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Dive into the research topics where Kathrin P. Lampert is active.

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Featured researches published by Kathrin P. Lampert.


Nature Genetics | 2002

A bisexually reproducing all-triploid vertebrate

Matthias Stöck; Dunja K. Lamatsch; Claus Steinlein; Jörg T. Epplen; Wolf-Rüdiger Grosse; Robert Hock; Thomas Klapperstück; Kathrin P. Lampert; Ulrich Scheer; Michael Schmid; Manfred Schartl

Green toads are common in the Palaearctic region, where they have differentiated into several taxa. The toads exist with variable amounts of ploidy, similar to other anuran species or reptiles. In vertebrate biology, the very rare occurrence of triploidy is coupled with infertility or unisexuality, or requires the coexistence of individuals of different ploidy in a reproductive community. The reproduction of naturally occurring triploids has been reported to occur only through parthenogenesis, gynogenesis or hybridogenesis. The bisexual reproduction of pure triploids has been considered to be impossible because of the problem of equally distributing three chromosome sets in meiosis. Here we report geographically isolated populations of green toads (Bufo viridis complex) that are all-triploid and reproduce bisexually.


Current Biology | 2010

Determination of onset of sexual maturation and mating behavior by melanocortin receptor 4 polymorphisms.

Kathrin P. Lampert; Cornelia Schmidt; Petra Fischer; Jean-Nicolas Volff; Carsten Hoffmann; Jenny Muck; Martin J. Lohse; Michael J. Ryan; Manfred Schartl

Polymorphisms in reproductive strategies are among the most extreme and complex in nature. A prominent example is male body size and the correlated reproductive strategies in some species of platyfish and swordtails of the genus Xiphophorus. This polymorphism is controlled by a single Mendelian locus (P) that determines the onset of sexual maturity of males. Because males cease growth after reaching puberty, this results in a marked size polymorphism. The different male size classes show pronounced behavioral differences (e.g., courtship versus sneak mating), and females prefer large over small males. We show that sequence polymorphisms of the melanocortin receptor 4 gene (mc4r) comprise both functional and non-signal-transducing versions and that variation in copy number of mc4r genes on the Y chromosome underlies the P locus polymorphism. Nonfunctional Y-linked mc4r copies in larger males act as dominant-negative mutations and delay the onset of puberty. Copy number variation, as a regulating mechanism, endows this system with extreme genetic flexibility that generates extreme variation in phenotype. Because Mc4r is critically involved in regulation of body weight and appetite, a novel link between the physiological system controlling energy balance and the regulation of reproduction becomes apparent.


Philosophical Transactions of the Royal Society B | 2008

The origin and evolution of a unisexual hybrid: Poecilia formosa

Kathrin P. Lampert; Manfred Schartl

Clonal reproduction in vertebrates can always be traced back to hybridization events as all known unisexual vertebrates are hybrids between recognized species or genetically defined races. Interestingly, clonal vertebrates often also rely on interspecific matings for their reproduction because gynogenesis (sperm-dependent parthenogenesis) and hybridogenesis are common modes of propagation. While in most cases these hybridization events leave no hereditary traces in the offspring, occasionally the genome exclusion mechanism fails and either small parts of male genetic material remain inside the oocyte in the form of microchromosomes, or fusion of the sperm nucleus with the oocyte nucleus leads to polyploid individuals. In this review, we highlight the important role of hybridization for the origin and evolution of a unisexual hybrid: the Amazon molly, Poecilia formosa.


Molecular Ecology | 2010

Monophyletic origin of multiple clonal lineages in an asexual fish (Poecilia formosa).

Matthias Stöck; Kathrin P. Lampert; Dirk Möller; Ingo Schlupp; Manfred Schartl

Despite the advantage of avoiding the costs of sexual reproduction, asexual vertebrates are very rare and often considered evolutionarily disadvantaged when compared to sexual species. Asexual species, however, may have advantages when colonizing (new) habitats or competing with sexual counterparts. They are also evolutionary older than expected, leaving the question whether asexual vertebrates are not only rare because of their ‘inferior’ mode of reproduction but also because of other reasons. A paradigmatic model system is the unisexual Amazon molly, Poecilia formosa, that arose by hybridization of the Atlantic molly, Poecilia mexicana, as the maternal ancestor, and the sailfin molly, Poecilia latipinna, as the paternal ancestor. Our extensive crossing experiments failed to resynthesize asexually reproducing (gynogenetic) hybrids confirming results of previous studies. However, by producing diploid eggs, female F1‐hybrids showed apparent preadaptation to gynogenesis. In a range‐wide analysis of mitochondrial sequences, we examined the origin of P. formosa. Our analyses point to very few or even a single origin(s) of its lineage, which is estimated to be approximately 120 000 years old. A monophyletic origin was supported from nuclear microsatellite data. Furthermore, a considerable degree of genetic variation, apparent by high levels of clonal microsatellite diversity, was found. Our molecular phylogenetic evidence and the failure to resynthesize the gynogenetic P. formosa together with the old age of the species indicate that some unisexual vertebrates might be rare not because they suffer the long‐term consequences of clonal reproduction but because they are only very rarely formed as a result of complex genetic preconditions necessary to produce viable and fertile clonal genomes and phenotypes (‘rare formation hypothesis’).


