Affiliations 

  • 1 Advanced Biotechnology and Breeding Centre, Malaysian Palm Oil Board (MPOB), P.O. Box 10620, 50720, Kuala Lumpur, Malaysia
  • 2 Quantitative and Computational Biology Section, University of Southern California, 1050 Childs Way, Los Angeles, CA, USA
  • 3 Codon Genomics Sdn. Bhd. Malaysia, No. 26, Jalan Dutamas 7, Taman Dutamas, Balakong, 43200, Seri Kembangan, Selangor, Malaysia
  • 4 United Plantations Bhd, Jendarata Estate, 36009, Teluk Intan, Perak, Malaysia
  • 5 Plant and Crop Sciences, Sutton Bonington Campus, Sutton Bonington, University of Nottingham, Loughborough, LE12 5RD, UK
  • 6 Biotechnology Research Centre, School of Biosciences, University of Nottingham Malaysia Campus, Jalan Broga, 43500, Semenyih, Selangor, Malaysia
  • 7 Molecular and Computational Biology Section, University of Southern California, 1050 Childs Way, Los Angeles, CA, USA
  • 8 Advanced Biotechnology and Breeding Centre, Malaysian Palm Oil Board (MPOB), P.O. Box 10620, 50720, Kuala Lumpur, Malaysia. [email protected]
Sci Rep, 2020 10 01;10(1):16296.
PMID: 33004875 DOI: 10.1038/s41598-020-73170-5

Abstract

Evaluation of transcriptome data in combination with QTL information has been applied in many crops to study the expression of genes responsible for specific phenotypes. In oil palm, the mesocarp oil extracted from E. oleifera × E. guineensis interspecific hybrids is known to have lower palmitic acid (C16:0) content compared to pure African palms. The present study demonstrates the effectiveness of transcriptome data in revealing the expression profiles of genes in the fatty acid (FA) and triacylglycerol (TAG) biosynthesis processes in interspecific hybrids. The transcriptome assembly yielded 43,920 putative genes of which a large proportion were homologous to known genes in the public databases. Most of the genes encoding key enzymes involved in the FA and TAG synthesis pathways were identified. Of these, 27, including two candidate genes located within the QTL associated with C16:0 content, showed differential expression between developmental stages, populations and/or palms with contrasting C16:0 content. Further evaluation using quantitative real-time PCR revealed that differentially expressed patterns are generally consistent with those observed in the transcriptome data. Our results also suggest that different isoforms are likely to be responsible for some of the variation observed in FA composition of interspecific hybrids.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.