| Literature DB >> 30827684 |
Christine R Beck1, Claudia M B Carvalho1, Zeynep C Akdemir1, Fritz J Sedlazeck2, Xiaofei Song1, Qingchang Meng2, Jianhong Hu2, Harsha Doddapaneni2, Zechen Chong3, Edward S Chen1, Philip C Thornton1, Pengfei Liu1, Bo Yuan1, Marjorie Withers1, Shalini N Jhangiani2, Divya Kalra2, Kimberly Walker2, Adam C English2, Yi Han2, Ken Chen4, Donna M Muzny2, Grzegorz Ira1, Chad A Shaw1, Richard A Gibbs5, P J Hastings6, James R Lupski7.
Abstract
DNA rearrangements resulting in human genome structural variants (SVs) are caused by diverse mutational mechanisms. We used long- and short-read sequencing technologies to investigate end products of de novo chromosome 17p11.2 rearrangements and query the molecular mechanisms underlying both recurrent and non-recurrent events. Evidence for an increased rate of clustered single-nucleotide variant (SNV) mutation in cis with non-recurrent rearrangements was found. Indel and SNV formation are associated with both copy-number gains and losses of 17p11.2, occur up to ∼1 Mb away from the breakpoint junctions, and favor C > G transversion substitutions; results suggest that single-stranded DNA is formed during the genesis of the SV and provide compelling support for a microhomology-mediated break-induced replication (MMBIR) mechanism for SV formation. Our data show an additional mutational burden of MMBIR consisting of hypermutation confined to the locus and manifesting as SNVs and indels predominantly within genes.Entities:
Keywords: CNVs; DNA repair; complex rearrangements; genomic characterization; genomic disorders; long-read sequencing; phasing
Mesh:
Year: 2019 PMID: 30827684 PMCID: PMC6438178 DOI: 10.1016/j.cell.2019.01.045
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582