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Early career researcher Stephanie Döpper awarded funding by Gerda Henkel Foundation to study abandoned mud-brick settlements in Oman
University is sending researchers to Oman: As the Gerda Henkel Foundation has
announced, Dr. Stephanie Döpper will receive funds of almost € 300,000 for the
duration of three years in the framework of its “Lost Cities" programme.
To this end, the archaeologists in the project will be
responsible over the coming years for mapping three mud-brick settlements in
Central Oman and documenting the history of their buildings. This will take
place in the framework of research visits lasting several months. In addition,
by examining the artefacts they find, such as ceramic shards, they will be able
to identify the former functions of the individual buildings in these
settlements. Of particular significance here are their later uses, for example
the repurposing of a house as a goat shed. The research team's hypothesis is
that the abandoned mud-brick settlements are not only the deserted backdrops of
a past way of life but instead still very lively and bustling places with a future.
Dr. Stephanie Döpper has been studying settlements and
settlement systems in Central Oman for several years now, starting from the
early Bronze Age in the 3rd millennium BC up until the mud-brick
settlements in the research project approved by the Gerda Henkel Foundation,
which were probably built in the 18th or 19th century AD
and are today abandoned. In the back of her mind is always the question of what
caused people in this region to settle and why such settlements were abandoned
Funding from the Gerda Henkel Foundation will make it
possible to finance a doctoral scholarship and the research visits on site.
In total, the foundation has included 53
new research projects in its sponsorship programme, for which its committees
approved € 8.6 million at their autumn meeting. This means support for researchers
from almost 30 countries.
can be downloaded under: http://www.uni-frankfurt.de/83770372
Picture 1: House in the abandoned mud-brick settlement of Al-Mudhaybi. Photo: Stephanie Döpper
Picture 2: Ceramic vessels in the abandoned mud-brick settlement of Al-Mudhaybi. Photo: Stephanie Döpper
Picture 3: House with collapsed ceilings in the abandoned mud-brick settlement of Sinaw.
Picture 4: Abandoned mud-brick settlement of Sinaw. Photo: Stephanie Döpper
Picture 5: Abandoned mud-brick settlement of Sinaw. Photo: Stephanie Döpper
courtesy of Stephanie Döpper.
Further information: Dr. Stephanie Döpper, Institute of Archaeological Sciences, Archaeology,
Westend Campus, Norbert-Wollheim-Platz 1, D-60629 Frankfurt am Main, +49(0)69-798-32320,
Prolongation of Collaborative Research Centre on selective autophagy led by Goethe University
FRANKFURT. Four years ago, Collaborative Research Centre (CRC) 1177 on selective autophagy was established under the leadership of Goethe University – now the German Research Foundation has given the green light for its further funding. A total of over € 12 million has been approved for the period up until 2023. Partners alongside Goethe University are the universities of Mainz, Munich, Tübingen and Freiburg, the Georg Speyer Haus and the Max Planck Institute of Biophysics in Frankfurt as well as the Institute of Molecular Biology (IMB) in Mainz.
Selective autophagy is part of the cell's waste disposal system. With its help, defective or potentially damaging cellular components are degraded and recycled. It plays a central role in maintaining cellular homeostasis and fulfils important functions in ageing and developmental processes. Errors in this system contribute to cancer, neurodegenerative disorders and infections. The objective of the research alliance is a better understanding of autophagy at molecular and cellular level in order to be able in future to counteract imbalances in the system. CRC 1177 is the first consortium in Germany to tackle this important topic systematically.
“This is very good news for Goethe University," said Professor Birgitta Wolff, President of Goethe University. Thanks to this CRC, Frankfurt has become a national hub for autophagy research over the past four years. Especially through the integration of new partners in Munich, Tübingen and Freiburg and at the MPI for Biophysics, it has been possible to substantially strengthen the existing partnership between Mainz (IMB/JGU) and Frankfurt (GSH/GU). We expect this research alliance to advance autophagy research significantly, which will help in the fight against many diseases," said the President.
Autophagy is found from simple organisms, such as yeasts, up to humans. The underlying molecular mechanisms are always similar: Cellular components that need to be removed are recognized in a highly specific manner, enveloped by membranes and degraded. This is how, for example, aggregated proteins are destroyed that would otherwise cause severe damage and trigger cell death. This can especially be observed in neurodegenerative disorders such as Alzheimer's disease, where toxic protein aggregates accumulate which then promote the massive destruction of nerve cells. Apart from proteins, autophagy can also target defective cell organelles and pathogens for removal. The cell can reutilize the recovered material as building blocks for synthesizing new components, which is why autophagy is also an important survival strategy in times of need.
