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Brazilian Archives of Biology and Technology

Print version ISSN 1516-8913On-line version ISSN 1678-4324

Braz. arch. biol. technol. vol.45 no.2 Curitiba June 2002

http://dx.doi.org/10.1590/S1516-89132002000200008 

Changes in Electrophoretic Profiles of Ipomoea batatas (Sweet Potato) Induced by Gamma Radiation

 

Celso Luiz Salgueiro Lage* ; Alexandre Guimarães Vasconcellos; Nina Claudia Barboza da Silva and Maria Apparecida Esquibel
Laboratório de Fisiologia Vegetal; Instituto de Biofísica Carlos Chagas Filho; Universidade Federal do Rio de Janeiro; CCS; Bloco G; Cidade Universitária; CEP 21941-590; Rio de Janeiro - RJ - Brazil

 

 

ABSTRACT

The ability of nodal segments of Ipomoea batatas to differentiate shoots and roots was evaluated after gamma irradiation. Shoot differentiation was less sensitive to irradiation than roots. However, at 90 Gy, no shoot was able to regenerate a new plant; in contrast 76 % of the roots from irradiated nodal segments continued to grow. The gamma radiation also induced changes in electrophoretic profiles of peroxidases of storage roots. Plants originated from irradiated storage roots presented changes in leaf peroxidase profiles very similar to those produced by leaves directly irradiated. The peroxidase profile of absorbent roots from irradiated storage roots was different from that obtained from directly irradiated absorbent roots.

Key words: Peroxidases; gamma radiation, sweet potato, Ipomoea batatas, convovulaceae

 

 

INTRODUCTION

Studies on the action of radiation on plant physiology frequently emphasize its direct deleterious effects, mainly on plant hormones (Skoog, 1934, 1935; Momiyama et al., 1999) or their biosynthesis (Gordon, 1957). The loss of reactivity of irradiated cells to a growth-promoting agent has been reported by Miura et al. (1974). In this paper, the effects of gamma radiation on Ipomoea batatas L. Lam (sweet potato) were evaluated in terms of the ability of nodal segments to form shoots and roots. Besides the evaluation of their ability to differentiate shoots and roots, issoperoxidases were analysed electrophoretically. These enzymes play a significant role in plant physiology (Van Huystee and Clarins, 1982; Van Huystee, 1987) as indicators of resistance and response to injury (Birecka et al., 1973; Birecka and Catafalmo, 1975; Luthra et al., 1988; Reuveni et al., 1992; Barabas et al., 1998; Kubo et al., 1999, Riedle-Bauer, 2000). As a consequence, peroxidases have been used as markers of differentiation in somatic embryogenesis (Joersbo et al., 1989; Hadrami et al., 1989), and leaf and root morphogenesis in barley calli culture, before initiation of the primordium (Coppens and Dewitte, 1990). Changes in plant peroxidases due to treatment with radiation had also been reported as marked increase in peroxidase activity of leaves from plants originated by irradiated nodal segments of sweet potato (Lage and Esquibel, 1997). Absorbent roots grown from irradiated sweet potato storage roots have also a modified electrophoretic profile of isoperoxidases (Lage and Esquibel, 1995).

The objective of the present study was to investigate the radiation effects on shoot and root differentiation, and also evaluate changes in electrophoretic profiles of peroxidases after treatment of I. batatas with gamma radiation.

 

MATERIAL AND METHODS

Plant material

Monoclonal plants regenerated from meristem tip culture (Alconero et al., 1975) of Ipomoea batatas L. Lam. cv. Roxinha were used in the experiments. Plantlets were subcultured every 60 days. At each subculture, nodal explants were excised and placed on fresh MS culture medium (Murashige and Skoog, 1962). Nodal explants, each containing a single dormant meristem, were obtained during the micropropagation phase. All cultures were maintained at 25 + 2 oC with an illumination rate of 23 mmol. cm-2.s-1 with a 16-h photoperiod.

