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. 2019 Jan 15;9(3):769–787. doi: 10.1534/g3.118.200805

Table 2. Normalized RNAseq quantification of pre-MIR828, TAS4, and target MYBA6 and -MYBA7 mRNAs in berry skins of five field-grown red and white cultivars during development (datasets of Massonnet et al. 2017).

Datasets/gene Berry Developmental Stage
Pea-sized Just prior veraison Soft Harvest
Red cultivars (reads per 100 Million*)
  pre-MIR828^ 1.1 0.0 0.2 0.0
  TAS4a^ 31.4 16.5 6.0 0.4
  TAS4b^ 0.3 0.2 0.0 0.0
  TAS4c& 0.0 0.0 13.6 8.7
  MYBA6$ 5.1 1.6 10.3 0.9
  MYBA7^ 19.9 13.3 0.0 0.0
  pre-MIR166e reference^ 26.5 20.2 13.2 7.8
White cultivars
  pre-MIR828^ 1.3 0.2 0.0 0.0
  TAS4a^ 53.8 41.7 19.1 3.9
  TAS4b^ 4.6 4.3 0.0 0.0
  TAS4c 0.0 0.0 0.0 0.0
  MYBA6$ 6.0 3.7 5.2 3.8
  MYBA7^ 8.2 0.0 0.2 0.0
  pre-MIR166e reference^ 23.0 14.4 5.8 3.9
*

96 nt reads mapping completely to amplicons quantified by qRT-PCR in Fig. S2, <= 4 mismatches. See Supplementary Table 7 for amplicon target details. Pre-vvi-MIR166e target sequence from miRBase22; TAS4b reads are for 105 bp amplicon plus 100 nts upstream and downstream because 96 nt read lengths precluded results.

^

The decreasing pre-MIR828, TAS4ab, MYBA7, and pre-MIR166e expressions as development progresses correlate with the derivative miR828*, TAS4 siRNA, MYBA7 mRNA, and mature miR166 abundances documented in field samples, Supplementary Table 3d and Supplementary Fig. S2.

&The increasing TAS4c expression as development progresses (bold) correlates with mRNA and derivative TAS4c tasiRNA 3′D4(-) abundances documented in field samples, Supplementary Table 3d and Fig. S2E.

$

The fluctuations of MYBA6 expressions at veraison and soft berry stages (italics) correlate with the derivative siRNA abundance documented in field samples, Supplementary Table 3d and Fig. S2F, left panel.