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Genetics and Molecular Biology

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

Genet. Mol. Biol. vol.27 no.4 São Paulo  2004

http://dx.doi.org/10.1590/S1415-47572004000400015 

ANIMAL GENETICS
RESEARCH ARTICLE

 

Cytogenetic variability in three species of the genus Cicindela (s.l.) (Coleoptera, Cicindelidae): karyotypes and localization of 18S rDNA genes

 

 

Sónia J. R. Proença; Maria João Collares-Pereira; Artur R. M. Serrano

Universidade de Lisboa, Faculdade de Ciências, Centro de Biologia Ambiental, Campo Grande, Lisboa, Portugal

Correspondence

 

 


ABSTRACT

Three tiger beetle species from the Cicindelini tribe were examined cytogenetically and found to have the following karyotypes: Cicindela argentata, 2n = 18 + X1X2Y/X1X1X2X 2; Cicindela aurulenta, 2n=18 + X1X2X3Y/X1X1X 2X2X3X3 and Cicindela suturalis, 2n = 18 + X1X2X3X4Y/X1X 1X2X2X3X3X4X 4. Fluorescence in situ hybridization (FISH) using a PCR-amplified 18S rDNA fragment as a probe showed the presence of ribosomal clusters in two autosomes in C. argentata, two autosomes and two heterosomes in C. aurulenta and in two heterosomes in C. suturalis (male configuration), revealing two new patterns of rDNA localization. Such results are representative of the cytogenetic variability observed in the species rich genus Cicindela (sensu lato) mainly as regards the localization of rDNA genes and the number and morphology of the heterosomes, in spite of the stability of autosome numbers. Changes in the localization and number of rDNA clusters were independent of changes in the number of sex chromosomes, indicating that several processes might have contributed to the great karyotypic diversity found within this speciose Coleopteran group.

Key words: chromosome evolution, Cicindela, multiple sex chromosomes, rDNA localization, tiger beetles


 

 

Introduction

The Coleopteran family Cicindelidae has about 2300 species distributed worldwide and is very successful in terms of species radiation (Cassola and Pearson, 2000; Pearson and Vogler, 2001). Several studies have been performed on the biology, ecology and geographical distribution of a great number of tiger beetle species (e.g. Pearson, 1988; Pearson and Vogler, 2001), although even so only about 80 species have until now been karyotyped (Serrano and Galián, 1998; Galián and Hudson, 1999; Galián et al., 2002; Proença et al., 2002a, b).

Tiger beetles have an unusually diverse karyotype, with a diploid chromosome number ranging from 12 to 44 and a great variety of both simple and multiple sex determination systems (Galián et al., 2002; Proença et al., 2002a, b). The most primitive tribes Manticorini, Omini and Megacephalini seem to be characterized by the presence of simple sex chromosome mechanisms of the X0 or XY types (Pearson and Vogler, 2001; Galián et al., 2002; Proença et al., 2002b). Multiple sex chromosome systems, XnY (where n varies from two to four) have been described in the Cicindelini and Collyrini tribes and were considered an apomorphy of a large clade that includes these two tribes (Galian et al., 2002). These multiple heterosomes form a non-chiasmatic multivalent during meiosis linked by telomeric connections (Giers, 1977) and differ from other multiple sex systems described in Coleoptera (Serrano, 1980a, 1984; Galián et al., 1990a; 1996; Vitturi et al., 1996). Even so, a few species of Cicindelini have been described with simple sex chromosome mechanisms (see Giers, 1977; Serrano et al. 1986; Proença et al., 2002a), which were hypothesized to be a secondary condition.

The direction in which diploid chromosome numbers and distinct sex chromosome determination systems have changed during karyotype evolution in tiger beetles can be determined by phylogenetic and cytogenetic analyses (Vogler and Pearson, 1996; Galián and Hudson, 1999; Proença et al., 1999, 2002a, b; Galián et al., 2002). Apparently, there has been a reduction in the number of autosomal pairs from the most plesiomorphic groups to the most derived groups, with the genus Cicindela (s.l.) being stable and commonly having 9 to 10 chromosome (Serrano and Galián, 1998) as well as non-chiasmatic multiple sex chromosome systems which presumably evolved from a simple chiasmatic system.

