Acid phosphatase polymorphism within and among populations of Cauliflower (Brassica oleracea var botrytis)

Acid phosphatase polymorphism within and among populations of Cauliflower (Brassica oleracea var botrytis)

Celso Luis Marino¹, Marcos Aparecido Gimenes¹, Norberto da Silva² and Catalina Romero Lopes ¹

1Departamento de Genética, Instituto de Biociências, UNESP, Botucatu, São Paulo, Brasil.

²Departamento de Agricultura e Melhoramento de Plantas, Faculdade de Ciências Agronômicas, UNESP, Botucatu, São Paulo, Brasil.

Send correspondence to Celso Luis Marino, Depto de Genética - IB - UNESP, 18610-000 Botucatu, São Paulo, Brasil. E-mail: [e-mail].

ABSTRACT

Eighty-one lines of cauliflower (Brassica oleracea var. botrytis) from 12 populations used to produce commercial hybrids in Brazil were screened for polymorphism in the acid phosphatase system, in order to evaluate the usefulness of this marker for the determination of the parental contamination level in hybrid seeds. Little polymorphism was detected in the examined lines, but the system appeared to be very useful for hybrid identification, since the only condition required was polymorphism between the two parental lines. If the analyzed lines were used for hybrid production, 8.4% and 12.3% of the possible crosses would result in hybrids which can be positively identified using the APS-1 and B₁ loci, respectively. If only one plant of each homozygous type (SS or FF) was analyzed in each population, 41% and 50% of the possible crosses would result in hybrids which can be positively identified using the APS-1 and B₁ loci, respectively.

Key words: isoenzyme, polymorphism, cauliflower.

Received: March 5, 2002; accepted: March 25, 2002.

INTRODUCTION

The use of F₁ hybrids is a very common procedure in breeding programs of Brassica species. Hybrids are grown in more than 90% of the Brazilian cauliflower fields (Ikuta, 1974; Ikuta and Paterniani, 1979). These hybrids are produced by crossing self-incompatible lines under open-field conditions. In spite of the self-incompatibility system found in the lines, a certain degree of self-crossing may happen, producing an undesirable number of non-hybrid seeds, which will determine their quality and price (Thompson, 1957; Haruta, 1962).

Isoenzymatic markers have been successfully used to identify hybrids and cultivars in many plant species (Heidrich-Sobrinho, 1982; Cardy and Kannenberg, 1982; Arús and Orton, 1983; Grossi et al., 1997). The isozyme method has proven to be one of the simplest ways to assess the level of parental contamination of seeds within a hybrid cauliflower seed lot (Nijenhius, 1977; Wills et al., 1979; Arus et al., 1985). Isoenzyme analysis is a low-cost and accessible technique (Kephart, 1990). The acid-phosphatase isoenzyme system has proven to be the most useful enzyme system for the detection of contamination within hybrid cauliflower seeds (Nijenhius, 1971; Woods, 1976; Wills et al., 1980).

The aim of this study was to analyze acid phosphatase polymorphism in cauliflower lines used to produce hybrids in Brazil, and to evaluate the usefulness of this enzyme system to identify hybrids between different lines.

MATERIAL AND METHODS

Plant material

Eighty-five lines from 12 cauliflower (Brassica oleracea var. botrytis) populations cultivated in Brazil were analyzed (Table I). The number of times the lines were self-crossed is listed in Table I. Hybrids resulting from the crossing of seven Piracicaba Precoce lines and one line from the Spring Snow population were analyzed to determine the genetic control of one acid phosphatase zone.

Isoenzyme analysis

Ten-day-old cotyledons were grounded in liquid nitrogen and transferred to 1.5 mL tubes, to which 50 mL of 0.01 M Tris-glycine buffer, pH 8.3, were added. The samples were centrifuged for 30 min at 4 °C, and 20 mL of the supernatants were loaded into a 10% polyacrylamide gel prepared in 0.37 M Tris-HCl, pH 9.1. The electrode buffer was 0.001 M Tris-glycine, pH 8.3. After 5 h of electrophoresis at 4 °C, acid phosphatase activity was detected in the gels using the histochemical techniques described by Allen et al. (1963).

Genetic control

The genetic control of the APS-5 zone was based on information about the secondary structure of APS in other plants (Kephart, 1990) and on the analysis of the band patterns of a Piracicaba Precoce line, of a Spring Snow line, and of a hybrid between them, as well as of 112 plants of an F2 population.

Usefulness of APS loci for hybrid identification

The usefulness of each APS locus for hybrid identification was estimated by calculating the expected frequencies of crossing between pairs of lines, which would produce hybrids with bands acquired from both parents. The proportion of possible crossings for one locus that would result in hybrids was calculated as being:

(p + q + r)² = p² + 2pq + 2pr + q² + 2qr + r²,

where p = frequency of genotype XX; q = frequency of genotype YY; and r = frequency of genotype XY. The desirable crossing would be XX x YY, or 2pq, according to the formula above.

