Hereditas 136: 51 57 (2002) Comparative cytogenetics and supernumerary chromosomes in the Brazilian lizard genus Enyalius (Squamata, Polychrotidae) CAROLINA ELENA VIN A BERTOLOTTO 1,3, KATIA CRISTINA MACHADO PELLEGRINO 1, MIGUEL TREFAUT RODRIGUES 2 and YATIYO YONENAGA-YASSUDA 1 1 Departamento de Biologia, Instituto de Biociências, Uni ersidade de São Paulo, São Paulo, SP, Brasil 2 Departamento de Zoologia, Instituto de Biociências and Museu de Zoologia, Uni ersidade de São Paulo, São Paulo, SP, Brasil 3 Uni ersidade Santo Amaro, Faculdade de Medicina Veterinária, São Paulo, SP, Brasil Bertolotto, C. E. V., Pellegrino, K. C. M., Rodrigues, M. T. and Yonenaga-Yassuda, Y. 2002. Comparative cytogenetics and supernumerary chromosomes in the Brazilian lizard genus Enyalius (Squamata, Polychrotidae). Hereditas 136: 51 57. Lund, Sweden. ISSN 0018-0661. Received August 13, 2001. Accepted January 24, 2002 Cytogenetical analyses based on conventional and differential staining were performed for the first time on five species of the Brazilian lizard genus Enyalius: E. bibronii, E. bilineatus, E. iheringii, E. leechii, and E. perditus. The species share a similar 2n=36 (12M+24m) karyotype, comprised of 12 metacentric or submetacentric macrochromosomes, except for an acrocentric pair 6 that characterizes E. bibronii. The 24 microchromosomes were acrocentrics, but in E. perditus two meta/submetacentric microchromosome pairs were unambiguously identified. Karyotypes with 2n=37 and 2n=37/38 chromosomes were also observed in some specimens of E. bilineatus as a result of the presence of supernumerary chromosomes (Bs). Ag-NORs were always located at the distal region of the long arm of the submetacentric pair 2. The constitutive heterochromatin was mostly restricted to the pericentromeric regions of some macrochromosomes and microchromosomes. A XX:XY mechanism of sex determination with a dot-like Y microchromosome occurs in E. bilineatus, E. leechii, ande. perditus. Carolina E. V. Bertolotto, Departamento de Biologia, Instituto de Biociências, Uni ersidade de São Paulo, São Paulo, SP, C.P. 11.461, CEP 05422-970, Brasil. E-mail: caroevb@usp.br Lizards of the genus Enyalius are predominantly inhabitants of eastern and central forested habitats of Brazil. JACKSON (1978) recognized a total of six species, two of them polytypic: E. bilineatus, E. brasiliensis (2 ssp.), E. catenatus (3 ssp.), E. iheringii, E. leechii, and E. perditus. A more recent inspection of additional specimens by one of us (MTR) suggests that a new revision for the genus is needed, and although we here adopt Jackson s scheme, we ignore subspecies and consider tentatively E. bibronii (a subspecies of E. catenatus) as a good species. Except for E. leechii, which occurs in the Amazon basin, all the others species are distributed throughout a wide range of the Brazilian Atlantic Forest, extending from state of Rio Grande do Norte (northeast) to Rio Grande do Sul (southern) (JACKSON 1978; ETHE- RIDGE and DE QUEIROZ 1988). Occasionally, some populations occur in gallery forests in the Cerrados of Central Brazil (E. bilineatus) or in isolated patches of forest in the Caatingas (E. bibronii ). Cytogenetic studies of pleurodont Iguania (former Iguanidae, ESTES et al. 1988; FROST and ETHERIDGE 1989) suggest that there are two distinct trends in chromosome evolution in these lizards. Considerable karyotype variability is found in species of the highly diverse genus Anolis (2n=25 to 2n=48), and among those of the genus Liolaemus (2n=30 to 2n=44). At the other extreme, there are species from several different families that share the same 2n=36 (12M+24m) karyotype with very similar macrochromosome complements, which has been considered as ancestral for pleurodont Iguania, which includes the family Polychrotidae (OLMO 1986). However, the use of differential staining reveal that these conventionally-stained conservative karyotypes are distinct with respect to C-banding patterns, Ag-NORs localization, morphology of microchromosomes, among other cytogenetic aspects (BERTOLOTTO et al. 1996; KASAHARA et al. 1996). Here, we describe the karyotypes of five species of the Brazilian lizard Enyalius based on banding patterns, and compare them with those reported for other pleurodont Iguania taxa. MATERIAL AND METHODS A total of 20 individuals from five species of Enyalius collected from different Brazilian localities were cytogenetically studied (Table 1), and deposited at the Museu de Zoologia of the Universidade de São Paulo (MZUSP), Brazil. Chromosome spreads were obtained from bone marrow, liver, spleen, testes according to routine techniques, or from fibroblast cultures (YONENAGA-YASSUDA et al. 1988). Mitotic and meiotic chromosomes were studied after standard
