Search bioRxiv⌕ Search

Biology subjects

Fabrice, F.

Publications and source records attributed to Fabrice, F..

4 recordsLinked to original sources

Proteomic Response of Thalassiosira pseudonana to Anoxia Reveals Alanine Fermentation Pathway and Reprogramming of Nitrogen Metabolism

O_LIDiatoms are key players in marine ecosystems and are frequently exposed to low-oxygen conditions in sediments and oxygen minimum zones. However, the metabolic strategies that enable their survival under anoxia remain poorly understood. C_LIO_LIUsing the model diatom Thalassiosira pseudonana, we investigated its response to dark anoxia. We first used proteomic approaches to identify differences between dark anoxia and dark oxic conditions combined with a phylogenetic analysis to decipher how the anoxic tolerance was acquired by this lineage. This approach revealed unexpected shunts involving amino acid pathways. We then correlated these findings with targeted metabolomic analysis on amino acids. C_LIO_LIOur results show that the diatom T. pseudonana undergoes a coordinated metabolic reprogramming under anoxia, centered on alanine production and tightly coupled to nitrogen metabolism. This work reveals how carbon and nitrogen fluxes are integrated to maintain cellular homeostasis in the absence of oxygen and provides a framework for understanding the resilience of diatoms in oxygen-depleted environments. C_LIO_LIWe identify three key features for anoxic adaptation in this lineage (i) alanine-centered metabolic reprogramming as a central component of acclimation to anoxia (ii) the involvement of an arginine-succinate shunt; and (iii) a critical contribution of lateral gene transfer (LGT) for anoxic tolerance. C_LI

plant biology↗

PAMPA: a software for peptide markers and taxonomic identification for ZooMS samples in Archaeology and Paleontology

ZooMS (Zooarchaeology by Mass Spectrometry) offers a rapid and cost-effective method for species identification of animal remains through peptide mass fingerprinting. After mass spectrum generation, a mostly used way to perform taxonomic identification is to compare the mass fingerprints to a reference database of diagnostic peptide markers to determine the species of origin. This analytical stage, however, is tedious and error-prone, often necessitating manual examination of spectra. In this paper, we present a comprehensive approach to automate and standardize the usage of peptide markers and the classification of ZooMS spectra. We have developed a software called PAMPA (Protein Analysis by Mass Spectrometry for Ancient Species), for which we demonstrate the effectiveness using a variety of spectral data from bone samples generated by MALDI-TOF and MALDI-FTICR. PAMPA is open-source and comes with a database of peptide markers and collection of curated COL1A1 and COL1A2 sequences. We believe it will be a valuable resource for the scientific community.

bioinformatics↗

AAV-delivery of diacylglycerol kinase kappa achieves long-term rescue of Fmr1-KO mouse model deficits of fragile X syndrome

Fragile X syndrome (FXS) is the most frequent form of familial intellectual disability. It results from the lack of the RNA binding protein FMRP and is associated with the overactivation of signaling pathways downstream of mGluRI receptors and upstream of mRNA translation. We previously found that diacylglycerol kinase kappa (DGKk) is a main mRNA target of FMRP in cortical neurons. Here we show that diacylglycerol kinase kappa (DGKk), when modified as to become FMRP-independent and delivered into the brain of adolescent mice using adeno-associated viral vectors, corrects brain diacylglycerol and phosphatidic acid homeostasis and the main phenotypic behaviors of the Fmr1-KO mouse model of FXS. Thus, DGKk appears as a key triggering factor of FXS pathomechanism while providing a possible means of intervention for FXS gene therapy. One sentence summaryDGKk gene therapy in Fmr1-KO mouse model

neuroscience↗

Extinct species identification from Upper Pleistocene bone fragments not identifiable from their osteomorphological studies by proteomics analysis

The ancient preserved molecules offer the opportunity to gain a better knowledge on the biological past. In recent years, bones proteomics has become an attractive method to study the animal biological origin, extinct species and species evolution as an alternative to DNA analysis which is limited by DNA amplification present in ancient samples and its contamination. However, the development of a proteomic workflow remains a challenge. The analysis of fossils must consume a low quantity of material to avoid damaging the samples. Another difficulty is the absence of genomic data for most of the extinct species. In this study, a proteomic methodology was applied to mammalian bones of 130,000 years old from the earlier Upper Pleistocene site of Scladina Cave (Belgium). Starting from 5 milligram samples, our results show a large majority of detected peptides matching collagen I alpha 1 and alpha 2 proteins with a sequence coverage up to 60%. Using sequence homology with modern sequences, a biological classification was successfully achieved and the associated taxonomic ranks to each bone were identified consistently with the information gained from osteomorphological studies and palaeoenvironmental and palaeodietary data. Among the taxa identified are the Felidae family, Bovinae subfamily, Elephantidae family and the Ursus genus. Amino acid substitutions on the collagens were identified providing new information on extinct species sequences and also helping in taxonomy-based clustering. Considering samples with no osteomorphological information, such as two bone retouchers, proteomics successfully identified the bovidae and ursidae families providing new information to the paleontologists on these objects. Combining osteomorphology studies and amino acid variations identified by proteomics, one retoucher was identified to be potentially from the Ursus spelaeus species.

paleontology↗