Autophagy is a very complex process which must be precisely regulated and is greatly dependent on the cellular context. Its analysis requires state-of-the-art technologies, the integration of a wide variety of data and close collaboration between researchers from different disciplines. “We will focus on novel concepts in autophagy research and its impact on major biological processes as well as pathogenesis and therapy of human diseases," explains Professor Ivan Dikic, CRC spokesperson and Director of the Institute of Biochemistry II at Goethe University. “Our vision includes close interactions between basic and translational research via centrally supported technology platforms."
The platforms with their ultramodern equipment are a key factor in the research alliance's success: Since 2016, over 20 scientific publications have been produced in cooperation with the proteomics platform alone. In the second funding period, centrally available technologies will be significantly extended to include modelling and simulation methods, genomic and chemical high-throughput screening, and imaging methods to quantify autophagy in model organisms. Another equally important matter within the consortium is support for early career researchers. To this end, the Research Training Group set up in the first funding period will be continued. “Training the next generation of autophagy researchers is a matter close to our hearts and for this reason we've planned a diverse and advanced training programme," said Dikic.
Participating in the CRC on the part of Goethe University – in addition to its faculties of Biological Sciences, Biochemistry, Chemistry and Pharmacy, and Medicine – is the Buchmann Institute for Molecular Life Sciences.
Further information: Dr. Kerstin Koch, Institute of Biochemistry II, Faculty of Medicine, Goethe University, Tel.: +49(0)69- 6301-84250, firstname.lastname@example.org.
Goethe University is a participant in a project receiving 3.2 million Horizon 2020 grant
European research project “Working, Yet Poor“ (WorkYP) was recently awarded 3.2
million euros for three years by the EU's Horizon 2020 programme. The project
will investigate the social and legal reasons behind the increasing number of
EU citizens who are at risk of living below the poverty line despite being
employed. Law Professor Bernd Waas from Goethe University is heading a
“Countries implement certain measures to
prevent in-work poverty, but there is not a set approach towards reducing or
eliminating it. EU Member States – individually and collectively – need a
better understanding of the problem, an understanding supported by pertinent
data and which allows them to monitor and successfully attack it," says Luca
Ratti, the WorkYP Project's coordinator and Associate Professor of European and
Comparative Labour Law at the University of Luxembourg.
The distribution of in-work poverty
differs substantially across Europe, due to different social and legal systems
or measures implemented to reduce poverty. For example, 13.4% of the working
population were at risk of poverty in Luxembourg in 2018, compared to 5.2% in
Belgium. The reasons for such differences have not been sufficiently
investigated. Therefore, the WorkYP Project will analyse seven representative
countries with different social and legal systems (Luxembourg. Belgium,
Germany, Italy, the Netherlands, Poland and Sweden) to document the problem and
to propose best practice solutions to combat in-work poverty across all
systems. “With this study, we intend to help EU Member States, and the EU as a
whole, to better target their policies and regulatory action," Ratti explains.
The WorkYP Project has identified specific
groups of people that are at greater risk of in-work poverty, on which the
analysis will focus. These include low wage workers; self-employed people;
those with temporary or flexible employment contracts; and casual or
“zero-hours" workers. Because women are more frequently employed in low-paid
jobs or are more vulnerable to unequal working conditions, the household's
composition and income will be considered in the research.
Luca Ratti will lead a multinational and
interdisciplinary research team comprised of researchers from eight European
universities (Frankfurt, Bologna, Leuven, Rotterdam, Tilburg, Gdansk and Lund)
as well as three social rights institutions active in Europe.
Goethe University will have a key role in
this project. It will assume project leadership for the part of the project
dedicated to consideration of employees with atypical work contracts. It will
furthermore coordinate the work of the experts in the comparative analysis of
the various models for combatting poverty at the workplace, and the system for
guaranteeing a minimum living standard and a minimum catalogue of social
rights. Overall, 320,000 euros in project funds will go to Goethe University.
