Identification of QTLs associated with callogenesis and embryogenesis in oil palm using genetic linkage maps improved with SSR markers

PLoS One. 2013;8(1):e53076. doi: 10.1371/journal.pone.0053076. Epub 2013 Jan 29.

Abstract

Clonal reproduction of oil palm by means of tissue culture is a very inefficient process. Tissue culturability is known to be genotype dependent with some genotypes being more amenable to tissue culture than others. In this study, genetic linkage maps enriched with simple sequence repeat (SSR) markers were developed for dura (ENL48) and pisifera (ML161), the two fruit forms of oil palm, Elaeis guineensis. The SSR markers were mapped onto earlier reported parental maps based on amplified fragment length polymorphism (AFLP) and restriction fragment length polymorphism (RFLP) markers. The new linkage map of ENL48 contains 148 markers (33 AFLPs, 38 RFLPs and 77 SSRs) in 23 linkage groups (LGs), covering a total map length of 798.0 cM. The ML161 map contains 240 markers (50 AFLPs, 71 RFLPs and 119 SSRs) in 24 LGs covering a total of 1,328.1 cM. Using the improved maps, two quantitative trait loci (QTLs) associated with tissue culturability were identified each for callusing rate and embryogenesis rate. A QTL for callogenesis was identified in LGD4b of ENL48 and explained 17.5% of the phenotypic variation. For embryogenesis rate, a QTL was detected on LGP16b in ML161 and explained 20.1% of the variation. This study is the first attempt to identify QTL associated with tissue culture amenity in oil palm which is an important step towards understanding the molecular processes underlying clonal regeneration of oil palm.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arecaceae / genetics
  • Chromosome Mapping
  • Microsatellite Repeats / genetics*
  • Plant Cells / physiology
  • Plant Development / genetics*
  • Polymorphism, Genetic
  • Polymorphism, Restriction Fragment Length / genetics
  • Quantitative Trait Loci / genetics*
  • Seeds / genetics*
  • Seeds / growth & development

Grants and funding

This project is funded by the Ministry of Science, Technology and Innovation (MOSTI), Malaysia under the project code MMBPP 04-03-T0045-TC3.2. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.