Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Published Erratum
. 2016 Jan 25;14(1):e1002374.
doi: 10.1371/journal.pbio.1002374. eCollection 2016 Jan.

Correction: A Novel Role for the TIR Domain in Association with Pathogen-Derived Elicitors

Published Erratum

Correction: A Novel Role for the TIR Domain in Association with Pathogen-Derived Elicitors

Tessa M Burch-Smith et al. PLoS Biol. .

Abstract

[This corrects the article DOI: 10.1371/journal.pbio.0050068.].

PubMed Disclaimer

Figures

Fig 4
Fig 4. N Co-Immunoprecipitates with p50-U1, but Not with p50-U1-Ob
Fig 4. N associates with p50-U1. Total protein extracts from N. benthamiana leaves transiently coexpressing gN-TAP (top panel, lanes 1–3) and Cerulean alone (middle panel, lane 1), p50-U1-Cerulean (middle panel, lane 2), or p50-U1-Ob-Cerulean (middle panel, lane 3) were pulled down using anti-GFP antibodies. gN-TAP was present in a complex with p50-U1-Cerulean (bottom panel, lane 2), but not with Cerulean (bottom panel, lane 1) or p50-U1-Ob-Cerulean (bottom panel, lane 3).
Fig 6
Fig 6. p50-U1 Fails to Associate with N TIR Mutants
(A) N and deletion mutants used to determine the domain required for association with p50. Numbers in parentheses are deleted amino acid residues. Not drawn to scale. (B) gN-TAP and gN-mutant-TAP proteins were tested for their association with p50-U1-Cerulean by coimmunoprecipitation. Input of N and its mutants are shown in top panel and Cerulean or Cerulean-tagged proteins are shown in the middle panel. Bottom panel shows coimmunoprecipitation results. gN-TAP + Cerulean (lane 1); gN TAP + p50-U1-Cerulean (lane 2); NΔTIR-TAP + p50-U1-Cerulean (lane 3); NΔP-loop-TAP + p50-U1-Cerulean (lane 4); NΔNB-TAP + p50-U1-Cerulean (lane 5); NΔLRR2–14-TAP + p50-U1-Cerulean (lane 6); N(D46H)TAP + p50-U1-Cerulean (lane 7); N(W141S)TAP + p50-U1-Cerulean (lane 8); and gN-TAP + p50-U1-Ob-Cerulean (lane 9). NΔTIR-TAP and N-TIR point mutants do not coimmunoprecipitate with p50-U1-Cerulean. Lane M is the size marker, and protein size is in kDa.
Fig 8
Fig 8. N's TIR Domain Is Sufficient for Association with p50-U1
(A) Co-immunoprecipitation of gN-TIR-TAP and p50-U1-Cerulean. N’s TIR domain was expressed under the control of N’s endogenous 5’ and 3’ regulatory regions. Extracts from tissue co-expressing N(TIR)-TAP (top panel, lanes 1 and 2) and p50-U1-Cerulean (middle panel, lane 1) or p50-U1-Ob-Cerulean (middle panel, lane 2) were pulled down with anti-GFP antibodies. N(TIR)-TAP was pulled down with p50-U1-Cerulean (bottom panel, lane 1), but not with p50-U1-Ob-Cerulean (bottom panel, lane 2). Lane M is the size marker, and protein sizes are shown in kDa. (B) BiFC between N(TIR)-YN and p50-U1-YC. N(TIR)-YN exhibits BiFC with p50-U1-YC (column 1), but not with p50-U1-Ob-YC (column 2). The TIR domains of two related R proteins, BS4 and RPP5, were tested for their ability to associate in vivo with p50-U1-YC. BS4(TIR)-YC and RPP5(TIR)-YC were coexpressed with p50-U1-YC, but were unable to exhibit BiFC (columns 3 and 4, respectively). Scale bar represents 20 μm.

Erratum for

References

    1. Burch-Smith TM, Schiff M, Caplan JL, Tsao J, Czymmek K, Dinesh-Kumar SP (2007) A Novel Role for the TIR Domain in Association with Pathogen-Derived Elicitors. PLoS Biol 5(3): e68 doi:10.1371/journal.pbio.0050068 - DOI - PMC - PubMed

Publication types