How do closely related neuron types establish and then maintain their functional differences ? And, how do genetic programs differ between individuals to create unique brains ? Colour photoreceptor neurons of the fly retina have proven to be an excellent system for addressing these question. Our lab focuses on the R8 photoreceptor type, with its two subtypes that express distinct Rhodopsins (G-protein coupled receptor that acts as a photon detectors). The two Rhodopsins, Rh5 and Rh6, are sensitive to blue and green wavelengths respectively and thus define the colours that the photoreceptor neurons respond to. Normally, these two subtypes of R8 cells are present in about 30%:70% (Rh5:Rh6) ratio, they are distributed stochastically, and Rh5 and Rh6 are never co-expressed. (See the figures and the reference 1 for images of what this looks like in the eye and for more details about the system.) The differentiation program that leads to this Rhodospin expression pattern has been relatively well understood (ref.1), yet a number of interesting and important questions remain unanswered. Also, we recently discovered that in the natural populations, individual flies can have eyes which deveate substantially from this standard laboratory Rhodopsin pattern and that much of this is due to the genetic differences among the flies.
Project 1 : Fly individuality : Identification and characterization of a wild-derived genetic variant affecting photoreceptor neuron identities in the adult Drosophila retina.
The mutually exclusive Rh5/Rh6 expression is established through a bistable positive feedback-driven genetic switch which turns ON (for Rh6) or OFF (for Rh5) the Hippo tumor supressor pathway. The involvement of this pathway is curious, because in most other systems, it regulates growth and cell prolifferation through negative feedbacks that drive the pathway towards equilibrium (like a thermostat, i.e. in sharp contrast to the bistability observed in the photoreceptors). To identify new genes involved in establishment and maintenance of Rh5/Rh6 expression pattern we took an unusual approach : we examined 200 fly lines recently derived from wild-caught flies. Surprisingly, many of them have interesting phenotypes that affect differentiation, maintenance and function of the R8 photoreceptor neurons.
One line in particular, has a reversed Rh5:Rh6 cell ratio (see figure) and is similar to the loss of the Hippo pathway phenotypes (which are normally lethal). Identification of the sequence change resulting in this phenotype will provide an interesting example of what type of natural genetic variation can affect a single function of this essential pathway without affecting its other roles. This is fundamental to understanding how pathways can independently evolve multiple functions.
The student will use powerful Drosophila genetics to identify the gene affected by the mutation and then will identify the mutation itself. In parallel, he or she will characterize the phenotype in order to understand the molecular mechanisms underlying it. The experiments will involve genetics, microdissection, immunohistochemistry (antibody stains), RNAscope-based in situ hybridization, confocal microscopy, and molecular biology.
Project 2 : Maintenance of neuronal functionality in an aging organism : molecular pathways that maintain the mutually exclusive Rhodopain5/Rhodopsin6 expression in the adult Drosophila retina.
How do terminally differentiated cells, particularly the long-living neurons, maintain their functionality throughout the life of the organism as it ages, is a fundamental biological question that is not well explored. We address it by asking what are the molecular mechanisms that maintain the mutually exclusive Rh5 vs. Rh6 expression in adult R8 neurons. We made a surprising discovery that a feedback signal from the Rh6 itself prevents transcription of Rh5 gene in the Rh6-expressing yR8 photoreceptors in adult flies (2). Furthermore, this signal does not involve key components of the phototransduction cascade, the molecular pathway by which light information is converted into an electrical signal. This implies a new unknown molecular signaling pathway downstream of Rh6.
What is also not known is how Rh6 expression is prevented in Rh5-expressing R8 photoreceptors. Recently we found a number of mutations in which, Rh6 is co-expressed with Rh5, the underlying genes normally function in repression of Rh6 in the “wrong” R8 photoreceptors.
This leads to a number of the “molecular pathway” questions which the student will address using powerful Drosophila genetics, microdissection, immunohistochemistry, RNAscope-based in situ hybridization, confocal microscopy, and molecular biology.
Relevant publications :
1. Rister, J., Desplan, C., and Vasiliauskas, D. (2013) Establishing and maintaining gene expression patterns : insights from sensory receptor patterning. Development 140, 493-503.
2. Vasiliauskas, D., Mazzoni, E.O., Sprecher, S.G., Brodetskiy, K., Johnston, R.J.Jr., Lidder, P., Vogt, N., Celik, A., and Desplan, C. (2011) Feedback from Rhodopsin controls rhodopsin exclusion in Drosophila photoreceptors. Nature, 479, 108-12.
3. Anderson, C., Reiss, I., Zhou, C., Cho, A., Siddiqi, H., Morman, B., Aviles, C.M., Deford, P., Bergland, A., Roberts, E., Taylor, J., Vasiliauskas, D., and Johnston, R.J., Jr. (2017)
Natural variation in stochastic photoreceptor specification and color preference in Drosophila. eLife, 6, e29593.
Functional studies of candidate pediatric cancers driver’s genes in a rare pediatric cancer.
The student will develop behavioral paradigms and new analyses based on the existing set ups in the lab (automated video-tracking, automated behavioral detection, quantitative behavioral analysis), by using both his/her ideas and existing protocols in the literature. This internship is also an opportunity to discover the Drosophila model, learn its advantages and other techniques used in the lab from Drosophula genetics to connectomics and functional imaging. The candidate will work in the team Neural Circuits and Behavior headed by Tihana Jovanic in Saclay (20 km south of Paris). NeuroPSI has state-of the art core facilities and the Saclay campus provides a highly interdisciplinary and collaborative environment mixing university and engineering schools, with excellent laboratories in fundamental and applied science. There will also be opprotunities for collaboration with the Janelia Research Campus (USA) and Institut Pasteur (Paris, France).
The hired individual (postdoctoral researcher) will contribute to research projects supported by an Equipe FRM grant, on morphogenetic mechanisms underlying eye malformations in the blind Mexican cavefish.
The « Computational Neuroscience » group of NeuroPSI Institute, and the European Institute for Theoretical Neuroscience (EITN), recruit a postdoctoral researcher for the computer modeling of neural networks implicated in decision making, in collaboration with Ruben Moreno-Bote (Barcelona).
The applicant will organize and undertake in-depth comparative studies of several mouse models holding distinct mutations in the DMD gene to address a range of cognitive and executive functions in a variety of behavioral paradigms. He/she will also perform statistical analyses, generate and archive results reports, and contribute to dissemination of the produced knowledge through scientific written and oral communications in French and/or English.