These authors contributed equally to this work.
Mechanisms of Formation of Structural Variation in a Fully Sequenced Human Genome
Article first published online: 19 NOV 2012
© 2012 WILEY PERIODICALS, INC.
Volume 34, Issue 2, pages 345–354, February 2013
How to Cite
Pang, A. W. C., Migita, O., MacDonald, J. R., Feuk, L. and Scherer, S. W. (2013), Mechanisms of Formation of Structural Variation in a Fully Sequenced Human Genome. Hum. Mutat., 34: 345–354. doi: 10.1002/humu.22240
Communicated by Peter K. Rogan
Contract grant sponsors: The University of Toronto McLaughlin Centre, Genome Canada and the Ontario Genomics Institute; the Canadian Institutes for Health Research (CIHR); The Canadian Institute for Advanced Research; The Canada Foundation for Innovation; The Government of Ontario; The Hospital for Sick Children Foundation.
- Issue published online: 29 JAN 2013
- Article first published online: 19 NOV 2012
- Accepted manuscript online: 19 OCT 2012 01:40PM EST
- Manuscript Accepted: 2 OCT 2012
- Manuscript Received: 20 JUN 2012
- The University of Toronto McLaughlin Centre
- Genome Canada and the Ontario Genomics Institute
- Canadian Institutes for Health Research (CIHR)
- Canadian Institute for Advanced Research
- Canada Foundation for Innovation
- Government of Ontario
- Hospital for Sick Children Foundation
- structural variation;
- mutational mechanism;
- inversion polymorphism;
- personal genomics
Even with significant advances in technology, few studies of structural variation have yet resolved to the level of the precise nucleotide junction. We examined the sequence of 408,532 gains, 383,804 losses, and 166 inversions from the first sequenced personal genome, to quantify the relative proportion of mutational mechanisms. Among small variants (<1 kb), we observed that 72.6% of them were associated with nonhomologous processes and 24.9% with microsatellites events. Medium-size variants (<10 kb) were commonly related to minisatellites (25.8%) and retrotransposons (24%), whereas 46.2% of large variants (>10 kb) were associated with nonallelic homologous recombination. We genotyped eight new breakpoint-resolved inversions at (3q26.1, Xp11.22, 7q11.22, 16q23.1, 4q22.1, 1q31.3, 6q27, and 16q24.1) in human populations to elucidate the structure of these presumed benign variants. Three of these inversions (3q26.1, 7q11.22, and 16q23.1) were accompanied by unexpected complex rearrangements. In particular, the 16q23.1 inversion and an accompanying deletion would create conjoined chymotrypsinogen genes (CTRB1 and CTRB2), disrupt their gene structure, and exhibit differentiated allelic frequencies among populations. Also, two loci (Xp11.3 and 6q27) of potential reference assembly orientation errors were found. This study provides a thorough account of formation mechanisms for structural variants, and reveals a glimpse of the dynamic structure of inversions.