Features of chromosomal abnormalities in spontaneous abortion cell culture failures detected by interphase FISH analysis
- 31 March 2004
- journal article
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 12 (7) , 513-520
- https://doi.org/10.1038/sj.ejhg.5201178
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.Keywords
This publication has 32 references indexed in Scilit:
- Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH)–Re-evaluation of chromosome aberration rates in early spontaneous abortionsEuropean Journal of Human Genetics, 2001
- The contribution of uniparental disomy to congenital development defects in children born to mothers at advanced childbearing ageAmerican Journal of Medical Genetics, 2000
- Comparative Genomic Hybridization in Combination with Flow Cytometry Improves Results of Cytogenetic Analysis of Spontaneous AbortionsAmerican Journal of Human Genetics, 2000
- Studies of non-disjunction in trisomies 2, 7, 15, and 22: does the parental origin of trisomy influence placental morphology?Journal of Medical Genetics, 1998
- Amniotic fluid culture failure: clinical significance and association with aneuploidyObstetrics & Gynecology, 1996
- Mosaicism of autosomes and sex chromosomes in morphologically normal, monospermic preimplantation human embryosPrenatal Diagnosis, 1995
- Early embryonic failure associated with uniparental disomy for human chromosome 21Human Molecular Genetics, 1994
- Abnormal maternal serum chorionic gonadotropin levels in pregnancies with fetal chromosome abnormalitiesPrenatal Diagnosis, 1987
- Morphology of early fetal deaths and their chromosomal characteristicsTeratology, 1985
- A cytogenetic study of 1000 spontaneous abortionsAnnals of Human Genetics, 1980