Acta Botanica Sinica 2004, 46 (2): 224 229 http://www.chineseplantscience.com Analysis of Transgenic Tobacco with Overexpression of Arabidopsis WUSCHEL Gene LI Jun-Hua 1, 2, XU Yun-Yuan 1, CHONG Kang 1*, WANG Hui 2 (1. Key Laboratory of Photosynthesis and Environmental Molecular Physiology, Institute of Botany, The Chinese Academy of Sciences, Beijing 100093, China; 2. College of Agronomy, Northwest Sci-Tech University of Agriculture and Forestry, Yangling 712100, China) Abstract: The Arabidopsis WUSCHEL (WUS) gene plays a key role in the specification of the stem cells in the shoot apical meristem (SAM). A cdna of WUS has been amplified with the RT-PCR approach from Arabidopsis. The plant overexpression vector was constructed. It was driven by a dual enhanced CaMV35S promoter. The construct was transformed into tobacco (Nicotiana tabacum L.) via Agrobacterium mediation. Dramatic phenotypic changes appeared in the WUS overexpression transgenic plants. Aberrant cell divisions and ectopic organogenesis could be found in almost every aerial parts of the transgenic tobacco except the meristems and the inner two floral whorls. The data showed a highly conserved function of WUS in tobacco, and suggested that WUS is involved in organogenesis. The leaves were malformed, which strongly matched those only described previously for plants grown in the presence of polar auxin transport inhibitors. It suggested a possible function of WUS in leaf development. These results provide useful information for functional analysis of WUS and important biotechnological implication as well. Key words: WUSCHEL; Nicotiana tabacum ; overexpression; phenotypic analysis Post-embryonic development in higher plants is characterized by continuous and repetitive formation of new structures and organs, which is different from most animals (Bowman and Eshed, 2000; Clark, 2001; Weigel and Jürgens, 2002). The derivatives of a shoot apical meristem (SAM) give rise to all the organs of the aerial parts of the plant except cotyledons. Genetic analysis in Arabidopsis has identified a central regulator of SAM, the WUSCHEL (WUS) gene. Shoot meristems of wus mutant terminate prematurely after producing only a few leaves, and flowers of the mutant are formed occasionally but lack carpel and most stamens. So WUS is required to keep the pool of stem cells (Laux et al., 1996). WUS encodes a homeodomain protein, which functions as a transcriptional regulator (Mayer et al., 1998). The observation of the constitutively overexpression of WUS in Arabidopsis is difficult, as it would preclude recovery of the seedlings (Schoof et al., 2000), an alteration is the use of the inducible system (Zuo et al., 2002). Here we constitutively overexpressed WUS in tobacco under the drive of the dual enhanced CaMV35S promoter. The transgene caused dramatic phenotypic changes, which provided useful information for functional analysis of WUS. 1 Materials and Methods 1.1 Plant and bacteria Nicotiana tabacum L. cv. W38 and Arabidopsis thaliana L. Wassilewskija-2 ecotype, as well as bacteria of Agrobacterium tumefaciens strain GV3101 (pmp90) (Koncz and Schell, 1986) were used in this study. 1.2 Construction of overexpression vector Total RNA was extracted using the TRIZOL kit (Gibco BRL, USA) from aerial parts of Arabidopsis plants. Firststrand cdnas were synthesized by reverse transcription kit (TaKaRa, Japan), open reading frame (ORF) of WUS was amplified using primers P 1 (5'-TTCTGGTACCATGGA- GCCGCCACAGCATCAG-3') and P 2 (5'-TCTTGGAGCTCC- TAGTTCAGACGTAGCTCAAG-3'), which were designed according to the sequence information of WUS (Mayer et al., 1998). The PCR products were cloned into pgem-t vector (Promega, USA) and sequenced. A dual enhanced CaMV35S promoter was inserted between Hind and Kpn sites of the pbib-kan plasmid (Becker et al., 1992) to produce vector pkan-35s kindly provided by Dr. LI. The WUS cdna was digested with Kpn and Sac and cloned between Kpn and Sst sites in binary vector pkan-35s to create the Received 23 Oct. 2003 Accepted 18 Dec. 2003 Supported by the State Key Basic Research and Development Plan of China (G19990116). * Author for correspondence. E-mail: <chongk@ns.ibcas.ac.cn>.
