Mouse Peg9/Dlk1 and human PEG9/DLK1 are paternally expressed imprinted genes closely located to the maternally expressed imprinted genes: Mouse Meg3/Gtl2 and human MEG3

Genes to Cells

Volumn 5, Issue 12, 2000, Pages 1029-1037

  Wagatsuma, Shin Kobayashi Irotaka ^a,f,g   Ono, Ryuichi ^a,b,c   Ichikawa, Hitoshi ^a,b   Yamazaki, Masaaki ^e   Tashiro, Hiroyuki ^d   Aisaka, Kohzo ^a   Miyoshi, Naoki ^a   Kohda, Takashi ^a,g   Ogura, Atsuo ^a   Ohki, Misao ^a,b   Kaneko Ishino, Tomoko ^a,b   Ishino, Fumitoshi ^a,b,c,g  

^a TOKYO INSTITUTE OF TECHNOLOGY   (Japan)

^b JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

^c NATIONAL CANCER CENTER RESEARCH INSTITUTE   (Japan)

^d Fujiya Co Ltd   (Japan)

^e TEIKYO UNIVERSITY   (Japan)

^f NATIONAL INSTITUTE OF INFECTIOUS DISEASES   (Japan)

^g TOKAI UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; EPIDERMAL GROWTH FACTOR; MEMBRANE PROTEIN; PROTEIN DLK 1; UNCLASSIFIED DRUG;

ARTICLE; CHROMOSOME 12; CHROMOSOME 14Q; CONTROLLED STUDY; DNA MICROARRAY; EMBRYO; FATHER; FEMALE; GENE CLUSTER; GENE EXPRESSION; GENE FUNCTION; GENE LOCATION; GENE SEQUENCE; GENE TECHNOLOGY; GENETIC ANALYSIS; GENETIC CODE; GENETIC DISORDER; GENETIC SCREENING; GENOME IMPRINTING; HUMAN; MALE; MOTHER; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; SCOLIOSIS; SEQUENCE HOMOLOGY; UNIPARENTAL DISOMY;

ANIMALS; CROSSES, GENETIC; EMBRYO; FEMALE; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION, DEVELOPMENTAL; GENE ORDER; GENOMIC IMPRINTING; HUMANS; MALE; MEMBRANE PROTEINS; MICE; MICE, INBRED C57BL; MICE, INBRED DBA; MOLECULAR SEQUENCE DATA; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PARTHENOGENESIS; PROTEINS;

DROSOPHILA MELANOGASTER; MAMMALIA; MELANOGASTER;

EID: 0034485081     PISSN: 13569597     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2443.2000.00390.x     Document Type: Article

References (38)

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2. Maternal uniparental disomy for human chromosome 14, due to loss of a chromosome 14 from somatic cells with t(13; 14) trisomy 14
3. Genetic and physical imprinting map of the mouse
4. Two cases of maternal uniparental disomy 14 with a phenotype overlapping with the Prader-Willi phenotype
5. Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis
6. Paternal uniparental disomy for chromosome 14: A case report and review
7. Maternal uniparental disomy for chromosome 14
8. Two fetal antigens (FA-1 and FA-2) and endometrial proteins (PP12 and PP14) isolated from amniotic fluid: Preliminary observations in fetal and maternal tissues
9. Assignment of DLK1 to human chromosome band 14q32 by in situ hybridization
10. Assignment of dlk (Dlk1) to mouse chromosome band 12E-F1 by in situ hybridization
11. Cloning of a membrane-spanning protein with epidermal growth factor-like repeat motifs from adrenal glomerulosa cells
12. Identification of an imprinted U2af binding protein related sequence on mouse chromosome 11 using the RLGS method
13. Molecular markers of neuroendocrine development and evidence of environmental regulation
14. Maintenance of somite borders in mice requires the Delta homologue DII1
15. Peg5/Neuronatin is an imprinted gene located on sub-distal chromosome 2 in the mouse
16. Systematic approaches for the identification of imprinted genes
17. Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization
18. Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein
19. The mouse pudgy mutation disrupts Delta homologue DII3 and initiation of early somite boundaries
20. The role of the epidermal growth factor-like protein dlk in cell differentiation
21. Dlk, a putative mammalian homeotic gene differentially expressed in small cell lung carcinoma and neuroendocrine tumor cell line
22. Partial deletion of 14q and partial duplication of 14q in sibs: Testicular mosaicism for t(14q;14q) as a common mechanism
23. Completion of mouse embryogenesis requires both the maternal and paternal genomes
24. Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene
25. Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q
26. Maternal uniparental disomy for chromosome 14 in a boy with intrauterine growth retardation
27. Expression and imprinting status of human PEG8/IGF2AS, a paternally expressed antisense transcript from the IGF2 locus, in Wilms' tumors
28. Uniparental isodisomy of chromosome 14 in two cases: An abnormal child and a normal adult
29. Maternal uniparental isodisomy of chromosome 14: Association with autosomal recessive rod monochromacy
30. Pref-1, a protein containing EGF-like repeats, inhibits adipocyte differentiation
31. Another case of maternal uniparental disomy chromosome 14 syndrome
32. Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis
33. Search for imprinted regions on chromosome 14: Comparison of maternal and paternal UPD cases with cases of chromosome 14 deletion
34. Maternal uniparental disomy for chromosome 14
35. Maternal uniparental isodisomy of human chromosome 14 associated with a parental t(13q14q) and precocious puberty
36. Short-limb dwarfism and hypertrophic cardiomyopathy in a patient with paternal isodisomy 14: 45,XY,idic(14)(p11)
37. Uniparental heterodisomy for chromosome 14 in a phenotypically abnormal familial balanced 13/14 Robertsonian translocation carrier
38. Genome-wide expression monitoring in Saccharomyces cerevisiae