52 C. E. V. Bertolotto et al. Hereditas 136 (2002) Table 1. Species, specimen number, sex, locality, diploid number and number of metaphases analysed for fi e species of Enyalius in this study. The regions of Brazil are: BA=Bahia, SP=São Paulo, MG=Minas Gerais, DF=Distrito Federal; MT=Mato Grosso. M=male and F=female; 2n=diploid number Species Specimen number Sex Locality 2n Number of metaphases E. bibronii LG 1377 F Serra da Jibóia (BA) (12 56 S, 39 31 W) 36 28 E. bilineatus LG 427 F São José do Rio Preto (SP) (20 49 S, 49 22 W) 36 21 LG 814 F 37 69 LG 815 M Nova Ponte (MG) (19 08 S, 47 40 W) 36 34 LG 816 F 36 52 LG 919 M 37/38 59/7 LG 1467 F Brasília (DF) (15 46 S, 47 55 W) 36 26 E. iheringii LG 421 F Santana de Parnaíba (SP) (23 26 S, 46 55 W) 36 12 LG 622 F Picinguaba (SP) (23 22 S, 44 50 W) 36 39 LG 625 F 35 LG 929 F Juréia, Peruíbe (SP) (24 19 S, 46 59 W) 36 20 LG 1383 F Pilar do Sul (SP) (23 48 S, 47 42 W 36 15 LG 1222 M Apiacás (MT) (09 32 S, 57 26 W) 4 LG 1223 M 36 5 E. leechii LG 1249 F 14 E. perditus LG 1135 F Piraju (SP) (23 11 S, 49 23 W) 36 33 LG 1500 F 10 LG 1501 F Serra da Cantareira (SP) (23 22 S, 46 36 W) 24 LG 1502 F 36 7 LG 1505 M 25 Total 5M;15F 539 Giemsa and Ag-NOR staining, and C-banding. Replication R-banding (RBG), after in vitro treatment with 5-bromodeoxyuridine (BrdU) and 5- fluorodeoxyuridine (FudR) followed by FPG staining (DUTRILLAUX and COUTURIER 1981) was carried out on metaphases of E. bilineatus RESULTS Comparati e analyses after con entional staining A similar karyotype of 2n=36 (12M+24m) comprised of 12 macrochromosomes and 24 microchromosomes characterized the five species of Enyalius (Fig. 1a e, Table 1). The macrochromosome pairs 1, 3, 4, and 5 are metacentrics, and the pairs 2 and 6 are submetacentrics in all species, except for E. bibronii which has an acrocentric pair 6 (Fig. 1a). An aberrant pair 6 formed by a submetacentric and an acrocentric was detected in one specimen (LG 1223) of E. leechii (data not shown). Pair 2 exhibits a typical secondary constriction at the distal end of the long arm. Some microchromosomes seem to be acrocentrics, and there are indubitably two distinct metacentric or submetacentric pairs in E. perditus (Fig. 1e). Supernumerary chromosomes (Bs) were observed in two specimens of E. bilineatus (Fig. 2a). The specimen LG 814 had a karyotype of 2n=37 chromosomes, while the specimen LG 919 was a mosaic composed of a major 2n=37 (one B) and a minor 2n=38 (two Bs) lineages, the latter representing about 10 % of its cells (Table 1). A mechanism of sex determination of XX:XY type was found in E. bilineatus, E. leechii and E. perditus. The Y is a dot-like microchromosome and the X is a medium-sized microchromosome which is indistinguishable from the other chromosomes of the same size (Fig. 1b, d, e and Fig. 2a). An evident heteromorphic microbivalent corresponding to the pairing of the X and Y was observed in some diakinesis cells from males of E. bilineatus and E. perditus (Fig. 2b). At metaphase II cells, 6 macrochromosomes and 12 microchromosomes were visualized. In the aberrant specimen of E. leechii (LG 1223), metaphase II cells contained either the submetacentric or the acrocentric macrochromosome 6. Analysis of seven diakinesis cells from the mosaic specimen LG 919 showed the presence of 6 macrobivalents, 12 microbivalents (one of them representing the pairing XY), and a probable univalent (Fig. 2b). Analyses after differential staining The Ag-NORs were detected at the distal end of the long arm of pair 2, corresponding to the conspicuous secondary constriction in all five species of Enyalius (Fig. 3b e). Out of 45 Ag-stained metaphases of one specimen of E. bilineatus (LG 815), 37 were heteromorphic with respect to the size of the NOR (Fig. 3b).
