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. 2007 Oct 19;318(5849):420-6.
doi: 10.1126/science.1149504. Epub 2007 Sep 27.

Paired-end mapping reveals extensive structural variation in the human genome

Jan O Korbel  1 , Alexander Eckehart Urban, Jason P Affourtit, Brian Godwin, Fabian Grubert, Jan Fredrik Simons, Philip M Kim, Dean Palejev, Nicholas J Carriero, Lei Du, Bruce E Taillon, Zhoutao Chen, Andrea Tanzer, A C Eugenia Saunders, Jianxiang Chi, Fengtang Yang, Nigel P Carter, Matthew E Hurles, Sherman M Weissman, Timothy T Harkins, Mark B Gerstein, Michael Egholm, Michael Snyder
Affiliations

Paired-end mapping reveals extensive structural variation in the human genome

Jan O Korbel et al. Science. .

Abstract

Structural variation of the genome involves kilobase- to megabase-sized deletions, duplications, insertions, inversions, and complex combinations of rearrangements. We introduce high-throughput and massive paired-end mapping (PEM), a large-scale genome-sequencing method to identify structural variants (SVs) approximately 3 kilobases (kb) or larger that combines the rescue and capture of paired ends of 3-kb fragments, massive 454 sequencing, and a computational approach to map DNA reads onto a reference genome. PEM was used to map SVs in an African and in a putatively European individual and identified shared and divergent SVs relative to the reference genome. Overall, we fine-mapped more than 1000 SVs and documented that the number of SVs among humans is much larger than initially hypothesized; many of the SVs potentially affect gene function. The breakpoint junction sequences of more than 200 SVs were determined with a novel pooling strategy and computational analysis. Our analysis provided insights into the mechanisms of SV formation in humans.

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Figures

Fig. 1
Fig. 1
(A) Flow chart illustrating PEM. (i) Genomic DNA was sheared to yield DNA fragments ~3 kb; (ii) biotinylated hairpin adapters were ligated to the fragment ends; (iii) fragments were circularized (iv) and randomly sheared; (v) linker (+) fragments were isolated; (vi) the library was subjected to 454 sequencing (13). (vii) Paired ends were analyzed computationally to determine (viii) the distribution of “paired-end spans” (shown for a single 454 sequencing pool). (B) Types of SVs. Deletions were predicted from paired-end spans larger than a specified cutoff D; simple insertions had a span < cutoff I; inversions are seen when ends map to the genome at different relative orientations; other types of insertions (defined in the text as mated and unmated) were detected with evidence of sequence integration from a distal locus.
Fig. 2
Fig. 2
SVs identified in two humans. (A) SVs mapped onto chromosomal ideograms (12). Right side: Red, deletion; blue, insertion; and yellow, inversion. Double length indicates SVs observed in both individuals. Left side: Log-scale size of an event (events ≥1 Mb are drawn at same length, corresponding to the maximum length of a line); unmated insertions [i.e., events lacking a predicted breakpoint and thus size information (12)] and simple insertions (12) are depicted with 1-kb lines; line colors indicate repetitive sequences in ±3-kb window of the predicted breakpoint junction (12): red, SDs; blue, LINEs; yellow, LTRs; green, satellites; black, two or more repetitive elements with equal frequency; gray, no repeat association. The arrow indicates the region in (B). A high-resolution image of this figure is available as fig. S1. (B) Amplified view of chromosome 4 region. SVs in NA18505 are indicated with dashed lines (validation: squares); NA15510, dotted lines (validation: circle). SVs shared between individuals are solid lines. Colors are as in (A).
Fig. 3
Fig. 3
SV size distribution, sequence coverage, genes, and distribution of gene categories. (A) Size distribution of SVs (NA15510 and NA18505 combined). Arrow indicates the lower size cutoff for deletions. (B) Cumulative number of base pairs affected by SVs in relation to SV size (NA18505 only). (C) Solid line indicates cumulative number of RefSeq genes intersecting with SVs in relation to SV size (NA18505 only). Dashed line, randomly shuffled SV locations within the local genomic context (±50-kb window) exhibit an increase in gene overlap. (D) Enrichment or depletion of GO (annotation level 3) biological processes for genes intersecting with SVs (NA15510 and NA18505 combined). Annotations represented by <10 genes are designated “other” and are gray. **Significant enrichment in genes belonging to a category (P < 1e−14)​(​12); *significant depletion (P < 0.001).
Fig. 4
Fig. 4
Validation of SVs. (A) A 170-kb deletion detected with both array-CGH and PEM. (B) PCR products validating SVs as originally predicted from NA18505 (lane 2). Lanes 1 to 4 use DNAs from NA15510, NA18505, NA11997 (HapMap CEU, cell lines derived from 30 trios of European descent), and NA18614 (HapMap CHB, Han Chinese from Beijing), respectively. Primer sequences can be found in table S6. (C) Fiber-FISH validation of heterozygous inversions in NA18505. The inversion in the upper panel was independently validated in NA15510. Alternating patterns of fluorescent labels from adjacent probes indicate genomic rearrangement.
Fig. 5
Fig. 5
Sequencing and analysis of SV breakpoint junctions. (A) PCR fragments spanning SVs were pooled and sequenced; breakpoints were determined from assembled contigs or ≥2 sequencing reads. (B) Representative sequenced SVs shown in relation to previous SV and/or CNV assignments [earlier SV and CNV assignments often extend outside of the depicted regions (3, 4)]. From top to bottom: SVs resulting from NHEJ, L1 retrotransposition, HERVK (retrovirus) insertion, (nonallelic) homologous recombination, gap closure (blue, insertions; red, deletions; orange, sequence gap; and yellow, inversions). Note that some SVs affect annotated genes. (C) Example breakpoint sequences (12). Upper case and green letters are for unaltered sequence; lower case for SV indel; solid arrows show microhomologies (indicative of NHEJ), duplication of target sequences (at retrotransposon or retrovirus insertion sites), and long stretches of sequence identity (12) (indicative of homologous recombination). Note that the fourth sequence (from top to bottom) shows an OR gene fusion in the main reading frame (breakpoints occurred in the long stretch of sequence identity).
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