Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene

American Journal of Human Genetics

Volumn 58, Issue 2, 1996, Pages 335-346

  Glenn, Christopher C ^b   Saitoh, Shinji ^b   Jong, Michelle T C ^b   Filbrandt, Michelle M ^b   Surti, Urvashi ^b   Driscoll, Daniel J ^a   Nicholls, Robert D ^b  

^a UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

DNA; MESSENGER RNA; SMALL NUCLEAR RIBONUCLEOPROTEIN;

ADULT; ALLELE; ARTICLE; BRAIN; CHILD; CHROMOSOME 15Q; CHROMOSOME MAP; DNA METHYLATION; EXON; FETUS; GENE; GENE EXPRESSION; GENE STRUCTURE; GENOME IMPRINTING; GERM CELL; HAPPY PUPPET SYNDROME; HUMAN; HUMAN CELL; HUMAN TISSUE; INFANT; INTRON; NORTHERN BLOTTING; PRADER WILLI SYNDROME; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SOMATIC CELL;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; ANGELMAN SYNDROME; AUTOANTIGENS; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CLONING, MOLECULAR; CODON, INITIATOR; CPG ISLANDS; DNA; EXONS; FEMALE; GENOMIC IMPRINTING; HUMANS; INFANT; MALE; METHYLATION; MOLECULAR SEQUENCE DATA; POLYMERASE CHAIN REACTION; PRADER-WILLI SYNDROME; RIBONUCLEOPROTEINS, SMALL NUCLEAR; RNA SPLICING;

EID: 0030052505     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (7)

1. Barr JA, Jones J, Glenister PH, Cattanach BM (1995) Ubiquitous expression and imprinting of Snrpn in the mouse. Mamm Genome 6:405-407
2. Brannan CI, Dees EC, Ingram RS, Tilghman SM (1990) The product of the H19 gene may function as an RNA. Mol Cell Biol 10:28-36
3. Brockdorff N, Ashworth A, Kay GF, McCabe VM, Norris DP, Cooper PJ, Swift S, et al (1992) The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus. Cell 71:515-526
4. Brown CJ, Hendrich BD, Rupert JL, Lafrenière RG, Xing Y, Lawrence J, Willard HF (1992) The human XIST gene: analysis of 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus. Cell 71:527-542
5. Buiting K, Dittrich B, Gro S, Greger V, Lalande M, Robinson W, Mutirangura A, et al (1993) Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene. Hum Mol Genet 2:1991-1994
6. Buiting K, Saitoh S, Gross S, Dittrich B, Schwartz S, Nicholls RD, Horsthemke B (1995) Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. Nat Genet 9:395-400
7. Cattanach BM, Barr JA, Evans EP, Burtenshaw M, Beechey CV, Leff SE, Brannan CI, et al (1992) A candidate mouse model for Prader-Willi syndrome which shown an absence of Snrpn expression. Nat Genet 2:270-274