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. 2013 Jan 10;64(4):991–1003. doi: 10.1093/jxb/ers374

Table 2.

Ratios of transcript levels of selected cell expansion-related genes in transgenic grape embryos compared with the control (C) and determination of the presence of bHLH-binding sites in the corresponding promoter regions.

Description Name Accession no. Ratio (35S/C)a bHLH-binding sitesb
Expansin VvEXPA1 XM_002269481.1 7.7
VvEXPA8 XM_002280264.1 38 +
VvEXPA11 XM_002285855.1 1154 +
VvEXPA12 XM_002284822.1 52 +
VvEXPA17 XM_002273247.1 252 ++
α-Amylase VvAMY1 XM_002285177.1 4.3
Xyloglucan endotransglycosylase VvXET2 XM_002274484.1 4 ++
Pectate lyase VvPECL1 XM_002285603.1 4.8 ++++++++
VvPECL8 XM_002275745.1 82 ++++++
Arabinogalactan protein VvAGP20 XM_002280458.1 5 +++
Aquaporin (TIP) VvAQP1 XM_002274502.1 8.3 +++++
VvAQP2 XM_002262942.1 0.2 +
VvAQP3 XM_002274691.1 4.1 ++
VvAQP4 XM_002274519.1 2.4 +

a Gene transcript levels were quantified by qRT-PCR in control (C, pFB8 empty vector) and VvCEB1-overexpressing (35S) grape 41B embryo lines. The embryos were collected 7 d after initiation of embryogenesis. Gene expression was normalized against VvEF1γ. Data are means of three independent experiments.

b The promoter regions (1000bp upstream of the transcription start site) for each gene were used as the target sequences for putative bHLH transcription factor recognition site identification using the MatInspector program (Genomatix software package). Each ‘+’ indicates the presence of one MYCL family binding site whereas ‘–’ indicates the absence of MYCL-binding site.