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Genetics and Molecular Biology

Print version ISSN 1415-4757On-line version ISSN 1678-4685

Genet. Mol. Biol. vol.27 no.2 São Paulo  2004

http://dx.doi.org/10.1590/S1415-47572004000200011 

ANIMAL GENETICS
RESEARCH ARTICLE

 

C-banding and fluorescent in situ hybridization with rDNA sequences in chromosomes of Cycloneda sanguinea Linnaeus (Coleoptera, Coccinellidae)

 

 

Eliane Mariza Dortas MaffeiI; Silvia das Graças PompoloII; Eduard PetitpierreIII

IUniversidade Estadual do Sudoeste da Bahia, Departamento de Ciências Naturais, Vitória da Conquista, BA, Brazil
IIUniversidade Federal de Viçosa, Departamento de Biologia Geral, Viçosa, MG, Brazil
IIIInstitut Mediterrani d' Estudis Avançats, Department de Recursos Naturals, Palma de Mallorca, Spain

Correspondence

 

 


ABSTRACT

The aim of this study was to describe mitotic and meiotic chromosomes of Cycloneda sanguinea using C-banding, fluorescent in situ hybridization (FISH) rDNA probes, and sequential FISH/Ag-NOR staining. The chromosome number was 2n = 18 + XX for females and 2n = 18 + Xy for males. The X chromosome was metacentric and the Y chromosome was very small. During meiosis, the karyotypic meioformula was n = 9 + Xyp, and sex chromosomes configured a parachute at metaphase I. At the beginning of pachytene, bivalents were still individualized, and sex chromosomes were associated end-to-end through the heteropycnotic region of the X chromosome. Later in pachytene, further condensation led to the formation of a pseudo-ring by the sex bivalent. All chromosomes showed pericentromeric heterochromatin. FISH and sequential FISH/Ag-NOR staining evidenced the location of the nucleolar organizer region in one pair of autosomes (at spermatogonial metaphase). During meiosis, these genes were mapped to a region outside the sex vesicle by FISH, although Xyp was deeply stained with silver at metaphase I. These results suggest that these argyrophilic substances are of a nucleolar protein nature, and seem to be synthesized by a pair of autosomes and imported during meiosis (prophase I) to the sex pair, during the association of the sex chromosomes.

Key words: in situ hybridization, rDNA sequences, sequential FISH/Ag-NOR staining, C-banding, Cycloneda sanguinea.


 

 

Introduction

The lady beetle Cycloneda sanguinea belongs to the family Coccinellidae, a cosmopolitan taxon that comprises 5000 species, 2000 of which are Neotropical species (Iabhlokoff-Khuzorian, 1982). Many species of this family are highly active predators and are intensively used for biological control (Borror and De Long, 1988; De Bach, 1964; Gordon, 1985; Levins and Wilson, 1980).

Cytogenetic analyses of the family Coccinellidae are scarce, and the karyotypes of only 4% of the species are known. All of them are characterized by meiosis with an n = 9 + Xyp in males. Sex chromosome association during metaphase shows the typical “parachute” shape that characterizes Coleoptera. This peculiar type of association has been traditionally explained as being due to the presence of the nucleolar organizer region (John and Lewis 1960; Smith and Virkki 1978; Virkki et al. 1991), and fluorescent in situ hybridization (FISH) using 18S-28S rDNA gene probes has corroborated this theory for some Australian species of Cicindela (Galián and Hudson, 1999) and for Olla v-nigrum (Maffei et al., 2001a). However, the nucleolar theory was questioned by other investigators, who found nucleoli in a pair of autosomes in other species (Drets et al., 1983; Postiglioni and Brum- Zorrilla 1988; Postiglioni et al. 1991).

Banded karyotypes of Coccinellidae are almost unknown, except for C-banding in six species of the genus Chilocorus, Epilachna paenulata, Eriopis connexa and seven species of lady-birds from Central Europe (Ennis, 1974; Drets et al., 1983; Maffei et al, 2000; Rošek and Holecová, 2002).

The aim of the present study was to describe the mitotic and meiotic chromosomes in females and males of Cycloneda sanguinea, establishing their C-banding pattern and physical mapping of rDNA sequences using FISH and sequential FISH/Ag-NOR staining.

 

Material and Methods

The Cycloneda sanguinea L. specimens were collected on the campus of the Universidade Federal de Viçosa (UFV). Mitotic and meiotic analyses were carried out in 12 prepupal larvae and 40 male adults, with a sample size of 10 mitotic metaphases per individual. Cytogenetic preparations of mitotic metaphase chromosomes (cerebral ganglion) and meiosis analysis were carried out as described by Imai et al. (1988) and adapted for Coccinellidae (Maffei et al., 2000).

