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    Transcriptome sequencing of different narrow-leafed lupin tissue types provides a comprehensive uni-gene assembly and extensive gene-based molecular markers

    Access Status
    Open access via publisher
    Authors
    Kamphuis, L.
    Hane, James
    Nelson, M.
    Gao, L.
    Atkins, C.
    Singh, K.
    Date
    2014
    Type
    Journal Article
    
    Metadata
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    Citation
    Kamphuis, L. and Hane, J. and Nelson, M. and Gao, L. and Atkins, C. and Singh, K. 2014. Transcriptome sequencing of different narrow-leafed lupin tissue types provides a comprehensive uni-gene assembly and extensive gene-based molecular markers. Plant Biotechnology Journal. 13 (1): pp. 14-25.
    Source Title
    Plant Biotechnology Journal
    DOI
    10.1111/pbi.12229
    ISSN
    14677644
    School
    Department of Environment and Agriculture
    URI
    http://hdl.handle.net/20.500.11937/17463
    Collection
    • Curtin Research Publications
    Abstract

    Narrow-leafed lupin (NLL; Lupinus angustifolius L.) is an important grain legume crop that is valuable for sustainable farming and is becoming recognized as a human health food. NLL breeding is directed at improving grain production, disease resistance, drought tolerance and health benefits. However, genetic and genomic studies have been hindered by a lack of extensive genomic resources for the species. Here, the generation, de novo assembly and annotation of transcriptome datasets derived from five different NLL tissue types of the reference accession cv. Tanjil are described. The Tanjil transcriptome was compared to transcriptomes of an early domesticated cv. Unicrop, a wild accession P27255, as well as accession 83A:476, together being the founding parents of two recombinant inbred line (RIL) populations. In silico predictions for transcriptome-derived gene-based length and SNP polymorphic markers were conducted and corroborated using a survey assembly sequence for NLL cv. Tanjil. This yielded extensive indel and SNP polymorphic markers for the two RIL populations. A total of 335 transcriptome-derived markers and 66 BAC-end sequence-derived markers were evaluated, and 275 polymorphic markers were selected to genotype the reference NLL 83A:476 × P27255 RIL population. This significantly improved the completeness, marker density and quality of the reference NLL genetic map.

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