12th International Meeting on Yeast Apoptosis

Bari, Italy • 14-18 May 2017

Preliminary Programme

Sessions

Fungal cell death pathways

Mitochondrial function and physiology

Metabolic regulation of cell stress response

Autophagy/Mitophagy

Protein aggregation and toxicity

Cellular ageing

Yeast models of human diseases

Yeast-based drug discovery

Systems-based model of cell death and ageing processes

Industrial yeast strain improvement

Confirmed Speakers

Maurizio Bettiga (Gothenburg, Sweden)

Maurizio Bettiga

Maurizio Bettiga was born in Italy and performed his graduate and post graduate studies at University of Milan-Bicocca (Milan, Italy), where he obtained his PhD in Industrial Biotechnology in 2006. After a post doctoral stay as Marie Curie Fellow at Lund University (Sweden), he joined the staff of Industrial Biotechnology at the department of Chemical and Biological Engineering, Chalmers University of Technology in Gothenburg (Sweden) as Assistant Professor.
His research focuses on the study and improvement of robustness of industrial microorganisms, in particular within the concept of Biorefinery for the conversion of lignocellulosic raw materials to fuels and chemicals.
He is currently leading a number of research projects on tolerance of yeast to lignocellulosic hydrolysate inhibitors including acetic acid, in addition to a project in the robustness of anaerobic microbial consortia involved in anaerobic digestion processes.

Charles Boone (Toronto, ON, Canada)

Charles Boone

Dr. Boone is Professor at the University of Toronto's Donnelly Centre and the Department of Molecular Genetics. His research is centered on the development and application of functional genomics approaches. In particular, applying an automated form of yeast genetics, he is investigating the general structure and topology of genetic interaction networks. Recently, Dr. Boone’s group generated a global synthetic genetic interaction map for yeast cells, testing most of the possible 18 million pairs of genes for genetic interactions. This global genetic network reveals a hierarchical model of cellular function, clustering genes and pathways into numerous different biological processes, and grouping bioprocesses into functional compartments. The global genetic network defines gene function, but it also provides a key for interpreting chemical-genetic profiles, linking bioactive compounds to their target pathways.

Carlo Bruschi (Salzburg, Austria)

Carlo Bruschi

Francesco Cecconi (Copenhagen, Denmark)

Francesco Cecconi

Francesco Cecconi is Full Professor of Developmental Biology at the University of Rome Tor Vergata, Unit Head at the Danish Cancer Society Research Center in Copenhagen, Denmark and member of the European Molecular Biology Organization (EMBO).
As a Max-Planck-Institute researcher (MPI of Biophysical Chemistry, Göttingen, Germany) in the field of developmental cell death, he has described the function in vivo of Apaf1 (1997), a master regulator of mitochondria-dependent apoptosis. In 1999, he was awarded a Telethon Scientist position, and since then he is the Head of the Molecular Embryology Lab at the Department of Biology, University of Tor Vergata, Rome, Italy. After his seminal work on the pro-autophagy molecule Ambra1 (2007), he became a world-leader in the field of autophagy, while producing in parallel key papers on the role played by apoptotic molecules in synaptic degeneration.
He is author of more than 150 publications in peer-reviewed journals, including Nature, Cell, and Nature Cell Biology. In recent years, he has developed a strong expertise in the role played by autophagy in cancer and his team is dissecting the regulatory network of this process by multidisciplinary approaches. 

Katrina Cooper (Stratford, NJ, USA)

