Search Results

You are looking at 1 - 6 of 6 items for

  • Author or Editor: Liping Wang x
Clear All Modify Search

Zinc finger–homeodomain (ZF-HD) proteins, a family of plant-specific transcription factors, play an important role in regulating plant growth and development, as well as responses to stress. Although ZF-HDs have been investigated in several model plants, no systematic studies have been reported in apple (Malus ×domestica). In this study, 14 putative ZF-HD genes were identified in the apple genome and characterized using bioinformatics tools. All members harbored complete canonical structures of the ZF-HD motif. Phylogenetic analysis demonstrated that ZF-HD genes in the genome of apple could be classified into four subfamilies, with high intragroup similarities. Gene-structure analysis revealed that although 11 MdZHDs had only one exon, MdZHD6 and MdZHD13 had two exons and MdZHD8 had six exons, suggesting limited variation among the apple ZHD genes. The expression profiles of MdZHD genes revealed their involvement in the growth and development of different tissues. Numerous binding sites for transcription factors, such as MYB, bZIP, and AP2, were found in the promoter region of the putative MdZHD genes. Nearly all putative MdZHDs were predicted to localize in the nucleus. Finally, the expression levels of the MdZHD genes under abiotic stress were examined in apple rootstock Malus hupehensis and the results showed that the expression of 10 MdZHD genes was induced in response to three abiotic stress factors. Exceptionally, the expression of MdZHD11 was not induced in response to any of the abiotic stress treatments, MdZHD12 was only induced in response to salt stress, and MdZHD7 and MdZHD9 were induced in response to both drought and salt stress. The present results provide valuable insights into the putative physiological and biochemical functions of MdZHDs in apple.

Open Access

In this study, in vitro induction of tetraploid Lychnis senno Siebold et Zucc. and its cytological and morphological characterization were conducted. For polyploid induction, nodal segments with axillary buds from in vitro grown plants were kept for 3 days in MS (Murashige and Skoog, 1962) liquid or solid media added with a series of concentrations of colchicine. Out of total 588 recovered plants, 15 tetraploids and 6 mixoploids determined by flow cytometry analysis were obtained. The tetraploid contained 48 chromosomes, twice the normal diploid number of 24, as observed under light microscope. The tetraploid plants exhibited much larger but less stomata than diploid plants. Moreover, significant differences in stem height and leaf size between the diploid and tetraploid plants were noted. The tetraploid plants were more compact than diploids.

Free access

Apple stem grooving virus (ASGV) and apple chlorotic leaf spot virus (ACLSV) are two major viruses of pear. In this study, in vitro thermotherapy was carried out at 37°C for 25, 30 and 35 days followed by subculturing of meristem tips of different sizes to eliminate ASGV and ACLSV from pear plants. Virus titers in heat-treated shoot tips were evaluated by ELISA testing of regenerated plants. Results showed that thermotherapy for 35 days significantly decreased the titer of ASGV and ACLSV in cultures regenerated from tips of main and axillary shoots, especially in those from explants 1 mm in length from the tip of meristems. Dot-blot hybridization of biotinylated cDNA probes derived from ACLSV and ASGV was used to detect these viruses in crude tissue extracts of in vitro-grown pear plants. Intense signals were consistently detected in untreated plant samples equivalent to less than 0.5 mg tissue. Comparison of signals from dot-blot hybridization and ELISA absorbance values (A405) confirmed that dot-blot hybridization had a higher sensitivity than PAS-ELISA. Dot-blot hybridization could detect viruses with a titer below the threshold level of ELISA. These results indicate that dot-blot hybridization is a useful tool for large-scale surveys of viruses, which facilitates the production of virus-free propagation materials in certification and sanitation programs. Results of PAS-ELISA and dot-blot hybridization showed that high virus elimination efficiency was achieved by a combination of thermotherapy for 35 days and in vitro culture of 1 mm meristem tips.