LI Jun-Hua et al.: Analysis of Transgenic Tobacco with Overexpression of Arabidopsis WUSCHEL Gene overexpression vector pbkb. The constructs were examined by PCR and Kpn /Sac double digestion. Plasmid extraction, digestion, electrophoresis, ligation and Escherichia coli transformation were according to Sambrook et al. (1989). 1.3 Plant transformation and identification pbkb and pkan-35s were introduced by electroporation into Agrobacterium strain GV3101. Transformation of tobacco leaf discs was performed as described previously (Horsch et al., 1985). The transformed plants were selected by kanamycin. Transgenic plants were transferred into greenhouse at about 25 under natural light. The positive lines were identified with tissue PCR as described by Klimyuk et al. (1993). Level of WUS expression was detected by RT-PCR. Total RNA from leaf, stem and flower was obtained respectively with the same method mentioned above. After quantification one microgramme of RNA was used in every RT-PCR reaction with One Step RNA PCR kit (TaKaRa, Japan) and primers P 1 and P 2. 1.4 Phenotypic analysis For conventional scanning electron microscopy (SEM), fresh materials were prepared as described by Chen et al. (2000), and examined with Hitachi S-2460 scanning electron microscope (Japan). The images were photographed on Lucky 120 films. Other photographs were taken with Sony DSC-F707 digital still camera (Japan). 2 Results 2.1 WUS cloning and transformations A cdna of WUS gene was obtained with the RT-PCR method, which was identified as 899 bp in length with a 879 bp ORF. The construct of pbkb was confirmed by PCR and Kpn /Sac double digestion (data not shown). The transgenic plants screened by kanamycin were identified with PCR amplication (Fig.1A), and target fragments were obtained from transformed but not from control plants. It showed that the target gene had been integrated into the genome of transformed tobacco. The transcripts were detected further with RT-PCR (Fig.1B). Again the target fragments were obtained from each parts of transgenic plant detected but not the control plant. 2.2 Phenotypic characterization of transgenic tobacco plants Eight independent lines of plants with ectopic WUS gene were obtained, they displayed a wide range of altered phenotype as early as at the in vitro regeneration stage. When the seeds were inseminated directly in soil, almost all of the T 1 progeny of transgenic plant showed Fig.1. Identification of transgenic plants. A. PCR assay of regenerated palnts from transgenic calluses. Lanes 1 4, transgenic plants harboring exogenous WUSCHEL (WUS); Lane 5, wildtype tobacco genomic DNA as template (negative control); Lane 6, pbkb plasmid DNA was used as template (positive control); Lane 7, DNA marker. B. Detection of 35S::WUS transcripts by RT-PCR. Lane 1, pbkb plasmid (positive control); Lanes 2, 4 and 6, leaf, stem and flower of wild-type tobacco respectively (negative control); Lanes 3, 5 and 7, leaf, stem and flower of one of the PCR positive plants, respectively. severe defects and did not develop beyond the seedling stage. Some wild-type seedlings developed normally in T 1 plants. This suggested that transgenic plants is lethal at young seedling stage. To overcome this difficulty, the transgenic seeds were germinated and cultured on MS medium till the seedlings had 4 leaves and the roots developed well. A higher viability of T 1 plants was obtained by this method and their phenotype was consistent with T 0 plants. The higher viability of T 0 and T 1 plants by in vitro culture could be due to the transgene having more defective effects on the seedlings and the adult shoots having a better tolerance. After planted in soil for three months, ectopic lateral outgrowths appeared on the laminas, the stems, and in the leaf axils of WUS overexpressing plants (Fig.2D, F, H). During flowering phase, ectopic outgrowths also appeared on the receptacles and even the corollas (Fig.2J, L). It should be noted that some of the outgrowths could develop into shoot meristems or flower buds (Fig.2G, H, J). The transgenic plants had flowers with shorter filaments and styli, and the stigmas are smaller than that of wildtype, but none ectopic outgrowth could be found (Fig.2K, L). The alterrance of leaves was also obvious. From the third or fourth leaf, the young leaves showed reduced expansion and upright position, subsequently, the laminas showed curled phenotypes and rolled up at their fringes, and the leaf vein pattern was also altered (Fig.2C). Sometimes conjointed leaves were formed, and trumpet-shaped