Katrina Cooper

Dr. Cooper is an Associate Professor in the Department of Molecular Biology, Rowan University, School of Medicine, USA. She received her D. Phil. in Biochemistry from The University of Oxford in 1992 where she studied in the laboratory of Professor Edwin Southern. She was awarded a SERC/NATO research fellowship to support her post-doctoral studies at the Fox Chase Cancer Center, Philadelphia in the laboratory of Dr. Randy Strich. She joined the Department of Biochemistry at Drexel University Medical School, Philadelphia, in 2001 as an Assistant Professor and moved to UMDNJ (now Rowan University) in 2005. The major focus of her research group is understanding how cells decide between life or death following environmental stress. To this end, she is investigating the conserved role of cyclin C in mitochondrial dynamics and apoptosis initiation. In unstressed cells, cyclin C is a transcription factor associating with the Mediator complex of RNA polymerase II. Here, accompanied by its cyclin dependent kinase Cdk8, this duo predominantly represses a subset of stress response genes. To relieve this repression, stress-induced activation of MAPK pathway(s) triggers cyclin C, but not Cdk8, relocalization to the mitochondrial outer membrane. Here it is required for stress-induced fission by associating with the conserved mitochondrial fission apparatus. It is also required for efficient programmed cell death. Currently, her research group investigates the molecular details governing cyclin C nuclear release as well as understanding its precise role in stress-induced fission and cell death. Finally, in collaboration with her former mentor, Dr. Randy Strich, she is investigating a tumor suppressor role for cyclin C in thyroid and pancreatic cancer mouse models. She has been the recipient of many awards including NIH funding and an American Cancer Society Research Scholar Grant.

Manuela Côrte-Real (Braga, Portugal)

Manuela Côrte-Real

Manuela Côrte-Real is a full professor at the Department of Biology, University of Minho, where she has been since 1992. She is also an investigator of the Centre of Molecular and Environmental Biology, Braga. Her research has been focused on the elucidation of apoptotic mechanisms and signalling pathways, namely those involving mitochondria membrane permeabilization and the release of apoptogenic factors, as well as the crosstalk between the mitochondria and the vacuole. Her group found for the first time the release of cytochrome c and the involvement of a mitochondrial mediated pathway in yeast wild-type cells independent of the heterologous expression of Bax. This finding, as well as the organization of the 1st International Meeting on Yeast Apoptosis in Braga, which gathered several researchers that started working on this topic, were relevant contributions to the emergence of the field of yeast apoptosis. Her Lab has also begun studies with mammalian cell lines and corroborated several of her major findings obtained with yeast cells, reinforcing this simple model system as a powerful tool in cell death research. In particular, the lysosomal protease Cathepsin D was shown to play a similar role in acetate-induced apoptosis in colorectal cancer cells as its orthologue Pep4p in acetic acid-induced apoptosis in yeast cells. More recently, and in collaboration with researchers from national and international institutions, she has been using yeast as an in vivo system for functional and molecular studies of individual mammalian apoptotic regulators.
Her global aim is to continue elucidating the regulatory network controlling regulated cell death in living organisms, and ultimately uncover attractive molecular targets for the development of novel therapeutics for Human pathologies associated with cell death dysfunctions, and cancer in particular.

Ali Gargouri (Sfax, Tunisia)

Ali Gargouri

Ali Gargouri is a group leader at the Center of Biotechnology of Sfax-Tunisia. In 1989 he obtained his « Doctorat d’Etat » from the University of Paris VI-France for a thesis work performed at the CNRS of Gif-sur-Yvette. During this stay, he worked on yeast mitochondrial introns, informational suppression and particularly on the reversion of mitochondrial mutations by intron retro-deletion, under the supervision of Pr Piotr Slonimski. Since 1989, he returned in Tunisia to lead a group working mainly, at that time, on fungal cellulases and the bioconversion of lignocellulosic materials into glucose to be converted in valuable by-products. They extended their activities to other hydrolytic fungal enzymes, such as pectinases, xylanases, lipases and proteases. Besides that, a sub-group of the laboratory is involved in another different field, dealing with cancer genetics and heterologous expression in yeast. They carried out several molecular studies on cancer patients searching for polymorphisms, mutations and epigenetic variations, including methylation status and miRNA expression. They have expressed the HBS (Hepatitis B Surface antigen), LMP1 (Latent Membrane Protein of Epstein Barr virus) and p53 gene in yeast and discovered that when over expressed, the p53 human gene triggers yeast apoptosis.

Campbell Gourlay (Canterbury, UK)

Campbell Gourlay

Campbell Gourlay began his career at The John Innes Centre in 1996 where he studied the genetic control of leaf development. Following this he began to work with budding yeast as a model eukaryote in the lab of Kathryn Ayscough, where he investigated the role of actin in the process of endocytosis. During this time he discovered a link between actin, the regulation of mitochondrial function and the control of ageing and apoptosis. This led to his involvement in the emerging field of yeast apoptosis, which has popularised the novel concept that unicellular organisms possess the ability to undergo programmed cell death as an altruistic act for the betterment of a population. In 2006 he was awarded a five year MRC Career Development Fellowship to establish his own lab within the Kent Fungal Group at the University of Kent where is now a senior lecturer in cell biology. The Gourlay lab maintains a strong interest in the role that actin plays in the control of homeostatic mechanisms that contribute to healthy ageing. The lab also uses yeast as a model eukaryote to study a number of aspects of human disease. The group has also diversified to apply its understanding of yeast stress signalling processes and death to the fields of fungal pathogenesis and drug resistance.

