Very short DNA segments can be detected and handled by the repair machinery during germline chromothriptic chromosome reassembly

• Published in: Human mutation Vol. 39; no. 5; pp. 709 - 716
• Main Authors: Slamova, Zuzana, Nazaryan‐Petersen, Lusine, Mehrjouy, Mana M., Drabova, Jana, Hancarova, Miroslava, Marikova, Tatana, Novotna, Drahuse, Vlckova, Marketa, Vlckova, Zdenka, Bak, Mads, Zemanova, Zuzana, Tommerup, Niels, Sedlacek, Zdenek
• Format: Journal Article
• Language: English
• Published: United States Hindawi Limited 01.05.2018
• Subjects: Adolescent; Adult; alternative non‐homologous end joining; Base Sequence; Breakpoints; Child, Preschool; Chromosome rearrangements; Chromosomes; Chromosomes, Human - genetics; Chromothripsis; complex chromosome aberration; Deoxyribonucleic acid; DNA; DNA - genetics; DNA microarrays; DNA Repair; Gene expression; Genomes; Germ Cells - metabolism; Humans; Infant; Infant, Newborn; Karyotype; Literature reviews; Male; small insertions; whole‐genome sequencing; complex chromosome aberration; alternative non-homologous end joining; DNA repair; small insertions; whole-genome sequencing; chromothripsis
• ISSN: 1059-7794; 1098-1004
• DOI: 10.1002/humu.23408

Analyses at nucleotide resolution reveal unexpected complexity of seemingly simple and balanced chromosomal rearrangements. Chromothripsis is a rare complex aberration involving local shattering of one or more chromosomes and reassembly of the resulting DNA segments. This can influence gene expression and cause abnormal phenotypes. We studied the structure and mechanism of a seemingly balanced de novo complex rearrangement of four chromosomes in a boy with developmental and growth delay. Microarray analysis revealed two paternal de novo deletions of 0.7 and 2.5 Mb at two of the breakpoints in 1q24.3 and 6q24.1‐q24.2, respectively, which could explain most symptoms of the patient. Subsequent whole‐genome mate‐pair sequencing confirmed the chromothriptic nature of the rearrangement. The four participating chromosomes were broken into 29 segments longer than 1 kb. Sanger sequencing of all breakpoint junctions revealed additional complexity compatible with the involvement of different repair pathways. We observed translocation of a 33 bp long DNA fragment, which may have implications for the definition of the lower size limit of structural variants. Our observations and literature review indicate that even very small fragments from shattered chromosomes can be detected and handled by the repair machinery during germline chromothriptic chromosome reassembly. Seemingly balanced rearrangements including chromothripsis (local chromosome shattering and random reassembly of segments) turn out to be more complex upon detailed analysis. De novo chromothripsis in a boy with developmental and growth delay was initially thought to involve 11 segments. Microarrays identified two large de novo deletions, and whole‐genome sequencing revealed the involvement of 29 segments, with a 33 bp fragment translocated to one junction. Therefore, even very small fragments can arise and be handled by the chromothriptic repair machinery.