Doris Lucyshyn1, Jeanette Moulinier-Anzola1, Muhammad Asaf Khan1,2, René Benjamins3,4,5, Elke Barbez1,6, Martina Ortbauer1, Inez Terpstra7, Johannes Leitner1, Nenad Malenica1,8, Haroon Butt1, Barbara Korbei1, Ben Scheres9, Jürgen Kleine-Vehn1, Christian Luschnig10. 1. Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Vienna (BOKU), Muthgasse 18, 1190, Wien, Austria. 2. Department of Bioinformatics and Biotechnology (BNB), Government College University, Faisalabad (GCUF), Allama Iqbal Road, Faisalabad, 38000, Pakistan. 3. Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Vienna (BOKU), Muthgasse 18, 1190, Wien, Austria. rene.benjamins@syngenta.com. 4. Plant Developmental Biology, Wageningen University Research, 6708 PB, Wageningen, The Netherlands. rene.benjamins@syngenta.com. 5. Syngenta Seeds B.V., Westeinde 62, 1601 BK, Enkhuizen, The Netherlands. rene.benjamins@syngenta.com. 6. Gregor Mendel Institute of Molecular Plant Biology, Dr. Bohr-Gasse 3, 1030, Vienna, Austria. 7. Swammerdam Institute for Life Sciences, Faculty of Science, University of Amsterdam, 1090 GE, Amsterdam, The Netherlands. 8. Faculty of Science, Department of Molecular Biology, University of Zagreb, Horvatovac 102a, 10000, Zagreb, Croatia. 9. Plant Developmental Biology, Wageningen University Research, 6708 PB, Wageningen, The Netherlands. 10. Department of Applied Genetics and Cell Biology, University of Natural Resources and Life Sciences, Vienna (BOKU), Muthgasse 18, 1190, Wien, Austria. christian.luschnig@boku.ac.at.
Retraction of: Scientific Reports 10.1038/srep32196, published online 24 August 2016The Authors have retracted this Article.In follow-up experiments on this work, we noticed a mix up of transgenic lines expressing N- and C-terminally tagged PPP1 reporter constructs under the 35S promoter. All the lines presented in the manuscript in Figure 4i–n correspond to the identical N-terminally tagged 35S::GFP:PPP1 expression cassette, and the GFP signal localizes to nucleus and cytoplasm. Expression of this construct results in a limited rescue of the ppp1-476 seedling phenotypes. However, the level of complementation is not comparable to complementation by a C-terminally GFP-tagged version of the protein that is in fact localized to the chloroplast, as reported by Manavski et al. [1]. As such, we are unable to support the conclusions presented as a nuclear regulator of PIN expression.René Benjamins, Elke Barbez, Martina Ortbauer, Inez Terpstra, Doris Lucyshyn, Jeanette Moulinier-Anzola, Muhammad Asaf Khan, Johannes Leitner, Nenad Malenica, Barbara Korbei, Ben Scheres, Jürgen Kleine-Vehn & Christian Luschnig agree with the retraction and its wording. Haroon Butt did not respond to the correspondence about the retraction.