Hereditas 136 (2002) Comparati e cytogenetics in Enyalius 53 Fig. 1a e. Karyotypes of species of Enyalius after conventional staining (2n=36, 12M+24m). a E. bibronii female; b E. bilineatus male; c E. iheringii female; d E. leechii female; e E. perditus female. For the sex chromosomes of the opposite sex, see the inset in b, d and e. Bar=10 m.
54 C. E. V. Bertolotto et al. Hereditas 136 (2002) Fig. 2a and b. Cells of the mosaic specimen of Enyalius bilineatus, male, after conventional staining. a Mitotic metaphase with 2n=37 (12M+24m+1B). Note the supernumerary chromosome (small arrow) and the dot-like Y microchromosome (large arrow); b Diakinesis cell presenting 6 macrobivalents, 12 microbivalents (one of them heteromorphic: small arrow), and one univalent (B chromosome: large arrow). Fig. 3a e. Chromosomes of species of Enyalius after differential staining. a C-banded metaphase of E. bilineatus. The labeled arrows indicate: (a) interstitial constitutive heterochromatin on pairs 1 and 2; (b) constitutive heterochromatin at the distal end of the long arm of pair 2. The supernumerary chromosome is indicated by a B; b Ag-NORs in E. bilineatus. Note the heteromorphism of size (arrows); c e Pairs 2 of E. perditus, E. iheringii and E. leechii after Ag-staining, respectively. All five species of Enyalius were characterized by a small amount of constitutive heterochromatin after C-banding, which was mostly restricted to the pericentromeric region of some chromosomes (Fig. 3a). The region of the secondary constriction of pair 2 was also positively stained in some metaphases of E. bibronii, E. bilineatus, and E. perditus. A proximal C-band equidistantly located on pair 1 and 2 was detected in the karyotypes of E. bilineatus and E. bibronii (Fig. 3a). The B chromosome detected in two specimens of E. bilineatus exhibits an intermediate staining between the darkest and the lightest C-positive blocks of the autosomes (Fig. 3a). RBG pattern was obtained for E. bilineatus, and allowed all its macrochromosomes to be unambiguously paired (Fig. 4a). A late replicating region at the distal end of the long arm of pair 2 was also observed. The B chromosome is late-replicating (Fig. 4a, b), and, interestingly, in two metaphases of the mosaic specimen LG 919 (2n=37/38; Table 1) bearing two Bs, only one of them was late replicating (Fig. 4c). DISCUSSION The five species of Enyalius share a common 2n=36 (12M+24m) karyotype which has been described among several taxa within pleurodont Iguania (BICK- HAM 1984; KASAHARA et al. 1996; PELLEGRINO et al. 1999). There is similarity among the macrochromo-
Hereditas 136 (2002) Comparati e cytogenetics in Enyalius 55 Fig. 4a c. RBG pattern from the mosaic specimen of E. bilineatus. a Partial karyotype showing the six pairs of macrochromosomes. A late-replicating B chromosome from a different metaphase is shown (inset); b Metaphase with one B chromosome (arrow); c Metaphase with two Bs (arrows), with only one of them late-replicating (large arrow). somes of the Enyalius species, with the exception of E. bibronii that present an acrocentric pair 6, making it distinct from its congeners, all other Polychrotidae, and related families within pleurodont Iguania that share the conservative karyotype usually with metacentric or submetacentric pair 6. We also detected the presence of a heteromorphic pair 6 in both somatic and meiotic cells of one specimen of E. leechii. This chromosome aberration could be explained by a deletion affecting the short arm of one homologue of this pair. It seems that the macrochromosome pair 6 might be a hot spot for karyotypic evolution in the genus Enyalius. A parallel example was reported in the genus Tropidurus (Tropiduridae) with three closely related species: T. nanuzae and T. amathites having a secondary constriction and NORs in the long arm of pair 6, while in T. di aricatus these regions are located in the short arm of the same pair due to the occurrence of a pericentric inversion (KASAHARA et al. 1987). All five species of Enyalius were very similar with respect to location of the NORs and the amount and distribution of constitutive heterochromatin. The distal end of the long arm of