Susanna Salvadori

Colocalization of (TTAGGG)n telomeric sequences and ribosomal genes in Atlantic eels.

The distribution of (TTAGGG)n telomeric repeats was studied in chromosomes of two Atlantic eels,Anguilla anguilla andA. rostrata. We found that these sequences hybridize to all the telomeres but also to the entire nucleolar organizer region (NOR) localized in both species at the short arm of chromosome 8. This was considered to be due to the interspersion of telomeric sequences within the NOR ones. Whatever the significance of this interspersion may be, it seems to be limited toA. anguilla andA. rostrata since inMuraena helena (family muraenidae), which also belongs to the Anguilliformes, no telomeric hybridization signals were found along the NOR regions.

The characterization of Muraena Helena L. mitotic chromosomes: karyotype, C-banding, nucleolar organizer regions, and in situ digestion with restriction endonucleases

We investigated the chromosome complement of Muraena Helena L. using C-banding, nucleolar organizer region silver staining, and restriction endonuclease digestion. We found a diploid number identical to that previously found in other Muraenidae (2n = 42). C-banding revealed the presence of constitutive heterochromatin in the centromeres of all chromosomes as well as in most telomeres of acrocentric chromosomes. Nucleolar organizer regions were detected only on the short arm of chromosome 7. Digestion with either HaeIII, MboI, or DdeI restriction endonucleases produced a clearcut, specific banding pattern for each enzyme and indicated the existence of at least two different classes of highly repetitive DNAs. The short arm of chromosome 7 varied in size and staining characteristics.

Major and 5S ribosomal sequences of the largemouth bass Micropterus salmoides (Perciformes, Centrarchidae) are localized in GC-rich regions of the genome

Major and 5S ribosomal genes have been localized in the chromosomes of Micropterus salmoides. By C-banding, Ag-staining, CMA3-staining and 45S and 5S fluorescence in-situ hybridization (FISH), we demonstrate that the 45S and 5S ribosomal genes are clustered in two different chromosome pairs and both are located in heterochromatic GC-rich regions. PCR amplification and sequencing of the 5S intergenic non-transcribed sequences have allowed us to identify variability essentially due to a trinucleotide tandem repeat (GCT).

Replication banding in two Mediterranean moray eels: chromosomal characterization and comparison

Early and late replication bandings have been obtained by in vitro BrdU incorporation in the Mediterranean Muraenidae species Muraena helena and Gymnothorax unicolor, and used to characterize their karyotypes. A comparative analysis of the banding patterns allowed to point out high karyotype similarity as well as chromosome rearrangements that occurred in karyotype evolution between these species.

The characterization of somatic chromosomes of Gymnothorax unicolor (Delaroche, 1809) by C-banding and NOR staining (Osteichthyes, Anguilliformes)

The diploid chromosome number of Gymnothorax unicolor (Delaroche, 1809) is 2n=42, the karyotype comprising six pairs of meta-submetacentric and fifteen pairs of acrocentric chromosomes. C-positive chromatin is present in the centromeres of all chromosomes as well as in the paracentromeric regions of some chromosomes. A nucleolar organizer region was identified on the long arm of chromosome 9, near the centromere. This region is also positive to C-banding.Cytotaxonomical relationships are evidenced between the described karyotype and that of the related species Muraena helena.

Mitochondrial DNA variability in Anguilla anguilla and phylogenetical relationships with congeneric species

Abstract To obtain genetic molecular markers, valuable for the explanation of intraspecific variability, we have sequenced and compared a region of the mitochondrial cytochrome b (Cyt‐b) of seven European eels, Anguilla anguilla (L.), from four different Italian sites. The alignment of the seven sequences shows the existence of 14 variable sites, due to nucleotidic substitutions which are evolutively neutral. Alignment of the A. anguilla Cyt‐b sequences with the corresponding sequences from A. rostrata and A. japonica (both available in the EMBL DNA database) identifies some interspecific differences. A phylogenetic analysis by the neighbour‐joining method clearly confirms the genetic separation and the monophyletic origin of the three species. Six and twenty base substitutions, which are common to all the samples of A. anguilla, can be diagnostic candidates for the interspecific differences of this species with A. rostrata and A. japonica, respectively.

Colocalization of the ribosomal gene families in Conger conger (Anguilliformes, Congridae)

The location of the major and minor ribosomal gene families in the conger eel (Conger conger) was investigated by in situ hybridization and CMA3 staining. The two gene families were localized in only one chromosome pair, on the short arm of pair 19, in an entirely CMA3‐positive region. Among the Anguilliformes, C. conger is the only species that shows the presence of the two gene families in the same chromosomal region.

B chromosomes in Crustacea Decapoda

Among crustacean Decapoda numerical chromosome variability is frequent, and it has been hypothesized that the presence of supernumerary chromosomes accounts for this variability. Thanks to the improvement of cytogenetic analysis by chromosomal banding techniques, supernumerary B chromosomes (Bs) have been demonstrated in Nephrops norvegicus, Homarus americanus,Palinurus elephas and P. mauritanicus, belonging to different crustacean families. In all four species Bs were variable in number, mainly heterochromatic and undigested by various endonucleases, and in meiosis they showed non-Mendelian segregation. Compared to the other chromosomes of the complement, the Bs are very small in almost all species, but some of them were very large in N. norvegicus.

Developmental changes in the content of dopamine in the olfactory bulb of the European eel (Anguilla anguilla)

The concentrations of dopamine (DA) and of its major metabolite, dihydroxyphenylacetic acid (DOPAC), were measured in discrete areas of the eel brain. To investigate the developmental changes in the content of DA and DOPAC, the assays were performed in yellow eels (i.e. at the feeding stage) and silver eels (i.e. at the migratory stage). DA and DOPAC were unevenly distributed in the eel brain. In yellow eels, the concentration of DA was highest (16-19 pmol/mg protein) in the olfactory bulb (OB), mesencephalic tectum-diencephalon (MT-D) and medulla oblongata (MO) and lowest in the cerebellum (CB, 1 pmol/mg protein), whereas intermediate values were measured in the telencephalon (TE; 10 pmol/mg protein). The metabolic rate of DA, as reflected by the DOPAC/DA ratio, was highest in the OB and CB, with progressively smaller values being observed in the TE, MT-D, and MO. A significant increase in the concentrations of DA (+80%) and DOPAC (+122%) was observed in the OB of silver eels compared with yellow eels, whereas no significant differences were detected in the concentrations of DA and DOPAC in the other brain areas as a function of the developmental stage. The results are discussed in terms of the possible involvement of environmental, behavioral and developmental factors.

Karyotype, C- and G-banding, and nucleolar organizer regions of Conger conger (Osteichthyes, Anguilliformes)

Abstract The diploid chromosome number of Conger conger L. was found to be 2n = 38, with the karyotype consisting of four pairs of metacentric, two of submetacentric and thirteen of acrocentric chromosomes. C‐ and G‐banding allowed the identification of homologous chromosomes. NOR was identified on the short arm of the smallest acrocentric pair.