Chromothripsis and ring chromosome 22: A paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome)

Nehir Kurtas, Filippo Arrigoni, Edoardo Errichiello, Claudio Zucca, Cristina Maghini, Maria Grazia D'Angelo, Silvana Beri, Roberto Giorda, Sara Bertuzzo, Massimo Delledonne, Luciano Xumerle, Marzia Rossato, Orsetta Zuffardi, Maria Clara Bonaglia

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Introduction Phelan-McDermid syndrome (PMS) is caused by SHANK3 haploinsufficiency. Its wide phenotypic variation is attributed partly to the type and size of 22q13 genomic lesion (deletion, unbalanced translocation, ring chromosome), partly to additional undefined factors. We investigated a child with severe global neurodevelopmental delay (NDD) compatible with her distal 22q13 deletion, complicated by bilateral perisylvian polymicrogyria (BPP) and urticarial rashes, unreported in PMS. Methods Following the cytogenetic and array-comparative genomic hybridization (CGH) detection of a r(22) with SHANK3 deletion and two upstream duplications, whole-genome sequencing (WGS) in blood and whole-exome sequencing (WES) in blood and saliva were performed to highlight potential chromothripsis/chromoanagenesis events and any possible BPP-associated variants, even in low-level mosaicism. Results WGS confirmed the deletion and highlighted inversion and displaced order of eight fragments, three of them duplicated. The microhomology-mediated insertion of partial Alu-elements at one breakpoint junction disrupted the topological associating domain joining NFAM1 to the transcriptional coregulator TCF20. WES failed to detect BPP-associated variants. Conclusions Although we were unable to highlight the molecular basis of BPP, our data suggest that SHANK3 haploinsufficiency and TCF20 misregulation, both associated with intellectual disability, contributed to the patient's NDD, while NFAM1 interruption likely caused her skin rashes, as previously reported. We provide the first example of chromoanasynthesis in a constitutional ring chromosome and reinforce the growing evidence that chromosomal rearrangements may be more complex than estimated by conventional diagnostic approaches and affect the phenotype by global alteration of the topological chromatin organisation rather than simply by deletion or duplication of dosage-sensitive genes.

Original languageEnglish
Pages (from-to)269-277
Number of pages9
JournalJournal of Medical Genetics
Volume55
Issue number4
DOIs
Publication statusPublished - Apr 1 2018

Fingerprint

Ring Chromosomes
Exome
Haploinsufficiency
Exanthema
Alu Elements
Genome
Mosaicism
Comparative Genomic Hybridization
Gene Dosage
Saliva
Cytogenetics
Intellectual Disability
Chromatin
Phenotype
Chromosome 22 ring
Perisylvian syndrome
Telomeric 22q13 Monosomy Syndrome
Chromothripsis

Keywords

  • NFAM1
  • polymicrogyria
  • SHANK3
  • TCF20
  • topologically associating domains

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Chromothripsis and ring chromosome 22 : A paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome). / Kurtas, Nehir; Arrigoni, Filippo; Errichiello, Edoardo; Zucca, Claudio; Maghini, Cristina; D'Angelo, Maria Grazia; Beri, Silvana; Giorda, Roberto; Bertuzzo, Sara; Delledonne, Massimo; Xumerle, Luciano; Rossato, Marzia; Zuffardi, Orsetta; Bonaglia, Maria Clara.

In: Journal of Medical Genetics, Vol. 55, No. 4, 01.04.2018, p. 269-277.

Research output: Contribution to journalArticle

Kurtas, Nehir ; Arrigoni, Filippo ; Errichiello, Edoardo ; Zucca, Claudio ; Maghini, Cristina ; D'Angelo, Maria Grazia ; Beri, Silvana ; Giorda, Roberto ; Bertuzzo, Sara ; Delledonne, Massimo ; Xumerle, Luciano ; Rossato, Marzia ; Zuffardi, Orsetta ; Bonaglia, Maria Clara. / Chromothripsis and ring chromosome 22 : A paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome). In: Journal of Medical Genetics. 2018 ; Vol. 55, No. 4. pp. 269-277.
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abstract = "Introduction Phelan-McDermid syndrome (PMS) is caused by SHANK3 haploinsufficiency. Its wide phenotypic variation is attributed partly to the type and size of 22q13 genomic lesion (deletion, unbalanced translocation, ring chromosome), partly to additional undefined factors. We investigated a child with severe global neurodevelopmental delay (NDD) compatible with her distal 22q13 deletion, complicated by bilateral perisylvian polymicrogyria (BPP) and urticarial rashes, unreported in PMS. Methods Following the cytogenetic and array-comparative genomic hybridization (CGH) detection of a r(22) with SHANK3 deletion and two upstream duplications, whole-genome sequencing (WGS) in blood and whole-exome sequencing (WES) in blood and saliva were performed to highlight potential chromothripsis/chromoanagenesis events and any possible BPP-associated variants, even in low-level mosaicism. Results WGS confirmed the deletion and highlighted inversion and displaced order of eight fragments, three of them duplicated. The microhomology-mediated insertion of partial Alu-elements at one breakpoint junction disrupted the topological associating domain joining NFAM1 to the transcriptional coregulator TCF20. WES failed to detect BPP-associated variants. Conclusions Although we were unable to highlight the molecular basis of BPP, our data suggest that SHANK3 haploinsufficiency and TCF20 misregulation, both associated with intellectual disability, contributed to the patient's NDD, while NFAM1 interruption likely caused her skin rashes, as previously reported. We provide the first example of chromoanasynthesis in a constitutional ring chromosome and reinforce the growing evidence that chromosomal rearrangements may be more complex than estimated by conventional diagnostic approaches and affect the phenotype by global alteration of the topological chromatin organisation rather than simply by deletion or duplication of dosage-sensitive genes.",
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AU - Errichiello, Edoardo

AU - Zucca, Claudio

AU - Maghini, Cristina

AU - D'Angelo, Maria Grazia

AU - Beri, Silvana

AU - Giorda, Roberto

AU - Bertuzzo, Sara

AU - Delledonne, Massimo

AU - Xumerle, Luciano

AU - Rossato, Marzia

AU - Zuffardi, Orsetta

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