TY - JOUR
T1 - Erratum
T2 - A Maternal System Initiating the Zygotic Developmental Program through Combinatorial Repression in the Ascidian Embryo (PLoS Genet (2016) 12:5 (e1006045) DOI: 10.1371/journal.pgen.1006045)
AU - Oda-Ishii, Izumi
AU - Kubo, Atsushi
AU - Kari, Willi
AU - Suzuki, Nobuhiro
AU - Rothbächer, Ute
AU - Satou, Yutaka
N1 - Publisher Copyright:
© 2016 Oda-Ishii 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 credited.
PY - 2016/10/1
Y1 - 2016/10/1
N2 - The number of embryos for the upper control reporter construct in panel E of S6 Fig is missing. This number is 90. Additionally, the percentages of expression of the lower reporter construct in panel E of S6 Fig are incorrect. The correct percentages are 5.8% in the AVD, and 61.6% in the PVD. Please view the correct S6 Fig here. Supporting Information S6 Fig. Repressive elements required for specific expression in the posterior vegetal cells. (A) While the reporter gene was expressed in the anterior and posterior vegetal blastomeres under the control of the 1241 bp upstream sequence of Foxd.b, (B) insertion of four repeats of the 22 bp sequence within the upstream region of Tbx6.b suppressed the expression in the anterior vegetal cells. Images are embryos expressing the third and fourth constructs shown in Fig 5G. (C) The repressive element of Tbx6.b directed specific expression in the posterior vegetal cells in a manner dependent on Zic-r.a activity. Constructs depicted in the illustrations on the left were injected with or without an MO against Zic-r.a. The green boxes indicate the Gfp reporter gene and SV40 polyadenylation signal. Graphs on the right show the percentage of blastomeres expressing the reporter gene in the anterior vegetal blastomeres and in the posterior vegetal blastomeres. (D) A series of deletion constructs using the Brachyury basal promoter revealed a repressive element in the upstream sequence of Wnttun5. Illustrations on the left depict the constructs. Graphs show the percentage of blastomeres expressing the reporter in the anterior vegetal blastomeres, and in the posterior vegetal blastomeres. (E) The repressive element, which was identified in (D), was inserted into-1041 of the upstream sequence of Foxd.b. The graphs indicate that this insertion made the expression of the reporter specific for the posterior vegetal cells. Because no expression in the animal hemisphere was observed with the constructs shown in (C), (D) and (E), graphs for expression in the animal hemisphere are omitted. (F) Image showing expression of the reporter with the second construct shown in (E).
AB - The number of embryos for the upper control reporter construct in panel E of S6 Fig is missing. This number is 90. Additionally, the percentages of expression of the lower reporter construct in panel E of S6 Fig are incorrect. The correct percentages are 5.8% in the AVD, and 61.6% in the PVD. Please view the correct S6 Fig here. Supporting Information S6 Fig. Repressive elements required for specific expression in the posterior vegetal cells. (A) While the reporter gene was expressed in the anterior and posterior vegetal blastomeres under the control of the 1241 bp upstream sequence of Foxd.b, (B) insertion of four repeats of the 22 bp sequence within the upstream region of Tbx6.b suppressed the expression in the anterior vegetal cells. Images are embryos expressing the third and fourth constructs shown in Fig 5G. (C) The repressive element of Tbx6.b directed specific expression in the posterior vegetal cells in a manner dependent on Zic-r.a activity. Constructs depicted in the illustrations on the left were injected with or without an MO against Zic-r.a. The green boxes indicate the Gfp reporter gene and SV40 polyadenylation signal. Graphs on the right show the percentage of blastomeres expressing the reporter gene in the anterior vegetal blastomeres and in the posterior vegetal blastomeres. (D) A series of deletion constructs using the Brachyury basal promoter revealed a repressive element in the upstream sequence of Wnttun5. Illustrations on the left depict the constructs. Graphs show the percentage of blastomeres expressing the reporter in the anterior vegetal blastomeres, and in the posterior vegetal blastomeres. (E) The repressive element, which was identified in (D), was inserted into-1041 of the upstream sequence of Foxd.b. The graphs indicate that this insertion made the expression of the reporter specific for the posterior vegetal cells. Because no expression in the animal hemisphere was observed with the constructs shown in (C), (D) and (E), graphs for expression in the animal hemisphere are omitted. (F) Image showing expression of the reporter with the second construct shown in (E).
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U2 - 10.1371/JOURNAL.PGEN.1006392
DO - 10.1371/JOURNAL.PGEN.1006392
M3 - Comment/debate
AN - SCOPUS:85127287393
SN - 1553-7390
VL - 12
JO - PLoS Genetics
JF - PLoS Genetics
IS - 10
M1 - e1006392
ER -