RESUMO
Recent molecular phylogenetic analyses have shown that the Mugil curema Valenciennes, 1836 species complex includes M. incilis Hancock, 1830, M. thoburni (Jordan & Starks, 1896) and at least four "M. curema" mitochondrial lineages, considered as cryptic species. The cytogenetic data on some representatives of the species complex have shown a high cytogenetic diversity. This research reports the results of cytogenetic and molecular analyses of white mullet collected in Ecuador. The analyzed specimens were molecularly assigned to the Mugil sp. O, the putative cryptic species present in the Pacific Ocean and showed a 2n = 46 karyotype, which is composed of 2 metacentric and 44 subtelocentric/acrocentric chromosomes. This karyotype is different from the one described for M. incilis (2n = 48) and from those of the two western Atlantic lineages Mugil curema (2n = 28), and Mugil margaritae (2n = 24). Data suggest the need for a morphological analysis to assign a species name to this Pacific lineage.
RESUMO
This study reports the description of the karyotype of Mugil incilis from Venezuela. The chromosome complement is composed of 48 acrocentric chromosomes, which uniformly decrease in size. Therefore, the homologues can not be clearly identified, with the exception of one of the largest chromosome pairs, classified as number 1, whose homologues may show a subcentromeric secondary constriction, and of chromosome pair number 24, which is considerably smaller than the others. C-banding showed heterochromatic blocks at the centromeric/pericentromeric regions of all chromosomes, which were more conspicuous on chromosomes 1, given the C-positive signals include the secondary constrictions. AgNO3 and fluorescent in situ hybridization (FISH) with 45S rDNA demonstrated that the nucleolus organizer regions are indeed located on the secondary constrictions of chromosome pair number 1. FISH with 5S rDNA revealed that the minor ribosomal genes are located on this same chromosome pair, near the NORs, though signals are closer to the centromeres and of smaller size, compared to those of the major ribosomal gene clusters. This is the first description of co-localization of major and minor ribosomal genes in the family. Data are discussed from a cytotaxonomic and phylogenetic perspective.
Se presenta la primera descripción del cariotipo de Mugil incilis de Venezuela. El complemento cromosómico está compuesto por 48 cromosomas acrocéntricos uniformemente decrecientes en tamaño. Por lo tanto, los homólogos no pueden ser claramente identificados, con excepción de uno de los pares de mayor tamaño, clasificado como número 1, cuyos homólogos poseen una constricción secundaria subcentromérica, y el par de cromosomas número 24, considerablemente más pequeño que los otros. El bandeo-C reveló bloques heterocromáticos en las regiones centroméricas/pericentroméricas de todos los cromosomas, más conspicuas en el cromosoma 1 en el que las señales C-positivas se encuentra localizada precisamente en la constricción secundaria. La tinción con AgNO3 y la Hibridación Fluorescente in situ (FISH) con sonda 45S rDNA revelaron que las regiones organizadoras del nucléolo están ciertamente localizadas sobre la constricción secundaria del cromosoma número 1. FISH con 5S rDNA reveló que los genes ribosomales menores están ubicados en este mismo par cromosómico, en posición proximal a las NORs, aunque cercanas al centrómero y de menor tamaño en comparación con los clúster de genes ribosomales mayores. Ésta es la primera descripción de co-localización de genes ribosomales mayores y menores en la familia Mugilidae. Los datos se discuten bajo perspectivas citotaxonómicas y filogenéticas.
Assuntos
Animais , Aberrações Cromossômicas , Peixes/classificação , Genes/genética , Ribossomos/genéticaRESUMO
This study reports the isolation and characterization of 11 polymorphic microsatellites from a sand smelt (Atherina boyeri) genomic library. Enrichment was performed with di-, tri- and tetranucleotide motifs following the FIASCO procedure (fast isolation by AFLP of sequences containing repeats). All loci were found to be in linkage and in Hardy-Weinberg equilibrium. This represents the first microsatellite isolation for the family Atherinidae and the isolated loci were accordingly tested on four additional species of the family: two recognized (A. presbyter and A. hepsetus) and two proposed ('punctata' and 'non-punctata' forms). Moreover their cross-species suitability on Menidia menidia, belonging to the same order but to the family Atherinopsidae, was also tested.
