Welcome to Acta Agronomica Sinica,

Acta Agron Sin ›› 2007, Vol. 33 ›› Issue (02): 292-296.

• ORIGINAL PAPERS • Previous Articles     Next Articles

Cloning and Sequence Analysis of Novel Drought-Tolerance Gene Coding LEA3 Protein in Tibetan Hulless Barley

QIAN Gang123,ZHAI Xu-Guang13,HAN Zhao-Xue13,PAN Zhi-Fen13,DENG Guang-Bing1,YU Mao-Qun1*   

  1. 1 Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, Sichuan; 2 Department of Biology, Zunyi Medical College, Zunyi 563003, Guizhou; 3 Graduate School, Chinese Academy of Sciences, Beijing 100039, China
  • Received:2006-04-07 Revised:1900-01-01 Online:2007-02-12 Published:2007-02-12
  • Contact: YU Mao-Qun

Abstract:

Late embryogenesis abundant (LEA) proteins were major group of proteins that were prominent in the stress response in various organisms including plants, algae, yeasts and bacteria. LEA3 protein was hydrophilic and accumulated in higher plants under conditions of extreme desiccation, during the last stage of seed formation, and during periods of water deficit in vegetative organs. In the present study, the most contrasting drought-tolerant genotypes were screened for comparing the differential sequences of gene coding LEA3 protein in Tibetan hulless barley, based on scoring of water loss rate (WLR), maldondialdehyde and proline measured. And Dongqing 8 with the highest scores and Pinbi 14 with the lowest ones were selected for analyzing the differences between the genes coding LEA3 protein in Tibetan hulless barley. Total RNA of two selected barley cultivars was extracted after treating with dehydration for 12 hours, and the first strand cDNA was synthesized by mRNA reverse transcription based on the primers designed according to the homologous sequence from Hordeum vulgare L. regiesterd in GenBank (No. X78205). RT-PCR products of gene coding LEA3 protein were cloned to pMD18-T vector. The recombinant pMD18-T plasmids, inserted interesting gene, were identified by PCR and restriction digestion, respectively. Results of sequence analysis revealed that both genes coding LEA3 protein contained entire open reading frames. The ORF of gene coding LEA3 protein from Dongqing 8 was composed of 606 bp, contrasting with 639bp from Pinbi 14. Accordingly, the deduced LEA3 protein in drought-tolerant genotype, Dongqing 8, was composed of 202 amino acid residues, while that of 213 amino acid residues in drought-sensitive genotype, Pinbi 14. The deduced LEA3 protein in the most tolerant genotype contains 8 repeats of an 11-amino acid motif that form amphiphilic α-helical structure, accordingly it shares the same characteristics as the third group of LEA protein. Comparing with LEA3 protein of the most sensitive genotype, the deduced LEA3 protein in Dongqing 8 was absent of the fourth motif because of absence of 33 nucleotides. In addition, there was a mutation of 6 differential amino acid residues appeared between in Dongqing 8. The polarity of LEA3 protein in drought-tolerant genotype could be stronger than that in Pinbi 14, due to those 6 mutant amino acid residues. Respectively, both materials shared 94.38% and 92.02% similarity by DNA and amino acid sequence homological comparison. In the present study, differential number of repeated motifs was related to the most contrasting drought-resistant genotypes in Tibetan hulless barley. The differential hydrophilic capability of LEA3 protein could be related to differential number of repeated motifs, mostly to the polarity of mutant amino acid residues. Accordingly, it was suggested that differential configuration of drought-tolerant proteins may be contributed to capability of drought resistance in plants.

Key words: Gene cloning, Sequence analysis, LEA3 protein, Tibetan hulless barley

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