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An Arabidopsis immunophilin, AtFKBP12, binds to AtFIP37 (FKBP interacting protein) in an interaction that is disrupted by FK506.
- Source :
-
The Plant journal : for cell and molecular biology [Plant J] 1998 Sep; Vol. 15 (6), pp. 783-9. - Publication Year :
- 1998
-
Abstract
- AtFKBP12 is an Arabidopsis cDNA that encodes a protein similar to the mammalian immunophilin, FKBP12. AtFKBP12 was used as 'bait' in a yeast 2-hybrid system to screen for cDNAs in Arabidopsis encoding proteins that bind to FKBP12. Two partial cDNAs were recovered encoding the C-terminus of a protein we have called Arabidopsis thaliana FKBP12 interacting protein 37 (AtFIP37). AtFIP37 is similar to a mammalian protein, FAP48, that also binds to FKBP12. The interaction between AtFKBP12 and AtFIP37 in the 2-hybrid system, as assessed by histidine auxotrophy and beta-galactosidase activity, was disrupted by FK506, but not by cyclosporin A, a drug that binds to cyclophilin A. AtFIP37 was also shown to bind in vitro to AtFKBP12 in GST-fusion protein binding assays. The binding was abolished by prior incubation of AtFKBP12 with FK506. These findings indicate that an Arabidopsis FKBP12 ortholog encodes a protein that binds FK506 and that the interaction between AtFKBP12 and AtFIP37 may involve the FK506 binding site of AtFKBP12. The interaction provides interesting new opportunities for controlling protein:protein interactions in vivo in plants.
- Subjects :
- Amino Acid Sequence
Cyclosporine pharmacology
DNA, Plant metabolism
Immunophilins chemistry
Immunophilins genetics
Molecular Sequence Data
Peptidylprolyl Isomerase metabolism
Sequence Alignment
Sequence Homology, Amino Acid
Tacrolimus Binding Proteins
Adaptor Proteins, Signal Transducing
Arabidopsis chemistry
Immunophilins metabolism
Immunosuppressive Agents pharmacology
Tacrolimus pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0960-7412
- Volume :
- 15
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- The Plant journal : for cell and molecular biology
- Publication Type :
- Academic Journal
- Accession number :
- 9807817
- Full Text :
- https://doi.org/10.1046/j.1365-313x.1998.00248.x