Professor Waas, who already heads the European Commission's labour law expert
network, and also coordinates the project on the restatement of labour law in
Europe, is pleased with his new task. “The days will be a bit longer, but it
will be worth it," he says. “In particular with regard to the rapid
digitalisation of the workplace and the emergence of completely new forms of
work, numerous problems have come about that are in urgent need of answers."
“I am happy that Goethe University is
involved in such an important European research project. Decent working and
living conditions in all countries of the Community are of critical
significance for Europe's future," says Professor Simone Fulda, who as Goethe
University Vice President is in charge of research.
Horizon 2020, the EU Framework Programme
for Research and Innovation launched in 2014, funds collaborative projects in
research and innovation. Research organisations, universities, and companies
are all eligible to participate. Horizon 2020 funds 6,000 projects each year
and Luxembourg entities have already received approximately 40 million euros
for more than 120 projects.
Caption: Professor Bernd Waas, labour law expert at Goethe University, heads
the Frankfurt subproject of the Horizon 2020 collaborative project “Working,
Further information: Professor Bernd Waas, Chair for Labour Law and Civilian Law, Institute
for Civil and Economic Law, Faculty of Law, Westend Campus, Phone+49 69-798
34232, E-Mail email@example.com
Sex-specific processes in schizophrenia and bipolar disorder
studies have found a high genetic similarity of the psychiatric diseases
schizophrenia and bipolar disorder, whose disease-specific changes in brain
cells show an overlap of more than 70 percent. These changes affect gene
expression, i.e., transcription of genes for the purpose of translation into
functional proteins. A collaborative study carried out by the Institute of Pharmacology
and Clinical Pharmacy at Goethe University (Professor Jochen Klein) and the
Institute of Neurosciences at the Hebrew University of Jerusalem (Professor
Hermona Soreq) now shows sex-specific biases in these changes, as well as in cellular
control mechanisms based on endogenous short ribonucleic acid (RNA) chains.
The scientists identified an important role of microRNAs, a special group of these small RNA molecules, known for their extensive control of gene expression in all human cells. Targeting of a gene by one of these microRNAs can lead to a significant restriction of its expression. “The main problem is the enormous variety of possible combinations," says Sebastian Lobentanzer, lead author of the article published in the journal Cell Reports. “The human expresses about 2,500 of these microRNAs, and a single one can influence hundreds, maybe even thousands of genes."
For this reason, the researchers
investigated gene expression in patient brains as well as human cultured nerve
cells with a combination of RNA sequencing and bioinformatics. They found a
difference in the expression of immune-related genes between men and women,
especially with regard to cytokines, the messenger substances of immune cells. Upon
exposition of the cultured male and female neuronal cells to some of these
cytokines, the researchers found a transformation of nerve cells into to cholinergic
neurons, defined by their use of the neurotransmitter “acetylcholine".
By sequencing the microRNAs at several time
points during this process, the scientists were able to paint a detailed
picture of the microRNA interface between the immune and neuronal systems. They
identified the involvement of 17 partially sex-dependent families of microRNAs
and generated an extensive network of 12,495 regulated genes. Using a multi-stage
selection process, the most influential of these microRNA families were
identified and confirmed in dedicated experiments. This led to the
identification of the two sex-specifically expressed families mir-10 and
mir-199 as interface between cytokines and cholinergic functions.
Psychiatric diseases are an important
field for new therapeutic approaches because of their high genetic complexity
and their inaccessibility to conventional forms of therapy. On the one hand, the
current study demonstrates molecular parallels to the long-observed but
previously unexplained clinical differences between disease-affected men and
women. On the other hand, mechanisms on the basis of small RNA molecules could
open up new avenues by influencing a large number of disease-relevant genes – a
promising approach in the search for alternatives to traditional antipsychotic drugs.
“Studies such as ours, which enable a comprehensive representation of microRNA interactions,
are the first step on the path to developing new therapeutic substances," says
Lobentanzer S, Hanin G, Klein J & Soreq H (2019). Integrative
Transcriptomics Reveals Sexually Dimorphic Control of the Cholinergic/Neurokine
Interface in Schizophrenia and Bipolar Disorder. CellReports. ElsevierCompany.
1–19. doi: 10.1016/j.celrep.2019.09.017.
