The THERMOSENSITIVE MALE STERILE 1 Interacts with the BiPs via DnaJ Domain and Stimulates Their ATPase Enzyme Activities in Arabidopsis
The THERMOSENSITIVE MALE STERILE 1 Interacts with the BiPs via DnaJ Domain and Stimulates Their ATPase Enzyme Activities in Arabidopsis
The Arabidopsis TMS1 encodes a heat shock protein identical to the Hsp40 protein AtERdj3A and plays important roles in the thermotolerance of pollen tubes and other plant tissues. Despite its importance to plant growth and reproduction, little has been known about its mechanisms underlying thermotolerance of plants. In this study, the relationship between TMS1 and the Hsp70 proteins, Binding Immunoglobulin Proteins (BiPs) was explored to understand the molecular mechanisms of TMS1 in thermotolerance of plants. The expression of TMS1 was induced not only by heat shock, but also by dithiothreitol (DTT) and L-azetidine-2-carboxylic acid (AZC), similarly to the three BiP genes, indicating that TMS1 may be involved in unfolded protein response (UPR). The firefly luciferase complementary imaging (LCI), GST pull-down and ATPase enzyme activity assays demonstrated that the DnaJ domain of TMS1 could interact with BiP1 and BiP3, and could stimulate their ATPase enzyme activities. In addition, the expression level of TMS1 was reduced in the bzip28 bzip60 double mutant. These results suggest that TMS1 may function at the downstream of bZIP28 and bZIP60 and be involved in termotolerance of plants, possibly by participating in refolding or degradation of unfolded and misfolded proteins through interaction with the BiPs.
- China Agricultural University China (People's Republic of)
- Wuhan University China (People's Republic of)
- National Center for Gene Research China (People's Republic of)
- Zhejiang Ocean University China (People's Republic of)
- Shanghai Municipal People's Government China (People's Republic of)
Nicotiana, Science, Molecular Sequence Data, Arabidopsis, Structure-Activity Relationship, Gene Expression Regulation, Plant, Luciferases, Firefly, Amino Acid Sequence, Adenosine Triphosphatases, Arabidopsis Proteins, Q, R, HSP40 Heat-Shock Proteins, Protein Structure, Tertiary, Plant Leaves, Dithiothreitol, Mutation, Medicine, Azetidinecarboxylic Acid, Heat-Shock Response, Research Article, Molecular Chaperones, Protein Binding
Nicotiana, Science, Molecular Sequence Data, Arabidopsis, Structure-Activity Relationship, Gene Expression Regulation, Plant, Luciferases, Firefly, Amino Acid Sequence, Adenosine Triphosphatases, Arabidopsis Proteins, Q, R, HSP40 Heat-Shock Proteins, Protein Structure, Tertiary, Plant Leaves, Dithiothreitol, Mutation, Medicine, Azetidinecarboxylic Acid, Heat-Shock Response, Research Article, Molecular Chaperones, Protein Binding
6 Research products, page 1 of 1
- IsSupplementTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).27 popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.Top 10% influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Average impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Average