RESUMO
This study reports the first description of the karyotype of Agonostomus monticola, a species belonging to a genus which is considered to be the most primitive among living mugilid fish. Specimens from Panama and Venezuela were cytogenetically analysed by conventional chromosome banding (Ag and base-specific-fluorochrome staining, C-banding) and by fluorescent in situ hybridization (FISH). Agonostomus monticola showed a chromosome complement of 2n = 48, composed of 23 acrocentric and one subtelocentric chromosome pairs and a pericentromeric distribution of the C-positive heterochromatin in all chromosomes. Major ribosomal genes were found to be located on the short arms of the subtelocentric chromosome pair number 24 and minor ribosomal genes in a paracentromeric position of a single medium-sized chromosome pair. All these observed cytogenetic features are similar to those previously described in four representatives of two genera, Liza and Chelon, which are considered to be among the most advanced in the family. Thus, this karyotypic form might represent the plesiomorphic condition for the mullets. This hypothesis regarding the plesiomorphic condition, if confirmed, would shed new light on the previously inferred cytotaxonomic relationships for the studied species of Mugilidae, because the karyotype with 48 acrocentric chromosomes, which has been so far regarded as primitive for the family, would have to be considered as derived.
Assuntos
RNA Ribossômico 18S/análise , RNA Ribossômico 5S/análise , Smegmamorpha/classificação , Smegmamorpha/genética , Animais , Antígenos Nucleares/análise , Bandeamento Cromossômico , Cromossomos/genética , Cromossomos/ultraestrutura , DNA Ribossômico/análise , Evolução Molecular , Heterocromatina/genética , Hibridização in Situ Fluorescente , Cariotipagem , Panamá , RNA Ribossômico 18S/genética , RNA Ribossômico 5S/genética , Especificidade da Espécie , VenezuelaRESUMO
Lutjanidae, commonly known as snappers, includes 105 species, grouped in four subfamilies. In spite of the high number of species and of its worldwide distribution, the family has been little investigated and the phylogenetic relationships among some of its genera and species are still cause for debate. Only a small number of the species has been cytogenetically analysed. This study reports the first description of the karyotype of Rhomboplites aurorubens as well as data concerning the distribution of the constitutive heterochromatin and the location of the 18S rRNA and the 5S rRNA genes. Specimens of Ocyurus chrysurus from Venezuela were also investigated for the same cytogenetic features. Both species have a 48 uniarmed karyotype, but R. aurorubens has a single subtelocentric chromosome pair, the smallest of the chromosome complement, among the other acrocentric chromosomes. The C-positive heterochromatin is limited to the pericentromeric regions of all chromosomes. Both species show a single chromosome pair bearing the Nucleolus Organizer Regions, but NORs are differently located, in a terminal position on the short arms of the smallest chromosomes in R. aurorubens and in a paracentromeric position in a chromosome pair of large size in O. chrysurus. In O. chrysurus, the 5S rDNA gene cluster is located on a medium-sized chromosome pair, whereas in R. aurorubens it is syntenic with the 18S rDNA gene cluster on chromosome pair number 24. The obtained cytogenetic data, along with previous cytogenetic, morphological and molecular data for the family, reinforce the proposal to synonymize genus Ocyurus with Lutjanus. A review of Lutjanidae cytogenetics is also included.
