A transcript profile comparison to evaluate purity of pollen samples used for RNA-Seq. A subset of 12 genes was used to compare relative purities of pollen samples in the current pollen transcriptome study to those from a RNA-Seq study from Loraine et al. [22] (yellow highlights) or a microarray experiment from Qin et al. 2009 [23] (purple highlights). Four references genes were chosen to generate normalization factors that could be used to adjust expression values in Loraine et al. [22] and Qin et al. 2009 [23] to allow a relative comparison of the three data sets for WT pollen under control (normal) conditions. For a control group, three CNGC genes were chosen that displayed low to moderate levels of expression (Tunc-Ozdemir et al. 2013 [...
Abstract Background In flowering plants, the male gametophyte (pollen) is one of the most vulnerable...
Figure S1. a. Order of developmental stages for anatomical samples. ACF, formation of archesporial c...
Table S1. List of binary plasmids used in this study. Table S2. Oligonucleotides used for RT-qPCR. F...
Normalized transcript expression counts for WT and cngc16 pollen with and without HS. Expression cou...
HS-dependent transcript abundance changes corresponding to transcription factors in WT and cngc16 po...
Raw expression counts for WT and cngc16 pollen with and without HS. Read counts generated via Featur...
A comparison of HS-dependent changes in pollen to 67 multi-stress response genes in vegetative tissu...
RNA-Seq validation using real-time Q-PCR. a. Comparison of expression values obtained from Q-PCR and...
Hot/Cold stress cycle. Diagram showing the Hot/Cold stress-cycle used here for growing plants from w...
GO analyses on HS-dependent changes in WT and cngc16. a. The number of genes in each GO category is ...
Library size and principal component analysis. a. Table showing library sizes of each sample. b. A p...
GO analysis on the 192 largest differences between WT and cngc16 under HS. A GO analysis pie chart i...
Predicted targets for HS-modulated microRNAs. Target predictions for microRNAs were conducted with p...
Integrated Genome Browser (IGB) screenshot showing cngc16 RNA-Seq reads primarily upstream of T-DNA ...
Figure S2. Pollen grains from BET11/12 mutants show reduced pollen tube growth in vivo but no develo...
Abstract Background In flowering plants, the male gametophyte (pollen) is one of the most vulnerable...
Figure S1. a. Order of developmental stages for anatomical samples. ACF, formation of archesporial c...
Table S1. List of binary plasmids used in this study. Table S2. Oligonucleotides used for RT-qPCR. F...
Normalized transcript expression counts for WT and cngc16 pollen with and without HS. Expression cou...
HS-dependent transcript abundance changes corresponding to transcription factors in WT and cngc16 po...
Raw expression counts for WT and cngc16 pollen with and without HS. Read counts generated via Featur...
A comparison of HS-dependent changes in pollen to 67 multi-stress response genes in vegetative tissu...
RNA-Seq validation using real-time Q-PCR. a. Comparison of expression values obtained from Q-PCR and...
Hot/Cold stress cycle. Diagram showing the Hot/Cold stress-cycle used here for growing plants from w...
GO analyses on HS-dependent changes in WT and cngc16. a. The number of genes in each GO category is ...
Library size and principal component analysis. a. Table showing library sizes of each sample. b. A p...
GO analysis on the 192 largest differences between WT and cngc16 under HS. A GO analysis pie chart i...
Predicted targets for HS-modulated microRNAs. Target predictions for microRNAs were conducted with p...
Integrated Genome Browser (IGB) screenshot showing cngc16 RNA-Seq reads primarily upstream of T-DNA ...
Figure S2. Pollen grains from BET11/12 mutants show reduced pollen tube growth in vivo but no develo...
Abstract Background In flowering plants, the male gametophyte (pollen) is one of the most vulnerable...
Figure S1. a. Order of developmental stages for anatomical samples. ACF, formation of archesporial c...
Table S1. List of binary plasmids used in this study. Table S2. Oligonucleotides used for RT-qPCR. F...