Studies on the structure of the Cicindelidae genome have mainly been restricted to the in situ localization of the 18S-28S ribosomal gene clusters (rDNA) using fluorescence in situ hybridization (FISH). The data available show that basal groups have higher number of chromosomes bearing rDNA copies located exclusively on the autosomes (three and four pairs). In the most derived groups these numbers decrease to a minimum of one pair of rDNA clusters, which are located on the autosomes, heterosomes or both (Galián et al., 1995; Galián and Hudson, 1999; Pearson and Vogler, 2001, Proença et al., 2002a, b). Such a pattern of localization for these highly repetitive and conserved genes seems to follow the reduction in the number of autosomal pairs and may suggest rearrangements between heterosomes and autosomes which could be associated with changes in the number of sex chromosomes.

In this paper we present the first report on the karyotypes, sex chromosome systems and localization of major rDNA sites (using FISH) for three Cicindela (s.l.) species and also discuss the cytogenetic variability within the cicindelids.

 

Material and Methods

Biological material

Adult tiger beetles were collected from natural populations in the localities listed in Table 1. They were identified by one of the authors (A.R.M. Serrano) and were deposited at the Department of Animal Biology of the Faculty of Sciences, University of Lisbon, Portugal. The species studied were: Cicindela (Brasiella) argentata (Fabricius, 1801), Cicindela (Cosmodela) aurulenta (Fabricius, 1801) and Cicindela (Cylindera) suturalis (Fabricius, 1798).

Chromosome preparations

Male and female gonads were dissected from ethyl-acetate anaesthetized adult beetles and then subjected to hypotonic treatment in distilled water and fixed using fresh ethanol-acetic acid solution (3:1) for one hour, with several changes of the fixative during the next day, the fixed gonads being kept at -20ºC until needed. Small sections of the gonads were squashed in 70% acetic acid and the air-dried slides stained in phosphate buffered 4% Giemsa (pH = 6.8) for karyotype analysis or kept in a 37º C incubator for at least three days before being subjected to FISH (Proença et al., 2002a).

In situ hybridization

FISH was carried out as described in Galián et al. (1999) with minor modifications. The hybridization probe used was obtained by amplification of an 18S rDNA fragment described in detail by De la Rúa et al. (1996) and labeled with biotin-16-dUTP by a second PCR reaction. The hybridization mixture contained 50% deionized formamide, 2xSSC, 50 mM sodium phosphate (pH = 7.0), 10% (w/v) aqueous dextran sulfate and 4 ng/µl of biotin-labeled probe. Probe hybridization sites were detected by treatment with avidin-fluorescein isothiocyanate (FITC) and the signal amplified twice with goat anti-avidin-biotin (Vector). Slides were counter-stained with propidium iodide and examined under epifluorescence, images being captured with a DP-50 Olympus digital camera.

 

Results

The karyotypes of the three species were: C. argentata, 2n = 18+X1X2Y/X1X1X 2X2; C. aurulenta, 2n = 18+X1X2X3Y/X1X 1X2X2X3X3; and C. suturalis, 2n = 18+X1X2X3X4Y/X1X 1X2X2X3X3X4X 4 (Table 1).

We found that C. argentata had nine homomorphic pairs of metacentric and submetacentric chromosomes (Figure 1A). The Y chromosome was the smallest chromosome of the complement and the X1 and X2 chromosomes were medium-sized metacentrics. Female mitosis gave 22 chromosomes (Figure 1B), except for one female which had 23 chromosomes in about 80% of the mitotic metaphases analyzed, probably due to trisomy of autosomic pair 8. Diakinetic and metaphase II figures were not observed.

 


 

The autosomes of C. aurulenta were metacentric and submetacentric and gradually decreased in size (Figure 2 A, B). The Y was acrocentric and one of the biggest chromosomes of the set, while the X chromosome was among the smallest. Spermatocyte metaphase I cells were made up of nine rod- or ring-shaped bivalents plus a sex chromosome complex with four elements (Figure 2C). Spermatocyte metaphase II cells were of two types with 10 (9+Y) and 12 (9+ X1X2X3) chromosomes (Figure 2D).

