ArticlePlant signaling & behavior2014
Intronic T-DNA insertion in Arabidopsis NBR1 conditionally affects wild-type transcript level.
Article in Plant signaling & behavior, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed, 11 citations in OpenAlex.
- Localization data of the T-DNA insertion site in Arabidopsis line SALK_146824C.Data in brief · 2024Article
- Intrinsically disordered protein AtDSS1(V) participates in plant defense response to oxidative stress.Protoplasma · 2021Article
- New insights into AtNBR1 as a selective autophagy cargo receptor in Arabidopsis.Plant signaling & behavior · 2021Article
- AtNBR1 Is a Selective Autophagic Receptor for AtExo70E2 in Arabidopsis.Plant physiology · 2020Article
- A selective autophagy cargo receptor NBR1 modulates abscisic acid signalling in Arabidopsis thaliana.Scientific reports · 2020Article
- Membrane Contact Sites and Organelles Interaction in Plant Autophagy.Frontiers in plant science · 2020Review
- A facile forward-genetic screen for Arabidopsis autophagy mutants reveals twenty-one loss-of-function mutations disrupting six ATG genes.Autophagy · 2019Article
- Herbivory-responsive calmodulin-like protein CML9 does not guide jasmonate-mediated defenses in Arabidopsis thaliana.PloS one · 2018Article
- Allele-Specific Interactions betweenFrontiers in plant science · 2016Article
Corrections and comments
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Authors and funding
3 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The SALK_135513 line of Arabidopsis thaliana is annotated by GenBank to have the T-DNA insertion in the fourth exon of NBR1 (At4g24690). Careful molecular analyses of the homozygous plants of SALK_135513 line indicated the place of T-DNA insertion in the fourth intron. Unexpectedly, 2 kinds of NBR1 transcripts, the wild-type and the mutated, resulting from alternative splicing events, were detected in those plants. Our findings explain the problems encountered by us with phenotypic evaluation of this line and emphasize the necessity for independent verification of the exact insertion site followed by careful expression studies when working with Arabidopsis T-DNA insertional mutants.
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