The E3 Ligase TaSAP5 Alters Drought Stress Responses by Promoting the Degradation of DRIP Proteins.

In Arabidopsis (Arabidopsis thaliana) plants growing under normal conditions, DEHYDRATION-RESPONSIVE ELEMENT BINDING PROTEIN2A (DREB2A) is present at low levels because it is ubiquitinated and destabilized by DREB2A INTERACTING PROTEIN1 (DRIP1) and DRIP2 through 26S proteasome-mediated proteolysis. Drought stress counteracts the ubiquitination and proteolysis of DREB2A, thus allowing the accumulation of sufficient amounts of DREB2A protein to activate downstream gene expression. The mechanisms leading to drought stress-mediated DREB2A accumulation are still unclear. Here, we report that the wheat (Triticum aestivum) TaSAP5 protein, which contains an A20/AN1 domain, acts as an E3 ubiquitin ligase to mediate DRIP degradation and thus increase DREB2A protein levels. Drought induces TaSAP5 expression in wheat, and TaSAP5 overexpression in Arabidopsis and wheat seedlings increased their drought tolerance, as measured by survival rate and grain yield under severe drought stress. TaSAP5 can interact with and ubiquitinate TaDRIP, as well as AtDRIP1 and AtDRIP2, leading to their subsequent degradation through the 26S proteasome pathway. Consistent with this, TaSAP5 overexpression enhances DRIP degradation and increases the levels of DREB2A protein and its downstream targets. These results suggest that TaSAP5 acts to link drought with DREB2A accumulation and illustrate the molecular mechanisms involved in this process.

Correlation between FUT4 expression and its promoter methylation in HaCaT cells.

The expression level of fucosyltransferase Ⅳ (FUT4) is low in normal cells. The mechanism underlying regulation of FUT4 expression in normal cells remains elusive. In this study, Western blot, immunofluorescence and real-time PCR were used to analyze FUT4 expression in the immortalized human keratinocytes cells HaCaT. Methylated-specific PCR was used to investigate methylation status of FUT4 promoter. The results showed that the FUT4 expression level was significantly lower in HaCaT cells than squamous carcinoma cells A431 and SCC12. FUT4 mRNA expression was increased in HaCaT cells treated by 5-aza-dC (5 µmol/L), an inhibitor of DNA methyltransferase. Furthermore, using the primers to amplify the methylated fragment yielded PCR products and no products were yielded by the primers to amplify the unmethylated fragment in HaCaT cells. Unmethylated PCR products were obtained in HaCaT cells treated by 5-aza-dC, while methylated PCR products were not detected. These results suggest that the lower expression of FUT4 in HaCaT cells may be correlated with the methylation of CpG island in FUT4 promoter.

[Cyclic changes of S100A10 expression in human endometrium].

OBJECTIVE: To explore the cyclic changes of S100A10 expression in human endometrium. METHODS: The gene and protein expression of S100A10 in human endometrium was examined by real-time polymerase chain reaction (PCR), immunohistochemical staining and Western blot. RESULTS: S100A10 protein was predominantly expressed in cytoplasm and cytomembrane of luminal and glandular epithelia. The S100A10 protein was continuously expressed from proliferative phase to secretory phase of menstrual cycle. However the expression in the secretory phase was much higher than in the proliferative phase (2.26 ± 0.17, 3.75 ± 0.22, 2.65 ± 0.20 vs 1.17 ± 0.11, 1.32 ± 0.14, both P < 0.05). Specifically, the highest level of S100A10 expression occurred during the mid-secretory phase. Then real-time PCR was used to analyze the mRNA expression of S100A10 in human endometrial samples at various points during the menstrual cycle. And the results confirmed the corresponding changes at the genetic level (0.50 ± 0.05, 1.02 ± 0.10, 0.55 ± 0.05 vs 0.25 ± 0.02, 0.30 ± 0.03, both P < 0.05). CONCLUSION: The endometrial expression of S100A10 increases during the window of embryo implantation. It suggests that it may increase the endometrial receptivity of uterine epithelial cells for embryos.

Constitutive and salt-inducible expression of SlBADH gene in transgenic tomato (Solanum lycopersicum L. cv. Micro-Tom) enhances salt tolerance.

