ArticlePlanta2013
Isolation of an abscisic acid senescence and ripening inducible gene from litchi and functional characterization under water stress.
Article in Planta, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 22 citations in OpenAlex.
- ThASR4 enhances salt tolerance in transgenic Tamarix and Arabidopsis by scavenging reactive oxygen species.BMC plant biology · 2026Article
- Genome-Wide Identification of the PeanutInternational journal of molecular sciences · 2024Article
- ThASR3 confers salt and osmotic stress tolerances in transgenic Tamarix and Arabidopsis.BMC plant biology · 2022Article
- Structural disorder in plant proteins: where plasticity meets sessility.Cellular and molecular life sciences : CMLS · 2017Review
- Overexpression of a Plasma Membrane-LocalizedFrontiers in plant science · 2017Article
- Identification of the ASR gene family from Brachypodium distachyon and functional characterization of BdASR1 in response to drought stress.Plant cell reports · 2016Article
- ASR5 is involved in the regulation of miRNA expression in rice.Plant cell reports · 2015Article
- The MaASR gene as a crucial component in multiple drought stress response pathways in Arabidopsis.Functional & integrative genomics · 2015Article
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Authors and funding
8 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A full-length abscisic acid (ABA) senescence and ripening inducible gene named LcAsr was obtained from litchi. Bioinformatic analysis showed that full-length LcAsr was 1,177 bp and contained an open reading frame (ORF) encoding 153 amino acids, 85- and 146-bp 5' and 3' UTRs, respectively. LcAsr was expressed in all organs, with preferential expression in the flower and low levels in pulp. The expression level of LcAsr in postharvest uncovered fruit reached a maximum at 24 h after harvest. When the litchi fruit was covered with plastic film, the LcAsr expression level remained constant. LcASR protein localized in the nucleus. LcAsr was transformed in Arabidopsis thaliana L. (ecotype Columbia) and four transgenic lines were obtained. One line, 35S::LcAsrD, was selected for drought tolerance analysis and showed higher tolerance to drought than the control. The activities of superoxide dismutase, catalase, ascorbate peroxidase, and glutathione reductase were much higher in the transgenic line than the control under drought conditions. The levels of several ABA/stress-regulated genes were investigated. The transcript level of responsive to ABA (RAB18) remained constant and responsive to dehydration (RD29A) displayed a slight decrease in the Columbia line (Col). However, the transcript levels of LcAsr, RAB18, and RD29A were greatly enhanced in the transgenic 35S::LcAsrD. The transcript levels of KAT1, KAT2, and SKOR were also markedly decreased in the transgenic line. These results suggest an important role of LcAsr as a protective molecule for water deficit and help to understand the molecular mechanism of postharvest litchi fruit dehydration.
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