Biology subjects

Wilinski, D.

Publications and source records attributed to Wilinski, D..

3 recordsLinked to original sources

bioRxiv2022

N6-Adenosine methylation regulates the translation of insulin mRNA

Relatively little is known about the first step of insulin synthesis: the translation of the mRNA. Here we show that the translation of D. melanogaster insulin 2 mRNA (dilp2) is controlled by methylation of N6-adenosine (m6A) in the 3 UTR. Mutations in the m6A writer Mettl3 and methylated-residues in the dilp2 3UTR decreased the levels of dilp2 mRNA associated with the polysomes, and the total amount of dilp2 protein produced. This resulted in aberrant energy homeostasis and diabetic-like phenotypes, consistent with the specific function of dilp2 in adult metabolism. Conserved m6A signatures were also identified in the 3 UTRs of vertebrate insulin mRNAs. These data identify m6A as a key regulator of insulin protein synthesis and energy homeostasis in metazoans and demonstrate an essential role for m6A in translation, with important implications for diabetes and metabolic disease. One-Sentence SummaryThe most abundant modification in eukaryotic mRNAs controls the synthesis of insulin protein in D. melanogaster.

molecular biology↗

bioRxiv2021

A nutriepigenetic pathway links nutrient information to sensory plasticity

Diet profoundly influences brain physiology, but how nutritional information is transmuted into neural activity and behavior changes remains elusive. Here we show that the metabolic enzyme O-GlcNAc Transferase (OGT) moonlights on the chromatin of the D. melanogaster gustatory neurons to instruct changes in chromatin accessibility and transcription that underlie sensory adaptations to a high sugar diet. OGT works synergistically with the Mitogen Activated Kinase/Extracellular signal Regulated Kinase (MAPK/ERK) rolled and its effector stripe (also known as EGR2 or Krox20) to integrate activity information. OGT also cooperates with the epigenetic silencer Polycomb Repressive Complex 2.1 (PRC2.1) to decrease chromatin accessibility and repress transcription in the high sugar diet. This integration of nutritional and activity information changes the taste neurons responses to sugar and flies ability to sense sweetness. Our findings reveal how nutrigenomic signaling generates cell-specific responses to global nutrient variations.

neuroscience↗

bioRxiv2017

Architecture and dynamics of overlapped RNA regulatory networks

A single protein can bind and regulate many mRNAs. Multiple proteins with similar specificities often bind and control overlapping sets of mRNAs. Yet, little is known about the architecture or dynamics of overlapped networks. We focused on three proteins with similar structures and related RNA-binding specificities - Puf3p, Puf4p, and Puf5p of S. cerevisiae. Using RNA Tagging, we identified a \"super-network\" comprised of four sub-networks: Puf3p, Puf4p, and Puf5p sub-networks, and one controlled by both Puf4p and Puf5p. The architecture of individual subnetworks, and thus the super-network, are determined by competition among particular PUF proteins to bind mRNAs, their affinities for binding elements, and the abundances of the proteins. The super-network responds dramatically: the remaining network can either expand or contract. These strikingly opposite outcomes are determined by an interplay between the relative abundance of the RNAs and proteins, and their affinities for one another. The diverse interplay between overlapping RNA-protein networks provides versatile opportunities for regulation and evolution.

molecular biology↗