Cloning Method for Stress-Resistant Gene of Conringia planisiliqua under Drought Stress

The low temperature, drought, high salt, and other environments influence crop production and development directly, so the gene cloning method has become an effective biological means. In order to effectively improve the cloning effect, a gene cloning method for Conringia planisiliqua based on mRNA differential display technology was proposed. Based on mRNA differential display technology, the gene of Conringia planisiliqua was transcribed. The present study expects gene cloning to be better than the traditional method. This will lay the basis for gene cloning and functional verification of the transcription and disease-resistant proteins in Conringia planisiliqua. According to homologous identification results, the homologous drought-resistant genes were determined and screened. The data of Conringia planisiliqua in the existing biological database were used to extract ESTs data of Conringia planisiliqua. Then, the heating environment was established and the concept of integral function was introduced to express the influence of growth environment of different genomes. The mass, momentum, energy, and turbulent flow situation of stress-resistant gene of Conringia planisiliqua during the growth were satisfied. Finally, the data search was carried out in the NCBI database and gene cloning was achieved by ESTs data sequence. Experimental results show that the proposed method can effectively reduce the gene data fitting and improve the quantity of gene fragments cloned in a cycle, so the overall cloning effect is better.

Prostate Cancer-Specific of DD3-driven oncolytic virus-harboring mK5 gene

Prostate cancer (PCa) is the second most diagnosed cancer in Western male population. In this study, we insert mK5 (the mutational kringle5 of human plasminogen) into a DD3-promoted (differential display code 3) oncolytic adenovirus to construct OncoAd.mK5.DD3. E1A.dE1B, briefly, OAd.DD3.mK5. DD3 is one of the most prostate cancer specific promoters which can transcriptionally control adenoviral replication. mK5 has been proved to be able to inhibit the tumor angiogenesis and inhibit cell proliferation. Our results suggested that targeting PCa with OAd.DD3.mK5 elicited strong antitumor effect.

Differential expression of genes in response to salinity stress in tree tomato (Solanum betaceum)

The Andean “tree tomato” (Solanum betaceum) is an exotic fruit crop endemic to the high Andes, but principally cultivated in Colombia, Peru and Ecuador. The species displays broad agro-ecological adaptability and has proven resilient to different marginality factors, including high soil-salinity. This study presents a preliminary exploration of the genetic mechanisms underlying salinity tolerance in S. betaceum. To this end, we selected two S. betaceum genotypes contrasting in their ability to tolerate high salinity in vitro, and used differential display analysis to compare overall differences in gene expression between salinity-stressed and unstressed (control) plants in both genotypes. Overall, 171 differentially expressed transcripts (DETs) were identified; 30 of which showed homology with candidate genes associated with abiotic stress tolerance in different species. These were ascribed putative roles in stressresponse, photosynthesis, cellular metabolism and cell wall metabolism. Several identified DETs (22 in total) also showed homology to proteins of unknown function. These sequences warrant further research for potentially novel abiotic stress tolerance mechanisms. Despite its inherent limitations, differential display analysis allowed us to identify and validate (via RT-qPCR) 3 salinity-stress induced DETs. Prospectively, expanding our analyses via the validation of additional DETs would likely contribute to the identification of genes which can be used as proxies for a better understanding of the regulatory, metabolic and physiological mechanisms used by S. betaceum to respond and adapt to salinity stress.