 

 

The chromosomes of C. suturalis gradually decreased in size with chromosome pairs 1,2 and 3 being metacentric and the remaining ones submetacentric. The heterosomes were among the smallest chromosomes of the complement, with the X1 chromosome larger than the Y chromosome (Figure 3A, B). Spermatocyte metaphase I cells had nine rod- or ring-shaped bivalents and a sex chromosome complex with five elements (Figure 3C). Spermatocyte metaphase II cells were of two types with 10 (9+Y) (Figure 3D) and 13 (9+X1X2X3X4) (Figure 3E) chromosomes.

 

 

In respect to the localization of rDNA sites, C. argentata showed two fluorescent signals on two medium-sized chromosomes (Figure 4A). FISH was not successful in male mitotic metaphases but hybridization of interphase nuclei showed fluorescent signals outside the sex vesicle, indicating rDNA clusters in the autosomes (not shown). Female mitotic plates of C. aurulenta had two small and four medium-sized labeled chromosomes (Figure 4B). Meiotic plates showed two hybridization sites in an autosomal pair and two additional signals in the sex vesicle which seemed to correspond to two of the X chromosomes (Figure 4C). We also found that C. suturalis had four fluorescent-labeled small-sized chromosomes in the female mitotic chromosome complement (Figure 4D) and two small fluorescent-labeled chromosomes in the male mitotic plates (Figure 4E). Male metaphases I chromosomes showed two hybridization sites in the sex complex (Figure 4F), corresponding to two of the X chromosomes, probably the X3 and X4 chromosomes taking into account the size of the labeled chromosomes.

 

Discussion

The three species of Cicindelini revealed the presence of nine pairs of autosomes and multiple sex chromosome systems, although with different numbers of X chromosomes.

Although having some specific variations in their morphology, the autosomal pairs of the species studied share some common features, such as the mediocentric morphology of the chromosomes (meta- and submetacentric) and the existence of two large pairs of autosomes with the remaining chromosomes gradually decreasing in size. A similar pattern has also been described for the autosomes of other Paleartic, Indian and Australian Cicindela species (Serrano 1980b; Yadav and Karamjeet, 1981; Yadav et al., 1985; Serrano and Collares-Pereira, 1989; Collares-Pereira and Serrano, 1990; Galián et al., 1990b; Yadav and Burra, 1991, 1994; Galián and Hudson, 1999). The heterosomes of the three species studied by us varied greatly in size, the Y chromosome being a small dot very difficult to identify in C. argentata but one of the biggest chromosomes in C. aurulenta. The X chromosomes were similar in size within each species but differed between species, being medium-sized in C. argentata but small in C. argentata and C. suturalis.

The karyotypes of C. argentata, C. aurulenta and C. suturalis can be used as an example of the three types of multiple sex chromosome systems found in the Cicindelini (2Xs, 3Xs and 4Xs), based on which several aspects related to the evolution of chromosomes within the family Cicindelidae can be discussed.

The generally accepted hypothesis for the development of the achiasmatic multiple sex chromosome systems in tiger beetles is that of a single-origin in a ancestor common to both Collyrinae and Cicindelini (Galián et al., 2002) before these two groups split. If we accept this single origin hypothesis, the multiple X system is remarkable within beetles because of its evolutionary antiquity (Galián et al., 2002). Phylogenetic and cytogenetic data support this hypothesis with the description of multiple sex chromosomes in Collyrini and Cicindelini but not in Megacephalini and in other basal groups (Sharma, 1988; Vogler and Pearson, 1996; Serrano and Galián, 1998; Galián and Hudson, 1999; Galián et al., 2002), with a few exceptions considered to be derived conditions. Also, the description of multiple sex chromosomes in the Cicindelini species (C. argentata, C. aurulenta and C. suturalis) discussed in this paper fits well into this pattern of chromosome evolution. The mechanisms underlying the development of such extraordinary multiple sex systems remain unknown, but several authors defended the theory of independent evolution of autosomes and heterosomes (Serrano and Collares-Pereira, 1989; Galián et al., 1990b) based on the following observations. In most of the Cicindela (s.l.) species so far described the number of autosomal pairs (9) remains unchanged while the number of heterosomes varies from two to four, as in the species now analyzed. Conversely, some African, Australian and Oriental Cicindelini species have 10, 11 and 12 autosomal pairs and share the same number of heterosomes (Galián and Hudson, 1999; Proença et al., 1999). Moreover, the absence of chiasmata between the sex chromosomes may constitute a barrier for the translocation of chromosomal material between the chromosomes.