Marie Hardwick (Baltimore, MD, USA)

Marie Hardwick

J. Marie Hardwick, PhD, is the David Bodian Professor in the Department of Molecular Microbiology & Immunology at the Johns Hopkins University Bloomberg School of Public Health, and holds joint appointments in the Departments of Biochemistry & Molecular Biology, Pharmacology & Molecular Sciences, Neurology, and Oncology, in the Johns Hopkins School of Medicine. Her research laboratory is best known for uncovering new functions of apoptotic cell death regulators that also alter disease pathogenesis. Her research group uses multiple model systems, including mammals, flies, yeast and viruses to determine the molecular details that govern life-death events: the activation of cell death in the epileptic brain, the failure of cancer cells to die, the apoptotic versus non-death functions of BCL-2 family proteins and caspase proteases, and the signals responsible for converting the pro-survival function of a protein into its pro-apoptotic function in a timely manner. Current projects include: non-apoptotic functions of caspases in the brain; novel membrane functions of apoptosis regulators of the BCL-2 protein family; gene mutation-driven genome evolution in yeast and in cancer cell survival, evolutionarily conserved nutrient-sensing pathways that control cell growth, autophagy defects in neurodegeneration, novel functions for new epilepsy genes, and the identification of yeast genes that can be unleashed to promote fungal cell death. Her research seeks to translate basic science knowledge to enhance the value of science to society, through discovery, education and innovation.

Paula Ludovico (Braga, Portugal)

Paula Ludovico

Paula graduated in Biology at the University of Porto (1994) and did her Master thesis on Molecular Genetics at the University of Minho (1999). In 2002 concluded her PhD in Biological Sciences at University of Minho. Paula was a visiting scientist at the Department of Biological Sciences, Columbia University, New York, USA and at the Department of Neurology, Miami University, Florida, USA. Since 2002, Paula is an Associate Professor at School of Medicine and a Principal Investigator at the Health and Life Sciences Research Institute (ICVS), School of Medicine, University of Minho. Paula was a pioneer on the study of programmed cell death in yeast and fungi and was one of the organizers of the 1st and the 11th International Meeting on Yeast Apoptosis. She has developed work in studying the mechanisms of programmed cell death in yeast and their link with autophagy and aging. Paula Ludovico is author or co-author of more than 56 publications in international Journals, 5 book chapters and participated as oral presenter/poster presenter in more than 50 International meetings related with the field. She has also been acting as referee for more than 20 international journals.

Frank Madeo (Graz, Austria)

Frank Madeo

Frank Madeo graduated in Tuebingen, Germany and is currently Professor for Molecular Biosciences at the University of Graz. He discovered and initiated the field of Programmed cell death in yeast and developed most of the techniques for its detection. He and his group has a long standing experience in phenotyping and molecular characterization of distinct causal metabolites of aging and longevity that are conserved across species. He discovered the role of spermidine in autophagy induction, cell protection and longevity.

Lynn Megeney (Ottawa, QC, Canada)

Lynn Megeney

Lynn Megeney is a Senior Scientist at the Sprott Centre for Stem Cell Research, at the Ottawa Hospital Research Institute, and he also holds academic appointments as Professor in the Dept. of Medicine (Division of Cardiology) and the Dept. of Cellular and Molecular Medicine at the University of Ottawa. Research from the Megeney group has had global impact in an area of basic cellular biology. Specifically, his group discovered that cell death or cell suicide pathways play vital roles in normal biologic processes such as stem cell differentiation and proteostasis. More recently, studies from the Megeney lab have shown that these same apoptotic proteins and pathways act as potent regulatory or mitigating factors in human disease. His laboratory is supported by provincial, national and international funding agencies and he has been the recipient of numerous awards and honors including the Mach Gaennslen Chair in Cardiac Research from 2005 to 2011 and an International Fellowship from the Chinese Academy of Sciences. In addition to his academic work, he maintains a keen interest in translational science and commercialization efforts, serving as a scientific founder of three biotechnology companies.

