CORRECTION article

Front. Plant Sci., 11 September 2020

Sec. Plant Membrane Traffic and Transport

Volume 11 - 2020 | https://doi.org/10.3389/fpls.2020.589954

Corrigendum: The GIP Gamma-Tubulin Complex-Associated Proteins are Involved in Nuclear Architecture in Arabidopsis Thaliana

  • 1. Centre National de la Recherche Scientifique, Institut de Biologie Moléculaire des Plantes, UPR 2357, Conventionné avec l’Université de Strasbourg, Strasbourg, France

  • 2. Biotechnologie et Signalisation cellulaire, Institut de Recherche de l’Ecole de Biotechnologie de Strasbourg, UMR 7242, Université de Strasbourg, Illkirch, France

  • 3. Institut de Génétique et Biologie Moléculaire et Cellulaire, Ecole Supérieure de Biotechnologie de Strasbourg, Illkirch, France

Errors in Supplementary Figures 3 and 4

In the original article, there were mistakes in Supplementary Figures S3andS4 as published.

In the original article, there were mistakes in the Supplementary Figure S3as published.

Positive growth controls on –LW medium in the yeast two-hybrid growth assay.

Pictures of the AH109 cells co-transformed with recombinant vectors expressing proteins fused to the GAL4 Binding and Activating domains (BD and AD, respectively) were not properly selected (GIP1/TSA1-D1; GIP2/TSA1-D1; GIP1/TSA1-D4; GIP2/TSA1-D4; empty/TSA1-D1; empty/TSA1-D4; GIP1/empty; GIP2/empty).

Negative growth controls on –HLW + 3-AT medium.

Pictures of the AH109 cells co-transformed with recombinant vectors expressing proteins fused to the GAL4 Binding and Activating domains (BD and AD, respectively) were not properly selected (empty/TSA1-D1; empty/TSA1-D4; GIP1/empty; GIP2/empty; empty vectors).

Negative growth controls on –AHLW medium.

Pictures of the AH109 cells co-transformed with recombinant vectors expressing proteins fused to the GAL4 Binding and Activating domains (BD and AD, respectively) were not properly selected (empty/TSA1-D1; empty/TSA1-D4; GIP1/empty; GIP2/empty; empty vectors).

The corrected Supplementary Figure S3 is now published.

In the original article, there were mistakes in the Supplementary Figure S4as published:

Character inversion in the name of the pGBKT7 yeast two-hybrid vector

Negative control in the β-galactosidase filter assay.

Part of the picture showing the Y187 cells co-transformed with recombinant vectors pGAD10-GIP1 and pGBKT7 was not properly selected.

GIP1-GIP1 interaction in the β-galactosidase filter assay.

Part of the picture showing the Y187 cells co-transformed with recombinant vectors pGAD10-GIP1 and pGBKT7-GIP1 was not properly selected.

The corrected Supplementary Figure S4 is now published.

The authors apologize for these errors and state that these do not change the scientific conclusions of the article in any way. The original article has been updated.

Statements

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2020.589954/full#supplementary-material

Summary

Keywords

gamma-tubulin complex, AtGIP1/MOZART1, AtTSA1, nuclear envelope, Arabidopsis thaliana

Citation

Batzenschlager M, Masoud K, Janski N, Houlné G, Herzog E, Evrard J-L, Baumberger N, Erhardt M, Nominé Y, Kieffer B, Schmit A-C and Chabouté M-E (2020) Corrigendum: The GIP Gamma-Tubulin Complex-Associated Proteins are Involved in Nuclear Architecture in Arabidopsis Thaliana. Front. Plant Sci. 11:589954. doi: 10.3389/fpls.2020.589954

Received

31 July 2020

Accepted

28 August 2020

Published

11 September 2020

Approved by

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Volume

11 - 2020

Updates

Copyright

*Correspondence: Anne-Catherine Schmit,

This article was submitted to Plant Traffic and Transport, a section of the journal Frontiers in Plant Science

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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