The Evolutionarily Conserved TOUGH Protein Is Required for Proper Development ofArabidopsis thaliana
Author(s) -
Luz Irina A. Calderón Villalobos,
Carola Kuhnle,
Esther M.N. Dohmann,
Hanbing Li,
Mike Bevan,
Claus Schwechheimer
Publication year - 2005
Publication title -
the plant cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.324
H-Index - 341
eISSN - 1532-298X
pISSN - 1040-4651
DOI - 10.1105/tpc.105.031302
Subject(s) - biology , arabidopsis , mutant , arabidopsis thaliana , saccharomyces cerevisiae , regulator , microbiology and biotechnology , rna binding protein , genetics , genetic screen , transcription (linguistics) , transcription factor , alternative splicing , rna splicing , rna , yeast , gene , messenger rna , linguistics , philosophy
In this study, we characterize the evolutionarily conserved TOUGH (TGH) protein as a novel regulator required for Arabidopsis thaliana development. We initially identified TGH as a yeast two-hybrid system interactor of the transcription initiation factor TATA-box binding protein 2. TGH has apparent orthologs in all eukaryotic model organisms with the exception of the budding yeast Saccharomyces cerevisiae. TGH contains domains with strong similarity to G-patch and SWAP domains, protein domains that are characteristic of RNA binding and processing proteins. Furthermore, TGH colocalizes with the splicing regulator SRp34 to subnuclear particles. We therefore propose that TGH plays a role in RNA binding or processing. Arabidopsis tgh mutants display developmental defects, including reduced plant height, polycotyly, and reduced vascularization. We found TGH expression to be increased in the amp1-1 mutant, which is similar to tgh mutants with respect to polycotyly and defects in vascular development. Interestingly, we observed a strong genetic interaction between TGH and AMP1 in that tgh-1 amp1-1 double mutants are extremely dwarfed and severely affected in plant development in general and vascular development in particular when compared with the single mutants.
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