Jens Nielsen (Gothenburg, Sweden)

Jens Nielsen

Jens Nielsen has an MSc degree in Chemical Engineering and a PhD degree (1989) in Biochemical Engineering from the Danish Technical University (DTU), and after that established his independent research group and was appointed full Professor there in 1998. He was Fulbright visiting professor at MIT in 1995-1996. At DTU he founded and directed Center for Microbial Biotechnology. In 2008 he was recruited as Professor and Director to Chalmers University of Technology, Sweden, where he is currently directing a research group of more than 50 people. At Chalmers he established the Area of Advance Life Science Engineering, a cross departmental strategic research initiative and was founding Head of the Department of Biology and Biological Engineering, which now encompass more than 170 people. Jens Nielsen has published so far more than 550 papers that have been cited more than 35,000 times (current H-factor 92), and co-authored more than 40 books. He is inventor of more than 50 patents and he has founded several biotech companies. He has received numerous Danish and international awards including the Nature Mentor Award, and is member of several academies, including the National Academy of Engineering in USA, the Royal Swedish Academy of Science, the Royal Danish Academy of Science and Letters, the Royal Swedish Academy of Engineering Sciences and the American Academy of Microbiology. He is a founding president of the International Metabolic Engineering Society.

Tiago Outeiro (Goettingen, Germany)

Tiago Outeiro

Prof. Tiago Outeiro graduated in Biochemistry at the University of Porto and was an Erasmus student at the University of Leeds in the UK. Prof. Outeiro did his PhD thesis at the Whitehead Institute for Biomedical research – MIT and worked as a Research Scientist at FoldRx Pharmaceuticals as a Research Scientist and Consultant. Prof. Outeiro was a Postdoctoral Research Fellow in the Department of Neurology of the Massachusetts General Hospital – Harvard Medical School where he focused on the study of Neurodegenerative disorders such as Parkinson’s and Alzheimer’s disease. Prof. Outeiro directed the Cell and Molecular Neuroscience Unit at IMM, Lisbon, from 2007 to 2014, and is currently Full Professor and the Director of the Department of Neurodegeneration and Neurorestoration at the University Medical Center Goettingen, in Germany. Prof. Outeiro has authored >130 research articles in international journals and participates in various international collaborative projects with the aim of identifying the molecular basis of neurodegenerative disorders such as Alzheimer’s and Parkinson’s disease.

Zdena Palkova (Prague, Czech Republic)

Zdena Palkova

Zdena Palkova is Professor and Group Leader at the Faculty of Science, Charles University in Prague, Czech Republic. ZP’s “Yeast Colony Group” studies molecular and cellular mechanisms that are involved in formation, differentiation and ageing of colonies of yeast coming from different environments. Current research is focused on i) function and regulation of processes involved in development of specialized colonial cells similar to cells of solid tumors of mammals; ii) differentiation of cells forming structured biofilm colonies of natural yeast strains; iii) regulations of processes involved in resistance of yeast biofilm colonies and biofilms against environmental attack (including drug treatment) and iv) development of new approaches to study multicellular structures.
Web page
Bibliography

Dina Petranovic (Gothenburg, Sweden)

Dina Petranovic

Dina Petranovic has a background in molecular biology from Zagreb University (1994-1999, Croatia), PhD in molecular microbiology from Paris University XI (2000-2004, France), two postdocs from Danish Technical University (2004-2007, Denmark) in microbial genetics and microbial biotechnology and sabbatical from Lindquist Lab at MIT (2012, USA). Dina has been an assistant (2008-2012) and then associate professor (since 2012) at Chalmers University of Technology, in Göteborg, Sweden.
Dina used to work with G+ bacteria and signal transduction mediated by phosphorelay (PTS) and protein-phosphorylation. Since 2007 she has been focusing on yeast Saccharomyces cerevisiae and how to use it to study proteostasis management. Her interest is to figure out how and why expression of some proteins that are not inherently toxic can damage the cell, and what is the fate of the cell in such circumstances. The proteins that she is interested in can have different origin and applications, for example she uses a fungal industrial enzyme (α-amylase) to study how secreting a large protein induces stress in the secretory pathway and how that influences the cell stress responses and eventually cell fate. She also uses other proteins, for example human insulin precursor, human globin proteins (hemoglobin, myoglobin, neuroglobin), human amyloid-β peptide (involved in Alzheimer’s disease) and human mutant ubiquitin. This approach is helping to learn about the fundamental roles of these proteins in vivo, the cell stress responses and additionally find engineering targets to use the yeast cell as a factory for production of proteins.
In her work Dina uses molecular and cell biology tools and approaches, microscopy, physiological characterizations, omics analyses, modeling and bioinformatics.
For more information please visit www.sysbio.se .

