Imprinting of PEG3, the human homologue of a mouse gene involved in nurturing behavior

Genomics

Volumn 71, Issue 1, 2001, Pages 110-117

  Murphy, Susan K ^a   Wylie, Andrew A ^a,b   Jirtle, Randy L ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b ASTRAZENECA   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ZINC FINGER PROTEIN;

ARTICLE; BEHAVIOR; CANCER GENETICS; CELL GROWTH; CHROMOSOME 19Q; EMBRYO; GENE EXPRESSION; GENOME IMPRINTING; HUMAN; HUMAN TISSUE; METHYLATION; NERVOUS TISSUE; PRIORITY JOURNAL; PROMOTER REGION;

EID: 0035140174     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2000.6419     Document Type: Article

References (35)

1. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH
2. Loss of heterozygosity in human ovarian cancer on chromosome 19q
3. γ2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome
4. Organization and expression of eucaryotic split genes coding for proteins
5. A truncated human peroxisome proliferator-activated receptor alpha splice variant with dominant negative activity
6. Promoter-region hypermethylation and gene silencing in human cancer
7. The role of histone acetylation in the allelic expression of the imprinted human insulin-like growth factor II gene
8. Imprinted genes, cognition and behaviour
9. CpG-island methylation in aging and cancer
10. Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization
11. Analysis and identification of imprinted genes
12. M6P/IGF2R imprinting evolution in mammals
13. The human homolog of a mouse-imprinted gene, Peg3, maps to a zinc finger generich region of human chromosome 19q13.4
14. Exon sharing of a novel human zinc-finger gene, ZIM2, and paternally expressed gene 3 (PEG3)
15. Zim 1, a maternally expressed mouse Kruppel-type zinc-finger gene located in proximal chromosome 7
16. Discovery of a novel, paternally expressed ubiquitin-specific processing protease gene through comparative analysis of an imprinted region of mouse chromosome 7 and human chromosome 19q13.4
17. RPGR transcription studies in mouse and human tissues reveal a retina-specific isoform that is disrupted in a patient with X-linked retinitis pigmentosa
18. Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein
19. Uniparental disomy in humans: Development of an imprinting map and its implications for prenatal diagnosis
20. Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest
21. Regulation of maternal behavior and offspring growth by paternally expressed Peg3
22. Organization and parent-of-origin-specific methylation of imprinted Peg3 gene on mouse proximal chromosome 7
23. Genetic mapping of a maternal locus responsible for familial hydatidiform moles
24. Genomic imprinting in mammalian development: A parental tug-of-war
25. A catalogue of imprinted genes and parent-of-origin effects in humans and animals
26. The impact of genomic imprinting for neurobehavioral and developmental disorders
27. Role of histone acetylation and DNA methylation in the maintenance of the imprinted expression of the H19 and Igf2 genes
28. Genetic changes in ovarian cancer
29. Imprinting mechanisms in mammals
30. Pw1/Peg3 is a potential cell death mediator and cooperates with Siahla in p53-mediated apoptosis
31. Peg3/Pw1 is an imprinted gene involved in the TNF-NFκB signal transduction pathway
32. A short isoform of the human growth hormone receptor functions as a dominant negative inhibitor of the full-length receptor and generates large amounts of binding protein
33. The putative tumor suppressor gene on chromosome 19q maps between APOc2 and HRC
34. Ocat, a paternally expressed gene closely linked and transcribed in the opposite direction to Peg3
35. Prenatal diagnosis of a partial trisomy 19q