Intact, unsprouted monoclonal storage roots collected in the field were selected according to weight, ranging from 250 to 270 g. These storage roots were produced by acclimated plants from in vitro meristem culture (Alconero et al.1975). The meristem-regenerated plants were used to avoid pathogen interference in the results.

Irradiation

Irradiation treatments were performed according to the method of Lage and Esquibel (1992) using a 60Co source, at a dose rate of 0.44 Gy/min. Plants were irradiated after 60 days of in vitro culture. Immediately after irradiation, the nodal segments were excised and placed in fresh medium. Three groups of 10 storage roots were prepared. Two of them were irradiated at 90 and 180 Gy of gamma radiation, respectively, and immediately immersed in water to allow shooting and rooting. The remaining group was left untreated and placed in water. Part of shoots and absorbent roots grown from the untreated group was irradiated to verify the direct effect of radiation in the studied organs. The immersion water was changed at intervals of 3 days in all treatments.

Peroxidase analysis

The electrophoretic runs were performed on 9.5 % starch gel at 7 oC for 4 hours, in nine parts of 0.2 M Tris-citrate buffer, pH 8.3, plus one part 0.2 M lithium-borate, pH 8.3. The lithium-borate buffer was used as the running buffer (Scandalios, 1969). Samples were applied in the middle of the gel. The gels were developed with 0.2 M sodium acetate buffer, pH 5.5, plus 0.6 ml 30 % H2O2 and 20 mg % 3-amino-9-ethyl-carbazole. The enzymes were extracted by homogenization in 0.1 M potassium phosphate buffer at 0oC.

Analysis of differentiation patterns

The nodal explants in vitro were periodically observed during 40 days in culture. The differentiation of shoots and roots was analyzed as percents of newly formed structures relatively to the total number of explants. Means and standard deviations reflect variation within each time that each experiment was conducted.

 

RESULTS

Radiation effects on differentiation

The radiation effects were evaluated in terms of the ability of nodal segments to differentiate shoots and roots. The nodal segments showed a dose-dependent decrease in their ability to differentiate both roots and shoots (Fig. 1). Compared to control plants, the efficiency to form shoots fell to 62 % and the ability to form roots was 20 % at 90 Gy. Although shoot differentiation was less sensitive to irradiation than root differentiation, at 90 Gy no shoot was able to regenerate a new plant. The differentiated shoots stopped growing in early developmental stages. In contrast, 76 % of the roots originated by the nodal segments irradiated at 90 Gy continued to grow.

 

 

A significant delay was found in the differentiation of shoots and roots in irradiated nodal segments, even at the lowest doses applied, and the lag phase increased proportionally with the radiation dose (Fig. 1, A,B,C and D). These results implicated the differentiation of aerial parts to be more strongly determinated than root ones.

Electrophoretic profile of peroxidases

Fig. 2 shows the electrophoretic profiles of peroxidases extracted from leaves of I. batatas cv Roxinha after different treatments. In this figure, the first run from left to right was control, second and third runs were the peroxidase patterns of leaves originated from irradiated storage roots at 90 and 180 Gy, respectively. Finally, the last one presented the peroxidase pattern of leaves directly irradiated with 90 Gy. All radiation treatments caused changes in peroxidase profiles when compared with the control.

 

 

It is interesting to observe that the profile of leaves directly irradiated with 90 Gy was very similar to that of leaves of plants originated from storage roots irradiated at 180 Gy. This result implied the gamma radiation as an agent able to induce changes in peroxidases of storage roots that would persist in the leaves of the plants grown from them. Furthermore, the changes in the peroxidase profile persisted during the differentiation process, and it still was present in the leaves of plants originated from the irradiated storage roots. All the radiation treatments also resulted in enhancement of the cathodic bands.

