Cloning and characterization of a flowering time gene from Thellungiella halophila
Article first published online: 12 AUG 2008
DOI: 10.1111/j.1745-7270.2008.00446.x
© 2008 Institute of Biochemistry and Cell Biology, SIBS, CAS
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How to Cite
Fang, Q., Liu, J., Xu, Z. and Song, R. (2008), Cloning and characterization of a flowering time gene from Thellungiella halophila. Acta Biochimica et Biophysica Sinica, 40: 747–753. doi: 10.1111/j.1745-7270.2008.00446.x
Publication History
- Issue published online: 12 AUG 2008
- Article first published online: 12 AUG 2008
- Received: April 9, 2008 Accepted: June 3, 2008
- Abstract
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Keywords:
- Thellungiella halophila;
- vernalization;
- FRIGIDA;
- ThFRI;
- Arabidopsis thaliana
Thellungiella halophila (T. halophila) (salt cress) is a close relative of Arabidopsis and a model plant for salt tolerance research. However, the nature of its later flowering causes some difficulties in genetic analysis. The FRIGIDA (FRT) gene plays a key role in the Arabidopsis vernalization flowering pathway, whose homolog in T. halophila may also be a key factor in controlling flowering time. In order to study the molecular mechanism of vernalization responses in T. halophila, a full length cDNA named ThFRI (Thellungiella halophila FRIGIDA) was isolated from the young seedlings of T. halophila by RT-PCR and RACE. The ThFRI cDNA was 2017 bp in length and contained an open reading frame encoding a putative protein of 605 ami no acids. The ThFRI showed significant homology to AtFRI (74.5% at the nucleotide level and 63.9% at the ami no acid level). To study its function, ThFRI cDNA was transformed into Arabidopsis thaliana, driven by CaMV 35S promoter. Transgenic plants expressing ThFRI exhibited late-flowering phenotype, which suggests that ThFRI is the funtional FRI homolog in T. halophila. The cloning and funtional characterization of the FRI homolog of T. halophila will faciliate further study of flowering time control in T. halophila.

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