14 research outputs found
El Diario de Pontevedra : periódico liberal: Ano LII Número 17828 - 1938 decembro 10
BinGO analysis of the top 500 DEGs with a positive difference between 26 and 20° Brix (26–20) (XLSX 73 kb)
El Diario de Pontevedra : periódico liberal: Ano XLII Número 12723 - 1927 xuño 6
Statistical results from gene set enrichment analysis of the DEGs using BinGO (XLSX 271 kb)
Additional file 5: of A comparison of heat-stress transcriptome changes between wild-type Arabidopsis pollen and a heat-sensitive mutant harboring a knockout of cyclic nucleotide-gated cation channel 16 (cngc16)
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 [24] and Frietsch et al. 2007 [25]). As markers for potential contamination from photosynthetic tissues, five different nuclear encoded genes were chosen that are associated with either photosystems I/II, or chlorophyll A-B binding proteins (Umate 2010 [26]). Average relative ratios are shown for each of the four different pollen samples in comparison to both Loraine et al. [22] and Qin et al. [23]. (XLSX 19 kb
Additional file 13: of A comparison of heat-stress transcriptome changes between wild-type Arabidopsis pollen and a heat-sensitive mutant harboring a knockout of cyclic nucleotide-gated cation channel 16 (cngc16)
A comparison of HS-dependent changes in pollen to 67 multi-stress response genes in vegetative tissues. From a list of 67 multi-stress genes curated by Swindell 2006 (PMCID: PMC1698639 [47]; highlighted in purple), 19 genes showed detectable expression in pollen. Among those, only three genes showed significant changes in pollen HS (red font). (XLSX 596 kb
Additional file 15: of A comparison of heat-stress transcriptome changes between wild-type Arabidopsis pollen and a heat-sensitive mutant harboring a knockout of cyclic nucleotide-gated cation channel 16 (cngc16)
GO analysis on the 192 largest differences between WT and cngc16 under HS. A GO analysis pie chart is shown for Molecular Function (a), Cellular Component (b), and Biological Process (c) generated using an upload of Additional file 3 or Additional file 9e column R listing the differences (≥ 2-fold and adjusted p-value ≤0.01) between WT and cngc16 HS-transcriptomes. Categories were defined using PANTHER Overrepresentation Test (release 2017–04-13 [61]) using a GO Ontology database (released 2017–08-14) with 27,060 reference genes for Arabidopsis thaliana. Gene categories shown displayed enrichments with a p-value of ≤0.05. (PPTX 993 kb
Additional file 2: of A comparison of heat-stress transcriptome changes between wild-type Arabidopsis pollen and a heat-sensitive mutant harboring a knockout of cyclic nucleotide-gated cation channel 16 (cngc16)
Raw expression counts for WT and cngc16 pollen with and without HS. Read counts generated via FeatureCounts, see Methods) for all 12 replicates are shown before normalization and exclusions. (XLSX 4358 kb
Additional file 3: of A comparison of heat-stress transcriptome changes between wild-type Arabidopsis pollen and a heat-sensitive mutant harboring a knockout of cyclic nucleotide-gated cation channel 16 (cngc16)
Normalized transcript expression counts for WT and cngc16 pollen with and without HS. Expression counts from Additional file 2 were subjected to exclusions/filters and normalized as described in methods. Expression data from other transcriptome studies (microarray and RNA-Seq) were added to the table for comparisons. These included an RNA-Seq data set for WT pollen and seedlings from Loraine et al. 2013 (PMCID: PMC3668042 [22]), two pollen microarray experiments from Qin et al. 2009 (PMCID: PMC2726614 [23]) and Borges et al. 2008 (PMCID: PMC2556834 [72]), and finally HS seedlings from Schmid et al. 2005 (PMID:15806101 [33]), respectively. Ratios of expression between pollen and seedling are based on Loraine et al. 2013 (PMCID: PMC3668042 [22]). In cases where the seedling value was below the limit of detection, a minimal value of 0.0019 was substituted in its place as a denominator (0.0019 was the RPKM for ATCG00860 and was the lowest value reported in Loraine et al. 2013 (PMCID: PMC3668042 [22]). Ratio of expression between semi-in vivo pollen tube over dry pollen is based on Qin et al. 2009 (PMCID: PMC2726614 [23]). HS dependent changes in transcript abundance in shoots were based on publicly available data using the AtGenExpress Visualization Tool (AVT) ( http://jsp.weigelworld.org/expviz/expviz.jsp , Schmid et al. 2005 (PMID:15806101 [33] for seedlings exposed to one hour HS at 38 °C). The log2-fold change was calculated based on a comparison of means of normalized values for two heat-stressed and two non-stressed seedling samples. NA stands for not available. Not Calculated, refers to a value not being calculated because one of the input sample read counts was considered to have an extreme outlier (see AT2G42540 and ATMG01360). (XLSX 8952 kb
Additional file 4: of A comparison of heat-stress transcriptome changes between wild-type Arabidopsis pollen and a heat-sensitive mutant harboring a knockout of cyclic nucleotide-gated cation channel 16 (cngc16)
Library size and principal component analysis. a. Table showing library sizes of each sample. b. A principal component analysis (PCA) of the filtered data showing that 87% of the variance of the samples can be explained by differences in the stress states. See methods for more details. Control and heat correspond to normal and HS conditions, respectively. (PPTX 43 kb
Additional file 6: of A comparison of heat-stress transcriptome changes between wild-type Arabidopsis pollen and a heat-sensitive mutant harboring a knockout of cyclic nucleotide-gated cation channel 16 (cngc16)
Integrated Genome Browser (IGB) screenshot showing cngc16 RNA-Seq reads primarily upstream of T-DNA insertion site. The green arrow identifies the position of T-DNA insertion in cngc16–2 (SAIL_726_B04). The observed reads aligning to cngc16 are primarily on the 5′ side of the T-DNA disruption site, with only a few reads observed at two disconnected downstream positions. This suggests that there were no detectable full-length transcripts. (PPTX 66 kb
Additional file 1: of A comparison of heat-stress transcriptome changes between wild-type Arabidopsis pollen and a heat-sensitive mutant harboring a knockout of cyclic nucleotide-gated cation channel 16 (cngc16)
Hot/Cold stress cycle. Diagram showing the Hot/Cold stress-cycle used here for growing plants from which pollen samples for RNA-Seq experiment were harvested at the end of HS-peak at 40 °C. See Methods and [20] for more details. (PPTX 50 kb