The peroxidase profiles of absorbent roots is presented in Fig. 3. All the radiation treatments resulted in changes in electrophoretic profiles, but differently from what occurred with leaves. The peroxidase pattern found in directly irradiated absorbent roots not similar to those of roots originated from irradiated storage roots. The cathodic bands lost intensity at 90 Gy, while at 180 Gy an enhancement occur. Similar results were found for cathodic peroxidase profiles of absorbent roots of another cultivar, Paty do Alferes (Fig. 4).

 

 

 

DISCUSSION

The first point to discuss are the differences found for both differentiation and peroxidase electrophoretic profiles in shoots and roots taking into account the origin of each one. Shoots are formed from a dormant meristem, a complex structure responsible for the organogenesis in the post-embryonic period, and the leaf primordium destiny is established in an extremely early stage (Steeves and Sussex, 1990a). In contrast, roots differentiate from pericicle cells - one or more layers of cells that constitute the outermost region of the vascular system (Steeves and Sussex, 1990b), where a single cell form an adventitious root meristem differentiates the new root. In the first case, the meristem that originates the aerial part is already formed before the shooting stimulus, and therefore is probably less affected by the radiation treatment. In the second case, the pericicle cells will generate a new meristem, in such a way that its formation could be affected by radiation by interfering with their epigenetic material. Changes in the epigenetic material may be related to permanent phenotypic modifications, defined as somaclonal variation (Larkin and Scrowcroft, 1981), commonly found in adventitiously regenerated plants. Lage and Rocha (1994) as defined by Waddington (1975) considered this phenomenon as an example of genetic assimilation. Changes in peroxidases must have direct effects in IAA turnover (Glaston et al., 1953; Kenten, 1955; Hokkinakis and Brooks, 1979; Acosta et al., 1989; Gazarian et al., 1998; Kubo et al.,1999), therefore affecting phenotype of the regenerated plant. Fields et al. (1989) reported heritable changes in flax peroxidases for two generations in response to modification in nitrogen levels. This indicates that changes in the peroxidase pattern could be maintained over long term, or even for generations.

Considering the possibility that induced changes in the peroxidases pattern is heritable, then a plant regenerated from a single enzymatically modified cell could have all its cells harboring this modification. Several forms of stress when given to plant tissue, in early developmental stages resulted in more vigorous or resistant plants, as, for instance, radiation (Lage and Esquibel, 1992), or methylene blue treatments (Lage and Esquibel, 1997).

The changes in peroxidase pattern seen in leaves and absorbent roots after irradiation may have common points with the results obtained for differentiation of irradiated nodal segments. In both cases leaves respond to radiation similarly, independently of the developmental stage when the treatment was applied - before or after leaf differentiation. The aerial part differentiation of nodal segments was significantly less sensible to radiation than root differentiation.

 

ACKNOWLEDGMENTS

This paper is dedicated to the memory of Dr. Carlos Chagas Filho. Financial support: CNPq, CAPES, Fundação Universitária José Bonifácio, FAPERJ.

 

 

RESUMO

A capacidade de Ipomoea batatas diferenciar parte aérea e raízes foi avaliada após irradiação com raios gama. A diferenciação da parte aérea foi menos sensível que a das raízes. Contudo, na dose de 90 Gy nenhum broto diferenciado regenerou planta, enquanto 76 % das raízes diferenciadas dos segmentos nodais irradiados manteve o crescimento. A radiação também induziu mudanças no perfil elotroforético de isoperoxidases. Plantas originadas de raízes tuberosas irradiadas apresentaram alteração no perfil de isoperoxidases foliares semelhantes ao perfil de folhas diretamente irradiadas. O perfil de isoperoxidases de raízes absorventes irradiadas diretamente não apresentou o mesmo padrão do perfil das raízes absorventes desenvolvidas de raízes tuberosas irradiadas.

 

 

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Received: July 20, 2000;
Revised: January 29, 2001;
Accepted: July 16, 2001.

 

 

* Author for correspondence

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