Sexual Development | 2008

Facultative Parthenogenesis in Vertebrates: Reproductive Error or Chance?

Kathrin P. Lampert

Parthenogenesis, the development of an embryo from a female gamete without any contribution of a male gamete, is very rare in vertebrates. Parthenogenetically reproducing species have, so far, only been found in the Squamate reptiles (lizards and snakes). Facultative parthenogenesis, switching between sexual and clonal reproduction, although quite common in invertebrates, e.g. Daphnia and aphids, seems to be even rarer in vertebrates. However, isolated cases of parthenogenetic development have been reported in all vertebrate groups. Facultative parthenogenesis in vertebrates has only been found in captive animals but might simply have been overlooked in natural populations. Even though its evolutionary impact is hard to determine and very likely varies depending on the ploidy restoration mechanisms and sex-determining mechanisms involved, facultative parthenogenesis is already discussed in conservation biology and medical research. To raise interest for facultative parthenogenesis especially in evolutionary biology, I summarize the current knowledge about facultative parthenogenesis in the different vertebrate groups, introduce mechanisms of diploid oocyte formation and discuss the genetic consequences and potential evolutionary impact of facultative parthenogenesis in vertebrates.


Evolution | 2005

EVIDENCE FOR A MONOPHYLETIC ORIGIN OF TRIPLOID CLONES OF THE AMAZON MOLLY, POECILIA FORMOSA

Kathrin P. Lampert; Dunja K. Lamatsch; Jörg T. Epplen; Manfred Schartl

Abstract Asexual reproduction in vertebrates is rare and generally considered an evolutionary dead end. Asexuality is often associated with polyploidy, and several hypotheses have been put forward to explain this relationship. So far, it remains unclear whether polyploidization in asexual organisms is a frequent or a rare event. Here we present a field study on the gynogenetic Amazon molly, Poecilia formosa. We used multilocus fingerprints and microsatellites to investigate the genetic diversity in 339 diploid and 55 triploid individuals and in 25 P. mexicana, its sexual host. A though multilocus DNA fingerprints found high clonal diversity in triploids, microsatellites revealed only two very similar clones in the triploids. Phylogenetic analysis of microsatellite data provided evidence for a monophyletic origin of the triploid clones of P. formosa. In addition, shared alleles within the triploid clones between the triploid and diploid genotypes and between asexual and sexual lineages indicate a recent origin of triploid clones in Poecilia formosa.


Current Biology | 2007

Automictic Reproduction in Interspecific Hybrids of Poeciliid Fish

Kathrin P. Lampert; Dunja K. Lamatsch; Petra Fischer; Jörg T. Epplen; Indrajit Nanda; Manfred Schartl

Automixis, the process whereby the fusion of meiotic products restores the diploid state of the egg, is a common mode of reproduction in plants but has also been described in invertebrate animals. In vertebrates, however, automixis has so far only been discussed as one of several explanations for isolated cases of facultative parthenogenesis. Analyzing oocyte formation in F1 hybrids derived from Poecilia mexicana limantouri and P. latipinna crosses (the cross that led to the formation of the gynogenetic Poecilia formosa), we found molecular evidence for automictic oocyte production. The mechanism involves the random fusion of meiotic products after the second meiotic division. The fertilization of diploid oocytes gives rise to fully viable triploid offspring. Although the automictic production of diploid oocytes as seen in these F1 hybrids clearly represents a preadaptation to parthenogenetic reproduction, it is also a powerful intrinsic postzygotic isolation mechanism because the resulting next generation triploids were always sterile. The mechanism described here can explain facultative parthenogenesis, as well as varying ploidy levels reported in different animal groups. Most importantly, at least some of the reported cases of triploidy in humans can now be traced back to automixis.