Ted Powers (Davis, CA, USA)

Ted Powers

Ted Powers received his PhD from the University of California at Santa Cruz in 1992, where he studied the structure and function of the ribosome with Professor Harry F. Noller. He then carried out postdoctoral studies at the University of California at San Francisco with Professor Peter Walter, where he examined the mechanism of protein targeting to biological membranes. During this time, he became interested in the regulation of cell growth in eukaryotic cells, in particular the role of the rapamycin-sensitive TOR signaling network. He carried these interests with him to the University of California at Davis, where he has been a faculty member since 1999. He is presently a Professor in the Department of Molecular and Cellular Biology in the College of Biological Sciences. His present research is aimed at understanding the architecture and scope of the TOR network in regulating cellular responses to intracellular as well as environmental cues, including conditions of stress.

Jared Rutter (Salt Lake City, UT, USA)

Jared Rutter

Dr. Jared Rutter is a Professor of Biochemistry and holds the Dee Glen and Ida Smith Endowed Chair for Cancer Research at the University of Utah where he has been on the faculty since 2003. As of September 2015, he is also an Investigator of the Howard Hughes Medical Institute. His laboratory employs a wide array of technologies to enable discovery related to metabolic control as well as fundamental aspects of mitochondrial biology. The Rutter laboratory has characterized the PAS kinase protein as an important factor in states of metabolic dysregulation—including obesity and diabetes. More recently, the Rutter laboratory and collaborators have identified the functions of a number of previously uncharacterized mitochondrial proteins, including the discovery of the long-sought mitochondrial pyruvate carrier. This knowledge has now enabled for the first time the interrogation of this critical metabolic step for impact in a variety of human diseases, including cancer and cardiovascular disease. Dr. Rutter is also actively involved in translating these academic discoveries into therapies for patients. Dr. Rutter also serves as co-Director of the Diabetes and Metabolism Center at the University of Utah and co-Leader of the Nuclear Control of Cell Growth and Differentiation at Huntsman Cancer Institute.

Hiroshi Takagi (Nara, Japan)

Hiroshi Takagi

Hiroshi Takagi was awarded the degrees of M.Sc. in immunology at Nagoya University in 1982. After his graduation, he worked at Ajinomoto Co, Inc. as a research scientist from 1982 to 1995. During the time, he studied at State University of New York at Stony Brook under Prof. Masayori Inouye in 1986 and received his Ph.D. degree at the University of Tokyo under Prof. Takahisha Ohta in 1988 for protein engineering of the Bacillus subtilis subtilisin E. He promoted to Chief Biochemist for protein engineering of microbial enzymes for industrial use and development of frozen dough. In 1995, Dr. Takagi left Ajinomoto and was appointed Associate Professor at Fukui Prefectural University. He then started his major fundamental research on novel stress-tolerant mechanisms of yeast, focusing on amino acid metabolism and ubiquitin system, and their applications to industrial yeast breeding. He promoted to full Professor in 2001 and moved to Nara Institute of Science and Technology (NAIST) ten years ago (2006). The Takagi lab is involved in Applied Molecular Microbiology including yeast big projects and the bacterial cysteine/sulfur metabolism. http://bsw3.naist.jp/takagi/English.htm

Benedikt Westermann (Bayreuth, Germany)

Benedikt Westermann

Benedikt Westermann obtained his doctoral degree in 1996 in the group of Walter Neupert at the University of Munich. After postdoctoral research in the lab of James E. Rothman at the Sloan-Kettering Institute in New York he returned to Munich to establish his own group working on mitochondrial dynamics in yeast. Since 2003 he is Professor of Cell Biology at the University of Bayreuth in Germany. His research focuses on fusion, fission, inheritance, and ultrastructure of mitochondria using state-of-the-art genetic methods, light and electron microscopy, and budding yeast as a major model organism. In several genome-wide screens his research group uncovered the genes that regulate mitochondrial distribution and morphology, inheritance of mitochondrial DNA, and mitophagy. Current projects analyze the molecular machinery orchestrating asymmetric inheritance of mitochondria in yeast and its role in aging and cell death.

