Journal
HUMAN GENETICS
Volume 140, Issue 5, Pages 775-790Publisher
SPRINGER
DOI: 10.1007/s00439-020-02242-3
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Funding
- Karolinska Institute
- SciLifeLab national sequencing projects
- Swedish Research Council [2017-02936, 2019-02078]
- Stockholm City Council
- Swedish Brain Foundation
- Karolinska Institutet funding for doctoral education (KID)
- Swedish Research Council [2017-02936, 2019-02078] Funding Source: Swedish Research Council
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This study reported a healthy female carrying two novel CCRs and characterized these complex rearrangements. The results were validated using multiple cytogenetic methods, revealing the highest number of breakpoint junctions (137) and indicating an association between CCR formation and active gene transcription.
Chromoanagenesis is a genomic event responsible for the formation of complex structural chromosomal rearrangements (CCRs). Germline chromoanagenesis is rare and the majority of reported cases are associated with an affected phenotype. Here, we report a healthy female carrying two de novo CCRs involving chromosomes 4, 19, 21 and X and chromosomes 7 and 11, respectively, with a total of 137 breakpoint junctions (BPJs). We characterized the CCRs using a hybrid-sequencing approach, combining short-read sequencing, nanopore sequencing, and optical mapping. The results were validated using multiple cytogenetic methods, including fluorescence in situ hybridization, spectral karyotyping, and Sanger sequencing. We identified 137 BPJs, which to our knowledge is the highest number of reported breakpoint junctions in germline chromoanagenesis. We also performed a statistical assessment of the positioning of the breakpoints, revealing a significant enrichment of BPJ-affecting genes (96 intragenic BPJs, 26 genes, p < 0.0001), indicating that the CCRs formed during active transcription of these genes. In addition, we find that the DNA fragments are unevenly and non-randomly distributed across the derivative chromosomes indicating a multistep process of scattering and re-joining of DNA fragments. In summary, we report a new maximum number of BPJs (137) in germline chromoanagenesis. We also show that a hybrid sequencing approach is necessary for the correct characterization of complex CCRs. Through in-depth statistical assessment, it was found that the CCRs most likely was formed through an event resembling chromoplexy-a catastrophic event caused by erroneous transcription factor binding.
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