To improve the stress tolerance of crops, many genes, including transcription factors, have been expressed in transgenic plants using either constitutive or stress-inducible promoters. However, transgenic plants that show strong constitutive expression of transcription factors often suffer from many undesirable phenotypes, such as stunted growth and reduced yield. In the present study, the betaine aldehyde dehydrogenase (BADH) gene, cloned from Suaeda liaotungensis and, controlled by the Cauliflower mosaic virus (CaMV) 35S promoter or stress-inducible promoter of BADH (P5: -300 to +62 bp), was transformed into tomato (Solanum lycopersicum). The transformants with single copy of SlBADH were determined by real time PCR. Expression of SlBADH in the P5:BADH transgenic plants exhibited salt induced and was higher than that in CaMV35S:BADH under salt stress. The SlBADH enhanced salt tolerance of P5:BADH and CaMV35S:BADH transformants. And SlBADH in P5:BADH plants did not affect the growth of transformants. Consequently, we conclude that the P5 promoter can drive increased expression of SlBADH in transgenic tomato under salt stress and increase salt tolerance without affecting plant growth.

Differential fucosyltransferase IV expression in squamous carcinoma cells is regulated by promoter methylation.

Enhanced fucosyltransferase IV (FUT4) expression correlates with increased tumor malignancy in many carcinomas. However, little is known about the regulation of FUT4 expression, and whether FUT4 expression is influenced by the methylation status of the FUT4 promoter is unclear. In this study, we demonstrated that FUT4 expression is negatively correlated with the methylation degree of a CpG island in the FUT4 promoter, suggesting that the methylation status of FUT4 promoter regulates the expression of FUT4. The results indicate that manipulating the methylation status of the FUT4 promoter to regulate FUT4 expression may be a novel approach in the treatment of malignant tumors.

[Advances in astaxanthin biosynthesis in Haematococcus pluvialis].

Astaxanthin is widely applied as a nutraceutical, pharmaceutical, and aquaculture feed additive because of its high antioxidant activity. Haematococcus pluvialis is a microalgal species that can largely accumulate astaxanthin under adverse environmental conditions. Here we review the research progress of astaxanthin biosynthesis in H. pluvialis, including the induction and regulation of massive astaxanthin, the relationship between astaxanthin synthesis, photosynthesis and lipid metabolism.

[Expression of Leafy Cotyledon 2 from Arabidopsis increased the content of lipid in Chlorella sorokiniana].

The low lipid content is one of the major bottlenecks to realize the industrialization of the algae biodiesel. Improvement of lipid content through global regulation to get high-yield generating algae is a good strategy. Leafy Cotyledon 2 (LEC2) is an important transcription factor for seed maturation and oil accumulation in Arabidopsis. However, there are few reports regarding adoption of LEC2 for lipid accumulation until now. In this study, LEC2 from Arabidopsis was cloned into the plant expression vector pCIMBIA1300 and transformed into C. sorokiniana through particle bombardment. One recombinant was screened by PCR, RT-PCR and Western blot analyses. Compared with the wild type one, the total lipid content in the recombinant increased one fold, which did not show effect on cell growth, indicating that LEC2 can efficiently enhance the lipid accumulation in C. sorokiniana.

Comparative Proteomic Analysis of Flag Leaves Reveals New Insight into Wheat Heat Adaptation.

Hexaploid wheat (Triticum aestivum L.) is an important food crop but it is vulnerable to heat. The heat-responsive proteome of wheat remains to be fully elucidated because of previous technical and genomic limitations, and this has hindered our understanding of the mechanisms of wheat heat adaptation and advances in improving thermotolerance. Here, flag leaves of wheat during grain filling stage were subjected to high daytime temperature stress, and 258 heat-responsive proteins (HRPs) were identified with iTRAQ analysis. Enrichment analysis revealed that chlorophyll synthesis, carbon fixation, protein turnover, and redox regulation were the most remarkable heat-responsive processes. The HRPs involved in chlorophyll synthesis and carbon fixation were significantly decreased, together with severe membrane damage, demonstrating the specific effects of heat on photosynthesis of wheat leaves. In addition, the decrease in chlorophyll content may result from the decrease in HRPs involved in chlorophyll precursor synthesis. Further analysis showed that the accumulated effect of heat stress played a critical role in photosynthesis reduction, suggested that improvement in heat tolerance of photosynthesis, and extending heat tolerant period would be major research targets. The significantly accumulation of GSTs and Trxs in response to heat suggested their important roles in redox regulation, and they could be the promising candidates for improving wheat thermotolerance. In summary, our results provide new insight into wheat heat adaption and provide new perspectives on thermotolerance improvement.