Imprinting of PEG1/MEST isoform 2 in human placenta

Placenta

Volumn 27, Issue 2-3, 2006, Pages 119-126

  McMinn, J ^a   Wei, M ^a   Sadovsky, Y ^b   Thaker, H M ^a   Tycko, B ^a  

^a NewYork Presbyterian Hospital   (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

DNA methylation; Epigenetics; Genomic imprinting; PEG1 gene; Placenta

Indexed keywords

GENE PRODUCT; MESSENGER RNA; PROTEIN PEG1; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; CELL ISOLATION; CHORION VILLUS SAMPLING; CONTROLLED STUDY; CPG ISLAND; CYTOTROPHOBLAST; DNA METHYLATION; EPIGENETICS; EXON; FEMALE; FETUS GROWTH; GENE EXPRESSION; GENE SEQUENCE; GENETIC VARIABILITY; GENOME IMPRINTING; HUMAN; HUMAN CELL; HUMAN TISSUE; PLACENTA DEVELOPMENT; PRIORITY JOURNAL; PROTEIN LOCALIZATION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SOUTHERN BLOTTING; TROPHOBLAST;

ADULT; ALLELES; CPG ISLANDS; DNA; DNA METHYLATION; EPIGENESIS, GENETIC; EXONS; FEMALE; GENETIC MARKERS; GENOMIC IMPRINTING; HUMANS; PLACENTA; PROTEIN ISOFORMS; PROTEINS; RNA, MESSENGER; TROPHOBLASTS; VARIATION (GENETICS);

EID: 28844445720     PISSN: 01434004     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.placenta.2004.12.003     Document Type: Article

References (22)

1. W. Mayer M. Hemberger H.G. Frank R. Grummer E. Winterhager P. Kaufmann et al. Expression of the imprinted genes MEST/Mest in human and murine placenta suggests a role in angiogenesis Dev Dyn 217 2000 1-10
2. L. Lefebvre S. Viville S.C. Barton F. Ishino E.B. Keverne M.A. Surani Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest Nat Genet 20 1998 163-9
3. J.G. Herman J.R. Graff S. Myohanen B.D. Nelkin S.B. Baylin Methylation-specific PCR: A novel PCR assay for methylation status of CpG islands Proc Natl Acad Sci U S A 93 1996 9821-6
4. S. Kobayashi T. Kohda N. Miyoshi Y. Kuroiwa K. Aisaka O. Tsutsumi et al. Human PEG1/MEST, an imprinted gene on chromosome 7 Hum Mol Genet 6 1997 781-6
5. H.J. Kliman J.E. Nestler E. Sermasi J.M. Sanger J.F. Strauss III Purification, characterization, and in vitro differentiation of cytotrophoblasts from human term placentae Endocrinology 118 1986 1567-82
6. D.M. Nelson R.D. Johnson S.D. Smith E.Y. Anteby Y. Sadovsky Hypoxia limits differentiation and up-regulates expression and activity of prostaglandin H synthase 2 in cultured trophoblast from term human placenta Am J Obstet Gynecol 180 1999 896-902
7. D.M. Nelson S.D. Smith T.C. Furesz Y. Sadovsky V. Ganapathy C.A. Parvin et al. Hypoxia reduces expression and function of system A amino acid transporters in cultured term human trophoblasts Am J Physiol Cell Physiol 284 2003 C310-5
8. W.T. Schaiff M.G. Carlson S.D. Smith R. Levy D.M. Nelson Y. Sadovsky Peroxisome proliferator-activated receptor-gamma modulates differentiation of human trophoblast in a ligand-specific manner J Clin Endocrinol Metab 85 2000 3874-81
9. A.M. Riesewijk L. Hu U. Schulz G. Tariverdian P. Hoglund J. Kere et al. Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses Genomics 42 1997 236-44
10. H. Cui M. Cruz-Correa F.M. Giardiello D.F. Hutcheon D.R. Kafonek S. Brandenburg et al. Loss of IGF2 imprinting: A potential marker of colorectal cancer risk Science 299 2003 1753-5
11. A.P. Feinberg B. Tycko The history of cancer epigenetics Nat Rev Cancer 4 2004 143-53
12. T. Moulton T. Crenshaw Y. Hao J. Moosikasuwan N. Lin F. Dembitzer et al. Epigenetic lesions at the H19 locus in Wilms' tumour patients Nat Genet 7 1994 440-7
13. T. Sakatani M. Wei M. Katoh C. Okita D. Wada K. Mitsuya et al. Epigenetic heterogeneity at imprinted loci in normal populations Biochem Biophys Res Commun 283 2001 1124-30
14. I. Sandovici M. Leppert P.R. Hawk A. Suarez Y. Linares C. Sapienza Familial aggregation of abnormal methylation of parental alleles at the IGF2/H19 and IGF2R differentially methylated regions Hum Mol Genet 12 2003 1569-78
15. K. Buiting S. Gross C. Lich G. Gillessen-Kaesbach O. el-Maarri B. Horsthemke Epimutations in Prader-Willi and Angelman syndromes: A molecular study of 136 patients with an imprinting defect Am J Hum Genet 72 2003 571-7
16. R. Weksberg A.C. Smith J. Squire P. Sadowski Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development Hum Mol Genet 12 Spec No 1 2003 R61-8
17. T. Kaneko-Ishino Y. Kuroiwa N. Miyoshi T. Kohda R. Suzuki M. Yokoyama et al. Peg1/Mest imprinted gene on chromosome 6 identified by cDNA subtraction hybridization Nat Genet 11 1995 52-9
18. K. Kosaki R. Kosaki W.J. Craigen N. Matsuo Isoform-specific imprinting of the human PEG1/MEST gene Am J Hum Genet 66 2000 309-12
19. I.S. Pedersen P. Dervan A. McGoldrick M. Harrison F. Ponchel V. Speirs et al. Promoter switch: A novel mechanism causing biallelic PEG1/MEST expression in invasive breast cancer Hum Mol Genet 11 2002 1449-53
20. S. Nishihara T. Hayashida K. Mitsuya T.C. Schulz M. Ikeguchi N. Kaibara et al. Multipoint imprinting analysis in sporadic colorectal cancers with and without microsatellite instability Int J Oncol 17 2000 317-22
21. T. Kaneko-Ishino T. Kohda F. Ishino The regulation and biological significance of genomic imprinting in mammals J Biochem (Tokyo) 133 2003 699-711
22. Y.S. Kanwar X. Pan S. Lin A. Kumar J. Wada C.S. Haas et al. Imprinted mesodermal specific transcript (MEST) and H19 genes in renal development and diabetes Kidney Int 63 2003 1658-70