The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes.

chromothripsis complex sSMC discontinuous sSMC molecular cytogenetics neocentric sSMC optical genome mapping (OGM) small supernumerary marker chromosomes (sSMC)

Journal

Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304

Informations de publication

Date de publication:
10 May 2022
Historique:
received: 14 04 2022
revised: 04 05 2022
accepted: 07 05 2022
entrez: 28 5 2022
pubmed: 29 5 2022
medline: 29 5 2022
Statut: epublish

Résumé

Background: The majority of small supernumerary marker chromosomes (sSMCs) are derived from one single chromosome. Complex sSMCs instead consist of two to three genomic segments, originating from different chromosomes. Additionally, discontinuous sSMCs have been seen; however, all of them are derived from one single chromosome. Here, we reported a 41 year-old patient with infertility, hypothyroidism, rheumatism, and degenerative spine and schizoaffective disorder, being a carrier of a unique, complex, and discontinuous sSMC. Methods: The sSMC was characterized in detail by banding and molecular cytogenetics including fluorescence in situ hybridization (FISH) and array-comparative genomic hybridization (aCGH), as well as by optical genome mapping (OGM). Results: The neocentric sSMC characterized here contained seven portions of five different chromosomes and was present in ~50% of both peripheral blood cells and buccal mucosa cells. aCGH and OGM revealed gains of 8q12.3q12.3, 8q22.3−8q23.1, 9q33.3−9q34.11, 14q21.1−14q21.1, 14q21.1−14q21.2, 15q21.2−15q21.2, and 21q21.1−21q21.1. Furthermore, glass-needle based microdissection and reverse FISH, as well as FISH with locus-specific probes confirmed these results. The exact order of the involved euchromatic blocks could be decoded by OGM. Conclusions: Among the >7000 reported sSMCs in the literature, this is the only such complex, discontinuous, and neocentric marker with a centric minute shape.

Identifiants

pubmed: 35625839
pii: biomedicines10051102
doi: 10.3390/biomedicines10051102
pmc: PMC9138958
pii:
doi:

Types de publication

Case Reports

Langues

eng

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Auteurs

André Weber (A)

Medicover Genetics, MVZ Humangenetik Berlin-Lichtenberg, 13053 Berlin, Germany.

Thomas Liehr (T)

Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Am Klinikum 1, 07747 Jena, Germany.

Ahmed Al-Rikabi (A)

Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Am Klinikum 1, 07747 Jena, Germany.

Simal Bilgen (S)

Medicover Bochum MVZ, 44879 Bochum, Germany.

Uwe Heinrich (U)

Medicover Humangenetik Martinsried, MVZ Martinsried, 81667 München, Germany.

Jenny Schiller (J)

Medicover Humangenetik Martinsried, MVZ Martinsried, 81667 München, Germany.

Markus Stumm (M)

Medicover Genetics, MVZ Humangenetik Berlin-Lichtenberg, 13053 Berlin, Germany.

Classifications MeSH