C-banding was performed as described by Sumner (1972) with modifications (Maffei et al., 2000). Slides were subjected to hydrolysis with 0.2 N HCl for 4 min at room temperature, washed in distilled water and incubated with 5% barium hydroxide at 60 °C for 8 min, then washed in 0.2 N HCl at room temperature for 30 s, incubated with 2xSSC at 60 °C for 10 min, and stained with 6.6% Giemsa in Sörensen buffer pH 6.8 for 50 min.

Sequential FISH/Ag-NOR staining followed the technique described by Maffei et al. (2001a). One drop of 2% gelatin (2 g gelatin diluted in 100 mL distilled water and 0.5 mL formic acid) and four drops of aqueous 50% Ag-NO3 solution (Merck) were added onto slides already hybridized with rDNA probes. The slides were then covered with a coverslip and incubated in a moist chamber at 38% humidity for 25 min. Finally, the material was thoroughly rinsed with a squirt bottle for approximately 5 min, air-dried and mounted with Entellan (Merck).

Ribosomal DNA sequences were mapped using FISH (Viegas-Péquignot, 1992). The rDNA probes (pDm 238) containing the 18S, 28S and 5.8S genes were labeled with biotin by nick translation using the Bionick kit (Gibco). Slides with fixed meiotic chromosomes were incubated with RNase (100 mg/mL) for 1 h in a moist chamber containing 70% formamide at 37 °C, followed by three incubations in 2xSSC for 3 min each, and dehydrated in 50%, 75% and 100% alcohol for 3 min each. After denaturation of the chromosomal DNA in 70% formamide for 2 min at 70 °C, the slides were dehydrated in ice-cold 2xSSC for 2 min and immersed in 50%, 75% and 100% alcohol for 2 min each. In parallel, the probe was incubated at 100 °C for 2 min and maintained on ice. Ten microliters of the probe (diluted in hybridization mixture) per hybridization area were then added onto the slides, which were incubated in a 70% formamide moist chamber at 37 °C for 36 h. After incubation, the slides were immersed twice in 50% formamide at 37 °C for 2 min each, and washed with 2xSSC at 37 °C for 2 min each, followed by two washes with PBT for 2 min each.

 

Immunological detection

The slides were incubated with anti-biotin (Vector SP3000) and anti-goat IgG-FITC (Vector FI5000). The DNA was counterstained with 100 mL propidium iodide for 1 min and washed with PBS. The slides were mounted in 13 mL Vectashield and photographed under an Olympus BX60 photomicroscope using appropriate fluorescence filters.

 

Results

Meiosis and mitosis

C. sanguinea cells in meiosis showed a large, single regular heteropycnotic chromocenter at prophase I (zygotene). At the beginning of pachytene, the bivalents were individualized and the sex chromosomes showed linear end-to-end association. As pachytene progressed, DNA condensation led to the formation of a pseudo-ring by the sex bivalents (Figure 1A). At metaphase I, the meioformula was n = 9 + Xyp (Figure 1B), followed by normal chromosome segregation at anaphase I.

 



 

The analysis of mitotic cells with standard staining showed a chromosome number of 2n = 18 + XX in 10 C. sanguinea females and of 2n = 18 + Xy in two males. The chromosomes of this species were mainly submetacentric and the y chromosome was very small (Figures 2A and 2B). C-banding revealed heterochromatin in the pericentromeric regions of all chromosomes, including the short arms (Figure 2C).

 





 

Location of rDNA genes and Ag-NOR banding

The location of rDNA sequences was evidenced by FISH as a large block at prophase I (early zygotene) (Figure 3A). Sequential FISH/Ag-NOR staining showed that the rDNA sequences were located outside the sex vesicle (Figures 3B and 3C). Sequential FISH/Ag-NOR treatment showed a marked silver staining of both the sex vesicles (prophase I) and the lumen of the sex chromosomes associated in a parachute format (metaphase I).

