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ACTA HORTICULTURAE SINICA ›› 2011, Vol. 38 ›› Issue (10): 1999-2004.

• Research Notes • Previous Articles     Next Articles

Cloning and Expression Analysis of Resistance Powdery Mildew Gene RmMlo in Rosa multiflora

QIU Xian-qin1,2,BAO Man-zhu1,ZHANG Hao1,2,JIAN Hong-ying2,WANG Qi-gang2,YAN Hui-jun2,ZHANG Ting2,and TANG Kai-xue2,*   

  1. (1College of Horticulture and Forestry,Huazhong Agricultural University,Key Laboratory of Horticultural Plant Biology,Ministry of Education,Wuhan 430070,China;2Flower Research Institute,Yunnan Academy of Agricultural Sciences,Yunnan Flower Breeding Key Lab,Kunming 650205,China)
  • Received:2011-04-09 Revised:2011-08-31 Online:2011-10-25 Published:2011-10-25
  • Contact: TANG Kai-xue2,*

Abstract: In this research,a full-length cDNA sequence of Mlo gene,named RmMlo(GenBank accession No. JF310747)was obtained from leaves of Rosa multiflora by RT-PCR and RACE. Sequence analysis indicated that RmMlo was 1 993 bp in full length containing a 5′-untranslated region(5′-UTR)of 49 bp,a 3′-UTR of 243 bp,and an opening reading frame(ORF)of 1 700 bp encoding 567 amino acids. Subsequently,amino acid sequence analysis revealed that RmMlo had two conserved MLO motifs in the protein C-terminal. Sequence alignment and phylogenetic analysis showed that RmMlo shared more than 90% homology with Mlo from Arabidopsis thaliana and other dicotyledon. Finally,semiquantitative RT-PCR analysis indicated that RmMlo showed the highest expression abundance in infected leaves and no expression in root,which was different from the expression pattern of AtMlo.

Key words: Rosa multiflora, rose, powdery mildew, Mlo, clone, tissue-specific expression

CLC Number: