Literature DB >> 15747166

Paternal uniparental disomy of chromosome 14 and unique exchange of chromosome 7 in cases of spontaneous abortion.

Sami Tsukishiro1, Qing Ying Li1, Mitsuyo Tanemura1, Mayumi Sugiura-Ogasawara1, Kaoru Suzumori1, Shin-Ichi Sonta2.   

Abstract

To investigate the involvement of uniparental disomies (UPDs) in spontaneous abortion, the polymorphic patterns of microsatellites on each chromosome were analyzed in 164 cases of abortion. Eighty-three of the 164 cases had chromosomal abnormalities. In 79 of the remaining 81 cases with normal karyotypes, the microsatellite analysis revealed that biparental patterns were present in the informative microsatellites in all chromosomes. In one of the remaining two cases, however, the polymorphic patterns of chromosome 14 appeared to be both of paternal origin. The patterns of the distal of the long arm were homozygous, and those of the remaining region were heterozygous. That is, this fetus had paternal UPD 14, originating from meiosis I nondisjunction. In the other case, the polymorphic patterns of the distal one third of the long arm of chromosome 7 were uniparental (maternal) in origin whereas those of the remaining region of this chromosome were biparental. These findings thus suggested that this chromosome might have originated from chromatid exchange between the long arms of paternal and maternal chromosome 7 at the first mitotic division. Microsatellite analysis, however, produced no evidence of duplication or deletion of any segments. The findings also suggest the possibility that some UPDs may cause spontaneous abortion.

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Year:  2005        PMID: 15747166     DOI: 10.1007/s10038-005-0229-9

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  49 in total

1.  Sex ratio and absence of uniparental disomy in spontaneous abortions with a normal karyotype.

Authors:  M J Smith; M R Creasy; A Clarke; M Upadhyaya
Journal:  Clin Genet       Date:  1998-04       Impact factor: 4.438

2.  The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32.

Authors:  M Fujimoto; P N Kantaputra; S Ikegawa; Y Fukushima; S Sonta; M Matsuo; T Ishida; T Matsumoto; S Kondo; H Tomita; H X Deng; M D'urso; M M Rinaldi; V Ventruto; T Takagi; Y Nakamura; N Niikawa
Journal:  J Hum Genet       Date:  1998       Impact factor: 3.172

3.  Immunological and genetic factors influencing pregnancy and development.

Authors:  T J Gill
Journal:  Am J Reprod Immunol Microbiol       Date:  1986-03

4.  Anatomic and chromosomal anomalies in 639 spontaneous abortuses.

Authors:  T Kajii; A Ferrier; N Niikawa; H Takahara; K Ohama; S Avirachan
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

5.  A narrow segment of maternal uniparental disomy of chromosome 7q31-qter in Silver-Russell syndrome delimits a candidate gene region.

Authors:  K Hannula; M Lipsanen-Nyman; T Kontiokari; J Kere
Journal:  Am J Hum Genet       Date:  2000-12-08       Impact factor: 11.025

Review 6.  Maternal uniparental disomy for chromosome 14 in a boy with a normal karyotype.

Authors:  R Hordijk; H Wierenga; H Scheffer; B Leegte; R M Hofstra; I Stolte-Dijkstra
Journal:  J Med Genet       Date:  1999-10       Impact factor: 6.318

7.  The importance of investigating for uniparental disomy in prenatally identified balanced acrocentric rearrangements.

Authors:  Kathryn D McGowan; Joseph J Weiser; Juli Horwitz; Sue Ann Berend; Christopher McCaskill; V Reid Sutton; Lisa G Shaffer
Journal:  Prenat Diagn       Date:  2002-02       Impact factor: 3.050

Review 8.  Paternal uniparental disomy for chromosome 14: a case report and review.

Authors:  P D Cotter; S Kaffe; L D McCurdy; M Jhaveri; J P Willner; K Hirschhorn
Journal:  Am J Med Genet       Date:  1997-05-02

9.  Maternal uniparental disomy for chromosome 14 with diabetes mellitus.

Authors:  Masahito Katahira; Tomohiko Kayashima; Tatsuya Kishino; Norio Niikawa
Journal:  Intern Med       Date:  2002-09       Impact factor: 1.271

Review 10.  Systematic search for uniparental disomy in early fetal losses: the results and a review of the literature.

Authors:  L G Shaffer; C McCaskill; K Adkins; T J Hassold
Journal:  Am J Med Genet       Date:  1998-10-12
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  2 in total

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Authors:  Elena A Sazhenova; Tatyana V Nikitina; Stanislav A Vasilyev; Ekaterina N Tolmacheva; Oksana Yu Vasilyeva; Anton V Markov; Sergey Yu Yuryev; Nikolay A Skryabin; Alexey A Zarubin; Nikita A Kolesnikov; Vadim A Stepanov; Igor N Lebedev
Journal:  J Assist Reprod Genet       Date:  2021-09-23       Impact factor: 3.412

2.  Diagnostic utility of novel combined arrays for genome-wide simultaneous detection of aneuploidy and uniparental isodisomy in losses of pregnancy.

Authors:  Stefanie Bug; Beate Solfrank; Felizitas Schmitz; Jana Pricelius; Mona Stecher; Andrew Craig; Marc Botcherby; Claudia Nevinny-Stickel-Hinzpeter
Journal:  Mol Cytogenet       Date:  2014-06-24       Impact factor: 2.009

  2 in total

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