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ACTA HORTICULTURAE SINICA ›› 2014, Vol. 41 ›› Issue (7): 1335-1343.

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Cloning and Expression Analysis of a GTP-binding Protein MiRab11 Gene from Mangifera indica

LIU Zhao-liang1,*,LUO Cong1,*,DONG Long1,HE Xin-hua1,2,**,CAN Van Toan1,LI Li-shu1,and WEI Peng-xiao1   

  1. 1College of Agriculture,Guangxi University,Nanning 530004,China;2Guangxi Crop Genetic Improvement and
    Biotechnology Key Laboratory,Nanning 530007,China
  • Online:2014-07-25 Published:2014-07-25

Abstract: A MiRab11 gene,which belonged to small GTP-binding proteins Rab gene family,was
cloned by RT-PCR and RACE from Mangifera indica mixed tissues(leaves,stems,flowers,and fruits).
The full-length cDNA sequence was 902 bp and contained an open reading frame of 654 bp,which
encoded a 218 amino acid protein. The deduced amino acid sequence exhibited high homology with Vitis
vinifera and Citrus sinensis(97% similarity). Real-time quantitative PCR detection showed that the
ubiquitously expressed MiRab11 in young stems and fruit of 70 d after flowering was much higher than in
other tissues;The expression level of the gene was down-regulated during early fruit development from 20
d to 50 d after flowering and up-regulated during fruit ripening from 50 d to 70 d after flowering;It could
be up-regulated under different stress treatments(low temperature,salt,and drought)and stimulated by
different signal molecules stimulation(abscisic acid,salicylic acid,and hydrogen peroxide). In a word,
a MiRab11 was identified from Mangifera indica,which might be associated with mango fruit ripening and play an important role in mango stress reaction.

Key words: Mangifera indica, MiRab11, cloning, expression analysis

CLC Number: