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Table 2 Genes and primers used in qRT-PCR assay

From: Transcriptome profiling of lentil (Lens culinaris) through the first 24 hours of Ascochyta lentis infection reveals key defence response genes

Target gene

Gene function

Primer sequences (5’-3’)

Amplification efficiencya

Tm (°C)

DELLA

SAR signalling

F: GTCTTCTAATTCAAACCA

1.926 ± 0.027

53

  

R: ATATCTGTTTACCCAAGTAA

  

RBP-hnRNP

Transcriptional factor

F: GAGAAAGATATTTGTTGGAG

1.947 ± 0.024

51

  

R: TGATCGTACATTACTACAACA

  

PGIP

Anti fungal compound

F: TGAAGGTGATGCTTCTATGCT

2.013 ± 0.026

53

  

R: GACTCACATCCAACGTTGCT

  

PR2

Anti fungal compound

F: GGCATGCTGGGAAACAATCT

2.018 ± 0.023

52

  

R: TGGCACACCTAACATGAGCT

  

PR10

Anti fungal compound

F: TGGCACTTCTGCTGTTAGATGGAC

2.017 ± 0.083

50

  

R: GGTAATCCATCCAGCCATTTGGAG

  

PP2A

Reference gene

F: GCCTCATTTGCAGCTGGTTT

2.002 ± 0.025

53

  

R: TACTCTCGTTCTAGGGTCCT

  
  1. aMean and standard deviation of the amplification efficiency for each gene were calculated from the coefficients of linear regression models fitted to each reaction (value of 2 equivalents to 100% efficiency, see [43])