Check-list of chromosome numbers of the family Hygromiidae (Gastropoda: Stylommatophora) with new data on Circassina frutis

Chromosome number data on the Hygromiidae (Gastropoda: Stylommatophora) are summarized and reviewed briefly in the context of the phylogeny of the family. In hygromiids, the haploid chromosome numbers range from 21 to 26. It is supposed that n = 21 is the ancestral chromosome number in the family. The modal haploid number for Hygromiidae is 23. Description of karyotype in terms of chromosome number and morphology of hygromiid land snail Circassina frutis is provided for the first time. The diploid chromosome number of this species is 2n = 46. The karyotype is symmetric and consists of 21 pairs of metacentric and 2 pairs of submetacentric chromosomes. The karyotype formula is as follows: 2n = 42m + 4sm (n = 21m + 2sm). The fundamental number (FN) is 92. Chromosomes range in length from 2.53 μm for the smallest pair to 6.00 μm for the largest pair. The total length of chromosomes in diploid complement (TCL) is 170.40 ± 3.22 μm.

Genetic System of Cucumis sativus var. hardwickii (Royle) Alef. – (wild cucumber) in Jammu, J&K, India

A small population of Cucumis sativus var. hardwickii (wild cucumber) has been localized for the first time from Billawar, Kathua (District) in UT of J&K. This variety as expected is monoecious in sex expression, but shows unique pattern of development of male and female flowers on the vine throughout its blooming period. Keeping provision for both both self and cross pollination, it is found to be self compatible, insect pollinated taxa with high reproductive output and a stable diploid complement (2n = 14). Small proportion of cells (9.92%) shows tetraploidy (2n = 28). The species exhibits high and healthy fruit set on open pollination as well as on manual self and cross pollination.

Mitosis without DNA replication in mammalian somatic cells

SUMMARYDNA replication initiates with pre-replication complex (pre-RC) formation at replication origins in G1 (replication origin licensing), followed by activation of a pre-RC subset in the S phase. It has been suggested that a checkpoint prevents S phase entry when too few origins are licensed. Yet, we found that in normal cells, complete DNA synthesis inhibition by overexpression of a non-degradable geminin variant, or by CDT1 silencing prevents DNA replication without inducing any checkpoint. Cells continue cycling and enter mitosis, despite the absence of replicated DNA. Most of these unlicensed cells exit mitosis without dividing and enter senescence; however, about 25% of them successfully divide without previous DNA replication, producing daughter cells with half the normal diploid complement of chromosomes (1C). This suggests a potentially attractive strategy to derive haploid cells from any somatic cell type and unveil undescribed aspects of the coordination between DNA replication and cell division in mammals.

The Ophryotrocha labronica group (Annelida: Dorvilleidae)— with the description of seven new species

This paper reviews the group of gonochoristic Ophryotrocha species, known as the “O. labronica group”. This informal group is chararacterised by its unique maxillary P- and K-forceps and dorsomedian rosette glands. All members of the group are primarily gonochoristic and almost all have the diploid complement of chromosomes of 2n = 6. External morphological differences within the group are very slight. In males and females of all species the P-type maxillae change at maturity to the K-type with the right forceps being bifid. A jaw fossil from the Upper Cretaceous, attributable to the O. labronica group, attests to the long history of the group. As herein defined, the group includes: O. labronica labronica, O. labronica pacifica, O. costlowi sp. nov., O. dimorphica, O. japonica sp. nov., O. macrovifera sp. nov., O. notoglandulata, O. permanae sp. nov., O. robusta sp. nov., O. rubra sp. nov., O. schubravyi, O. vellae sp. nov., O. olympica, nom. nud., O. prolifica, nom. nud., and O. sativa, nom. nud.. Seven species are formally described and diagnoses are provided for all remaining taxa in the taxonomic section. This is followed by an illustrated discussion of the morphology, reproductive traits, and relationships of the members of the informal group.

Evolution of haploid selection in predominantly diploid organisms

Diploid organisms manipulate the extent to which their haploid gametes experience selection. Animals typically produce sperm with a diploid complement of most proteins and RNA, limiting selection on the haploid genotype. Plants, however, exhibit extensive expression in pollen, with actively transcribed haploid genomes. Here we analyze models that track the evolution of genes that modify the strength of haploid selection to predict when evolution intensifies and when it dampens the “selective arena” within which male gametes compete for fertilization. Considering deleterious mutations, evolution leads diploid mothers to strengthen selection among haploid sperm/pollen, because this reduces the mutation load inherited by their diploid offspring. If, however, selection acts in opposite directions in haploids and diploids (“ploidally antagonistic selection”), mothers evolve to reduce haploid selection to avoid selectively amplifying alleles harmful to their offspring. Consequently, with maternal control, selection in the haploid phase either is maximized or reaches an intermediate state, depending on the deleterious mutation rate relative to the extent of ploidally antagonistic selection. By contrast, evolution generally leads diploid fathers to mask mutations in their gametes to the maximum extent possible, whenever masking (e.g., through transcript sharing) increases the average fitness of a father’s gametes. We discuss the implications of this maternal–paternal conflict over the extent of haploid selection and describe empirical studies needed to refine our understanding of haploid selection among seemingly diploid organisms.

