A potential imprint control element: Identification of a conserved 42 bp sequence upstream of H19

Trends in Genetics

Volumn 15, Issue 6, 1999, Pages 216-218

  Frevel, Mathias A E ^a   Hornberg, Jorrit J ^a   Reeve, Anthony E ^a  

^a UNIVERSITY OF OTAGO   (New Zealand)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ANIMAL CELL; DIAGNOSTIC VALUE; DNA FLANKING REGION; DNA METHYLATION; GENE DELETION; GENE LOCATION; GENETIC CONSERVATION; GENOME IMPRINTING; HUMAN; HUMAN CELL; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SHORT SURVEY; TRANSCRIPTION REGULATION;

ANIMALIA;

EID: 0033152214     PISSN: 01689525     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-9525(99)01752-7     Document Type: Article

References (10)

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3. Zhang Y.et al. Imprinting of human H19: allele-specific CpG methylation, loss of the active allele in Wilms tumor, and potential for somatic allele switching. Am. J. Hum. Genet. 53:1993;113-124.
4. Overall M.et al. Genomic imprinting in the rat: linkage of Igf2 and H19 genes and opposite parental allele-specific expression during embryogenesis. Genomics. 45:1997;416-420.
5. Tremblay K.D.et al. A paternal-specific methylation imprint marks the alleles of the mouse H19 gene. Nat. Genet. 9:1995;407-413.
6. Tremblay K.D.et al. A 5′ 2-kilobase-pair region of the imprinted mouse H19 gene exhibits exclusive paternal methylation throughout development. Mol. Cell Biol. 17:1997;4322-4329.
7. Jinno Y.et al. Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus. Hum. Mol. Genet. 5:1996;1155-1161.
8. Thorvaldsen J.L.et al. Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2. Genes Dev. 12:1998;3693-3702.
9. Hark A.T., Tilghman S.M. Chromatin conformation of the H19 epigenetic mark. Hum. Mol. Genet. 7:1998;1979-1985.
10. Stadnick M.P.et al. Role of a 461-bp G-rich repetitive element in H19 transgene imprinting. Dev. Genes Evol. 209:1999;239-248.