Selection and characterization of somatic hybrids between Lycopersicon esculentum and Lycopersicon peruvianum

Somatic hybrids of the cultivated tomato, Lycopersicon esculentum, and a wild species, L. peruvianum, were obtained by fusion of leaf protoplasts from both species in the presence of poly-ethylene-glycol (PEG) or in an electric field. The somatic hybrids were selected on the basis of kanamycin resistance of L. esculentum and the plant regeneration capacity of L. peruvainum. Chromosome counts in root tips and the determination of the number of chloroplasts in guard cell pairs revealed that the majority of these hybrids was tetraploid (2n = 4x = 48). The remaining hybrids were at the hexaploid level with chromosome numbers between 64 and 72. The hybrid nature of the regenerated plants was confirmed by analysis of isozyme markers and by their morphology. Most hybrids did flower and set fruits and seeds after selfing. According to RFLP analysis 6 out of the 10 hexaploid hybrids contained two genomes of L. esculentum and four genomes of L. peruvianum. One of these hexaploids had genomes of two different L. peruvianum genotypes and was therefore considered to be derived from a triple protoplast fusion. The hexaploid plants were less fertile than the tetraploids and more resembled L. peruvianum.     

Cytogenetic studies of 1-29 translocation carrying cows and their embryos

An examination has been made of embryos from infertile 1-29 translocation carrying heifers. Cytogenetic measurements of C-banded chromosomes from these cattle, together with those from fertile 1-29 cows, have been made and compared with those from normal karyotypes. There are relative differences between normal animals and translocation carriers in the ratios of total to C-banded material throughout the karyotypes: their possible effects on mitosis and meiosis are discussed. Of the embryos recovered from the infertile heifers, one did not survive transplantation and others had various indications of inviability.     

The genetics of sympatric Arctic charr [Salvelinus alpinus (L.)] populations from Loch Rannoch, Scotland

Two morphologically and ecologically distinct forms of Arctic charr, Salvelinus alpinus , are found in Loch Rannoch, Scotland. The differences in morphology are adaptations to different modes of life, one being pelagic, the other benthic. Both forms have been the subjects of extensive genetic studies including cytogenetics, nuclear and mitochondrial DNA analysis, and protein electrophoresis. Significant differences between the two forms are revealed by some techniques but not others and provide evidence for the reproductive isolation of these two morphs. The findings are discussed in relation to the derivation of sympatry and the phylogenetics of Arctic charr.     

NUCLEOTYPIC EFFECT IN HOMEOTHERMS: BODY-MASS-CORRECTED BASAL METABOLIC RATE OF MAMMALS IS RELATED TO GENOME SIZE

The body-mass-corrected rate of basal metabolism in mammals is found to be negatively correlated with genome size, which is possibly linked to average cell size. The correlation, already significant at the species level (r_sp = –0.61, P < 0.0002), gradually strengthens as mean values for higher taxonomic levels (genera, families, and orders) are substituted in place of the species points (r_gen = –0.65, P < 0.0002; r_fam = –0.71, P < 0.0004; r_ord = –0.81, P < 0.008). This finding suggests that a sizeable part of the mammalian (above 25% of human) genome can be used for evolutionary adjustment of metabolic rate resulting from nucleotypic effect independently of body size. The total variance of mammalian genome-size values is found to be divided into two parts: within genera (43%) and taxonomic levels higher than order (57%), with no tangible variance being added between these taxonomic levels; whereas the body-mass-corrected rate of basal metabolism varies mainly at family (42%) and order (53%) levels. The only order for which there seems to be a necessary minimum of data for intraorder analysis (rodents) shows a not statistically significant correlation at the species level (r_sp = –0.47; P < 0.09), significant at the genus level (r_gen = –0.74; P < 0.04), and very high at the family level (r_fam = –0.98; P < 0.03). The concept of ultimate (distant) characters consolidation is proposed. In birds, with average genome sizes 40% of those of mammals, and similarly narrower ranges both of genome sizes and of body-mass-corrected metabolic rates, the correlation was not significant.     

Evolutionary implications of meiotic chromosome behavior, reproductive biology, and hybridization in 6x and 9x cytotypes of Andropogon gerardii (Poaceae)

Andropogon gerardii, big bluestem, has 60 and 90 chromosome cytotypes. Meiosis in the hexaploid was shown to be regular, although some secondary associations of bivalents form. Meiosis in the enneaploid (2n = 9z = 90) is irregular, leading to most gametes having unbalanced chromosome complements. Both cytotypes show considerable self-incompatibility. Cytotypes crossed freely, forming a variety of fertile euploids and aneuploids. Indistinguishable exomorphology, intermixing in natural populations, and compatibility suggest that A. gerardii is best understood as a cytotypically complex single species.     

The effect of B chromosomes and T-DNA on chromosomal variation in callus cells and regenerated roots of Crepis capillaris

The chromosome behaviour has been compared in three Crepis capillaris callus culture lines and the roots regenerated from these calli. The calli were obtained from explants derived from plants without and with two B chromosomes and the hairy roots were obtained from plants transformed with Agrobacterium rhizogenes. Cytological studies demonstrated that the presence of additional DNA as B chromosomes or as T-DNA had an influence on the numerical and structural variability of the standard chromosome in long-term callus cultures and in regenerated organs. The callus with two B chromosomes displayed higher levels of polyploidyzation than callus without B chromosomes. The roots regenerated from both these calli were only diploid, while roots regenerated from transformed callus were also polyploid. This revised version was published online in June 2006 with corrections to the Cover Date.     