In our research, the localization of major rDNA sites by FISH revealed different patterns for C. argentata, C. aurulenta and C. suturalis, with ribosomal clusters located in the autosomes, the heterosomes or in both. Different patterns regarding the localization of rDNA genes have been described in other Cicindela species : two clusters located in one autosomal pair (C. flexuosa, C. paludosa and C. hispanica); two clusters located in one autosomal pair and one in an X chromosome (C. littoralis and C. maura); two clusters located in one autosomal pair and two in the heterosomes (XY) (C. deserticoloides and C. circumdata) and three clusters located in the heterosomes (XXY) (C. trisignata) (see Proença et al., 2000; Proença and Galián, 2003). In our study we found two new rDNA localization patterns, i.e. the existence of copies of rDNA exclusively in two X chromosomes in C. suturalis and in one autosomal pair and in two Xs in C. aurulenta. The absence of descriptions of heterosomal copies located only on Y chromosomes may suggest that the heterosomal copies are functionally active and are also needed in females.

Basal groups of Cicindelidae exhibit the highest number of rDNA copies solely located on the autosomes, the number of copies ranging from three to four pairs (Galián and Hudson, 1999; Galián et al., 2002). The tendency for these genes to transfer from autosomes to heterosomes is seen from the most primitive cicindelid species to the derived cicindelid species, with subsequent diversification in the genus Cicindela (s.l.). Taking into account the apparent lack of interaction between the heterosomes and autosomes in the species with these multiple sex chromosome systems it has been suggested that the diversity of 18S-28S rDNA clusters in terms of localization could be due to non-genetic transposition mechanisms rather than simple translocations or other structural rearrangements. This was proposed by Mandrioli (2000) for the pufferfish Tetraodon fluviatilis where mariner-like transposable elements were found interspersed within the rDNA-associated heterochromatin. Such transposable elements have been considered to be responsible for a significant proportion of the observed karyotypic variation in many groups (revised in Kidwell, 2002) and mariner-like transposable elements have also been successfully amplified in some Cicindela species (S. Proença and J. Galián, unpublished results).

Future research on the genes located on the sex chromosomes (especially the Xs) and on the genetic control of sex determination and the evolutionary consequences of differential gene expression in males and females may provide insights into the patterns and processes of chromosome evolution in this speciose Coleopteran group.

 

Acknowledgments

This work was supported by grant number PRAXIS XXI/BD/15986/98 (Fundação para a Ciência e Tecnologia, Portugal) to SJRP. Thanks are due to José Galián for training in the FISH technique and Deodália Dias for allowing the use of PCR and in situ hybridization facilities. We also thank the Instituto Humbold (Colombia), Instituto de Ciências Naturales, Universidad Nacional de Colombia and Universidade Federal de Pernambuco, Brazil for field assistance in Colombia and Brazil. Rita Moura (Brazil) and A. Ali (Malaysia) are also kindly acknowledged for their help in collecting and sending material.

 

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Correspondence to
Maria João Collares-Pereira
Universidade de Lisboa, Faculdade de Ciências, Centro de Biologia Ambiental
Campo Grande, Edifício C2 - 3° Piso
1749-016 Lisboa, Portugal
E-mail address: mcolares@fc.ul.pt

Received: October 24, 2003; Accepted: May 5, 2004

 

 

Associate Editor: Yatiyo Yonenaga-Yassuda

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