SRX3504148 d2ctl3 SRP127376 PRJNA414660 Sterile, pre-chilled mortar and pestles were used to grind leaf tissue into fine powder in liquid nitrogen. RNA was extracted from 80 130 mg of fresh weight leaf tissue using an Ambion PureLink RNA Mini kit (Fisher Scientific) and an Ambion PureLink DNase Set (Thermo Fisher Scientific). The quantity and quality of the extracted RNA was measured using a 2100 Bioanalyzer Instrument (Agilent Technologies). All RIN (RNA Integrity) numbers were above 7, indicating high quality material was used for sequencing. mRNA was isolated from total RNA using a TruSeq mRNA Stranded Total Library Prep Kit (Illumina) and then sequenced using the HiSeq2500 System (Illumina) at The Australian Cancer Research Foundation (ACRF) Biomolecular Resource Facility (BRF), Australian National University. SRS2781738 SAMN07807075 d2ctl3 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2500 SRX3504149 d2ll1 SRP127376 PRJNA414660 Sterile, pre-chilled mortar and pestles were used to grind leaf tissue into fine powder in liquid nitrogen. RNA was extracted from 80 130 mg of fresh weight leaf tissue using an Ambion PureLink RNA Mini kit (Fisher Scientific) and an Ambion PureLink DNase Set (Thermo Fisher Scientific). The quantity and quality of the extracted RNA was measured using a 2100 Bioanalyzer Instrument (Agilent Technologies). All RIN (RNA Integrity) numbers were above 7, indicating high quality material was used for sequencing. mRNA was isolated from total RNA using a TruSeq mRNA Stranded Total Library Prep Kit (Illumina) and then sequenced using the HiSeq2500 System (Illumina) at The Australian Cancer Research Foundation (ACRF) Biomolecular Resource Facility (BRF), Australian National University. SRS2781739 SAMN07807076 d2ll1 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2500 SRX3504150 d2ctl1 SRP127376 PRJNA414660 Sterile, pre-chilled mortar and pestles were used to grind leaf tissue into fine powder in liquid nitrogen. RNA was extracted from 80 130 mg of fresh weight leaf tissue using an Ambion PureLink RNA Mini kit (Fisher Scientific) and an Ambion PureLink DNase Set (Thermo Fisher Scientific). The quantity and quality of the extracted RNA was measured using a 2100 Bioanalyzer Instrument (Agilent Technologies). All RIN (RNA Integrity) numbers were above 7, indicating high quality material was used for sequencing. mRNA was isolated from total RNA using a TruSeq mRNA Stranded Total Library Prep Kit (Illumina) and then sequenced using the HiSeq2500 System (Illumina) at The Australian Cancer Research Foundation (ACRF) Biomolecular Resource Facility (BRF), Australian National University. SRS2781742 SAMN07807073 d2ctl1 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2500 SRX3504151 d2ctl2 SRP127376 PRJNA414660 Sterile, pre-chilled mortar and pestles were used to grind leaf tissue into fine powder in liquid nitrogen. RNA was extracted from 80 130 mg of fresh weight leaf tissue using an Ambion PureLink RNA Mini kit (Fisher Scientific) and an Ambion PureLink DNase Set (Thermo Fisher Scientific). The quantity and quality of the extracted RNA was measured using a 2100 Bioanalyzer Instrument (Agilent Technologies). All RIN (RNA Integrity) numbers were above 7, indicating high quality material was used for sequencing. mRNA was isolated from total RNA using a TruSeq mRNA Stranded Total Library Prep Kit (Illumina) and then sequenced using the HiSeq2500 System (Illumina) at The Australian Cancer Research Foundation (ACRF) Biomolecular Resource Facility (BRF), Australian National University. SRS2781740 SAMN07807074 d2ctl2 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2500 SRX3504152 d6ctl1 SRP127376 PRJNA414660 Sterile, pre-chilled mortar and pestles were used to grind leaf tissue into fine powder in liquid nitrogen. RNA was extracted from 80 130 mg of fresh weight leaf tissue using an Ambion PureLink RNA Mini kit (Fisher Scientific) and an Ambion PureLink DNase Set (Thermo Fisher Scientific). The quantity and quality of the extracted RNA was measured using a 2100 Bioanalyzer Instrument (Agilent Technologies). All RIN (RNA Integrity) numbers were above 7, indicating high quality material was used for sequencing. mRNA was isolated from total RNA using a TruSeq mRNA Stranded Total Library Prep Kit (Illumina) and then sequenced using the HiSeq2500 System (Illumina) at The Australian Cancer Research Foundation (ACRF) Biomolecular Resource Facility (BRF), Australian National University. SRS2781741 SAMN07807079 d6ctl1 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2500 SRX3504153 d6ctl2 SRP127376 PRJNA414660 Sterile, pre-chilled mortar and pestles were used to grind leaf tissue into fine powder in liquid nitrogen. RNA was extracted from 80 130 mg of fresh weight leaf tissue using an Ambion PureLink RNA Mini kit (Fisher Scientific) and an Ambion PureLink DNase Set (Thermo Fisher Scientific). The quantity and quality of the extracted RNA was measured using a 2100 Bioanalyzer Instrument (Agilent Technologies). All RIN (RNA Integrity) numbers were above 7, indicating high quality material was used for sequencing. mRNA was isolated from total RNA using a TruSeq mRNA Stranded Total Library Prep Kit (Illumina) and then sequenced using the HiSeq2500 System (Illumina) at The Australian Cancer Research Foundation (ACRF) Biomolecular Resource Facility (BRF), Australian National University. SRS2781743 SAMN07807080 d6ctl2 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2500 