Karyotypic study of titi monkeys,Callicebus moloch brunneus

A karyotypic study on a subspecies of the dusky titi,Callicebus moloch brunneus, was carried out and a third karyotype ofC. moloch was discovered. The chromosome number of this subspecies is 48. The autosomes consist of 5 subtelocentric, 5 submeta- or metacentric, and 13 acrocentric chromosome pairs. The X chromosome and the Y chromosome are submetacentric and metacentric, respectively. A comparative study with other subspecies of theC. moloch group (i.e.,C. m. cupreus andC. m. ornatus with 2n=46 andC. m. donacophilus with 2n=50) suggests that the karyotype ofbrunneus occupies a position intermediate between the two other karyotypes ofC. moloch, but nearer to that of 2n=50. The presumed total differences betweenbrunneus andcupreus comprise one Robertsonian rearrangement, one centromeric transposition and four pericentric inversions, and those betweenbrunneus anddonacophilus involve one translocation or breakage (possibly corresponding to two events, that is, one Robertsonian rearrangement and one centromeric transposition).     

C-banding in 6x-Triticale xSecale cereale L. hybrid cytogenetics

Summary The meiotic behaviour of F₁ hybrids of hexaploid Triticale that differed in their genotypic or chromosomic constitution, and diploid rye, was investigated. Meiotic analysis were done by Feulgen and C-banding staining methods. A differential desynaptic effect in the hybrids was detected and explained in terms of genetic differences in pairing regulators. The high homoeologous pairing (A-B wheat chromosomes and wheat-rye chromosomes) observed in the hybrids can be explained in terms of an inhibition of the effect of a single dose of thePh allele of the 5B chromosome produced by two doses of the 5R chromosome. The higher homoeologous pairing detected in the hybrid 188 x Canaleja could be the overall result of the balance between thePh diploidizing system (1 dose), the pairing promoter of the 5R chromosome (2 doses) and that of the 3D chromosome (1 dose coming from the parental line Triticale with the substitution 3R by 3D).     

Cytological investigations on two species of allocreadiid trematodes with special reference to the occurrence of triploidy and parthenogenesis in Allocreadium fasciatusi

Karyotypes and cytological details of gametogenesis were analysed for Allocreadium handiai and A. fasciatusi. Mitotic plates studied in squashes of testes, ovary, eggs and intramolluscan stages showed that A. handiai is a diploid (2n = 14) with six pairs of submetacentrics and one pair of subtelocentrics. Total chromosome length of the diploid complement was 86.57 μm, the largest chromosome measured 8.87 μm (10.24% total chromosome length [TCL]) and the smallest was 2.83 μm (3.28% TCL). Squashes of testes revealed the presence of all stages of spermatogenesis with spermatocytes in various stages of meiotic activity and spermatids containing bundles of spermatozoa. Stages of development of the ovum conclusively proved that reproduction takes place by amphimixis. Mitotic figures of A. fasciatusi, on the other hand, revealed that it is a triploid (3n = 21) with three metacentrics, 12 submetacentrics and six subtelocentrics. The mean total chromosome length of the triploid complement was 137.54 μm. The largest chromosome measured 10.37 μm (7.54% TCL) and the smallest measured 2.67 μm (1.94% TCL). Spermatogenesis was abortive with no evidence of synaptic pairing and spermatozoa were not produced. Eggs remained unfertilized and reproduction was achieved by parthenogenesis which is of mitotic type. The karyotypes of the two species differed not only in the ploidy level but also in the centromeric indexes of certain chromosomes.     

Molecular phylogenetics provides a novel hypothesis of chromosome evolution in Neotropical fishes of the genus Potamorhina (Teleostei,Curimatidae)

Potamorhina includes the largest species in the Neotropical fish family Curimatidae. They perform long-distance migrations in large schools and represent relative importance for regional fisheries in South American lowlands. A morphology-based phylogenetic study recognized five species and proposed interspecific phylogenetic relationships mostly based on osteology, squamation, and morphology of the gasbladder. Subsequent cytogenetic studies revealed extreme variability in diploid numbers and other cytomolecular structures and hypothesized multiple events of chromosome rearrangements with centric fissions followed by reversed fusions. However, neither the taxonomic revision and phylogeny nor the cytogenetic hypothesis of chromosome evolution in Potamorhina was tested using molecular phylogenetic approaches. Here, we use mitochondrial and nuclear DNA sequences to delimit species of Potamorhina with an extensive sampling across the Amazon basin and use phylogenetic methods to test prior hypothesis of multiple events of chromosome rearrangements during the evolution of the genus. Phylogenetic and species delimitation methods clearly support the presence of five species but reveal novel interspecific relationships allowing a reinterpretation of the morphological characters relative to the number of vertebrae, caudal peduncle pigmentation, and modifications in the gasbladder chambers. With the new phylogenetic arrangement, we propose a novel hypothesis of occurrence of a single chromosome fission in the lineage of P. latior followed by an extraordinary event that involved more than 20 chromosome-pair fissions during the evolution of the ancestor of P. altamazonica and P. squamoralevis. This novel hypothesis represents a simpler and more conceivable explanation for the achievement of these elevated chromosome numbers during the evolution of Potamorhina.