPRESSION; GENE FUNCTION; GENE SEQUENCE; GENETIC ANALYSIS; GENOME IMPRINTING; METHYLATION; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN DOMAIN; SEQUENCE ANALYSIS; TISSUE SPECIFICITY;

ALLELES; ANIMALS; CELLS, CULTURED; CPG ISLANDS; DNA METHYLATION; FEMALE; GENE EXPRESSION REGULATION; GENOMIC IMPRINTING; INSULIN-LIKE GROWTH FACTOR II; MALE; MICE; MICE, INBRED C57BL; MICE, MUTANT STRAINS; RNA, UNTRANSLATED; SEQUENCE DELETION; TISSUE DISTRIBUTION;

ANIMALIA; RODENTIA;

EID: 0036211514     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.22.8.2450-2462.2002     Document Type: Article

References (56)

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18. The H19 methylation imprint is erased and reestablished differentially on the parental alleles during male germ cell development
19. Deletion of a silencer element disrupts H19 imprinting independently of a DNA methylation epigenetic switch
20. The gene encoding the mouse ribosomal protein L32 contains a uniquely expressed intron-containing gene and an unmutated processed gene
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31. Translating the histone code
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