Conserved domains control heterochromatin localization and silencing properties of SU(VAR)3-7

The Drosophila protein SU(VAR)3-7 is essential for fly viability, chromosome structure, and heterochromatin formation. We report that searches in silico and in vitro for homologues of SU(VAR)3-7 were successful within, but not outside, the Drosophila genus. Protein sequence homology between the distant sibling species Drosophila melanogaster and Drosophila virilis is low, except for the general organization of the protein and three conserved motives: seven widely spaced zinc fingers in the N-terminal half and the BESS and BoxA motives in the C-terminal half of the protein. We have undertaken a fine functional dissection of SU(VAR)3-7 in vivo using transgenes encoding truncations of the protein. BESS mediates interaction of SU(VAR)3-7 with itself, and BoxA is required for specific heterochromatin association. Both are necessary for the silencing properties of SU(VAR)3-7. The seven zinc fingers, widely spaced over the N-terminal half of SU(VAR)3-7, are required for binding to polytene chromosomes. One finger is necessary and sufficient to determine the appropriate chromatin association of the C-terminal half of the protein. Conferring a function to each of the conserved motives allows us to better understand the mode of action of SU(VAR)3-7 in triggering heterochromatin formation and subsequent genomic silencin

A novel approach to volcano surveillance using gas geochemistry

The aim of this paper is to test a simple damage model of a cohesive granular medium to study the relationship between the damage and velocity of elastic waves. Our numerical experiments of edometric compression show that the mi- croscopic deformation quickly becomes very heterogeneous, while our simulations of elastic waves propagation show that a small amount of damage induces a dra- matic decrease in the elastic velocity. This shows that cohesive discrete media are very sensitive to strain field heterogeneity, and that the wave velocities in these media can measure subtle transient deformation processes, such as earthquake initiation phases

The contrasting origins of glauconite in the shallow marine environment highlight this mineral as a marker of paleoenvironmental conditions

Glauconite is an authigenic mineral reputed to form during long-lasting contact between a nucleus (a pre-existing phyllosilicate) and seawater. This protracted contact makes it possible to subtract the ions necessary for the construction of the neoformed phyllosilicate, here, glauconite (a mineral very close to an illite, rich in K and Fe). As a result, glauconite is often associated with sediments deposited in a transgressive context with a strong slowdown in the rate of sedimentation and a relatively large water layer thickness. This is the case of the Cenomanian chalk of Boulonnais (north of France). Being chemically and physically resistant, glauconite is a mineral that is often reworked, like quartz grains. This is frequently the case of the Jurassic deposits of the Boulonnais, where glauconite, almost ubiquitous, either in traces or in significant proportions of the sediments, presents a grain size sorting attesting to its transport and reworking. However, these Jurassic deposits are shallow (shoreface, upper offshore), which supports the idea that the “glauconite factory” was itself in the shallow areas of the Boulonnais. The only identified Jurassic facies of the Boulonnais where glauconite is both relatively abundant, large in size and unsorted (non reworked) are oyster reefs that formed at the outlet of cold seeps linked to a late-Jurassic synsedimentary tectonic (Kimmeridgian, Tithonian). Our work makes it possible to hypothesize that isolated oyster reefs were environments combining the redox conditions and in contact with seawater favoring the authigenic formation of glauconite. The weakly reducing conditions necessary for the formation of glauconite here are attested by the contents of metallic trace elements sensitive to redox conditions (vanadium, germanium, arsenic, in this case). Our work thus adds a new element to the understanding of the mechanisms of formation of glauconite in shallow environments

CRAL-MUS – Musique

Élizabeth Claire, chargée de recherche au CNRSEmmanuelle Delattre, doctorante à l’Université Versailles Saint-Quentin-en-YvelinesMarie Glon, Juan Ignacio Vallejos, doctorantsSophie Jacotot, postdoctoranteVannina Olivesi, doctorante à l’Université de ProvenceMarion Rhéty, doctorante à l’Université Paris 1-Panthéon-Sorbonne Histoire culturelle de la danse Cette année, le séminaire a exploré les contours d’un projet collectif intitulé Danse et morale, à l’époque moderne et contemporaine. Plusieu..

