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Genetic Interactions of Arabidopsis thaliana Damaged DNA Binding Protein 1B (DDB1B) With DDB1A, DET1, and COP1
Damaged DNA Binding protein 1 (DDB1)–CULLIN4 E3 ubiquitin ligase complexes have been implicated in diverse biological processes in a range of organisms. Arabidopsis thaliana encodes two homologs of DDB1, DDB1A, and DDB1B. In this study we use a viable partial loss of function allele of DDB1B, ddb1b-...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Genetics Society of America
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583456/ https://www.ncbi.nlm.nih.gov/pubmed/23450167 http://dx.doi.org/10.1534/g3.112.005249 |
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author | Ganpudi, Ashwin L. Schroeder, Dana F. |
author_facet | Ganpudi, Ashwin L. Schroeder, Dana F. |
author_sort | Ganpudi, Ashwin L. |
collection | PubMed |
description | Damaged DNA Binding protein 1 (DDB1)–CULLIN4 E3 ubiquitin ligase complexes have been implicated in diverse biological processes in a range of organisms. Arabidopsis thaliana encodes two homologs of DDB1, DDB1A, and DDB1B. In this study we use a viable partial loss of function allele of DDB1B, ddb1b-2, to examine genetic interactions with DDB1A, DET1 and COP1. Although the ddb1b-2 ddb1a double mutant is lethal, ddb1a ddb1b-2/+ and ddb1b-2 ddb1a/+ heterozygotes exhibit few developmental phenotypes but do exhibit decreased tolerance of ultraviolet light. In addition, germination in ddb1a and ddb1a ddb1b-2/+ was found to be sensitive to salt and mannitol, and both DDB1 single mutants as well as the heterozygotes exhibited heat sensitivity. DE-ETIOLATED1 (DET1) and CONSTITUTIVE PHOTOMORPHOGENIC1 (COP1) are negative regulators of light development which interact with DDB1-CUL4 complexes. Although ddb1a strongly enhances det1 phenotypes in both dark- and light-grown seedlings, ddb1b-2 weakly enhanced the det1 short hypocotyl phenotype in the dark, as well as enhancing anthocyanin levels and suppressing the det1 low chlorophyll phenotype in light-grown seedlings. In adults, ddb1a suppresses det1 early flowering and enhances the det1 dwarf phenotype. A similar trend was observed in ddb1b-2 det1 double mutants, although the effects were smaller in magnitude. In cop1 mutants, ddb1b-2 enhanced the cop1-4 short hypocotyl phenotype in dark and light, enhanced anthocyanin levels in cop1-1 in the light, but had no effect in adults. Thus the requirement for DDB1B varies in the course of development, from COP1-specific effects in hypocotyls to DET1-specific in adults. |
format | Online Article Text |
id | pubmed-3583456 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-35834562013-03-01 Genetic Interactions of Arabidopsis thaliana Damaged DNA Binding Protein 1B (DDB1B) With DDB1A, DET1, and COP1 Ganpudi, Ashwin L. Schroeder, Dana F. G3 (Bethesda) Investigations Damaged DNA Binding protein 1 (DDB1)–CULLIN4 E3 ubiquitin ligase complexes have been implicated in diverse biological processes in a range of organisms. Arabidopsis thaliana encodes two homologs of DDB1, DDB1A, and DDB1B. In this study we use a viable partial loss of function allele of DDB1B, ddb1b-2, to examine genetic interactions with DDB1A, DET1 and COP1. Although the ddb1b-2 ddb1a double mutant is lethal, ddb1a ddb1b-2/+ and ddb1b-2 ddb1a/+ heterozygotes exhibit few developmental phenotypes but do exhibit decreased tolerance of ultraviolet light. In addition, germination in ddb1a and ddb1a ddb1b-2/+ was found to be sensitive to salt and mannitol, and both DDB1 single mutants as well as the heterozygotes exhibited heat sensitivity. DE-ETIOLATED1 (DET1) and CONSTITUTIVE PHOTOMORPHOGENIC1 (COP1) are negative regulators of light development which interact with DDB1-CUL4 complexes. Although ddb1a strongly enhances det1 phenotypes in both dark- and light-grown seedlings, ddb1b-2 weakly enhanced the det1 short hypocotyl phenotype in the dark, as well as enhancing anthocyanin levels and suppressing the det1 low chlorophyll phenotype in light-grown seedlings. In adults, ddb1a suppresses det1 early flowering and enhances the det1 dwarf phenotype. A similar trend was observed in ddb1b-2 det1 double mutants, although the effects were smaller in magnitude. In cop1 mutants, ddb1b-2 enhanced the cop1-4 short hypocotyl phenotype in dark and light, enhanced anthocyanin levels in cop1-1 in the light, but had no effect in adults. Thus the requirement for DDB1B varies in the course of development, from COP1-specific effects in hypocotyls to DET1-specific in adults. Genetics Society of America 2013-03-01 /pmc/articles/PMC3583456/ /pubmed/23450167 http://dx.doi.org/10.1534/g3.112.005249 Text en Copyright © 2013 Ganpudi, Schroeder http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigations Ganpudi, Ashwin L. Schroeder, Dana F. Genetic Interactions of Arabidopsis thaliana Damaged DNA Binding Protein 1B (DDB1B) With DDB1A, DET1, and COP1 |
title | Genetic Interactions of Arabidopsis thaliana Damaged DNA Binding Protein 1B (DDB1B) With DDB1A, DET1, and COP1 |
title_full | Genetic Interactions of Arabidopsis thaliana Damaged DNA Binding Protein 1B (DDB1B) With DDB1A, DET1, and COP1 |
title_fullStr | Genetic Interactions of Arabidopsis thaliana Damaged DNA Binding Protein 1B (DDB1B) With DDB1A, DET1, and COP1 |
title_full_unstemmed | Genetic Interactions of Arabidopsis thaliana Damaged DNA Binding Protein 1B (DDB1B) With DDB1A, DET1, and COP1 |
title_short | Genetic Interactions of Arabidopsis thaliana Damaged DNA Binding Protein 1B (DDB1B) With DDB1A, DET1, and COP1 |
title_sort | genetic interactions of arabidopsis thaliana damaged dna binding protein 1b (ddb1b) with ddb1a, det1, and cop1 |
topic | Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583456/ https://www.ncbi.nlm.nih.gov/pubmed/23450167 http://dx.doi.org/10.1534/g3.112.005249 |
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