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note
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AG genomic sequences (nucleotides 44,331 to 47,358 of BAC F13C5, GenBank AL021711) were from pCIT526 (11). The fragment used in Fig. 4B spans nucleotides 46,832 to 46,992.
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0344796164
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note
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Lines used were lfy-12 (3) and LFY:VP16 DW245.2.7 (10).
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24
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0345227059
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note
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KB45 deletes nucleotides 46,873 to 46,901; KB46 deletes 46,873 to 46,949 (12).
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GUS fusions were in pDW294, a pCGN1547 derivative [K. E. McBride, K. R. Summerfelt, Plant Mol. Biol. 14, 269 (1990)] with the minimal -46-bp cauliflower mosaic virus promoter [P. N. Benfey and N.-H. Chua, Science 250, 959 (1990)] upstream of GUS [R. A. Jefferson, T. A. Kavanagh, M. W. Sevan, EMBO J. 6, 3901 (1987)]. Transgenic plants in the Columbia ecotype were generated by vacuum infiltration [N. Bechtold, J. Ellis, G. Pelletier, C.R. Acad. Sci. 316, 1194 (1993)]. GUS staining was as described [M. A. Blázquez, L. Soowal, I. Lee, D. Weigel, Development 124, 3835 (1997)].
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GUS fusions were in pDW294, a pCGN1547 derivative [K. E. McBride, K. R. Summerfelt, Plant Mol. Biol. 14, 269 (1990)] with the minimal -46-bp cauliflower mosaic virus promoter [P. N. Benfey and N.-H. Chua, Science 250, 959 (1990)] upstream of GUS [R. A. Jefferson, T. A. Kavanagh, M. W. Sevan, EMBO J. 6, 3901 (1987)]. Transgenic plants in the Columbia ecotype were generated by vacuum infiltration [N. Bechtold, J. Ellis, G. Pelletier, C.R. Acad. Sci. 316, 1194 (1993)]. GUS staining was as described [M. A. Blázquez, L. Soowal, I. Lee, D. Weigel, Development 124, 3835 (1997)].
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1842369623
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GUS fusions were in pDW294, a pCGN1547 derivative [K. E. McBride, K. R. Summerfelt, Plant Mol. Biol. 14, 269 (1990)] with the minimal -46-bp cauliflower mosaic virus promoter [P. N. Benfey and N.-H. Chua, Science 250, 959 (1990)] upstream of GUS [R. A. Jefferson, T. A. Kavanagh, M. W. Sevan, EMBO J. 6, 3901 (1987)]. Transgenic plants in the Columbia ecotype were generated by vacuum infiltration [N. Bechtold, J. Ellis, G. Pelletier, C.R. Acad. Sci. 316, 1194 (1993)]. GUS staining was as described [M. A. Blázquez, L. Soowal, I. Lee, D. Weigel, Development 124, 3835 (1997)].
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40
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0345227056
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note
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Electromobility shift assays were performed with purified His-tagged LFY protein (10).
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-
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41
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0344796162
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note
-
We are grateful to T. Nguyen for technical assistance. We thank M. Blázquez, M. Deyholos, R. Hong, K. Jones, O. Nilsson, F. Parcy, L. Sieburth, D. Wagner, and M. Yanofsky for discussion, review of the manuscript, and communicating unpublished results. Supported by a fellowship from the Human Frontier Science Program Organization (M.B.), and grants from the NSF and Department of Energy (D.W.). D.W. is a NSF Young Investigator.
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