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. 2011 Oct 21;2:67. doi: 10.3389/fpls.2011.00067

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Copyright © 2011 Narayanan, Ihemere, Chiu, Siritunga, Rajamani, Singh, Oda and Sayre.

This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.

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RT-PCR analysis of expression in FEA1 transgenic plants. (A) Modified pKYLX–FEA1 vector used for transformation of wild-type Arabidopsis thaliana. Two separate plasmids were used for transforming plants with the FEA1 gene driven by the 35S promoter (constitutive) and patatin (storage organ) promoter. (B) RT-PCR analysis of FEA1 expression in leaves of independent 2 × 35S–FEA1 transgenic plants. (C) RT-PCR analysis of FEA1 expression in roots of independent patatin-FEA1 transgenic plants.