tpj12128-sup-0001-FigS1.tifimage/tif1264KFigure S1. PCR analysis showing T–DNA insertion into the 180 bp repeat array.
tpj12128-sup-0002-FigS2.tifimage/tif2983KFigure S2. Five images of fiber FISH for estimating the size of the 180 bp repeat array interrupted by T–DNA insertion on chromosome 2, and the calculated lengths of the 180 bp repeat array.
tpj12128-sup-0003-FigS3.tifimage/tif757KFigure S3. Schematic illustration showing the original T–DNA insertion site on CEN2 and the re-inserted positions of the DLD cassette identified by TAIL–PCR or inverse PCR.
tpj12128-sup-0004-FigS4.tifimage/tif573KFigure S4. PCR analysis for detecting an artificial ring chromosome (AtARC1).
tpj12128-sup-0005-FigS5.tifimage/tif899KFigure S5. A DAPI-stained pachytene cell containing a mini-chromosome.
tpj12128-sup-0006-FigS6.tifimage/tif401KFigure S6. The process of conversion from a monocentric ring chromosome to a double-size dicentric ring chromosome.
tpj12128-sup-0007-TableS1.docWord document38KTable S1. WiscDsLox lines used in this study and their estimated number of T–DNA insertion sites and number of copies per site.
tpj12128-sup-0008-TableS2.docWord document51KTable S2. PCR primers used in this study.
tpj12128-sup-0009-SM-legends.docxWord document16K 

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