Abstract:We review the different modes of meiosis and its deviations encountered in polyploid animals. Bisexual reproduction involving normal meiosis occurs in some allopolyploid frogs with variable degrees of polyploidy. Aberrant modes of bisexual reproduction include gynogenesis, where a sperm stimulates the egg to develop. The sperm may enter the egg but there is no fertilization and syngamy. In hybridogenesis, a genome is eliminated to produce haploid or diploid eggs or sperm. Ploidy can be elevated by fertilizatio… Show more
“…We suppose that two species studied are not only triploids but contain a tetraploids admixture, as was demonstrated earlier for O. scaber (Stenberg et al, 1997). At the moment, it is known that the ploidy level of the genus Otiorhynchus parthenogenetic forms varies from 2 n to 10 n (Stenberg, Saura, 2013). For this reason, the hypothesis of the presence in the population species we studied allotetraploids admixture is seemed to be quite probable.…”
Clonal Diversity of Otiorhynchus ligustici and O. raucus (Coleoptera, Curculionidae) in Central Ukraine. Morozov-Leonov, S. Yu., Nazarenko, V. Yu. -Th e clonal diversity in four weevil populations of two species, Otiorhynchus ligustici (Linnaeus, 1758) and O. raucus (Fabricius, 1777), from vicinity of Kyiv is analyzed. Polyclonality and inter-population diff erentiation in both species is demonstrated. Th e obtained data about two weevil species clonal diversity are compared with those known for European species O. scaber (Linnaeus, 1758).
“…We suppose that two species studied are not only triploids but contain a tetraploids admixture, as was demonstrated earlier for O. scaber (Stenberg et al, 1997). At the moment, it is known that the ploidy level of the genus Otiorhynchus parthenogenetic forms varies from 2 n to 10 n (Stenberg, Saura, 2013). For this reason, the hypothesis of the presence in the population species we studied allotetraploids admixture is seemed to be quite probable.…”
Clonal Diversity of Otiorhynchus ligustici and O. raucus (Coleoptera, Curculionidae) in Central Ukraine. Morozov-Leonov, S. Yu., Nazarenko, V. Yu. -Th e clonal diversity in four weevil populations of two species, Otiorhynchus ligustici (Linnaeus, 1758) and O. raucus (Fabricius, 1777), from vicinity of Kyiv is analyzed. Polyclonality and inter-population diff erentiation in both species is demonstrated. Th e obtained data about two weevil species clonal diversity are compared with those known for European species O. scaber (Linnaeus, 1758).
“…Maintenance of heterozygosity during parthenogenesis can result from several types of modified meiosis: (1) pre-meiotic genome doubling where the entire genetic material from the mother along with its heterozygosity is preserved in the first meiotic division, which thus loses its reductional property; (2) central fusion, where two genetically distinct meiotic end-products fuse, forming a diploid heterozygous embryo; or (3) skipping of the first reductional division (Meiosis I), whereby the mother’s entire genetic material and its heterozygosity are also maintained [64, 65]. Complete heterozygosity is maintained unless crossing over or gene conversion occurs (in type 2 or 3) [64, 65]. …”
SUMMARY
Asexual reproduction in animals, though rare, is the main or exclusive mode of reproduction in some long-lived lineages. The longevity of asexual clades may be correlated with the maintenance of heterozygosity by mechanisms that rearrange genomes and reduce recombination. Asexual species thus provide an opportunity to gain insight into the relationship between molecular changes, genome architecture and cellular processes. Here, we report the genome sequence of the parthenogenetic nematode Diploscapter pachys with only one chromosome pair. We show that this unichromosomal architecture is shared by a long-lived clade of asexual nematodes closely related to the genetic model organism Caenorhabditis elegans. Analysis of the genome assembly reveals that the unitary chromosome arose through fusion of six ancestral chromosomes, with extensive rearrangement among neighboring regions. Typical nematode telomeres and telomeric protection-encoding genes are lacking. Most regions show significant heterozygosity; homozygosity is largely concentrated to one region and attributed to gene conversion. Cell-biological and molecular evidence are consistent with the absence of key features of Meiosis I, including synapsis and recombination. We propose that D. pachys preserves heterozygosity and produces diploid embryos without fertilizationthrough a truncated meiosis. As a prelude to functional studies, we demonstrate that D. pachys is amenable to experimental manipulation by RNA interference.
There is a close association between parthenogenesis and polyploidy. For this reason, we undertook a karyological analysis to test whether the parthenogenetic Marmorkrebs, Procambarus fallax forma virginalis, possesses an enlarged set of chromosomes. For this purpose, we karyotyped the Marmorkrebs, the sexual form of P. fallax (together called P. fallax complex), and the closely related species P. alleni. The latter shows 94 chromosomes in the haploid condition. In contrast to this, we found a haploid set of 92 chromosomes in individuals of the P. fallax complex. However, in mitotic metaphases the sexual form shows 184 chromosomes, whereas the Marmorkrebs possesses 276 chromosomes. Hence, the parthenogenetic Marmorkrebs reveals a triple amount of the haploid chromosome number. In addition, we detected a strikingly large subtelocentric chromosome which appears once in haploid and twice in diploid cells of sexual individuals of the P. fallax complex. In the parthenogenetic Marmorkrebs, this prominent chromosome occurs thrice. All this clearly reveals that the Marmorkrebs is a triploid organism. The applicability of the used methods, the significance of polyploidy in evolution of Decapoda, putative pathways to parthenogenetic triploidy, a possible hybrid origin and the scientific and ecological consequences of an increased chromosome set in Marmorkrebs are discussed.
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