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. 2016 Feb 11;67(8):2139–2150. doi: 10.1093/jxb/erw029

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© The Author 2016. Published by Oxford University Press on behalf of the Society for Experimental Biology.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

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Fig. 2. — Map-based cloning of SRL2. (A) The srl2 locus was mapped to a 56-kb DNA region on chromosome 3. The SRL2 gene comprises 20 exons (boxes) and 19 introns (line). (B) Constructs used for complementary analysis; pCSRL2 and pCSRL2-CK were used to transform srl2 plants. The dotted line in pCSRL2-CK indicates the deleted genomic region. (C) Constructs used for RNAi analysis; pSRL2RNAi was used to transform wild-type plants. (D, E) Results of complementary analysis. Scale bars=10cm (D) and 1cm (E).