Large-scale collection of full-length cDNA and transcriptome analysis in Hevea brasiliensis
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作者:
Makita, Yuko
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RIKEN, Ctr Sustainable Resource Sci, Synthet Genom Res Grp, Biomass Engn Res Div, Yokohama, Kanagawa 2300045, JapanRIKEN, Ctr Sustainable Resource Sci, Synthet Genom Res Grp, Biomass Engn Res Div, Yokohama, Kanagawa 2300045, Japan
Makita, Yuko
[1
]
Ng, Kiaw Kiaw
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RIKEN, Ctr Sustainable Resource Sci, Synthet Genom Res Grp, Biomass Engn Res Div, Yokohama, Kanagawa 2300045, Japan
Univ Sains Malaysia, Sch Biol Sci, Mol Ecol & Evolut Res Lab, Minden 11800, Pulau Pinang, MalaysiaRIKEN, Ctr Sustainable Resource Sci, Synthet Genom Res Grp, Biomass Engn Res Div, Yokohama, Kanagawa 2300045, Japan
Ng, Kiaw Kiaw
[1
,2
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Singham, G. Veera
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RIKEN, Ctr Sustainable Resource Sci, Synthet Genom Res Grp, Biomass Engn Res Div, Yokohama, Kanagawa 2300045, Japan
Univ Sains Malaysia, Ctr Chem Biol, Bayan Lepas 11900, Pulau Pinang, MalaysiaRIKEN, Ctr Sustainable Resource Sci, Synthet Genom Res Grp, Biomass Engn Res Div, Yokohama, Kanagawa 2300045, Japan
Singham, G. Veera
[1
,4
]
Kawashima, Mika
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RIKEN, Ctr Sustainable Resource Sci, Synthet Genom Res Grp, Biomass Engn Res Div, Yokohama, Kanagawa 2300045, JapanRIKEN, Ctr Sustainable Resource Sci, Synthet Genom Res Grp, Biomass Engn Res Div, Yokohama, Kanagawa 2300045, Japan
Kawashima, Mika
[1
]
Hirakawa, Hideki
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Kazusa DNA Res Inst, 2-6-7 Kazusa Kamatari, Kisarazu, Chiba 2920818, JapanRIKEN, Ctr Sustainable Resource Sci, Synthet Genom Res Grp, Biomass Engn Res Div, Yokohama, Kanagawa 2300045, Japan
Hirakawa, Hideki
[3
]
Sato, Shusei
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Kazusa DNA Res Inst, 2-6-7 Kazusa Kamatari, Kisarazu, Chiba 2920818, JapanRIKEN, Ctr Sustainable Resource Sci, Synthet Genom Res Grp, Biomass Engn Res Div, Yokohama, Kanagawa 2300045, Japan
Sato, Shusei
[3
]
Othman, Ahmad Sofiman
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Univ Sains Malaysia, Sch Biol Sci, Mol Ecol & Evolut Res Lab, Minden 11800, Pulau Pinang, Malaysia
Univ Sains Malaysia, Ctr Chem Biol, Bayan Lepas 11900, Pulau Pinang, MalaysiaRIKEN, Ctr Sustainable Resource Sci, Synthet Genom Res Grp, Biomass Engn Res Div, Yokohama, Kanagawa 2300045, Japan
Othman, Ahmad Sofiman
[2
,4
]
Matsui, Minami
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RIKEN, Ctr Sustainable Resource Sci, Synthet Genom Res Grp, Biomass Engn Res Div, Yokohama, Kanagawa 2300045, JapanRIKEN, Ctr Sustainable Resource Sci, Synthet Genom Res Grp, Biomass Engn Res Div, Yokohama, Kanagawa 2300045, Japan
Matsui, Minami
[1
]
机构:
[1] RIKEN, Ctr Sustainable Resource Sci, Synthet Genom Res Grp, Biomass Engn Res Div, Yokohama, Kanagawa 2300045, Japan
[2] Univ Sains Malaysia, Sch Biol Sci, Mol Ecol & Evolut Res Lab, Minden 11800, Pulau Pinang, Malaysia
[3] Kazusa DNA Res Inst, 2-6-7 Kazusa Kamatari, Kisarazu, Chiba 2920818, Japan
[4] Univ Sains Malaysia, Ctr Chem Biol, Bayan Lepas 11900, Pulau Pinang, Malaysia
Natural rubber has unique physical properties that cannot be replaced by products from other latex-producing plants or petrochemically produced synthetic rubbers. Rubber from Hevea brasiliensis is the main commercial source for this natural rubber that has a cis-polyisoprene configuration. For sustainable production of enough rubber to meet demand elucidation of the molecular mechanisms involved in the production of latex is vital. To this end, we firstly constructed rubber full-length cDNA libraries of RRIM 600 cultivar and sequenced around 20,000 clones by the Sanger method and over 15,000 contigs by Illumina sequencer. With these data, we updated around 5,500 gene structures and newly annotated around 9,500 transcription start sites. Second, to elucidate the rubber biosynthetic pathways and their transcriptional regulation, we carried out tissue- and cultivar-specific RNA-Seq analysis. By using our recently published genome sequence, we confirmed the expression patterns of the rubber biosynthetic genes. Our data suggest that the cytoplasmic mevalonate (MVA) pathway is the main route for isoprenoid biosynthesis in latex production. In addition to the well-studied polymerization factors, we suggest that rubber elongation factor 8 (REF8) is a candidate factor in cis-polyisoprene biosynthesis. We have also identified 39 transcription factors that may be key regulators in latex production. Expression profile analysis using two additional cultivars, RRIM 901 and PB 350, via an RNA-Seq approach revealed possible expression differences between a high latex-yielding cultivar and a disease-resistant cultivar.