An image may
be downloaded here: www.uni-frankfurt.de/83258617
The illustration shows a network of 212 microRNAs and their 12,495 targeted genes, deconstructed into four fields according to their sex-specific changes. (Copyright: Sebastian Lobentanzer)
Further information: Sebastian Lobentanzer, research scientist; Professor Jochen Klein;
Institute for Pharmacology and Clinical Pharmacy, Riedberg Campus; firstname.lastname@example.org, email@example.com. https://slobentanzer.github.io/cholinergic-neurokine.
Scientists from Goethe University and Senckenberg Society for Nature Research are developing maps on the Zika virus infection risk
How the Zika virus can spread
Scientists from Goethe University and Senckenberg Society for Nature Research are developing maps on the Zika virus infection risk
FRANKFURT. The spread of infectious diseases such as Zika depends on many different factors. Environmental factors play a role, as do socioeconomic factors. Recently, several attempts have be made to predict the transmission risk of the Zika virus at a global and local level, but the spatial and temporal patterns of transmission are still not well understood. Researchers from Goethe University and the Senckenberg Society for Nature Research in Frankfurt were now able to generate reliable maps for the transmission risk of the Zika virus in South America.
The results have been published in the scientific journal “PeerJ". Based on the models for South America, they will use the method to determine the Zika risk for Europe as well. In most cases, mosquitoes of the genus Aedes transmit the Zika virus to humans. Primary vectors are the yellow fever mosquito (Aedes aegypti) and the Asian tiger mosquito (Aedes albopictus). Both mosquito species are widespread in South America. Whereas the yellow fever mosquito (Aedes albopictus) is nearly absent in Europe, the Asian tiger mosquito is widespread in the Mediterranean region.
“With our new modelling approaches we can illustrate the risk areas for Zika infections in Latin America," says Sven Klimpel Professor for Parasitology and Infection Biology at Goethe University in Frankfurt and the Senckenberg Biodiversity and Climate Research Centre. “The models additionally allow us to illustrate Zika risk areas for Europe. For example, our models indicate the two autochthonous cases in southern France in Département Var (see illustration)." At the end of October, French authorities announced the first Zika case in Europe; about a week later, a second case was made public.
According to the researcher's calculations, the Zika infection risk in South America is highest along the Brazilian East Coast and in Central America. The risk is moderate in the Amazon region and lowest in the southern areas of the continent. The following countries are especially affected according to the model: Brazil, Columbia, Cuba, the Dominican Republic, El Salvador, Guatemala, Haiti, Honduras, Jamaica, Mexico, Puerto Rico and Venezuela. In Europe, a risk of infection exists mainly in the Mediterranean region, but also in the inland regions of France and in the Rhine areas of Baden-Württemberg.
To determine the infection risk of a specific area, the researchers Dr Sarah Cunze and Professor Sven Klimpel modelled the potential spread of the two species of mosquito, Aedes aegypti and Aedes albopictus. Since the mosquitoes can only transmit the Zika virus in regions where the virus is present in the first place, the researchers included an Evidence Consensus Map in their risk model. This map categorises the number of reported Zika illnesses at the regional level. The average temperature of the warmest quarter was also incorporated in the model, since temperature has a significant influence on whether the virus can survive and multiply in the mosquito. Finally, the scientists added socioeconomic factors such as population density and gross domestic product to their risk model
Publication: Cunze S, Kochmann J, Koch LK, Genthner E, Klimpel S. 2019. Vector distribution and transmission risk of the Zika virus in South and Central America. PeerJ 7:e7920 DOI 10.7717/peerj.7920
An image maybe downloaded here: http://www.uni-frankfurt.de/83225123
Illustration 1: Correlative modelling approach for regions with increased Zika infection risk in South America. In addition to the modelled expansion of the two main vector types (Aedes aegypti a1 and Ae. albopictus a2), the model incorporates the average temperature of the warmest quarter (b), the occurrence of the Zika virus (c) and the Dengue virus (e), population density (f) and the gross domestic product.
Illustration 2: Zika infection risk modelled for South America.
Illustration 3: Regions where an autochthonous transmission of the Zika virus through the bite of an infected tiger mosquito is possible, since the temperature conditions are suitable (red areas) and the tiger mosquito is already present as vector species (hatched areas).
Further information: Professor Sven Klimpel, Institute for Ecology, Evolution and Diversity, Faculty 15 (Biosciences), Riedberg Campus, phone +49 69 798-42237, E-Mail firstname.lastname@example.org