Given that soil salinity significantly limits plant growth and production in agricultural land, research on salt stress is of particular agricultural relevance. In this study, for the purposes of functional screening of genes involved in salt stress responses, we selected approximately 651 transgenic Arabidopsis lines (157 independent full-length) from a transgenic Arabidopsis population overexpressing full-length Brassica rapa cDNAs. Initial screening indicated that the transgenic lines of 12 genes showed apparent salt tolerance phenotypes when exposed to NaCl at a concentration of 125 mM, among which, two genes (BrATL30 and BrZHD10) were selected for detailed characterization. The T₃ progeny of these transgenic lines exhibited accelerated seed germination, often accompanied by faster root growth and higher survival rate, compared with wild-type plants under salt stress. Additionally, in order to examine the agricultural potential of the two selected B. rapa genes, we constructed BrATL30- and BrZHD10-overexpressing Brassica napus transgenic plants (BrATL30-OX and BrZHD10-OX), which showed apparent high salt stress-tolerant phenotypes compared with wild-type plants. Furthermore, we found that the basal expression of several salt- and abiotic stress-responsive genes was higher in transgenic plants than in wild-type plants. Taken together, this study will provide two valuable functional genes related to salt stress tolerance.

AbstractThe SHORT VEGETATIVE PHASE (SVP) gene encodes a MADS-box gene family of transcription factors that repress floral transition. To explore the function of the Brassica rapa SVP (BrSVP) gene during the flowering time of this species, a construct containing BrSVP under the control of the cauliflower mosaic virus 35S promoter was introduced into B. rapa via Agrobacterium-mediated transformation. The resulting transgenic plants showed delayed flowering time, and RT-PCR analyses further revealed that BrSVP repressed the expression of the floral integrator genes AGL20, AGL24, and FT during vernalization. Our data indicated that BrSVP acts as a negative regulator in the flowering time of B. rapa and that it may therefore be a useful genetic source for crop improvement with respect to flowering time regulation.

In recent years, new plant breeding technologies (NPBT) have had enormous effects on breeding and the agricultural industry. In particular, genome editing technology, including site-directed nuclease technologies, has progressed dramatically since the first-generation Zinc finger nucleases to the third-generation clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9 (CRISPR/Cas9). CRISPR/Cas9 technology has yielded a revolutionary breakthrough in the accurate, efficient, and user-friendly genome editing of eukaryotes. Several methods for basic research and applications, such as knock-out, base editing, gene targeting, and transcriptional activation or repression have been derived from CRISPR/Cas9 technology. Herein, we will describe the current progress in NPBTs and also summarize the crops developed by NPBTs. After analyzing the current status of NPBTs and crop development, we have proposed potential strategies for crop development using NPBTs.