Joris Winderickx (Leuven, Belgium)

Joris Winderickx

Joris Winderickx obtained his degree Master of Science in Biology at the Katholieke Universiteit Leuven (KU Leuven, Belgium) in 1984 and a PhD in Sciences at the same university in 1990. He then went as a Senior Fellow to the University of Washington, Seattle for a Post-Doc at the Dept of Genetics (Prof. S. Deeb) and the Dept of Human Genetics (Prof. A. Motulsky). At the end of 1992 he returned to the KU Leuven is now full professor at the Dept. of Biology at the KU Leuven, Belgium, and head of the research group Functional Biology (http://www.kuleuven.be/bio/funbio). He is an expert in molecular cell biology and genetics and is internationally known for his research on signal transduction in yeast and the use of humanized yeast models for medical applications, as further illustrated by an outstanding publication record in high-ranked international journals. His research is embedded in a well-established network of national and international collaborations with academia, biotech and pharmaceutical companies. Joris Winderickx also co-founded the KU Leuven spin-offs reMYND, that focusses on drug discovery (http://www.remynd.com), and ADx NeuroSciences, a company dedicated to biomarker identification and diagnostics (http://www.adxneurosciences.com). Since August 2014, Joris Winderickx is heading the Biology Department of KU Leuven.

Richard Y. Zhao (Baltimore, MD, USA)

Richard Y. Zhao

I am currently a Professor of Pathology, Microbiology-Immunology and Human Virology, and a Division Head of Molecular Pathology at the University of Maryland School of Medicine, Baltimore, Maryland, USA. My basic science research interest is in the area of host-pathogen interactions specifically to study the effects of viral infections on host innate cellular responses. I use a unique approach in my research by combining the tools of molecular biology, fission yeast genetics, mammalian biology and virology into a single theme. Studies supported with such a distinctive combination of tools often give rise to unique perspectives of scientific findings that are otherwise difficult to obtain based solely on a single approach or organism. The adaptation of this special research approach was rooted from my scientific training and working experiences. I was initially trained in molecular biology and microbial genetics at Oregon State University. My postdoctoral training was in molecular biology and fission yeast genetics at Columbia University College of Physicians and Surgeons. I started my own independent research laboratory in 1994 at Northwestern University Feinberg School of Medicine where I came up the idea of using fission yeast as a model to study human immunodeficiency virus type 1 (HIV-1). Because of my scientific achievements, I was awarded with an endowed research Chair as the Bernard L. Mirkin PhD/MD Research Scholar at the Children’s Memorial Institute of Education and Research, Northwestern University Feinberg School of Medicine. Through these research efforts, I have built extensive experiences and a strong track record of scientific achievements in the described scientific areas with a total of greater than 120 peer-reviewed publications. I have been invited to serve on many scientific journal editorial boards including Cell Research, Cell and Biosciences, Frontiers in Virology, Microbial Cell, PLoS One and Retrovirology. In addition, I have been invited to review scientific grant applications for funding agencies of over 10 different countries and have chaired or served on a number of NIH grant review study panels or sections. I have been invited to give scientific and clinical lectures world-wide.

Sunday, 14 May

17:00

Registration opening

17:30-18:00

Opening and Welcome

Alessandro Ambrosi (President of Bari Chamber of Commerce)

Antonio Felice Uricchio (Rector of the University "Aldo Moro", Bari)

Graziano Pesole (Director of the Institute of Biomembranes and Bioenergetics, CNR, Bari)

18:00-19:00

Opening Lecture

Frank Madeo (Austria)
From dying yeasts to longevity drugs

19:00-20:00

Get together party – mingling

Monday, 15 May

8:00-12:00

Late Registration

8:30-11:00

Session 1: Fungal Cell Death pathways I

Marie Hardwick (USA)
Yeast cell death and nutrient-sensing pathways merge

Campbell Gourlay (UK)
Actin and the mitochondria co-ordinate MAPK signalling to control cell health