RESULTS AND DISCUSSION

Three zones of enzyme activity were detected in the gels (Figure 1), as previously described and named by Arus et al. (1985). The most anodic zone was named APS-1, the intermediate zone APS-3, and the most cathodic zone APS-5 (Figure 1). Two alleles were detected in APS-1, differently from Wills and Wiseman (1980), who detected four alleles in APS-1 in an analysis of 19 F₁ hybrids and inbred lines of cabbage and Brussels sprouts. Two alleles were also detected in APS-3. In the third zone (APS-5), up to five bands and three band patterns were seen (Figure 1). Pattern 1 contained three bands (e, d, and c), pattern 2 contained four bands (e, c, b, and a), and pattern 3 contained bands e, d, c, b, and a. Since the genetic control of APS-5 was not described previously, there are no reports on alleles in this zone.

The APS-5 zone was not used for hybrid identification in previous studies (Wills and Wiseman, 1980; Arus et al., 1985). The usefulness of this zone for hybrid identification was tested in this study, because of the very clear and easy to score band patterns. Crosses between plants with band patterns 1 and 2 in APS-5 always resulted in a hybrid with pattern 3, and an F₂ population in which one-quarter had pattern 1, one-half had pattern 2, and one-quarter had pattern 3. A chi-square test showed that there was no significant difference between the observed and the expected phenotype frequencies for a cross between two plants which are heterozygous for the same two alleles (Table II). This observation indicates that there is at least one segregating locus in this zone.

The genetic control of the APS-5 zone was proposed based on the band patterns detected in 112 plants from a cross between plants with band patterns 1 and 2 (Figure 1), and on hypothetical phenotypes of electrophoresed enzymes, as described by Kephart (1990). Pattern 1 would be formed by (i) the overlapping of two homodimers, formed by the products of alleles A₁¹ and B₁¹ (band e), (ii) interlocus heterodimers resulting from the combination of chains coded by alleles B₁¹ and B₂² (band d), and (iii) by a homodimer coded on locus B₂ (band c). Pattern 2 would be formed by (i) a homodimer formed from the product of allele A₁¹ (band e), (ii) a homodimer formed from products coded by allele B₂ (band c), (iii) an interlocus heterodimer formed from products coded by alleles B₂² and B₁³ (band b), and (iv) a homodimer formed from products coded by allele B₁³ (band a). Pattern 3 would be formed by the overlapping of two homodimers, formed by (i) products of alleles A₁¹ and B₁¹ (band e), (ii) interlocus heterodimers resulting from the combination of chains coded by alleles B₁¹ and B₂² (band d), (iii) the overlapping of a homodimer coded on locus B₂ and an intralocus heterodimer formed by chains coded by alleles B₁¹ and B₁³ (band c), (iv) a heterodimer formed from chains coded by allele B₂²B₁³ (band b), and (v) a homodimer formed by the product of allele B₁³ (band a). Thus, the isoenzymes observed in the APS-5 zone were coded in loci A₁, B_1, and B_2, and some of them were interlocus heterodimers. B₁ was the only locus segregating in this zone. The similar electrophoretic mobility observed among the isozymes coded by the analyzed loci and the occurrence of interlocus heterodimers suggested gene duplication. Gene duplications have also been reported in other plant species (Stuber and Goodman, 1980; Massey and Hamrick, 1998).

Different frequencies were found for each allele of the two loci in the 12 analyzed populations (Table III). The frequencies of each phenotype in zones APS-1 and APS-3 were very similar, suggesting that APS-3 is most probably formed by interlocus heterodimers, as suggested previously by Arus and Shields (1983). In APS-1, the frequencies detected for phenotypes SF and SS were similar and much higher than the frequency of phenotype FF. In B₁, the frequencies of phenotypes SS and FF were a little lower than that of SF, and more similar to each other than to APS-1. The frequencies of each phenotype varied in the population, that of SS generally being higher than those of SF and FF. The polymorphism within and among populations was generally very low, since only up to two alleles were found at the two loci analyzed. The populations differed from each other in the frequencies of these alleles.

The proportion of crosses using all analyzed lines resulting in hybrids that may be identified using loci APS-1 and B₁ was calculated based on the total frequency of each phenotype (SS, FF, FS) (Table IV). The most useful locus was B₁, by which 14.3% of the possible hybrids between any pair of the analyzed lines could be detected based on their band patterns, whereas APS-1 would allow the detection of no more than 8.8% of hybrids. If the crosses were done using the lines with genotypes FF or SS of each population (Table V), the proportion of crosses resulting in hybrids that might be identified using APS-1 and B₁ would be 41% and 50%, respectively (Table VI). These results indicate that the acid phosphatase system can be very useful for hybrid identification in the analyzed lines, and that the genotyping of these lines could increase the efficiency of this marker.

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Publication Dates

• Publication in this collection
  02 Aug 2002
• Date of issue
  2002

History

• Accepted
  25 Mar 2002
• Received
  05 Mar 2002