pair 2 bearing the NORs and a positive C-band has been described across several species of pleurodont Iguania families: Tropiduridae (Tropidurus, KASAHARA et al. 1987, 1996; Strobilurus, RODRIGUES et al. 1989; Liolaemus, BERTOLOTTO et al. 1996), Polychrotidae (Pristidactylus, PELLEGRINO 1993; Urostrophus, PELLEGRINO et al. 1999), and Phrynosomatidae (Sceloporus, PORTER et al. 1994), indicating that it is a conservative region shared by these related families. Studies involving comparative analyses of microchromosomes are usually limited because their reduced size prevents precise definition of their morphology in most cases, with few exceptions (PINNA- SENN et al. 1987; PELLEGRINO et al. 1994; BERTOLOTTO et al. 1996; KASAHARA et al. 1996). In all species of Enyalius, the 24 microchromosomes seem to be acrocentrics, but E. perditus has at least two biarmed pairs. Increase in quality of the chromosome preparations should allow these chromosomes to be used more often in comparative analyses, and indeed facilitate the detection of mechanisms of sex determination that involve these microchromosomes. A mechanism of the XX:XY type was detected in E. bilineatus, E. leechii, ande. perditus. A heteromorphic microbivalent, representing the pairing of X and Y, was observed in meiotic cells of E. bilineatus and E. perditus, and allowed us to evaluate the size of the X chromosome. In pleurodont Iguania, both simple (XX:XY) and multiple (X 1 X 1 X 2 X 2 :X 1 X 2 Y) mechanisms of sex determination involving microchromosomes occur, including the polychrotids Pristidactylys (PELLEGRINO 1993), Anolis (GORMAN and ATKINS 1968; GORMAN and STAMM 1975; our unpublished data), Polychrus (BERTOLOTTO et al. 2001) and Urostrophus (PELLEGRINO et al. 1999).
56 C. E. V. Bertolotto et al. Hereditas 136 (2002) Supernumerary chromosomes of intermediate size between the microchromosomes and macrochromosomes are present in two specimens of E. bilineatus. They do not exhibit a heterochromatic pattern, but they are almost entirely late-replicating after R-banding, which is typical for the heterochromatin of the Bs. Few reports of occurrence of supernumerary chromosomes have been made among lizards, compared to those from plants and other animals. Besides the present study, these chromosomes have been found in ten other genera, which represent eight different families including the polychrotid Anolis (GORMAN et al. 1968). The function, composition, and origin the supernumerary chromosomes are not completely known, with the most intriguing questions regarding their origin. Several molecular cytogenetic studies utilizing restriction endonucleases, fluorochromes, in situ hybridization, and chromosome microdissection techniques have been used to elucidate the composition, structure, origin and evolution of the supernumerary chromosomes (LOPEZ-LEON et al. 1994; BRINKMAN et al. 2000; MAISTRO et al. 2000). The present study extends the knowledge on karyotypes of the yet poorly known lizard family Polychrotidae. Considering that the relationships within this family are still unresolved, studies employing banding techniques on the remained taxa should allow the identification of synapomorphies that can be useful in a phylogenetic context. ACKNOWLEDGEMENTS The authors are grateful to Maria José de Jesus Silva, Vinícius Xavier da Silva, Gabriel Skuk, Dante Pavan, Patrícia Narvaes, José Manoel Martins, Claudia Silva, Cristiano Nogueira, Paula Valdujo and Sandra Favorito for collecting specimens, and to Dr. Tien Hsi Chu and Mrs. Miriam Romeo for technical assistance. We thank Dr. Elizabeth Sinclair for helpful comments in the early versions of the manuscript. Grants for this study were provided by Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) and Consórcio Nacional de Engenheiros Consultores (CNEC). REFERENCES Bertolotto CEV, Rodrigues MT, Skuk G and Yonenaga- Yassuda Y, (1996). Comparative cytogenetic analysis with differential staining in three species of Liolaemus (Squamata, Tropiduridae). Hereditas 125: 257 264. Bertolotto CEV, Rodrigues MT and Yonenaga-Yassuda Y, (2001). Banding patterns, multiple sex chromosomes system and localization of telomeric (TTAGGG)n sequences