Selected lectures from submitted abstracts

11:00-11:30

Coffee break

11:30-13:00

Session 2: Fungal Cell Death pathways II

Katrina Cooper (USA)
MAPK and SCF choreograph the 2-step dance to cyclin C mediated cell death

Carlo Bruschi (Austria)
Apoptotic dynamics ensuing Bridge-Induced chromosome Translocation

Selected lectures from submitted abstracts

13:00-14:00

Lunch

14:00-15:00

Poster session I

15:00-17:30

Session 3: Mitochondrial function and physiology

Jared Rutter (USA)
Functionalizing the unannotated mitochondrial proteome

Benedikt Westermann (Germany)
Asymmetric inheritance of mitochondria in yeast

Selected lectures from submitted abstracts

17:30-18:00

Coffee break

18:00-19:30

Session 4: Metabolic regulation of cell stress response

Jens Nielsen (Sweden)
Adaptation of the yeast proteome to stress: Insights from systems analysis

Hiroshi Takagi (Japan)
Nitric oxide in yeast: a double-edged sword "cell protection vs. cell death"

Selected lectures from submitted abstracts

Tuesday, 16 May

8:30-10:30

Session 5: Autophagy/Mitophagy

Francesco Cecconi (Denmark)
Autophagy fine regulation: key molecules in a destroy-to-create pathway

Ted Powers (USA)
Autophagy and stress: intersection of TOR, mitochondria, and Calcium signaling

Selected lectures from submitted abstracts

10:30-11:00

Coffee break

11:00-13:00

Session 6: Cellular Ageing

Zdena Palková (Czech Republic)
Mitochondria, important players in ageing and metabolic differentiation of yeast colonies

[Plenary speaker tba]

Selected lectures from submitted abstracts

13:00-14:00

Lunch

14:00-16:00

Session 7: Protein aggregation and toxicity

Tiago Outeiro (Germany)
The yeast toolbox to determine the role of posttranslational modifications in Parkinson's disease

Dina Petranovic (Sweden)
Physiological characterisation of Amyloid-beta expressing strains

Selected lectures from submitted abstracts

16:00-16:30

Coffee break

16:30-18:00

Session 8: Yeast models of human deaseases I

Joris Winderickx (Belgium)
On nutrient signaling, second messengers and the use of yeast as disease model

Richard Zhao (USA)
The use of fission yeast as a surrogate system for the discovery of cytopathic factors through genome-wide analysis of Zika viral proteins

Selected lectures from submitted abstracts

18:00-19:00

Poster session II

19:00-20:00

Meeting of the IMYA Scientific Advisory Board

Wednesday, 17 May

8:30-10:00

Session 9: Yeast models of human deaseases II

Ali Gargouri (Tunisia)
Cell death induced by p53 expression in yeast: detection and suppression

Manuela Corte-Real (Portugal)
Mechanistic insights on the selective antitumoral activity of lactoferrin unveiled by yeast

Selected lectures from submitted abstracts

10:00-10:30

Coffee break

10:30-12:30

Session 10: Yeast-based drug discovery

Ralf Braun (Germany)
Neurotoxic 43 kDa TAR DNA-binding protein (TDP-43) interferes with its own degradation via the endolysosomal pathway

Paula Ludovico (Portugal)
Supplemented metabolites as anti-aging strategies in yeast

Selected lectures from submitted abstracts

12:30-14:00

Lunch

15:00

Excursion and gala dinner

Thursday, 18 May

9:00-11:00

Session 11: Systems-based model of cell death and ageing processes

Charles Boone (Canada)
A global genetic interaction network maps a wiring diagram of cellular function

Duccio Cavalieri (Italy)
Dead yeast cells as common goods: cooperation and competition at the community level: a systems biology approach

Selected lectures from submitted abstracts

11:00-11:30

Coffee break

11:30-13:15

Session 12: Industrial yeast strain improvement

Maurizio Bettiga (Sweden)
Membrane permeability as a key determinant of acetic acid tolerance in yeast

[Plenary speaker tba]

Selected lectures from submitted abstracts

 

Closing remarks

13:15-14:15

Lunch and Departure

14:30-17:00

Meeting of the Italian yeast research community