Lutjanidae, comumente conhecidos como snappers, inclui 105 espécies, reunidas em quatro subfamílias. A despeito do grande número de espécies e de sua distribuição mundial, a família tem sido pouco estudada e as relações filogenéticas entre alguns de seus gêneros e espécies ainda é motivo de debates. Apenas um pequeno número de espécies foi citogeneticamente analisada. Esse estudo apresenta a primeira descrição do cariótipo de Rhomboplites aurorubens assim como dados relativos à distribuição de heterocromatina constitutiva e localização dos genes 18S rRNA e 5S rRNA. Espécimes de Ocyurus chrysurus da Venezuela foram também analisados quanto às mesmas características citogenéticas. Ambas as espécies têm cariótipos compostos de 48 cromossomos com um único braço, entretanto R. aurorubens tem um único par de cromossomos subtelocêntrico, o menor do complemento cromossômico, entre os outros cromossomos acrocêntricos. A heterocromatina C-positiva é limitada à região pericentromérica de todos os cromossomos. Ambas as species apresentam um único par com Regiões Organizadoras de Nucléolo, mas as RONs são localizadas em posições diferentes, em posição terminal no braço curto dos menores cromossomos de R. aurorubens e em posição paracentromérica no braço longo de um par de cromossomos grandes de O. chrysurus. Em O. chrysurus, os genes 5S rDNA estão localizados em um par de cromossomos de tamanho médio, enquanto em R. aurorubens eles são sintenicamente localizados com os genes 18S rDNA no par de cromossomos número 24. Os dados citogenéticos obtidos, junto com os dados morfológicos e moleculares disponíveis para a família reforçam a proposta de sinonimizar o gênero Ocyurus com Lutjanus. Uma revisão da citogenética dos Lutjanidae é também apresentada
Assuntos
Animais , Perciformes/genética , Citogenética/classificação , Heterocromatina , Genes de RNAr/genéticaRESUMO
In the present study, three species of Lutjaninae, Lutjanus analis, L. griseus and L. synagris, were analyzed by conventional Giemsa staining, C-banding and silver staining, to reveal active Nucleolus Organizer Regions (NORs). Fluorescent in situ hybridization (FISH) was also applied to establish the number and location of the ribosomal gene clusters (18S and 5S rRNA genes). Counts of diploid metaphasic cells revealed a diploid modal chromosome complement composed of 48 acrocentric chromosomes in both L. analis and L. griseus. Two cytotypes were observed in L. synagris: cytotype I, with 2n=48 acrocentric chromosomes, found in 19 specimens, and cytotype II, with 46 acrocentric chromosomes and one large metacentric, found in two specimens. The large metacentric, which possibly originated from a Robertsonian rearrangement, was not found to be sex-related. In the three species, constitutive heterochromatin is located in the centromeres of all chromosomes. NORs were detected on the short arms of a single chromosome pair, number 24 in L. analis and number 6 in both cytotypes of L. synagris. In L. griseus, a polymorphism of the NORs number was detected, by both Ag-staining and FISH, as females show a maximum of three NORs, and males a maximum of six NORs. In all species, minor ribosomal genes were found located on a single chromosome pair. The obtained data, along with those previously reported for other five Lutjanidae species, show that a general chromosome homogeneity occurs within the family, but that derived karyotypes based on Robertsonian rearrangements as well as multiple and variable NORs sites can also be found.
No presente estudo três espécies de Lutjaninae, Lutjanus analis, L. griseus e L. synagris foram analisadas através da coloração convencional com Giemsa, banda C e coloração com nitrato de prata para identificar as Regiões Organizadoras de Nucléolo (NORs) ativas. Hibridação fluorescente in situ (FISH) foi também aplicada para estabelecimento do número e localização dos agrupamentos de genes ribossômicos (18S e 5S rRNA). A contagem de células metafásicas revelou um número diplóide modal de 48 cromossomos acrocêntricos em L. analis e L. griseus. Dois citótipos foram observados em L. synagris: citótipo I com 2n=48 cromossomos acrocêntricos, encontrado em 19 espécimes, e citótipo II com 46 cromossomos acrocêntricos e um grande metacêntrico, encontrado em dois espécimes. O grande metacêntrico, que possivelmente se originou por um rearranjo Robertsoniano, não está relacionado com o sexo. Nas três espécies a heterocromatina constitutiva está localizada nas regiões centroméricas de todos os cromossomos. NORs foram detectadas no braço curto de um único par cromossômico, número 24 em L. analis e número 6 em ambos os citótipos de L. synagris. Em L. griseus, um polimorfismo de número de NORs foi observado, após coloração com prata e por FISH, as fêmeas apresentaram um máximo de três NORs e os machos um máximo de seis NORs. Em todas as espécies os genes ribossômicos 5S foram encontrados em um único par cromossômico. Os dados obtidos, somados aos demais previamente publicados para cinco outras espécies de Lutjanidae, mostram que na família há uma homogeneidade cromossômica, porém também são encontrados cariótipos derivados, originados por rearranjos Robertsonianos, assim como pela ocorrência de sítios múltiplos e variados de NORs.
