Novel pericentric inversion inv(9)(p23q22.3) in unrelated individuals with fertility problems in the Southeast European population
Autor: | Pavlina Iliopoulou, Efstathios Tsitsopoulos, Ioannis Papaevripidou, Voula Velissariou, Dagmar Huhle, Maria Syrrou, Rozalia Neroutsou, Angelos Alexandrou, Stamatia-Maria Rapti, Monika Ziegler, Ludmila Kousoulidou, Marianna Robola, Sigrid Fuchs, Maja Hempel, Carolina Sismani, Athina Theodosiou, Max Duesberg, Magdalini Lagou, Thomas Liehr, Anastasia Spring |
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Rok vydání: | 2020 |
Předmět: |
Adult
Male 0301 basic medicine Proband Heterozygote Perinatal Death Population Chromosome 9 030105 genetics & heredity Biology Identity by descent 03 medical and health sciences Pregnancy Germany Genetics Humans Child education In Situ Hybridization Fluorescence Genetics (clinical) Chromosomal inversion education.field_of_study Greece Haplotype Infant Newborn Karyotype Oligospermia Microarray Analysis Abortion Spontaneous Fertility 030104 developmental biology Karyotyping Chromosome Inversion Cyprus Female Chromosomes Human Pair 9 Founder effect |
Zdroj: | Journal of Human Genetics. 65:783-795 |
ISSN: | 1435-232X 1434-5161 |
DOI: | 10.1038/s10038-020-0769-z |
Popis: | Pericentric inversions are among the known polymorphisms detected in the general population at a frequency of 1-2%. Despite their generally benign nature, pericentric inversions affect the reproductive potential of carriers by increasing the risk for unbalanced live-born offspring, miscarriages, or other fertility problems. Here we present a novel large pericentric inversion of chromosome 9, inv(9)(p23q22.3), detected in 30 heterozygote carriers, 24 from seven apparently unrelated families and 6 isolated patients, where the probands were mainly referred for fertility and prenatal problems. The inversion carries a significant risk for recombinant abnormal chromosomes, as in two families one supernumerary rec(9)dup(9p) and one rec(9)dup(9q) were identified, leading to neonatal death and miscarriage, respectively. The inversion carriers were identified by three different laboratories in Greece, Cyprus and Germany respectively, however all carriers have Southeast European origin. The inversion appears to be more frequent in the Greek population, as the majority of the carriers were identified in Greece. We were able to determine that the inversion is identical in all individuals included in the study by applying a combination of several methodologies, such as karyotype, fluorescence in situ hybridization (FISH), chromosomal microarrays (CMA) and haplotype analysis. In addition, haplotype analysis supports that the present inversion is identical by descent (IBD) inherited from a single common ancestor. Our results are, therefore, highly indicative of a founder effect of this inversion, presumably reflecting an event that was present in a small number of individuals that migrated to the current Southeast Europe/Northern Greece from a larger population. |
Databáze: | OpenAIRE |
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