Luc Courchesne : observateur du monde

Catalogue préparé sous la direction de Christine Bernier.Catalogue de l’exposition tenue au Carrefour des arts et des sciences, Université de Montréal, du 13 avril au 19 juin 2022

SU(VAR)3-7 Links Heterochromatin and Dosage Compensation in Drosophila

In Drosophila, dosage compensation augments X chromosome-linked transcription in males relative to females. This process is achieved by the Dosage Compensation Complex (DCC), which associates specifically with the male X chromosome. We previously found that the morphology of this chromosome is sensitive to the amounts of the heterochromatin-associated protein SU(VAR)3-7. In this study, we examine the impact of change in levels of SU(VAR)3-7 on dosage compensation. We first demonstrate that the DCC makes the X chromosome a preferential target for heterochromatic markers. In addition, reduced or increased amounts of SU(VAR)3-7 result in redistribution of the DCC proteins MSL1 and MSL2, and of Histone 4 acetylation of lysine 16, indicating that a wild-type dose of SU(VAR)3-7 is required for X-restricted DCC targeting. SU(VAR)3-7 is also involved in the dosage compensated expression of the X-linked white gene. Finally, we show that absence of maternally provided SU(VAR)3-7 renders dosage compensation toxic in males, and that global amounts of heterochromatin affect viability of ectopic MSL2-expressing females. Taken together, these results bring to light a link between heterochromatin and dosage compensation

CRAL – Centre de recherches sur les arts et le langage

Esteban Buch, Giovanni Careri, directeurs d’étudesMarielle Macé, chargée de recherche au CNRS L’art et l’esthétique en questions Le CRAL a proposé cette année un rendez-vous collectif autour de questions-clés de l’esthétique contemporaine. Autour d’une série d’interventions d’invités et de membres du centre, on a construit des séances-débats privilégiant les partis pris ou les conflits de disciplines qui animent le champ de l’esthétique. La première séance, inaugurale, était un entretien (men..

CRAL – Centre de recherches sur les arts et le langage

Esteban Buch, Giovanni Careri, directeurs d’étudesMarielle Macé, chargée de recherche au CNRS L’art et l’esthétique en questions Le CRAL a proposé cette année un rendez-vous collectif autour de questions-clés de l’esthétique contemporaine. Autour d’une série d’interventions d’invités et de membres du centre, on a construit des séances-débats privilégiant les partis pris ou les conflits de disciplines qui animent le champ de l’esthétique. La première séance, inaugurale, était un entretien (men..

ALK germline mutations in patients with neuroblastoma: a rare and weakly penetrant syndrome

Neuroblastic tumours may occur in a predisposition context. Two main genes are involved: PHOX2B, observed in familial cases and frequently associated with other neurocristopathies (Ondine's and Hirschsprung's disease); and ALK, mostly in familial tumours. We have assessed the frequency of mutations of these two genes in patients with a presumable higher risk of predisposition. We sequenced both genes in 26 perinatal cases (prebirth and o1 month of age, among which 10 were multifocal), 16 multifocal postnatal (41 month) cases, 3 pairs of affected relatives and 8 patients with multiple malignancies. The whole coding sequences of the two genes were analysed in tumour and/or constitutional DNAs. We found three ALK germline mutations, all in a context of multifocal tumours. Two mutations (T1151R and R1192P) were inherited and shared by several unaffected patients, thus illustrating an incomplete penetrance. Younger age at tumour onset did not seem to offer a relevant selection criterion for ALK analyses. Conversely, multifocal tumours might be the most to benefit from the genetic screening. Finally, no PHOX2B germline mutation was found in this series. In conclusion, ALK deleterious mutations are rare events in patients with a high probability of predisposition. Other predisposing genes remain to be discovered