Free access

The spicas of Prunella vulgaris are widely used in the medical, beverage, and ornamental fields. Temperature and photoperiod are the two main ecological factors that determine the transformation of many plants from vegetative growth to reproductive growth. To explore the response of P. vulgaris flowering to temperature and photoperiod induction, we adopted vernalization long-day, vernalization short-day, nonvernalization long-day, and nonvernalization short-day treatments. The results showed that the morphology (total number of leaves, number of branches, number of leaves per branch, and branch length) of the vernalization treatment groups was significantly different from that of other nonvernalization groups, and the photosynthetic pigments, net photosynthetic rate, water use efficiency, stomatal conductance, intercellular CO2 concentration, and transpiration rate increased in the vernalization treatment group. However, the gibberellin 3 (GA3), indole-3-acetic acid and zeatin riboside (ZR) contents were significantly increased under the short-day treatments groups, and the results were the same for the expression of endogenous hormone synthesis genes, except for abscisic acid (ABA). The flowering-related genes soc1, elf3, svp, ga20ox, and cry1 were highly expressed under the vernalization short-day. Therefore, the induction of vernalization is more conducive to the increase in the photosynthetic rate. Temperature and photoperiod synergistically induced the synthesis and accumulation of starch, sugar, amino acids, and protein and affected the content of endogenous hormones and the expression of genes involved in their synthesis. GA3 and ZR had thresholds for their regulation of the flowering process in P. vulgaris, and high concentrations of ABA promoted flowering. Temperature and photoperiod coordinate the expression of the flowering-related genes soc1, elf3, svp, ga20ox, and cry1, thereby affecting the flowering process in P. vulgaris.

Open Access

Heat tolerance is considered to be an essential feature for cucumber (Cucumis sativus) production, and it has been suggested that higher antioxidant ability could prevent the oxidative damage in plants caused by high-temperature stress. We aimed to investigate whether the application of exogenous spermidine (Spd) increases antioxidant activities and, therefore, elevates the heat tolerance of cucumber. Cucumber seedlings (cv. Jinchun No. 4) showing moderate heat tolerance were grown in climate chambers to investigate the effects of exogenous Spd (1 mm) foliar spray treatment on the activities and isozyme levels of antioxidative enzymes under both high-temperature stress 42/32 °C (day/night) and normal temperature 28/18 °C (day/night). On high-temperature stress, the activities of superoxide dismutase and ascorbate peroxidase were significantly reduced; the catalase activity was initially lower and then increased, whereas the peroxidase activity was initially higher and then decreased. The levels of these isozymes also changed differently. On treatment with exogenous Spd, the activities of these antioxidant enzymes were noticeably enhanced, and the isozyme zymogram expression had some changes. It was concluded that foliar spray with Spd effectively improved the total antioxidant ability of cucumber seedlings and, therefore, enhanced the tolerance of the plants to high-temperature stress.

Free access

As one of the most important fruit tree crops, apple (Malus ×domestica), is faced with the serious impact of soil salinization. However, the underlying genetic and regulatory network remains elusive. Here, we adopted time-course RNA sequencing to decipher the genetic basis and regulatory module of apple in response to salt stress. Among a series of intense changes in genes at each time point, the critical genes in the mitogen-activated protein kinase signaling pathway were highly consistent with the duration of the stress treatment. Moreover, Salt Overly Sensitive 1 (SOS1) genes were identified and predicted to play important roles in the response process. We constructed coexpression modules and explored modules significantly associated with stress. SOS genes were identified in the hub genes, suggesting a critical role. Interestingly, transcription factors were also identified and predicted to cointeract with SOS genes in the hub genes of the coexpression module [e.g., HB7 (MD01G1226600), WRKY33 (MD12G1181000), and ERF106 (MD07G1248700)]. Collectively, our exploration and findings provide a reference and data resource for the study of genetic and salt regulatory networks in apple.

Open Access