 





 

Discussion

Mitosis and meiosis

The lady-beetle Cycloneda sanguinea has a chromosome number of 2n = 18 + XX for females and a meioformula of n = 9 + Xyp for males, characteristic of most Coleopteran species. This may also represent the basic (ancestral) karyotype, especially in the suborder Polyphaga (Smith, 1950; Smith and Virkki, 1978). As recently reported for Eriopis connexa (Maffei et al., 2000) and Olla v-nigrum (Maffei et al., 2001a), all members of the family Coccinellidae (42%) apparently share the same chromosomal behavior: at prophase I (pachytene) of the male meiosis, sex chromosomes appear associated end-to-end, with the short arm of the X chromosome joining the y chromosome in a linear fashion followed by a pseudo-ring and, finally, a parachute is visible at metaphase I, with the expanded chromatin of the short arm of the X chromosome contributing to the parachute. These results are in agreement with the model of Xyp sex chromosome association proposed by Drets et al. (1983) for Epilachna paenulata (Coleoptera, Coccinellidae). In this species, C-banding analysis revealed a sex chromosome association different from other Coleopteran species studied, due to the extensive role played by constitutive heterochromatin segments in chromosome association and Xyp formation. The authors proposed a model where the parachutes consist of three different segments: two corpuscles showing intense heterochromatin upon C-banding and a euchromatic segment that forms the parachute. The euchromatic segment is acknowledged as the long arm of the X chromosome in the parachute, and the formation of the parachute itself is the result of the association between the X and y chromosomes. It has been suggested that this association is not mediated by the nucleolar organizer region, since no nucleolar material associated with the sex chromosomes was detected. The observations made by Virkki et al. (1991) on the behavior of Xyp association in six Coleopteran species by silver staining supported the interpretation of Drets et al. (1983).

In the present study, the heterochromatin of C. sanguinea was mainly located in the pericentromeric region of all chromosomes and in the short arms, as observed for most Coleopterans studied with C-banding technique (Ennis, 1974; Angus, 1982, 1983; Drets et al., 1983; Juan and Petitpierre, 1989; Holecová et al., 1997; Rošek and Holecová, 2000; 2002).

Location of rDNA sequences (FISH) and gene activity

Meiotic chromosomes (prophase I) and NOR-banding analysis in spermatogonial metaphase of C. sanguinea are described for the first time in the present work. In an earlier study using NOR-banding techniques in mitotic cells of adult males, Maffei et al. (2001b) reported active regions as restricted to one pair of autosomes. They also indicated that rDNA sequences occur in a region outside the sex vesicle (prophase I). Sequential FISH/Ag-NOR confirmed the result obtained by silver staining regarding the Xyp bivalent. FISH using rDNA probes has been little applied in Coleoptera. Juan et al. (1993) applied rDNA FISH to Tenebrio molitor and Misolampus goudoti, both bearing 2n = 20 chromosomes and an Xyp sex chromosome system. In T. molitor, mitotic metaphases showed that the nucleolar organizer regions were located on two pairs of autosomes and on one pair of sex chromosome, thus supporting the classic hypothesis of the nucleolar origin of the Xyp association. In contrast, in M. goudoti, the rDNA sequences were restricted to one pair of autosomes. In Cicindela melancholica, FISH mapped the rDNA sequences to one of three X chromosomes and to the y chromosome (multiple sex system). However, in Cicindela paludosa (a related species), which has an X0 sex determination system, the rDNA sequences were restricted to one pair of autosomes (Galián et al., 1995). FISH for the 18S-28S rDNA genes was applied to other Cicindela species (Cicindelini tribe), and in three species of them, Cicindela cardinalba, Cicindela sp. (saetigera group) and Cicindela gillesensis, these genes were mapped to two of the four sex chromosomes that contributed to the sex vesicle. On the other hand, in Megacephala whelani, fluorescent hybridization during meiosis and mitosis revealed that the rDNA sequences were located on three pairs of autosomes (Galián and Hudson, 1999). This result does not support the classic nucleolar theory. The detection of argyrophilic substances in C. sanguinea during mitosis and meiosis by FISH and sequential FISH/Ag-NOR suggests that these substances are nucleolar proteins synthesized by a pair of autosomes and imported at prophase I, during sex chromosome association.

 

Acknowledgements

We are grateful to Dr. Shirlei M. Recco-Pimentel, Klélia Santos, and Dr. Luciana B. Lourenço for providing the labeled Drosophila rDNA probe and for technical assistance, and to Dr. Lúcia Massutti de Almeida (Departamento de Zoologia, Universidade Federal do Paraná, Curitiba, PR) for identifying the species used in the present study. This research was supported by Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG), Coordenação de Aperfeiçoamento de Pessoal de Ensino Superior (CAPES) and Universidade Federal de Viçosa, Viçosa, MG, Brazil.

 

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Editor Associado: Yatiyo Yonenaga-Yassuda

 

 

Correspondence to
E.M.D. Maffei
Universidade Estadual do Sudoeste da Bahia, Departamento de Ciências Naturais
Estrada do Bem Querer, km 4, Vitória da Conquista
45050-200 Bahia, Ba, Brazil
E-mail: maffeiemd@hotmail.com

Received: March 19, 2003;
Accepted: November 14, 2003.

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