Recurrent biparental hydatidiform mole: Additional evidence for a 1.1-Mb locus in 19q13.4 and candidate gene analysis

Journal of the Society for Gynecologic Investigation

Volumn 12, Issue 5, 2005, Pages 376-383

  Panichkul, Prisana C ^a   Al Hussaini, Tarek K ^d   Sierra, Rebecca ^d   Kashork, Catherine D ^b   Popek, Edwina J ^d   Stockton, David W ^d   Van Den Veyver, Ignatia B ^c  

^a PHRAMONGKUTKLAO HOSPITAL   (Thailand)

^b Signature Genomic Laboratories LLC   (United States)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d NONE

Author keywords

19q13.4; Biparental inheritance; Hydatidiform mole; Maternal imprinting

Indexed keywords

ARTICLE; CONTROLLED STUDY; EXON; FEMALE; GENE; GENE CONTROL; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENE TARGETING; GENETIC CODE; GENETIC POLYMORPHISM; GENOMICS; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; HUMAN TISSUE; HYDATIDIFORM MOLE; INHERITANCE; MOLECULAR PROBE; NALP5 GENE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 19; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC MARKERS; HUMANS; HYDATIDIFORM MOLE; IN SITU HYBRIDIZATION, FLUORESCENCE; INHERITANCE PATTERNS; MICROSATELLITE REPEATS; PEDIGREE; PREGNANCY; RECURRENCE; UTERINE NEOPLASMS;

EID: 20544431959     PISSN: 10715576     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jsgi.2005.02.011     Document Type: Article

References (38)