Chromosome evolution in fishes: a new challenging proposal from Neotropical species

We present a database containing cytogenetic data of Neotropical actinopterygian fishes from Venezuela obtained in a single laboratory for the first time. The results of this study include 103 species belonging to 74 genera assigned to 45 families and 17 out of the 40 teleost orders. In the group of marine fishes, the modal diploid number was 2n=48 represented in 60% of the studied species, while in the freshwater fish group the modal diploid complement was 2n=54, represented in 21.21 % of the studied species. The average number of chromosomes and the mean FN were statistically higher in freshwater fish than in marine fish. The degree of diversification and karyotype variation was also higher in freshwater fish in contrast to a more conserved cytogenetic pattern in marine fish. In contrast to the assumption according to which 48 acrocentric chromosomes was basal chromosome number in fish, data here presented show that there is an obvious trend towards the reduction of the diploid number of chromosomes from values near 2n=60 with high number of biarmed chromosomes in more basal species to 2n=48 acrocentric elements in more derived Actinopterygii.

Restricted development of mouse triploid fetuses with disorganized expression of imprinted genes

SummaryEukaryotic species commonly contain a diploid complement of chromosomes. The diploid state appears to be advantageous for mammals because it enables sexual reproduction and facilitates genetic recombination. Nonetheless, the effects of DNA ploidy on mammalian ontogeny have yet to be understood. The present study shows phenotypic features and expression patterns of imprinted genes in tripronucleate diandric and digynic triploid (DAT and DGT) mouse fetuses on embryonic day 10.5 (E10.5). Measurement of crown–rump length revealed that the length of DGT fetuses (1.87 ± 0.13 mm; mean ± standard error of the mean) was much smaller than that of diploid fetuses (4.81 ± 0.05 mm). However, no significant difference was observed in the crown–rump length between diploid and DAT fetuses (3.86 ± 0.43 mm). In DGT fetuses, the expression level of paternally expressed genes, Igf2, Dlk1, Ndn, and Peg3, remained significantly reduced and that of maternally expressed genes, Igf2r and Grb10, increased. Additionally, in DAT fetuses, the Igf2 mRNA expression level was approximately twice that in diploid fetuses, as expected. These results provide the first demonstration that imprinted genes in mouse triploid fetuses show distinctive expression patterns independent of the number of parental-origin haploid sets. These data suggest that both DNA ploidy and asymmetrical functions of parental genomes separately influence mammalian ontogeny.

Karyotype traits in Grindelia squarrosa (Pursh) Dunal (Asteraceae), an invasive plant in Romania

The description of the karyotype features and idiogram in Grindelia squarrosa (Pursh) Dunal (Asteraceae), an invasive plant in Romania, are reported here for the first time. The diploid chromosome number is 2n=2x=12, in agreement with the data published for the other species of the genus. The karyomorphological data show that the complements of the studied genotypes have small chromosomes (mean chromosome length is X̅±SE=2.56±0.10 μm, and mean length of haploid complements is X̅±SE=15.33±0.69 μm, with a range of variability comprised between 12.87-17.51 μm). The karyotypes are made up of six pairs of metacentric and submetacentric chromosomes, with an identical formula of the diploid complement: KF=2n=12=8m+ 2sm + 2sm-SAT. Satellites are located on the short arms of the chromosomes of pair III. The karyotypes show a relatively high level of intra-specific uniformity as well as similar symmetry patterns (R=1.29-1.53; TF%=38.78-41.57%; AsI%=54.54-57.61%; A1 = 0.24- 0.32; A2=0.08-0.16), belonging to 1A and 2A classes of symmetry. The small size of the chromosomes, the presence of only two chromosome morphometric types, and the preponderance of metacentrics confer a relatively high degree of symmetry to the karyotypes studied.

Hepatocytes Polyploidization and Cell Cycle Control in Liver Physiopathology

Most cells in mammalian tissues usually contain a diploid complement of chromosomes. However, numerous studies have demonstrated a major role of “diploid-polyploid conversion” during physiopathological processes in several tissues. In the liver parenchyma, progressive polyploidization of hepatocytes takes place during postnatal growth. Indeed, at the suckling-weaning transition, cytokinesis failure events induce the genesis of binucleated tetraploid liver cells. Insulin signalling, through regulation of the PI3K/Akt signalling pathway, is essential in the establishment of liver tetraploidization by controlling cytoskeletal organisation and consequently mitosis progression. Liver cell polyploidy is generally considered to indicate terminal differentiation and senescence, and both lead to a progressive loss of cell pluripotency associated to a markedly decreased replication capacity. Although adult liver is a quiescent organ, it retains a capacity to proliferate and to modulate its ploidy in response to various stimuli or aggression (partial hepatectomy, metabolic overload (i.e., high copper and iron hepatic levels), oxidative stress, toxic insult, and chronic hepatitis etc.). Here we review the mechanisms and functional consequences of hepatocytes polyploidization during normal and pathological liver growth.

Mitotic and polytene chromosome analysis in the Mexican fruit fly, Anastrepha ludens (Loew) (Diptera: Tephritidae)

The present study constitutes the first attempt to construct a polytene chromosome map of an Anastrepha species, Anastrepha ludens (Loew), a major agricultural pest. The mitotic karyotype has a diploid complement of 12 acrocentric chromosomes, including five pairs of autosomes and an XX/XY sex chromosome pair. The analysis of salivary gland polytene chromosomes has shown a total number of five polytene elements that correspond to the five autosomes. The characteristic features and the most prominent landmarks of each chromosome are described. By comparing chromosome banding patterns, the possible chromosomal homology between A. ludens and Ceratitis capitata (Wiedemann) is presented. This work shows that polytene maps of A. ludens are suitable for cytogenetic studies in this species and may be used as reference for other Anastrepha species, most of which are also serious agricultural pests.