versión impresa ISSN 1415-4757versión On-line ISSN 1678-4685
Genet. Mol. Biol. v.23 n.1 São Paulo mar. 2000
Luciana Bolsoni Lourenço1, Shirlei M. Recco-Pimentel1 and Adão José Cardoso2*
Departamentos de 1Biologia Celular and 2Zoologia, Instituto de Biologia, Universidade Estadual de Campinas (UNICAMP), 13083-970 Campinas, SP, Brasil. Send correspondence to S.M.R.-P. Fax: +55-19-788-7821. E-mail: firstname.lastname@example.org
We analyzed the meiotic chromosomes of specimens from the two karyological groups of Physalaemus petersi (Jiménez de la Espada, 1872) described in the literature. Multivalent configurations (rings or chains) were observed in both groups. This meiotic organization resulted from the terminal association of non-homologous chromosomes, and an analysis of C-banded multivalents indicated no involvement of heterochromatic regions in these associations. A possible explanation for such meiotic configurations is the occurrence of heterozygous translocations. Thus, multivalents may indicate the involvement of translocation events in the karyotypic evolution of P. petersi.
Terminal association of non-homologous bivalents at first meiosis has been described in many organisms. In some cases, such meiotic configurations arise from non-chiasmate interactions between C-band positive ends and either euchromatic ends or other heterochromatic blocks of non-homologues (Drets and Stoll, 1974; John and King, 1982, 1985). On the other hand, several studies have shown multivalent configurations at first meiosis as a result of heterozygosity for either interchange or Robertsonian fusion or fission (John, 1987; Bidau and Mirol, 1988; Haaf et al., 1989; Moss and Murray, 1990; Mirol and Bidau, 1991, 1992, 1994; Reed et al., 1992). In all these cases, the associations between non-homologues were chiasmate. Meiotic configurations formed in this way can lead to irregular segregation and a high rate of non-disjunction, with a consequent reduction in reproductive potential (Eichenlaub-Ritter and Winking, 1990), although sometimes there may be no apparent negative influence on fertility (Mirol and Bidau, 1994).
In Anura, multivalent meiotic configurations formed by homologous chromosomes have been described in some polyploid species (Beçak et al., 1966, 1967, 1970; Schmid et al., 1985), but terminal association of non-homologous bivalents in meiosis was observed only in the leptodactylids Eleutherodactylus binotatus (2n = 22) (Beçak and Beçak, 1974) and Odontophrynus americanus (4n = 44) (Beçak and Beçak, 1998). In E. binotatus, such configurations were considered to be indicative of multiple translocations and/or centric fusions, important mechanisms possibly related to the diploidization of an ancestral polyploid karyotype, giving rise to the diploid karyotype of this species (Beçak and Beçak, 1974). In the polyploid O. americanus, the multivalent configurations involving non-homologous chromosomes were attributed to a 4/11 translocation (Beçak and Beçak, 1998).
We have previously reported two distinct karyotypes (I and II), as well as C-band and NOR polymorphisms in the anuran Physalaemus petersi (Jiménez de la Espada, 1872) (Lourenço et al., 1998, 1999). The multiple NOR sites and non-centromeric C-bands detected could have resulted from translocation events. In the present work, we describe multivalent configurations in both karyological groups of P. petersi from the Brazilian Amazon and suggest that these arrangements provide cytological evidence for translocation events during the evolution of the two karyotypes.
MATERIAL AND METHODS
The meiotic chromosomes of 13 P. petersi males belonging to karyological group I (ZUEC 9584, 9586, 9588, 9589, 9593, 9595, 9596, 9597, 9598, 9613, 9632, 9633, 9625) and two males belonging to karyological group II (ZUEC 9584, 9654) were examined. The group II specimens were collected in the Alto Juruá Reserve (Acre State, Brazil) in February, 1994, and January, 1996. Five group I animals were also collected in this region at the same time; the other eight specimens of this group were obtained from the Humaitá Reserve (Acre State, Brazil) in December, 1994, and April, 1995. All of the specimens were deposited in the Museum of Zoology at the State University of Campinas (ZUEC). Cytological preparations were obtained from cell suspensions of testes removed from animals treated with colchicine for 4 h (Schmid, 1978). Conventional staining with Giemsa and C-banding were done as described elsewhere (King, 1980).