Assuntos
Animais , Biodiversidade , Citogenética , Especificidade da Espécie , Polimorfismo Conformacional de Fita Simples , Peixes/classificaçãoRESUMO
A cytogenetical study was carried out on 34 specimens of the European bitterling Rhodeus amarus (Teleostei: Cyprinidae, Acheilognathinae) from four rivers of the Venice district (NE Italy). This allochthonous fish species was accidentally introduced in the North-East of Italy about 20 years ago and is now rapidly spreading all over the rivers of the Northern part of the country. All the studied specimens are characterised by the same karyotype (2n = 48: 8M + 20SM + 20ST), i.e., the typical one of the native populations of the species. However, a polymorphism in the number of NOR bearing chromosomes has been found. In fact, in addition to the main species-specific NORs, on the short arms of chromosome pair 7, two to five additional 18S rDNA sites have been revealed by FISH in different specimens. Sequential staining with silver nitrate, chromomycin A(3) and DAPI revealed that most of the additional sites are inactive and CMA(3)-positive. Data herein reported confirm that in spite of an overall morphological karyological conservativeness, significant differences for the finer cytogenetic features can be found within the Acheilognathinae with the 2n = 48 and NF = 76 karyotype.
Assuntos
Cyprinidae/genética , Animais , Cromossomos/genética , Citogenética , Hibridização in Situ Fluorescente , Itália , CariotipagemRESUMO
Se presentan los resultados del análisis comparativo citogenético y aloenzimático entre las especies simpátricas Mugil rubrioculus y M. curema de Venezuela. Los especímenes de M. rubrioculus presentan un cariotipo con 2n=48 cromosomas exclusivamente acrocéntricos (NF=48), NORs intersticiales localizados en el par cromosómico número 8 y heterocromatina constitutiva distribuida en posición pericentromérica en todos los cromosomas. Los especímenes de M. curema presentan características citogenéticas significativamente diferentes de M. rubrioculus en términos de número cromosómico y morfología (2n=24 cromosomas de dos brazos y NF=48) y localización de las NORs (región terminal del par metacéntrico más grande). El análisis electroforético en gel de almidón de 20 loci presuntivos reveló una diferenciación genética reducida entre las dos especies. De hecho, aún cuando un total de diez alelos específicos hayan sido identificados, no hay loci que no compartan alelos entre las dos especies y el valor de distancia genética (Nei) obtenido (D= 0,060) es más bajo que el obtenido entre otras especies congenéricas de mugílidos. Así, los datos citogenéticos y los alozímicos indican diversos grados de divergencia entre el M. rubrioculus y M. curema. Esto podría reflejar una subestimación de la divergencia molecular por variación críptica o diferentes tasas de evolución molecular y cromosómica. De cualquier manera, este estudio confirma el poder de los datos cariotípicos para discriminar especies de Mugilidae.
Assuntos
Cromossomos , Análise Citogenética , Genética , Biologia , VenezuelaRESUMO
The family Mugilidae (Pisces, Mugiliformes) includes species which are present in all tropical and temperate regions. Six species, Chelon labrosus, Mugil cephalus, Liza aurata, L. ramada, L. saliens, Oedalechilus labeo, are commonly found in the Mediterranean. These species have been widely studied through morphological, biochemical, and molecular markers. However, their phylogenetic relationships, and therefore the assumed monophyly of Liza species, still remain unclear: To further investigate this topic, gene-enzyme systems and sequences of the partial 16S rRNA mitochondrial gene were analyzed in Italian samples of all six Mediterranean species. The phylogenetic reconstructions indicated M. cephalus as being the most divergent species and the existence of a main cluster including all the Mediterranean species of Liza and C. labrosus. The parametric bootstrap approach adopted to test alternative phylogenetic hypotheses indicated that the Mediterranean species of Liza do not form a monophyletic group exclusive of Chelon.