Literature DB >> 15054396

Features of chromosomal abnormalities in spontaneous abortion cell culture failures detected by interphase FISH analysis.

Igor N Lebedev1, Nadezhda V Ostroverkhova, Tatyana V Nikitina, Natalia N Sukhanova, Sergey A Nazarenko.   

Abstract

Cytogenetic analysis of reproductive wastage is an important stage in understanding the genetic background of early embryogenesis. The results of conventional cytogenetic studies of spontaneous abortions depend on tissue culturing and are associated with a significant cell culture failure rate. We performed interphase dual-colour FISH analysis to detect chromosomal abnormalities in noncultured cells from two different tissues-cytotrophoblast and extraembryonic mesoderm-of 60 first-trimester spontaneous abortions from which cells had failed to grow in culture. An original algorithm was proposed to optimize the interphase karyotype screening with a panel of centromere-specific DNA probes for all human chromosomes. The overall rate of numerical chromosomal abnormalities in these cells was 53%. Both typical and rare forms of karyotype imbalance were found. The observation of six cases (19%) of monosomy 7, 15, 21 and 22 in mosaic form, with a predominant normal cell line, was the most unexpected finding. Cell lines with monosomies 21 and 22 were found both in cytotrophoblast and mesoderm, while cells with monosomy 7 and 15 were confined to the cytotrophoblast. The tissue-specific compartmentalization of cell lines with autosomal monosomies provides evidence that the aneuploidy of different human chromosomes may arise during different stages of intrauterine development. The effect of aneuploidy on selection may differ, however, depending on the specific chromosome. The abortions also revealed a high frequency of intratissue chromosomal mosaicism (94%), in comparison with that detected by conventional cytogenetic analysis (29%; P<0.001). Confined placental mosaicism was found in 25% of the embryos. The results of molecular cytogenetic analysis of these cell culture failures illustrate that the diversity and phenotypic effects of chromosomal abnormalities during the early stages of human development are underestimated.

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Year:  2004        PMID: 15054396     DOI: 10.1038/sj.ejhg.5201178

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  13 in total

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3.  Karyotype evaluation of repeated abortions in primary and secondary recurrent pregnancy loss.

Authors:  T V Nikitina; E A Sazhenova; D I Zhigalina; E N Tolmacheva; N N Sukhanova; I N Lebedev
Journal:  J Assist Reprod Genet       Date:  2020-02-03       Impact factor: 3.412

Review 4.  From contemplation to classification of chromosomal mosaicism in human preimplantation embryos.

Authors:  Igor N Lebedev; Daria I Zhigalina
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5.  NLRP7 variants in spontaneous abortions with multilocus imprinting disturbances from women with recurrent pregnancy loss.

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Review 6.  Stem Cell-Based Trophoblast Models to Unravel the Genetic Causes of Human Miscarriages.

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Review 7.  Chromosomal instability in mammalian pre-implantation embryos: potential causes, detection methods, and clinical consequences.

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Journal:  Cell Tissue Res       Date:  2015-11-21       Impact factor: 5.249

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Journal:  PLoS One       Date:  2014-03-20       Impact factor: 3.240

10.  LINE-1 retrotransposon methylation in chorionic villi of first trimester miscarriages with aneuploidy.

Authors:  Stanislav A Vasilyev; Ekaterina N Tolmacheva; Oksana Yu Vasilyeva; Anton V Markov; Daria I Zhigalina; Lada A Zatula; Vasilissa A Lee; Ekaterina S Serdyukova; Elena A Sazhenova; Tatyana V Nikitina; Anna A Kashevarova; Igor N Lebedev
Journal:  J Assist Reprod Genet       Date:  2020-11-10       Impact factor: 3.412

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