Journal of Herpetology | 2011

Putting Toe Clipping into Perspective: A Viable Method for Marking Anurans

T. Ulmar Grafe; Margaret M. Stewart; Kathrin P. Lampert; Mark-Oliver Rödel

Abstract Toe clipping is widely used in studies of amphibian ecology and behavior, but its impact on return rates and survival remains controversial. We evaluated the effect of toe clipping on apparent survival, using four comprehensive mark–recapture data sets of four anuran species covering four different time scales and varying life histories. The effect of toe clipping was evaluated by comparing frogs with different numbers of toes removed. Two species, Eleutherodactylus coqui and Hemisus marmoratus, showed minimal effects of toe clipping on apparent survival with seasonal and annual apparent survival decreasing by 0.1% and 1.5% with toe removal, respectively. In Hyperolius nitidulus, daily apparent survival increased on average by 4.1% with toe removal, an effect than can be attributed to disproportionate emigration of the lowest toe-removal group. Finally, in Phrynobatrachus guineensis, individuals with three toes clipped showed an additional 5.0–19.7% decreased apparent survival between weeks when compared to individuals with only one toe clipped. However, the data set was characterized by an interaction between the number of toes clipped and week of marking, thus confounding interpretation. To minimize any effects of toe clipping, we recommend that not more than four toes should be clipped and at most a single toe removed on each leg. In addition, functionally important toes such as the proximal toes of front feet and fourth toes of hind feet should be spared. Furthermore, toe-removal groups should be equally distributed over time to facilitate the analysis of potential toe-clipping effects.


PLOS ONE | 2012

Exploring Pandora's Box: Potential and Pitfalls of Low Coverage Genome Surveys for Evolutionary Biology

Florian Leese; Philipp Brand; Andrey Rozenberg; Christoph Mayer; Shobhit Agrawal; Johannes Dambach; Lars Dietz; Jana Sophie Doemel; William P. Goodall-Copstake; Christoph Held; Jennifer A. Jackson; Kathrin P. Lampert; Katrin Linse; Jan Niklas Macher; Jennifer Nolzen; Michael J. Raupach; Nicole T. Rivera; Christoph D. Schubart; Sebastian Striewski; Ralph Tollrian; Chester J. Sands

High throughput sequencing technologies are revolutionizing genetic research. With this “rise of the machines”, genomic sequences can be obtained even for unknown genomes within a short time and for reasonable costs. This has enabled evolutionary biologists studying genetically unexplored species to identify molecular markers or genomic regions of interest (e.g. micro- and minisatellites, mitochondrial and nuclear genes) by sequencing only a fraction of the genome. However, when using such datasets from non-model species, it is possible that DNA from non-target contaminant species such as bacteria, viruses, fungi, or other eukaryotic organisms may complicate the interpretation of the results. In this study we analysed 14 genomic pyrosequencing libraries of aquatic non-model taxa from four major evolutionary lineages. We quantified the amount of suitable micro- and minisatellites, mitochondrial genomes, known nuclear genes and transposable elements and searched for contamination from various sources using bioinformatic approaches. Our results show that in all sequence libraries with estimated coverage of about 0.02–25%, many appropriate micro- and minisatellites, mitochondrial gene sequences and nuclear genes from different KEGG (Kyoto Encyclopedia of Genes and Genomes) pathways could be identified and characterized. These can serve as markers for phylogenetic and population genetic analyses. A central finding of our study is that several genomic libraries suffered from different biases owing to non-target DNA or mobile elements. In particular, viruses, bacteria or eukaryote endosymbionts contributed significantly (up to 10%) to some of the libraries analysed. If not identified as such, genetic markers developed from high-throughput sequencing data for non-model organisms may bias evolutionary studies or fail completely in experimental tests. In conclusion, our study demonstrates the enormous potential of low-coverage genome survey sequences and suggests bioinformatic analysis workflows. The results also advise a more sophisticated filtering for problematic sequences and non-target genome sequences prior to developing markers.


Genetics | 2007

Stable Inheritance of Host Species-Derived Microchromosomes in the Gynogenetic Fish Poecilia formosa

Indrajit Nanda; Ingo Schlupp; Dunja K. Lamatsch; Kathrin P. Lampert; Manfred Schartl

B chromosomes are additional, usually unstable constituents of the genome of many organisms. Their origin, however, is often unclear and their evolutionary relevance is not well understood. They may range from being deleterious to neutral or even beneficial. We have followed the genetic fate of B chromosomes in the asexual, all-female fish Poecilia formosa over eight generations. In this species, B chromosomes come in the form of one to three tiny microchromosomes derived from males of the host species that serve as sperm donors for this gynogenetic species. All microchromosomes have centromeric heterochromatin but usually only one has a telomere. Such microchromosomes are stably inherited, while the telomereless are prone to be lost in both the soma and germline. In some cases the stable microchromosome carries a functional gene lending support to the hypothesis that the B chromosomes in P. formosa could increase the genetic diversity of the clonal lineage in this ameiotic organism and to some degree counteract the genomic decay that is supposed to be connected with the lack of recombination.

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Ralph Tollrian

University of Duisburg-Essen

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Florian Leese

University of Duisburg-Essen

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Jean-Nicolas Volff

École normale supérieure de Lyon

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