In addition to 11 isolated bivalents (Figures 1a and 2a), multivalent rings and chains formed by the association of bivalent chromosomes were observed in diakinetic spermatocytes from eight group I and two group II specimens of P. petersi (Figures 1b-g and 2b). In two specimens (ZUEC 9588 and 9589) there were multivalent configurations that appeared to involve most of the chromosome pairs of the karyotypes (Figure 1d-f).
Both alternate and adjacent multivalents were seen in group I specimens (Figure 1b-d and 1g, respectively) whereas in group II animals only open chains were observed. The association between bivalents involved terminal regions and the C-banded figures showed no participation of heterochromatic regions in these interactions (Figure 1g).
As previously reported (Lourenço et al., 1999), non-centromeric C-bands interfered with homologous chromosome behavior in meiosis. The heterozygosity of the telomeric and interstitial heterochromatic blocks seen in karyological group I specimens of P. petersi probably prevented pairing and/or crossing-over between homologous chromosome arms. Nevertheless, there was no evidence to support the involvement of non-centromeric heterochromatic blocks in the formation of multivalent configurations at first meiosis in this karyological group. The C-banding technique showed no heterochromatin in the region of the bivalent associations. Generally, in cases where C-bands play a role in the origin of multivalent meiotic arrangements, the associations between two non-homologous chromosome pairs involve at least one terminal C-band (John and King, 1985). Although we did not conclusively determine the C-banding pattern of all the specimens examined here, the haploid karyotype of group I P. petersi usually showed a maximum of four telomeric C-bands (Lourenço et al., 1999). This suggests that there are probably not enough C-blocks to support heterochromatic associations that can give rise to configurations such as that shown in Figure 1d, for example.
One possible explanation for these meiotic associations could be the existence of limited homology between non-homologous chromosomes in the group I karyotype. The pairing of such segments and the formation of chiasma between them would arrange the chromosomes in multiple configurations in the first meiosis. We hypothesize that multiple translocations could have been involved in the origin of such homologous segments in non-homologous chromosomes, as also suggested for the leptodactylid Eleutherodactylus binotatus (Beçak and Beçak, 1974). The variable relative size and arm ratio of the different morphs of chromosomes 6 and 8 (Lourenço et al., 1998, 1999) agree with this hypothesis since multiple translocations are expected to change the morphology of the chromosomes involved. Such multiple translocations probably played an important role in the karyotypic evolution of this species and could provide a mechanism for the appearance of multiple NOR and C-bands in P. petersi, particularly in the group I karyotype. Although the occurrence of heterozygotes for translocations could also account for the multivalent chains observed in group II specimens, the absence of C-banded configurations precludes a reliable interpretation of this event. In any case, these unusual meiotic configurations make this group an interesting model for future cytological investigations.
We thank the Brazilian agencies CAPES and CNPq for financial support, and Moisés Barbosa de Souza for helping in the field work. Publication supported by FAPESP.
Nós analisamos os cromossomos meióticos de espécimes dos dois grupos cariotípicos de Physalaemus petersi (Jiménez de la Espada, 1872) descritos na literatura. Configurações multivalentes (anéis e cadeias) foram descritas em ambos os grupos. Essa organização meiótica resultou da associação terminal de cromossomos não-homólogos e a análise de preparações meióticas submetidas ao bandamento C não indicou o envolvimento de regiões heterocromáticas nessas associações. Uma possível explicação para tais configurações meióticas consiste na presença de translocações heterozigotas. Nesse caso, os multivalentes observados evidenciariam o envolvimento de eventos de translocação na evolução cariotípica em P. petersi.
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(Received December 7, 1998)
*This paper is dedicated to the memory of Adão José Cardoso, who died before this work was completed.