1. Volume 1, Issue 1, Pages 89-97 (February 2002)
A role for common fragile site induction in amplification of human oncogenes 
Asaf Hellman, Eitan Zlotorynski, Stephen W Scherer, Joseph Cheung, John B Vincent, David I Smith, Luba Trakhtenbrot, Batsheva Kerem 
Cancer Cell 
Volume 1, Issue 1, Pages (February 2002)
DOI: /S (02)00017-X

2. Figure 1
A scheme illustrating gene amplification via breakage-fusion-bridge cycles
Amplicons, yellow triangles; telomeres, orange (p-arm) or black (q-arm) circles; centromeres, orange rectangles. A: Interphase—an initial break gives rise to an uncapped chromatid carrying the selected gene. B: Metaphase—fusion of the 2 uncapped sister chromatids results in a dicentric chromosome. C: Anaphase—the dicentric chromosome forms a bridge between the opposite poles. A break of this chromosome leaves one daughter cell (D) with 3 copies of the selected gene, and only one copy in the other cell (E). Under a selection, recurrent cycles of BFB will occur, resulting in further accumulation of amplicon copies.
Cancer Cell 2002 1, 89-97DOI: ( /S (02)00017-X)

3. Figure 2 Organization of the MET amplicons relative to FRA7G region
A: The organization of the MET amplicons along a GTL-16 metaphase chromosome, analyzed by FISH using clone V193A as a probe. Insert: Computational representation of the FISH signals (red) and the DAPI staining (blue) along the amplified marker chromosome. B: FISH analysis of the FRA7G region. Upper panels: metaphase chromosomes expressing FRA7G (white triangles), stained with propidium iodide (PI). FRA7G are seen as unstained gaps. Bottom: the same chromosomes probed with a MET clone (cosmid c169h6, green arrow) and a reference clone from 7q32 to mark chromosome 7. The MET signals appear telomeric (left) or centromeric (right) to FRA7G gaps. C: Upper panel: A metaphase chromosome stained with PI, expressing both FRA7H and FRA7G. Bottom: The same chromosome probed with YAC HSC7E125 (FRA7H) and BAC AC (FRA7G). Note the opposite orientation of both clones relative to the physical map. D: The order of clones along the FRA7G region, analyzed by FISH on interphase nuclei from the GM00847 cells (each has 4–6 chromosomes 7). Left: AC (green); AC (red); AC (green); AC (red). Right: HSC7E160 (7q31.1) (red); AC (green); AC (green); AC (red). Inserts: a magnification of one chromosome from each nucleus. Note that the order found in these FISH experiments is the expected order, based on the sequenced contigs (Figure 3).
Cancer Cell 2002 1, 89-97DOI: ( /S (02)00017-X)

4. Figure 3 Maps of the FRA7G region
A: Reference genes and polymorphic markers at 7q31.1–7q31.3. B: A region spanning the cytogenetic gaps and constrictions (dark blue), and a region showing telomeric signals of clones that are located more centromeric on the physical map (“opposite oriented”) (light blue). C: Regions showing normal (synchronous) and early replication pattern in orange, normal and late in dark green, and unusual (asynchronous) and early in pink. D: The boundaries of the GTL-16 amplicons, 5× region in red, 10× in green. Below are indicated the YAC clones used in the analysis of the telomeric boundary. E: The set of Celera DNA sequence scaffolds (upper line) connect-ed by BAC clones (bottom lines). The numbers indicate the size of each sequence in Mb. The sequence names from left to right are: i-GA_x8Y8FG7; ii-GA_x8Y8FKQ; iii-GA_X2HTBKNJPOH; iv-GA_x2HTBL4GTR2; v-GA-x8WU11E; vi-GA_x2HTBKNGALA; vii-GA_x2HTBI2VJAN. The BAC clones or accession numbers from left to right are: AC073346; CIT-2172F3; AC032017; AC073901; CIT-2012G19; AC015621; NH032P06; NH516A21; AC F: Clones used for the cytogenetic analysis of FRA7G gaps and constrictions. G: Clones used for the replication analysis. H: Clones used for the analysis of the amplicon boundaries and the copy number within the amplified region. The colors of the clones in F–H are the same as in B–D.
Cancer Cell 2002 1, 89-97DOI: ( /S (02)00017-X)

5. Figure 4
The organization of the amplified chromosome in the GTL-16 cells
A: FISH analysis of the amplicon boundaries. Left: an interphase nucleus hybridized with the MET clone c169h6 (green) and with clone V193A (red). The signals of both probes colocalize and appear yellow. Right: an interphase nucleus hybridized with V193A (red) and HSC7E137 (green). HSC7E137 signals appear only on the 4 nonamplified copies of chromosome 7 (arrowheads), indicating that this clone is not included in the amplicon. B: The level of amplification of clones encompasses the amplified region, determined by counting FISH signals in interphase nuclei. Only nuclei in which the analyzed region was replicated were considered. C: Left: SKY analysis of the amplified chromosome. Chromosome 12 sequences in green, chromosome 7 in orange. Right: G-banding of the same chromosome. D: An interphase nucleus from GTL-16 cells hybridized with a chromosome 12 centromeric probe (green) and V193A (red).
Cancer Cell 2002 1, 89-97DOI: ( /S (02)00017-X)

6. Figure 5
Reconstruction of the events which led to the MET amplification in GTL-16 cells
A: The sequence of events, leading to amplification of MET in the GTL-16 cells. The 5× region is shown in red, the 10× region in green, induced FRA7G as black rectangles, uninduced as empty rectangles. Only intact (nonrearranged) fragile regions are marked. Other elements have the same color code as in Figure 1. B: Upper: The expected hybridization pattern along one chromatid of the amplified chromosome. Bottom: A replicated amplified chromosome of a GTL-16 interphase, hybridized with clone AC025297, from the 5× amplified region (red) and AC from the 10× amplified region (green).
Cancer Cell 2002 1, 89-97DOI: ( /S (02)00017-X)