Cloning and characterization of a cDNA encoding Ran binding protein from wheat

Abstract

Ran, which functions in nucleocytoplasmic transport and mitosis, binds to and is regulated in part by Ran binding protein (RanBP). A RanBP cDNA (TaRanBP1) was isolated from a wheat cDNA library using RT-PCR product as a probe. The predicted amino acid sequence of TaRanBP1 is over 60% identity to AtRanBP1 from Arabidopsis and also with considerable similarity to human and fungi RanBPs. TaRanBP1 gene was expressed ubiquitously in roots, leaves and stems, with a similar abundance in these tissues. Phylogenetic reconstruction of TaRanBP1 with 32 other RanBPs from 26 species of organisms revealed that RanBPs from plants, animals and fungi clustered as the distinct groups, intraspecies isoforms were not developed for RanBPs, contrast with most other ancestral genes. Structural analysis revealed that all RanBPs were highly conserved in the middle region of their amino acid sequence, which included Ran binding domain and the three conserved motifs that have the essential roles in binding with Ran protein and promotion of GTP hydrolysis by the Ran/RanGAP/RanBP complex. However, N-terminus and C-terminus exhibited very low similarity between the different RanBPs. The different structures in N-terminus and C-terminus of RanBPs are likely to direct the Ran into the specific physiological processes and subsequently exhibit the different roles in different organisms.

• Ran binding protein
• phylogenetic reconstruction
• structural analysis, Triticum aestivum

Acknowledgements

This work was supported by the National Natural Science Foundation of China (No. 30400222), the Chinese National Special Foundation for Transgenic Plant Research and Commercialization (J2002-B007), the State Key Basic Research and Development Plan of China (G1999016002) and the Innovation Project of the Chinese Academy of Sciences.

Notes

^† The first two authors (B. Tian and Z. B. Lin) contributed equally to this work.