Low-temperature stresses limit the sustainability and productivity of grapevines when early spring frosts damage young grapevine leaves. Spring conditions often expose grapevines to low, but not damaging, chilling temperatures and these temperatures have
Heat map of CCCH gene expression inC. bungeiunder low temperature stress. CK refers to 0 h of treatment under 4 degrees low temperature stress, 0.5 h refers to 0.5 h of treatment under 4 degrees low temperature stress, and so on. The more a color approaches red, the higher the expression...
because transcripts encoding theArabidopsissigma factorsSIG1,SIG4andSIG5accumulate in response to low temperatures (Extended Data Fig.1)23,28. We focused on the role of SIG5 in low-temperature responses because published microarray data indicate that it has the greatest transcriptional...
, 1994). It contained a cis-acting element responsible for drought and low-temperature responsivity, subsequently named the drought-responsive element (DRE; Yamaguchi-Shinozaki & Shinozaki, 1994). This motif (also known as the C-repeat or CRT) was later found in the promoters of many other ...
In turn, AtERF012 is involved in the response to abiotic stress, such as low temperature stress [55]. The homologous gene PsAP2/ERF88 contained many cis-acting elements involved in defense and stress responsiveness and was highly expressed in the transcriptome; consequently, PsAP2/ERF88 may ...
The present invention provides a gene participating in the low temperature germinability in rice and utilization of the same, and the invention relates to a gene for a low temperatu
Promoter regions of the up-regulated genes were enriched in the GCCGGC motif also contained in the AtHAK5 promoter. These results suggest that RAP2.11 regulates AtHAK5 expression under low-K+ conditions and also contributes to a coordinated response to low-potassium conditions through the regulation...
0.625 mL of 16% formaldehyde was added and the samples were incubated on a shaker for 5 min at room temperature. The samples were then quenched with 0.667 mL of 2 M glycine and incubated for 5 min at room temperature on a rotator. The cells were then centrifuged at 1600...
Recently, it has been shown that prolonged exposure to high temperature promotes primary root elongation in a BRI1-dependent manner48. However, in our study, the root phenotypes of two bri1 mutants indicate that a BRI1-independent mechanism modulates root foraging in response to N (Supplementary...