SRX3504154 d2ll2 SRP127376 PRJNA414660 Sterile, pre-chilled mortar and pestles were used to grind leaf tissue into fine powder in liquid nitrogen. RNA was extracted from 80 130 mg of fresh weight leaf tissue using an Ambion PureLink RNA Mini kit (Fisher Scientific) and an Ambion PureLink DNase Set (Thermo Fisher Scientific). The quantity and quality of the extracted RNA was measured using a 2100 Bioanalyzer Instrument (Agilent Technologies). All RIN (RNA Integrity) numbers were above 7, indicating high quality material was used for sequencing. mRNA was isolated from total RNA using a TruSeq mRNA Stranded Total Library Prep Kit (Illumina) and then sequenced using the HiSeq2500 System (Illumina) at The Australian Cancer Research Foundation (ACRF) Biomolecular Resource Facility (BRF), Australian National University. SRS2781745 SAMN07807077 d2ll2 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2500 SRX3504155 d2ll3 SRP127376 PRJNA414660 Sterile, pre-chilled mortar and pestles were used to grind leaf tissue into fine powder in liquid nitrogen. RNA was extracted from 80 130 mg of fresh weight leaf tissue using an Ambion PureLink RNA Mini kit (Fisher Scientific) and an Ambion PureLink DNase Set (Thermo Fisher Scientific). The quantity and quality of the extracted RNA was measured using a 2100 Bioanalyzer Instrument (Agilent Technologies). All RIN (RNA Integrity) numbers were above 7, indicating high quality material was used for sequencing. mRNA was isolated from total RNA using a TruSeq mRNA Stranded Total Library Prep Kit (Illumina) and then sequenced using the HiSeq2500 System (Illumina) at The Australian Cancer Research Foundation (ACRF) Biomolecular Resource Facility (BRF), Australian National University. SRS2781744 SAMN07807078 d2ll3 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2500 SRX3504156 d6ctl3 SRP127376 PRJNA414660 Sterile, pre-chilled mortar and pestles were used to grind leaf tissue into fine powder in liquid nitrogen. RNA was extracted from 80 130 mg of fresh weight leaf tissue using an Ambion PureLink RNA Mini kit (Fisher Scientific) and an Ambion PureLink DNase Set (Thermo Fisher Scientific). The quantity and quality of the extracted RNA was measured using a 2100 Bioanalyzer Instrument (Agilent Technologies). All RIN (RNA Integrity) numbers were above 7, indicating high quality material was used for sequencing. mRNA was isolated from total RNA using a TruSeq mRNA Stranded Total Library Prep Kit (Illumina) and then sequenced using the HiSeq2500 System (Illumina) at The Australian Cancer Research Foundation (ACRF) Biomolecular Resource Facility (BRF), Australian National University. SRS2781746 SAMN07807081 d6ctl3 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2500 SRX3504157 d6ll1 SRP127376 PRJNA414660 Sterile, pre-chilled mortar and pestles were used to grind leaf tissue into fine powder in liquid nitrogen. RNA was extracted from 80 130 mg of fresh weight leaf tissue using an Ambion PureLink RNA Mini kit (Fisher Scientific) and an Ambion PureLink DNase Set (Thermo Fisher Scientific). The quantity and quality of the extracted RNA was measured using a 2100 Bioanalyzer Instrument (Agilent Technologies). All RIN (RNA Integrity) numbers were above 7, indicating high quality material was used for sequencing. mRNA was isolated from total RNA using a TruSeq mRNA Stranded Total Library Prep Kit (Illumina) and then sequenced using the HiSeq2500 System (Illumina) at The Australian Cancer Research Foundation (ACRF) Biomolecular Resource Facility (BRF), Australian National University. SRS2781747 SAMN07807082 d6ll1 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2500 SRX3504158 d6ll2 SRP127376 PRJNA414660 Sterile, pre-chilled mortar and pestles were used to grind leaf tissue into fine powder in liquid nitrogen. RNA was extracted from 80 130 mg of fresh weight leaf tissue using an Ambion PureLink RNA Mini kit (Fisher Scientific) and an Ambion PureLink DNase Set (Thermo Fisher Scientific). The quantity and quality of the extracted RNA was measured using a 2100 Bioanalyzer Instrument (Agilent Technologies). All RIN (RNA Integrity) numbers were above 7, indicating high quality material was used for sequencing. mRNA was isolated from total RNA using a TruSeq mRNA Stranded Total Library Prep Kit (Illumina) and then sequenced using the HiSeq2500 System (Illumina) at The Australian Cancer Research Foundation (ACRF) Biomolecular Resource Facility (BRF), Australian National University. SRS2781748 SAMN07807083 d6ll2 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2500 SRX3504159 d6ll3 SRP127376 PRJNA414660 Sterile, pre-chilled mortar and pestles were used to grind leaf tissue into fine powder in liquid nitrogen. RNA was extracted from 80 130 mg of fresh weight leaf tissue using an Ambion PureLink RNA Mini kit (Fisher Scientific) and an Ambion PureLink DNase Set (Thermo Fisher Scientific). The quantity and quality of the extracted RNA was measured using a 2100 Bioanalyzer Instrument (Agilent Technologies). All RIN (RNA Integrity) numbers were above 7, indicating high quality material was used for sequencing. mRNA was isolated from total RNA using a TruSeq mRNA Stranded Total Library Prep Kit (Illumina) and then sequenced using the HiSeq2500 System (Illumina) at The Australian Cancer Research Foundation (ACRF) Biomolecular Resource Facility (BRF), Australian National University. SRS2781749 SAMN07807084 d6ll3 RNA-Seq TRANSCRIPTOMIC PCR Illumina HiSeq 2500