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Biology subjects

Marques, G. S.

Publications and source records attributed to Marques, G. S..

2 recordsLinked to original sources

FLYNC: A Machine Learning-Driven Framework for Discovering Long Non-Coding RNAs in Drosophila melanogaster

Non-coding RNAs have increasingly recognized roles in critical molecular mechanisms of disease. However, the non-coding genome of Drosophila melanogaster, one of the most powerful disease model organisms, has been understudied. Here, we present FLYNC - FLY Non-Coding discovery and classification - a novel machine learning-based model that predicts the probability of a newly identified RNA transcript being a long non-coding RNA (lncRNA). Integrated into an end-to-end bioinformatics pipeline capable of processing single-cell or bulk RNA sequencing data, FLYNC outputs potential new non-coding RNA genes. FLYNC leverages large-scale genomic and transcriptomic datasets to identify patterns and features that distinguish non-coding genes from protein-coding genes, thereby facilitating lncRNA prediction. We demonstrate the application of FLYNC to publicly available Drosophila adult head bulk transcriptome and single-cell transcriptomic data from Drosophila neural stem cell lineages and identify several novel tissue- and cell-specific lncRNAs. We have further experimentally validated the existence of a set of FLYNC positive hits by qPCR. Overall, our findings demonstrate that FLYNC serves as a robust tool for identifying lncRNAs in Drosophila melanogaster, transcending current limitations in ncRNA identification and harnessing the potential of machine learning.

genomics↗

Fate transitions in Drosophila neural lineages: a single cell road map to mature neurons.

Neuron specification and maturation are essential for proper central nervous system development. However, the precise mechanisms that govern neuronal maturation remain poorly understood. Here, we use single-cell RNA sequencing, combined with a conditional genetic strategy to analyse neuronal lineages and their new born neurons in the Drosophila larval brain. A focused analysis on the transcriptional alterations that occur right after neuron generation revealed that neuron maturation starts shortly after neuronal birth, with transcription, but no translation, of mature neuronal features such as neurotransmitter (NT) genes. Using NT gene Choline acetyltransferase as an example, we show that the timings of translation initiation are not solely dependent on neuron age but are rather coordinated with the animal developmental stage. This study is the first characterization of the initial phases of neuron maturation, supporting a model where neuron maturation is coordinated with the animal developmental stage through post-transcriptional regulation of terminal effector genes.

neuroscience↗