Verification of legitimate tenera oil palm hybrids using SSR and propagation of hybrids by somatic embryogenesis

Oil palm planting material consists solely of tenera hybrids, originating from crosses between dura and pisifera types.To confirm the parentage of the tenera hybrids, we used a DNA molecular marker approach based on simple sequence repeat(SSR). 6 parental lines of pisifera and 2 of dura were used to...

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Bibliographic Details
Main Authors: Supawadee Thawaro, Sompong Te-chato
Format: Article
Language:English
Published: Prince of Songkla University 2010-03-01
Series:Songklanakarin Journal of Science and Technology (SJST)
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Online Access:http://www.rdoapp.psu.ac.th/html/sjst/journal/32-1/0125-3395-32-1-1-8.pdf
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Summary:Oil palm planting material consists solely of tenera hybrids, originating from crosses between dura and pisifera types.To confirm the parentage of the tenera hybrids, we used a DNA molecular marker approach based on simple sequence repeat(SSR). 6 parental lines of pisifera and 2 of dura were used to produce 6 independent progenies. SSR markers were tested(8 SSR primers) to valid the progenies from crosses #77 [366 (D)  172 (P)], #58 [366 (D)  72 (P)], #118 [366 (D)  206 (P)],#119 [865 (D)  206 (P)], #130 [865 (D)  110 (P)], and #137 [366 (D)  777 (P)]. All primers tested could amplify parentalDNA. Secondly, half mature zygotic embryos consisting of the coleoptile region of those combinations was cultured on Murashige and Skoog (MS) medium plus various kinds and concentrations of auxins for callus induction. The results revealed that primers mEgCIR008 provided a clear DNA pattern and could be used for hybrid verification of the crosses 366 (D)  172 (P). The highest frequency of nodular callus formation at 65% was obtained on MS medium supplemented with 2.5 mg/l3, 6-dichloro-o-anisic acid (dicamba), significantly superior to the other kinds and concentrations of auxins. Moreover, somatic embryo formations at the globular and haustorium stages were achieved at 7.17% and 4.59%, respectively whencultured on MS medium supplemented with 0.2 M of sorbitol and 200 mg/l ascorbic acid for 3 months.
ISSN:0125-3395