LI Jun-Hua et al.: Analysis of Transgenic Tobacco with Overexpression of Arabidopsis WUSCHEL Gene Fig.3. Scanning electron micrograph of the leaf epidermis. A. Fully-grown wild-type epidermis. B. Leaf primordium-like outgrowths on the leaf of transgenic line with small and dense cells. Bars = 1 900 µm. leaves were seen at in vitro stage (data not shown). To character the ectopic cells described above, the leaf outgrowths were observed by SEM. Results showed that the outgrowths were leaf primordia-like, with small and dense cells resembled the meristematic cells (Fig.3). The meristems of the plants were examined by histological sections and no evident histological differences were observed between the wild-type and transgenic plants. 3 Discussion 3.1 Overexpression of WUS in tobacco leads to ectopic organogenesis Owing to the results above, WUS overexpression is sufficient to promote aberrant cell divisions and ectopic organogenesis de novo in differentiated tissue in tobacco (Fig.2D L). However, it is reported that WUS overexpression only induces aberrent cell divisions and embryonic cell clusters but not organogenesis in Arabidopsis (Gallois et al., 2002; Zuo et al., 2002). We consider the difference in the phenotypic effect of WUS in tobacco and Arabidopsis reported is due to an enough period of overproduction of WUS protein in tobacco, but not a difference in the molecular function of the WUS gene that maintains SAM activity as reported (Noriko et al., 2003), because the similar multiple shoots phenotype have been observed in Arabidopsis (unpublished data). This result suggested a new definition of the function of WUS in organ formation, that is, WUS is involved in organogenesis. This effect of WUS could also have important biotechnological implications for vegetative propagation from differentiated cells. 3.2 WUS and meristem cells Several observations suggested that the size of the stem cell population in the SAM and the floral meristem of Arabidopsis are regulated by a negative feedback loop between WUS and CLAVATA3 (CLV3), the stem cell marker gene. In this loop, WUS activates the expression of CLV3, and CLV3 repress WUS expression (Brand et al., 2000; Fig.2. Phenotypic characterization of tobacco plants overexpressing the Arabidopsis WUSCHEL (WUS) gene. A. Gross morphology of wild-type tobacco plant (the left one) and WUS overexpression transgenic plants (the right one). B. Leaf of the wild-type plants. C. Leaf of WUS transgenic plants, the lamina curled up at fringes and leaf vein pattern altered. D. Leaf surface of a transgenic line with outgrowths. E. Wild-type internote with only one axillary bud per axil. F. Internote of a WUS overexpression transgenic tobacco with ectopic outgrowths on the stem and the leaf axils. G. Stem of a transgenic tobacco with a ectopic shoot meristem. H. Leaf axil of a transgenic line with additional shoot meristems besides the axillary bud, the insert is the higher-magnification image of the ectopic buds. I. Rachis of wild-type plants. J. Rachis of a transgenic line with ectopic columned outgrowths and flower buds on the receptacles, the insert is a epiclinal flower. K. Mature wide-type flowers, the right one has been partly moved. L. flowers of a transgenic line, the right one has been partly moved, with columned outgrowths on the receptacles and the corollas. Bars = 0.5 m (A), 10 cm (B,C), 2 cm (D L) and 0.5 cm (H inset).
Schoof et al., 2000). A initially similar self regulating circuitry is established between WUS and AGAMOUS (AG), the floral homeotic gene which plays a key role in floral meristem termination and specifies organ identity in whorls 3 (stamens) and 4 (carpels) (Bowman et al., 1989). The transgenic plants have abnormal flowers with shorter filaments, styli and smaller stigmas, which indicated an unclear effect of transgene on these two organs, but no ectopic outgrowth was seen (Fig.2L). Histological section analysis of transgenic plant showed that the cells of the meristem still positioned properly (data not shown). Therefore, in spite of the widespread expression directed by the 35S promoter, it seems that WUS can not promote excess cell division or organogenesis in the shoot apical and floral meristems. Similar meristematic phenotype was reported when WUS was overexpressed ectopically in Arabidopsis under the drive of inducible or meristem-specific promoters (Schoof et al., 2000; Lenhard et al., 2001; Lohmann et al., 2001; Zuo et al., 2002). It was known that the level of WUS expression was increased in mutants clv3 and ag because of loss of its suppressor. In these mutants, the enlarged shoot apical and floral meristems in clv3 and indeterminate flowers with pepals in ag mutant formed (Bowman et al., 1989; Yanosky et al., 1990; Clark et al., 1995). One conceivable interpretation for this difference is that the similar repressors of WUS exist and functioning in tobacco, as CLV3 and AG in Arabidopsis, and this kind of suppression is strong. This is also proof of the high conservation of the function of WUS in tobacco. 3.3 WUS and auxin The malformed leaves showed by the WUSoverexpressing plants matched those only described previously for plants grown in the presence of polar auxin transport inhibitors (Liu et al., 1993; Sieburth, 1999). Therefore, these changes probably result specifically from the loss of auxin polar transport or the decrease of auxin synthesis level due to widespread expression of WUS. This observation suggested that WUS may function non-cellautonomously in leaf development, and auxin is mediated here. Previous study suggested that WUS regulates stem cells and integument initiation in the chalaza by a non-cellautonomous way, but the mechanism is unknown (Mayer et al., 1998; Gross-Hardt et al., 2002), our results provide a possible hint for this research. 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