Gaia Tavosanis

Prof. Dr. Gaia Tavosanis

orcid

Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
1 November 2010 in Current Biology
Verified
Journal Article
Closed access
MKMalte C. Kremer
Malte C. Kremer
FCFrauke Christiansen
Frauke Christiansen
FLFlorian Leiss
Florian Leiss
MPMoritz Paehler
Moritz Paehler
SKStephan Knapek
Stephan Knapek
GTGaia Tavosanis
Gaia Tavosanis

21 January 2009 in Developmental Neurobiology
Verified
Journal Article
Open access
PDF file
FLFlorian Leiss
Florian Leiss
EKEwa Koper
Ewa Koper
IHIrina Hein
Irina Hein
WFWernher Fouquet
Wernher Fouquet
JLJana Lindner
Jana Lindner
GTGaia Tavosanis
Gaia Tavosanis
Dendritic spines are a characteristic feature of a number of neurons in the vertebrate nervous system and have been implicated in processes that include learning and memory. In spite of this, there has been no comprehensive analysis of the presence of spines in a classical genetic system, such as Drosophila, so far. Here, we demonstrate that a subset of processes along the dendrites of visual system interneurons in the adult fly central nervous system, called LPTCs, closely resemble vertebrate spines, based on a number of criteria. First, the morphology, size, and density of these processes are very similar to those of vertebrate spines. Second, they are enriched in actin and devoid of tubulin. Third, they are sites of synaptic connections based on confocal and electron microscopy. Importantly, they represent a preferential site of localization of an acetylcholine receptor subunit, suggesting that they are sites of excitatory synaptic input. Finally, their number is modulated by the level of the small GTPase dRac1. Our results provide a basis to dissect the genetics of dendritic spine formation and maintenance and the functional role of spines. © 2009 Wiley Periodicals, Inc. Develop Neurobiol, 2009

6 August 2009 in Journal of Comparative Neurology
Verified
Journal Article
Closed access
PDF file
FLFlorian Leiss
Florian Leiss
CGClaudia Groh
Claudia Groh
NBNancy J. Butcher
Nancy J. Butcher
IMIan A. Meinertzhagen
Ian A. Meinertzhagen
GTGaia Tavosanis
Gaia Tavosanis

1 February 2003 in Developmental Cell
Verified
Journal Article
Closed access
CPClaudia Petritsch
Claudia Petritsch
GTGaia Tavosanis
Gaia Tavosanis
CTChristoph W. Turck
Christoph W. Turck
LJLily Y. Jan
Lily Y. Jan
YJYuh Nung Jan
Yuh Nung Jan

29 June 2011 in Journal of Neuroscience
Verified
Journal Article
Open access
PDF file
FCFrauke Christiansen
Frauke Christiansen
CZChristina Zube
Christina Zube
TATill Andlauer
Till Andlauer
CWCarolin Wichmann
Carolin Wichmann
WFWernher Fouquet
Wernher Fouquet
SSStephan J. Sigrist
Stephan J. Sigrist
Plastic changes at the presynaptic sites of the mushroom body (MB) principal neurons called Kenyon cells (KCs) are considered to represent a neuronal substrate underlying olfactory learning and memory. It is generally believed that presynaptic and postsynaptic sites of KCs are spatially segregated. In the MB calyx, KCs receive olfactory input from projection neurons (PNs) on their dendrites. Their presynaptic sites, however, are thought to be restricted to the axonal projections within the MB lobes. Here, we show that KCs also form presynapses along their calycal dendrites, by using novel transgenic tools for visualizing presynaptic active zones and postsynaptic densities. At these presynapses, vesicle release following stimulation could be observed. They reside at a distance from the PN input into the KC dendrites, suggesting that regions of presynaptic and postsynaptic differentiation are segregated along individual KC dendrites. KC presynapses are present in γ-type KCs that support short- and long-term memory in adult flies and larvae. They can also be observed in α/β-type KCs, which are involved in memory retrieval, but not in α′/β′-type KCs, which are implicated in memory acquisition and consolidation. We hypothesize that, as in mammals, recurrent activity loops might operate for memory retrieval in the fly olfactory system. The newly identified KC-derived presynapses in the calyx are, inter alia, candidate sites for the formation of memory traces during olfactory learning.

1 May 2015 in Neuron
Verified
Journal Article
Closed access
ASAtsushi Sugie
Atsushi Sugie
SHSatoko Hakeda-Suzuki
Satoko Hakeda-Suzuki
ESEmiko Suzuki
Emiko Suzuki
MSMarion Silies
Marion Silies
MSMai Shimozono
Mai Shimozono
GTGaia Tavosanis
Gaia Tavosanis