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Hermann M.,University of Bonn | Schunke A.C.,MPI for Evolutionary Biology | Schultz T.,University of Bonn | Klein R.,University of Bonn
IEEE Pacific Visualization Symposium | Year: 2014

Gaining insight into anatomic co variation helps the understanding of organismic shape variability in general and is of particular interest for delimiting morphological modules. Generation of hypotheses on structural co variation is undoubtedly a highly creative process, and as such, requires an exploratory approach. In this work we propose a new local anatomic covariance tensor which enables interactive visualizations to explore co variation at different levels of detail, stimulating rapid formation and (qualitative) evaluation of hypotheses. The effectiveness of the presented approach is demonstrated on a μCT dataset of mouse mandibles for which results from the literature are successfully reproduced, while providing a more detailed representation of co variation compared to state-of-The-Art methods. © 2014 IEEE. Source


News Article
Site: http://phys.org/biology-news/

The "mini mouse" Mus mattheyi is one of ten mouse species that researchers have studied at the Max Planck Institute for Evolutionary Biology in their gene expression. Just like in other mammals, 95% of the genome is not translated into proteins. Credit: MPI for Evolutionary Biology Every region of DNA codes for a gene. Well, not quite. Although an organism's genome contains some regions that are read and transcribed into RNA, many of those do not give rise to functional genes. Scientists at the Max Planck Institute for Evolutionary Biology in Plön have now studied the genome of the house mouse Mus musculus and its relatives and have found that new functional genes can evolve from such putatively useless DNA regions within a short time. Mice are popular experimental animals for behavioural and genetic studies. But not all mice are the same. The house mouse, Mus musculus, which is often used in European laboratories, is one of 39 known species in its genus. The genus Mus arose around ten million years ago, whereas the house mouse has only been a distinct species for 500,000 years. New species often emerge as a result of changes to existing genes. Three years ago, however, scientists at the Max Planck Institute in Plön discovered that many genes are created entirely from scratch and are not just modified copies of older genes. In their recent study, the researchers analyzed the genome of the mouse, concentrating on regions without known genes. In some mouse species, many of these regions are read and transcribed into RNA, while in others they are not. The scientists analyzed RNA molecules from various tissues of ten mouse species of the genus Mus and compared them to molecules that occur in a "reference mouse", a laboratory mouse of the species Mus musculus, the genome of which is known to the researchers in detail. The researchers determined what proportion of the genome in each species and each tissue is transcribed into RNA. They found that each species synthesizes approximately the same amount of RNA. However, the genome regions that are read are not always the same. The genome can be thought of as an office and the regions that are read as workers. Accordingly, different companies have the same number of workers, but their jobs would be differently distributed. The potential of becoming a gene The results show that only very closely related species share a high percentage of RNA molecules. The researchers' analyses also showed that overall there are very few regions in the genome that are not transcribed into RNA molecules. "We used to interpret the additional molecules as faulty measurements or biological junk, as we have no idea why these regions are read. In fact, these transcripts could serve as candidates for new genes," Rafik Neme of the Max Planck Institute for Evolutionary Biology explains. DNA segments that are read but have no known function or gene designation are known as protogenes. The scientists assume that any DNA segment which can be transcribed into RNA has the potential to act as a gene. If a gene with an important function arises, it is permanently retained. If the entire genome is transcribed into RNA, nearly every segment is a protogene. Most inactive regions of a given species are active in related species. "This indicates that such regions can be activated or deactivated relatively easily," Neme says. In the course of evolution, varying amounts of RNA arise in different tissues. The researchers suspect that RNA molecules tend to evolve rapidly within a short period rather than in the long term, because if they fail to perform important functions, they are lost again. In conclusion, the genome can be very easily transcribed into RNA. Each part of the genome can be, and is, read. "The genome therefore consists almost entirely of genes and protogenes," Neme says. "Extensive transcription into RNA enables protogenes to be tested continuously to determine whether they are suitable candidates for new genes." "The molecular apparatus for reading and transcribing DNA automatically involves the creation of new genes. Any part of the genome containing no genes could therefore become important at some time in the course of evolution," Diethard Tautz, Director at the Max Planck Institute in Plön explains. Explore further: Genes without templates: Many genes are completely new inventions and not just modified copies of old genes More information: Rafik Neme et al. Fast turnover of genome transcription across evolutionary time exposes entire non-coding DNA to gene emergence , eLife (2016). DOI: 10.7554/eLife.09977


Yun Y.,Research Center Borstel | Srinivas G.,MPI for Evolutionary Biology | Srinivas G.,University of Lubeck | Kuenzel S.,MPI for Evolutionary Biology | And 9 more authors.
PLoS ONE | Year: 2014

Commensal bacteria control the micro-ecology of metazoan epithelial surfaces with pivotal effect on tissue homeostasis and host defense. In contrast to the upper respiratory tract, the lower respiratory tract of healthy individuals has largely been considered free of microorganisms. To understand airway micro-ecology we studied microbiota of sterilely excised lungs from mice of different origin including outbred wild mice caught in the natural environment or kept under non-specificpathogen- free (SPF) conditions as well as inbred mice maintained in non-SPF, SPF or germ-free (GF) facilities. High-throughput pyrosequencing of reverse transcribed 16S rRNA revealed metabolically active murine lung microbiota in all but GF mice. The overall composition across samples was similar at the phylum and family level. However, species richness was significantly different between lung microbiota from SPF and non-SPF mice. Non-cultivatable Betaproteobacteria such as Ralstonia spp. made up the major constituents and were also confirmed by 16S rRNA gene cloning analysis. Additionally, Pasteurellaceae, Enterobacteria and Firmicutes were isolated from lungs of non-SPF mice. Bacterial communities were detectable by fluorescent in situ hybridization (FISH) at alveolar epithelia in the absence of inflammation. Notably, higher bacterial abundance in non-SPF mice correlated with more and smaller size alveolae, which was corroborated by transplanting Lactobacillus spp. lung isolates into GF mice. Our data indicate a common microbial composition of murine lungs, which is diversified through different environmental conditions and affects lung architecture. Identification of the microbiota of murine lungs will pave the path to study their influence on pulmonary immunity to infection and allergens using mouse models. Copyright: © 2014 Yun et al. Source

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