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Parental origin of deletions and duplications - about the necessity to check for cryptic inversions
- Source :
- Molecular Cytogenetics, Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-8 (2018)
- Publication Year :
- 2018
-
Abstract
- Background Copy number variants (CNVs) are the genetic bases for microdeletion/ microduplication syndromes (MMSs). Couples with an affected child and desire to have further children are routinely tested for a potential parental origin of a specific CNV either by molecular karyotyping or by two color fluorescence in situ hybridization (FISH), yet. In the latter case a critical region probe (CRP) is combined with a control probe for identification of the chromosome in question. However, CNVs can arise also due to other reasons, like a recombination-event based on a submicroscopic, cryptic inversion in one of the parents. Results Seventy-four patients with different MMSs and overall 81 CNVs were studied here by a novel three color FISH approach. The way how three locus-specific probes are selected (one is the CRP and two are flanking it in a distance of 5-10 Mb) enables to detect or exclude two possible parental conditions as origins of the CNV seen in the index: (i) direct parental origin of the CNV (deletion or duplication) or (ii) a parental cryptic inversion. Thus, for overall 51/81 CNVs (63%) a parental origin could be determined. 36/51 (70.5%) inherited the CNV directly from one of the parents, but 15/51 (29.5%) were due to an exclusively by three color FISH detectable parental inversion. A 2:1 ratio of maternal versus paternal inheritance was found. Also almost two times more male than female were among the index patients. Conclusion The new, here suggested three color FISH approach is suited for more comprehensive parental studies of patients with MMS. The detection rate for parental origin was increased by 140% in this study. Still, for 30/81 cases (37%) no reason for the ‘de novo’ MMS in the affected index patient could be found by the here suggested FISH-probe set. Electronic supplementary material The online version of this article (10.1186/s13039-018-0369-1) contains supplementary material, which is available to authorized users.
- Subjects :
- 0301 basic medicine
medicine.medical_specialty
lcsh:QH426-470
Duplication
Copy number variants (CNVs)
Medizin
030105 genetics & heredity
Biology
Biochemistry
Deletion
03 medical and health sciences
Gene duplication
Genetics
medicine
Copy-number variation
Three color fluorescence in situ hybridization (FISH)
Paternal Inheritance
Molecular Biology
Genetics (clinical)
medicine.diagnostic_test
Research
Biochemistry (medical)
Cytogenetics
Inversion
Chromosome
Karyotype
Human genetics
lcsh:Genetics
030104 developmental biology
Molecular Medicine
Fluorescence in situ hybridization
Microdeletion/microduplication syndromes (MMSs)
Subjects
Details
- ISSN :
- 17558166
- Volume :
- 11
- Database :
- OpenAIRE
- Journal :
- Molecular cytogenetics
- Accession number :
- edsair.doi.dedup.....b68c279ca05381ad2f6d3d5d41b7010e