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. 2015 Apr 21;10(4):e0123170. doi: 10.1371/journal.pone.0123170

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© 2015 He et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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Fig 3 — (A) The product of NbS3-inserted PCR amplification in four strains, SD1 and SD2 represent one pair of segmental duplication in N. bombycis. (B) The product of NbS24-inserted PCR amplification in three strains and the illustration. M, DNA marker, CQ1: Chongqing isolate, YN: Yunnan isolate, GD: Guangdong isolate, GX: Guangxi isolate. Black arrowhead: MITE-inserted PCR-amplified products. Gray arrowheads: PCR-amplified product without MITEs insertion. Rectangular arrowheads: genes in the syntenic region among several N. bombycis isolates and N. antheraeae. Same color rectangles correspond to homologous genes.