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Transcript abundance profiles reveal larger and more complex responses of grapevine to chilling compared to osmotic and salinity stress

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Abstract

Cabernet Sauvignon grapevines were exposed to sudden chilling (5°C), water deficit (PEG), and an iso-osmotic salinity (120 mM NaCl and 12 mM CaCl2) for 1, 4, 8, and 24 h. Stomatal conductance and stem water potentials were significantly reduced after stress application. Microarray analysis of transcript abundance in shoot tips detected no significant differences in transcript abundance between salinity and PEG before 24 h. Chilling stress relates to changes in membrane structure, and transcript abundance patterns were predicted to reflect this. Forty-three percent of transcripts affected by stress vs control for 1 through 8 h were affected only by chilling. The functional categories most affected by stress included metabolism, protein metabolism, and signal transduction. Osmotic stress affected more protein synthesis and cell cycle transcripts, whereas chilling affected more calcium signaling transcripts, indicating that chilling has more complex calcium signaling. Stress affected many hormone (ABA, ethylene, and jasmonate) and transcription factor transcripts. The concentrations and transporter transcripts of several anions increased with time, including nitrate, sulfate, and phosphate. The transcript abundance changes in this short-term study were largely the same as a gradually applied long-term salinity and water-deficit study (Cramer et al. Funct Integr Genomics 7:111–134, 2007), but the reverse was not true, indicating a larger and more complex response in the acclimation process of a gradual long-term stress.

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Acknowledgments

This work was supported by grants from the National Science Foundation (NSF) Plant Genome program (#0217653), and a graduate student fellowship to E.A.R. Tattersall from the NSF EPSCoR Integrated Approaches to Abiotic Stress program (#0132556). The Nevada Genomics Center is supported by grants from the NIH Biomedical Research Infrastructure Network (NIH-NCRR, P20 RR16464) and NIH IDeA Network of Biomedical Research Excellence (INBRE, RR-03-008).

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Correspondence to Grant R. Cramer.

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Supplemental Figure 1S

Percent of transcripts representing significantly different abundance (p < 0.01) in stress versus control (1, 4 and 8 hours) that were assigned to MIPS functional categories. Results are given as a percentage of the total number of transcripts in the set to reflect relative differences among treatments (GIF 15 kb)

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Supplemental Figure 2S

Concentrations of anions found in shoot tips (peak area/hippuric acid standard). Mean and s.d of three biological replicates. Square (■), chilling. Triangle (▲), PEG. Inverted triangle (▼), salinity. Diamond (◆), control (GIF 22 kb)

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Supplemental Figure 3S

Percentage of transcripts with significant differences in abundance (p < 0.01) for salinity and PEG/water-deficit versus control at 24 hours and day 16 that were assigned to MIPS functional categories. Transcripts common to both 24 hours and day 16 for either stress were omitted from this analysis (GIF 20 kb)

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Tattersall, E.A.R., Grimplet, J., DeLuc, L. et al. Transcript abundance profiles reveal larger and more complex responses of grapevine to chilling compared to osmotic and salinity stress. Funct Integr Genomics 7, 317–333 (2007). https://doi.org/10.1007/s10142-007-0051-x

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