Cloning a novel reduced-height (Rht) gene TaOSCA1.4 from a QTL in wheat.

Reducing plant height (PH) is one of the core contents of the "Green Revolution", which began in the 1960s in wheat. A number of 27 reduced-height (Rht) genes have been identified and a great number of quantitative trait loci (QTLs) for PH have been mapped on all 21 chromosomes. Nonetheless, only several genes regulated PH have been cloned. In this study, we found the interval of QTL QPh-1B included an EST-SSR marker swes1079. According to the sequence of swes1079, we cloned the TaOSCA1.4 gene. We developed a CAPS marker to analyze the variation across a natural population. The result showed that the PH was significantly different between the two haplotypes of TaOSCA1.4-1B under most of the 12 environments and the average values of irrigation and rainfed conditions. This result further demonstrated that TaOSCA1.4 was associated with PH. Then, we validated the TaOSCA1.4 via RNAi technology. The average PHs of the wild-type (WT), RNAi lines 1 (Ri-1) and 2 (Ri-2) were 94.6, 83.6 and 79.2 cm, respectively, with significant differences between the WT and Ri-1 and Ri-2. This result indicated that the TaOSCA1.4 gene controls PH. TaOSCA1.4 is a constitutively expressed gene and its protein localizes to the cell membrane. TaOSCA1.4 gene is a member of the OSCA gene family, which regulates intracellular Ca2+ concentration. We hypothesized that knock down mutants of TaOSCA1.4 gene reduced regulatory ability of Ca2+, thus reducing the PH. Furthermore, the cell lengths of the knock down mutants are not significantly different than that of WT. We speculate that TaOSCA1.4 gene is not directly associated with gibberellin (GA), which should be a novel mechanism for a wheat Rht gene.

First Record of Paramyrothecium roridum Causing Leaf Spot on Physostegia virginiana in China.

Physostegia virginiana Benth. (false dragon head flower), belonging to the family Lamiaceae, is a perennial plant and is usually used as landscape plant in parks and wetlands in China. It is also widely used as an ornamental plant for cut-flower all over the world (Cardin et al. 2007). In June 2019, leaf spot symptoms were observed on P. virginiana in Zibo botanical garden of Shandong Province, China (36.79°N, 118.02°E). We surveyed about 200 square meters of planting area, and most of the infected plants were close to the water or wet places, with ~20% disease incidence which were concentrated in the lower leaves of plants. The symptoms appeared on leaves were mostly round or oval spots, light to dark brown in color, and 3 to 8 mm in diameter. Severe leaf lesions were linked together, causing early fall of leaves. Small pieces of 15 infected leaves were collected to confirm the causal pathogen. The samples were sterilized by 70% ethanol for 30 s, 5% NaClO for 1 min, then rinsed in sterile water three times, plated on potato dextrose agar (PDA) and incubated at 25℃ in the dark for 7 days (Zhu et al. 2013), and 7 isolates were obtained from 10 diseased samples. The stroma of fungal mycelium was initially white, gradually turning dark green to black, while the margin of colony was regular, with concentric rings which were black sporodochia aggregates. Conidiophore hyaline, produce 2-3 order complex branches, arising as 3-4 conidiogenous cells from the tip of the branches, conidiogenous cells ampulliform to cylindrical. Conidia were aseptate, unicellular, hyaline, cylindrical, and their dimensions varied from 4.8 to 8.2 × 1.7 to 2.4 µm with rounded tips. The morphological characteristics of the isolates matched features described for Paramyrothecium roridum (Tode) L. Lombard & Crous, comb. nov. (Lombard et al. 2016). For molecular identification, genomic DNA was extracted from five representative single spore isolates. The partial coding genes of internal transcribed spacer (ITS) and calmodulin (cmdA) from the original isolates were amplified with primers ITS1/ITS4 and CALDF1/CALDR1 (White et al. 1990; Lawrence et al. 2013), respectively. The sequenced genes (GenBank accession no. MT318535, and MT454826) exhibited 98.71%, and 100.00% homology with type specimen of P. roridum strain CBS372.50 (GenBank accession no. MH856665.1, and KU846271.1), respectively, confirming the morphological identification. Pathogenicity of the fungus was tested indoor by inoculating 5 living, healthy P. virginiana plants with 3 leaves, which were inoculated with 10 µl of conidial suspension (2 × 105 conidia/ml) from a 10-day-old cultures on PDA, while 5 other inoculated plants with 10 µl of sterile water were served as controls. Treated plants with the inoculated leaves were covered by plastic bags in the greenhouse of 14 h light/10 h dark with ~80% relative humidity at 25℃. As time went by (about 3-7 days), the leaves inoculated with conidial suspension appeared similar symptoms as described above, whereas negative controls were still healthy. The same pathogens were isolated from the diseased leaves and repeated three times with same results as those that were obtained previously from the outdoor plants, including morphological and molecular results which confirm Koch's postulates. To our knowledge, this is the first record of P. roridum causing leaf spot on P. virginiana in China. The finding is beneficial to the better application of P. virginiana, a very common ornamental plant.