1. R.A. Fisher, M.D. Hodges, H.C. Rees The maternally transcribed gene p57(KIP2) (CDNK1C) is abnormally expressed in both androgenetic and biparental complete hydatidiform moles Hum Mol Genet 11 2002 3267 3272
2. A.E. Szulman, U. Surti The syndromes of hydatidiform mole. I. Cytogenetic and morphologic correlations Am J Obstet Gynecol 131 1978 665 671
3. A.E. Szulman Trophoblastic diseases Complete and partial hydatidiform moles 2nd ed. 1999 Churchill Livingstone New York, NY
4. B.W. Kovacs, B. Shahbahrami, D.E. Tast, J.P. Curtin Molecular genetic analysis of complete hydatidiform moles Cancer Genet Cytogenet 54 1991 143 152
5. M.N. Helwani, M. Seoud, L. Zahed, G. Zaatari, A. Khalil, R. Slim A familial case of recurrent hydatidiform molar pregnancies with biparental genomic contribution Hum Genet 105 1999 112 115
6. L.M. Ambani, R.A. Vaidya, C.S. Rao, S.D. Daftary, N.D. Motashaw Familial occurrence of trophoblastic disease - Report of recurrent molar pregnancies in sisters in three families Clin Genet 18 1980 27 29
7. F. Parazzini, C. La Vecchia, S. Franceschi, G. Mangili Familial trophoblastic disease case report Am J Obstet Gynecol 149 1984 382 383
8. R. Kircheisen, T. Schroeder-Kurth [Familial hydatidiform mole syndrome and genetic aspects of this disturbed trophoblast development] Geburtshilfe Frauenheilkd 51 1991 569 571
9. M. Seoud, A. Khalil, A. Frangieh, L. Zahed, G. Azar, N. Nuwayri-Salti Recurrent molar pregnancies in a family with extensive intermarriage report of a family and review of the literature Obstet Gynecol 86 1995 692 695
10. A. Sensi, F. Gualandi, M.C. Pittalis Mole maker phenotype Possible narrowing of the candidate region Eur J Hum Genet 8 2000 641 644
11. H. Judson, B.E. Hayward, E. Sheridan, D.T. Bonthron A global disorder of imprinting in the human female germ line Nature 416 2002 539 542
12. M.D. Hodges, H.C. Rees, M.J. Seckl, E.S. Newlands, R.A. Fisher Genetic refinement and physical mapping of a biparental complete hydatidiform mole locus on chromosome 19q13.4 J Med Genet 40 2003 e95
13. Y.B. Moglabey, R. Kircheisen, M. Seoud, N. El Mogharbel, I. Van den Veyver, R. Slim Genetic mapping of a maternal locus responsible for familial hydatidiform moles Hum Mol Genet 8 1999 667 671
14. M. Shannon, L.K. Ashworth, M.L. Mucenski, J.E. Lamerdin, E. Branscomb, L. Stubbs Comparative analysis of a conserved zinc finger gene cluster on human chromosome 19q and mouse chromosome 7 Genomics 33 1996 112 120
15. L. Stubbs, E.A. Carver, M.E. Shannon Detailed comparative map of human chromosome 19q and related regions of the mouse genome Genomics 35 1996 499 508
16. J. Kim, L. Ashworth, E. Branscomb, L. Stubbs The human homolog of a mouse-imprinted gene, Peg3, maps to a zinc finger gene-rich region of human chromosome 19q13.4 Genome Res 7 1997 532 540
17. J. Kim, A. Bergmann, L. Stubbs Exon sharing of a novel human zinc-finger gene, ZIM2, and paternally expressed gene 3 (PEG3) Genomics 64 2000 114 118
18. J. Kim, A. Bergmann, E. Wehri, X. Lu, L. Stubbs Imprinting and evolution of two Kruppel-type zinc-finger genes, ZIM3 and ZNF264, located in the PEG3/USP29 imprinted domain Genomics 77 2001 91 98
19. L. Sunde, L.O. Vejerslev, M.P. Jensen, S. Pedersen, J.M. Hertz, L. Bolund Genetic analysis of repeated, biparental, diploid, hydatidiform moles Cancer Genet Cytogenet 66 1993 16 22
20. T.K. Al-Hussaini, D.M. Abd el-Aal, I.B. Van den Veyver Recurrent pregnancy loss due to familial and non-familial habitual molar pregnancy Int J Gynaecol Obstet 83 2003 179 186
21. O. El-Maarri, M. Seoud, P. Coullin Maternal alleles acquiring paternal methylation patterns in biparental complete hydatidiform moles Hum Mol Genet 12 2003 1405 1413
22. T.K. Al-Hussaini, M.A. Abdel-Alim Habitual complete molar pregnancy a case report Reprod Biomed Online 3 2001 133 135
23. D.W. Stockton, R.A. Lewis, E.B. Abboud A novel locus for Leber congenital amaurosis on chromosome 14q24 Hum Genet 103 1998 328 333
24. I.B. Van den Veyver, S. Subramanian, H.Y. Zoghbi Genomic structure of a human holocytochrome c-type synthetase gene in Xp22.3 and mutation analysis in patients with Rett syndrome Am J Med Genet 78 1998 179 181
25. L.G. Shaffer, G.M. Kennedy, A.S. Spikes, J.R. Lupski Diagnosis of CMT1A duplications and HNPP deletions by interphase FISH Implications for testing in the cytogenetics laboratory Am J Med Genet 69 1997 325 331
26. R.A. Fisher, R. Khatoon, F.J. Paradinas, A.P. Roberts, E.S. Newlands Repetitive complete hydatidiform mole can be biparental in origin and either male or female Hum Reprod 15 2000 594 598
27. E.S. Lander, L.M. Linton, B. Birren Initial sequencing and analysis of the human genome Nature 409 2001 860 921
28. D. Karolchik, R. Baertsch, M. Diekhans The UCSC Genome Browser Database Nucleic Acids Res 31 2003 51 54
29. C.Y. Howell, T.H. Bestor, F. Ding Genomic imprinting disrupted by a maternal effect mutation in the Dnmt1 gene Cell 104 2001 829 838
30. Z.B. Tong, C.A. Bondy, J. Zhou, L.M. Nelson A human homologue of mouse Mater, a maternal effect gene essential for early embryonic development Hum Reprod 17 2002 903 911
31. Z.B. Tong, L. Gold, K.E. Pfeifer Mater, a maternal effect gene required for early embryonic development in mice Nat Genet 26 2000 267 268
32. T. Miyamoto, S. Hasuike Isolation and expression analysis of the human RNH2 gene encoding ribonuclease inhibitor 2 J Assist Reprod Genet 19 2002 394 397
33. J.M. Grenier, L. Wang, G.A. Manji Functional screening of five PYPAF family members identifies PYPAF5 as a novel regulator of NF-kappaB and caspase-1 FEBS Lett 530 2002 73 78
34. P.J. Wang, J.R. McCarrey, F. Yang, D.C. Page An abundance of X-linked genes expressed in spermatogonia Nat Genet 27 2001 422 426
35. A. Rajkovic, J.H. Lee, C. Yan, M.M. Matzuk The ret finger protein-like 4 gene, Rfpl4, encodes a putative E3 ubiquitin-protein ligase expressed in adult germ cells Mech Dev 112 2002 173 177
36. N. Suzumori, K.H. Burns, W. Yan, M.M. Matzuk RFPL4 interacts with oocyte proteins of the ubiquitin-proteasome degradation pathway Proc Natl Acad Sci U S A 100 2003 550 555
37. K. Hata, M. Okano, H. Lei, E. Li Dnmt3L cooperates with the Dnmt3 family of de novo DNA methyltransferases to establish maternal imprints in mice Development 129 2002 1983 1993
38. B.E. Hayward, M. De Vos, H. Judson Lack of involvement of known DNA methyltransferases in familial hydatidiform mole implies the involvement of other factors in establishment of imprinting in the human female germline BMC Genet 4 2003 2