Isolation and characterization of floral transcripts from mangosteen (Garcinia mangostana L.)

ArticleinTrees 23(5):899-910 · October 2009with27 Reads
Impact Factor: 1.65 · DOI: 10.1007/s00468-009-0331-2


    The understanding of flower initiation, development, and maturation in mangosteen is of paramount importance to shorten its
    long juvenile phase and to synchronize its flowering or fruiting time. In this study, we have identified 97 tentative unique
    genes with higher expression levels in young flower buds compared to young shoots by using suppressive subtraction hybridization
    and reverse northern analysis. Sequence analysis showed that 63.9% of these transcripts had non-significant matches to sequences
    in the non-redundant protein database in GenBank, 19.6% had significant matches to unknown proteins while the remaining 16.5%
    had putative functions in transcription, stress, signal transduction, cell wall biogenesis, photosynthesis and miscellaneous.
    The full-length cDNA of GmAGMBP encoding AG-motif binding protein (a zinc finger transcriptional factor), and 3′ termini cDNA
    sequences of GmHSA32 and GmBZIP, encoding heat-stress-associated 32 (HSA32) and bZIP transcription factor, respectively; were
    cloned and further analysed. Real-time PCR analysis revealed that these three genes have different transcript profiles in
    flowers of different developmental stages and young shoots. The highest abundance of transcripts was achieved in flowers with
    diameters ranging from 0.5 to 0.9cm for GmAGMBP and GmBZIP and in flowers with diameters less than 0.5cm for GmHSA32. Southern
    analysis suggested that GmAGMBP might be single copy gene while GmHSA3A could possibly belong to a small gene family in the
    mangosteen genome.