by FISH on two species of Polychrus (Squamata, Polychrotidae). Caryologia 54: 217 226. Bickham JW, (1984). Patterns and modes of chromosomal evolution in reptiles. In: Chromosomes in evolution of eukaryotic groups (eds A Sharma and A Sharma). CRC Press, Florida, p. 13 40. Brinkman JN, Sessions SK, Houben A and Green DM, (2000). Structure and evolution of supernumerary chromosomes in the Pacific giant salamander, Dicamptodon tenebrosus. Chromosome Res. 8: 477 485. Dutrillaux B and Couturier J, (1981). La pratique de l analyse chromosomique. Masson, Paris. Estes R, de Queiroz K and Gauthier J, (1988). Phylogenetic relationships within Squamata. In: Phylogenetic relationships of the lizard families (eds E Estes and G Pregill). Stanford Univ., California, p. 119 281. Etheridge R and de Queiroz K, (1988). A phylogeny of Iguanidae. In: Phylogenetic relationships of the lizard families (eds R Estes and G Pregill). Stanford Univ., California, p. 283 367. Frost D and Etheridge R, (1989). A phylogenetic analysis and taxonomy of iguanian lizards (Reptilia: Squamata). Misc. Publ. Univ. Kansas. Mus. Nat. Hist. 81: 65. Gorman GC and Atkins L, (1968). Confirmation of an X-Y sex determining mechanism in lizards (Anolis). Copeia 1: 159 160. Gorman GC and Stamm B, (1975). The Anolis lizards of Mona, Redonda, and La Blanquilla: chromosomes, relationships, and natural history notes. J. Herpet. 9: 197 205. Gorman GC, Thomas R and Atkins L, (1968). Intra- and interspecific chromosome variation in the lizard Anolis cristatellus and its closest relatives. Breviora 293: 1 13. Jackson JF, (1978). Differentiation in the genera Enyalius and Strobilurus (Iguanidae): implications for Pleistocene climatic changes in eastern Brazil. Arq. Zool. S. Paulo 30: 1 79. Kasahara S, Yonenaga-Yassuda Y and Rodrigues MT, (1987). Geographical karyotypic variations and chromosome banding patterns in Tropidurus hispidus (Sauria, Iguanidae) from Brazil. Caryologia 40: 43 57. Kasahara S, Pellegrino KCM, Rodrigues MT and Yonenaga-Yassuda Y, (1996). Comparative cytogenetic studies of eleven species of the Tropidurus torquatus group (Sauria, Tropiduridae), with banding patterns. Hereditas 125: 37 46. Lopez-Leon MD, Neves N, Schwarzacher T, Heslop-Harrison TS, Hewitt GM and Camacho JPM, (1994). Possible origin of abchromosomededuced from its DNA composition using double FISH technique. Chromosome Res. 2: 87 92. Maistro EL, Oliveira C and Foresti F, (2000). Cytogenetic analysis of A- and B-chromosomes of Prochilodus lineatus (Teleostei, Prochilodontidae) using different restriction enzyme banding and staining methods. Genetica 108: 119 125. Olmo E, (1986). Reptilia. In: Animal Cytogenetics (ed. B John). Gebruder Borntraeger, Berlin, Vol. 4/3A, p. 1 100. Pellegrino KCM, (1993). Caracterização cromossômica em 16 espécies das famílias Tropiduridae, Polychrotidae e Gekkonidae (Sauria) pela aplicação de técnicas de coloração diferencial. Rev. Bras. Genet. 16: 1140 1141(Thesis abstract). Pellegrino KCM, Yonenaga-Yassuda Y and Rodrigues MT, (1994). Cytogenetic studies in six species of Tropiduridae (Sauria). Brazil. J. Genetics 17: 401 408. Pellegrino KCM, Bertolotto CEV, Rodrigues MT and Yonenaga-Yassuda Y, (1999). Banding patterns, hetero-
Hereditas 136 (2002) morphic sex chromosomes and Ag-stained NORs after pachytene stage in the meiosis of the Brazilian lizard Urostrophus vautieri (Squamata, Polychrotidae). Caryologia 52: 21 26. Pinna-Senn E, Tada IE and Lisanti JA, (1987). Polymorphism of the microchromosomes and the nucleolar organizer region in Pristidactylus achalensis (Sauria: Iguanidae). Herpetological 43: 120 127. Porter CA, Haiduk MW and Queiroz K, (1994). Evolution and phylogenetic significance of ribosomal gene location Comparati e cytogenetics in Enyalius 57 in chromosomes of Squamata reptiles. Copeia 2: 302 313. Rodrigues MT, Yonenaga-Yassuda Y and Kasahara S, (1989). Notes on the ecology and karyotypic description of Strobilurus torquatus (Sauria, Iguanidae). Rev. Bras. Genet. 12: 747 759. Yonenaga-Yassuda Y, Kasahara S, Chu TH and Rodrigues MT, (1988). High-resolution RBG-banding pattern in the genus Tropidurus (Sauria, Iguanidae). Cytogenet. Cell Genet. 48: 68 71.