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Refined Requirements for Protein Regions Important for Activity of the TALE AvrBs3
AvrBs3, the archetype of the family of transcription activator-like (TAL) effectors from phytopathogenic Xanthomonas bacteria, is translocated by the type III secretion system into the plant cell. AvrBs3 localizes to the plant cell nucleus and activates the transcription of target genes. Crucial for...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4363659/ https://www.ncbi.nlm.nih.gov/pubmed/25781334 http://dx.doi.org/10.1371/journal.pone.0120214 |
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author | Schreiber, Tom Sorgatz, Anika List, Felix Blüher, Doreen Thieme, Sabine Wilmanns, Matthias Bonas, Ulla |
author_facet | Schreiber, Tom Sorgatz, Anika List, Felix Blüher, Doreen Thieme, Sabine Wilmanns, Matthias Bonas, Ulla |
author_sort | Schreiber, Tom |
collection | PubMed |
description | AvrBs3, the archetype of the family of transcription activator-like (TAL) effectors from phytopathogenic Xanthomonas bacteria, is translocated by the type III secretion system into the plant cell. AvrBs3 localizes to the plant cell nucleus and activates the transcription of target genes. Crucial for this is the central AvrBs3 region of 17.5 34-amino acid repeats that functions as a DNA-binding domain mediating recognition in a “one-repeat-to-one base pair” manner. Although AvrBs3 forms homodimers in the plant cell cytosol prior to nuclear import, it binds DNA as a monomer. Here, we show that complex formation of AvrBs3 proteins negatively affects their DNA-binding affinity in vitro. The conserved cysteine residues at position 30 of each repeat facilitate AvrBs3 complexes via disulfide bonds in vitro but are also required for the gene-inducing activity of the AvrBs3 monomer, i.e., activation of plant gene promoters. Our data suggest that the latter is due to a contribution to protein plasticity and that cysteine substitutions to alanine or serine result in a different DNA-binding mode. In addition, our studies revealed that extended parts of both the N-terminal and C-terminal regions of AvrBs3 contribute to DNA binding and, hence, gene-inducing activity in planta. |
format | Online Article Text |
id | pubmed-4363659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43636592015-03-23 Refined Requirements for Protein Regions Important for Activity of the TALE AvrBs3 Schreiber, Tom Sorgatz, Anika List, Felix Blüher, Doreen Thieme, Sabine Wilmanns, Matthias Bonas, Ulla PLoS One Research Article AvrBs3, the archetype of the family of transcription activator-like (TAL) effectors from phytopathogenic Xanthomonas bacteria, is translocated by the type III secretion system into the plant cell. AvrBs3 localizes to the plant cell nucleus and activates the transcription of target genes. Crucial for this is the central AvrBs3 region of 17.5 34-amino acid repeats that functions as a DNA-binding domain mediating recognition in a “one-repeat-to-one base pair” manner. Although AvrBs3 forms homodimers in the plant cell cytosol prior to nuclear import, it binds DNA as a monomer. Here, we show that complex formation of AvrBs3 proteins negatively affects their DNA-binding affinity in vitro. The conserved cysteine residues at position 30 of each repeat facilitate AvrBs3 complexes via disulfide bonds in vitro but are also required for the gene-inducing activity of the AvrBs3 monomer, i.e., activation of plant gene promoters. Our data suggest that the latter is due to a contribution to protein plasticity and that cysteine substitutions to alanine or serine result in a different DNA-binding mode. In addition, our studies revealed that extended parts of both the N-terminal and C-terminal regions of AvrBs3 contribute to DNA binding and, hence, gene-inducing activity in planta. Public Library of Science 2015-03-17 /pmc/articles/PMC4363659/ /pubmed/25781334 http://dx.doi.org/10.1371/journal.pone.0120214 Text en © 2015 Schreiber et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited. |
spellingShingle | Research Article Schreiber, Tom Sorgatz, Anika List, Felix Blüher, Doreen Thieme, Sabine Wilmanns, Matthias Bonas, Ulla Refined Requirements for Protein Regions Important for Activity of the TALE AvrBs3 |
title | Refined Requirements for Protein Regions Important for Activity of the TALE AvrBs3 |
title_full | Refined Requirements for Protein Regions Important for Activity of the TALE AvrBs3 |
title_fullStr | Refined Requirements for Protein Regions Important for Activity of the TALE AvrBs3 |
title_full_unstemmed | Refined Requirements for Protein Regions Important for Activity of the TALE AvrBs3 |
title_short | Refined Requirements for Protein Regions Important for Activity of the TALE AvrBs3 |
title_sort | refined requirements for protein regions important for activity of the tale avrbs3 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4363659/ https://www.ncbi.nlm.nih.gov/pubmed/25781334 http://dx.doi.org/10.1371/journal.pone.0120214 |
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