Binding of dsRNA by D. melanogaster Dicer-2 is substrate-dependent and regulated by Loquacious-PD
Abstract
Drosophila melanogaster Dicer-2 is a large, multidomain protein that cleaves double-stranded RNA (dsRNA) into small interfering RNAs in a terminus-dependent manner as part of the RNA interference pathway. We characterize the local binding environment involved in this substrate-selective molecular recognition event by monitoring the time-resolved photophysics of a cyanine dye linked to the dsRNA terminus. We observe substantial changes in the molecular rigidity and local freedom of motion of the probe as a function of distinct conformations of the biomolecular complex between Dicer-2 and dsRNA as a function of dsRNA termini, the presence of regulatory proteins, and the addition of a biochemical energy source (ATP) or a non-hydrolysable equivalent (ATP-{gamma}S). With a clustering analysis based solely on these molecular-scale measures of the local binding environment at the dsRNA terminus, we identify sub-populations of similar conformations that define distinct modes of molecular recognition which are correlated with biochemical activity. These observations reveal the important role of substrate-selective molecular recognition properties for proteins with multiple domains that can bind RNA, regulatory proteins, and cofactors. STATEMENT OF SIGNIFICANCEThe molecular-scale determinants of protein-RNA binding remain elusive, particularly when different subunits of a single protein confer specificity toward small structural differences of their RNA partners. An important case is that of Drosophila melanogaster Dicer-2, a critical component of the antiviral RNA interference response. Dicer-2 discriminates between double stranded RNA with blunt or 3 overhang termini, a feature suggested to mediate recognition of "self" vs. "non-self" substrates. We study these interactions at the binding site with a fluorescent label at the RNA terminus, monitoring intramolecular and collective measures of flexibility to report on the local environment. Dicer-2 has distinct modes of molecular recognition which are regulated by accessory proteins and ATP, leading to different conformations and tuning biochemical activity.
02 /Specification & Classification
Click any tag to browse matching papers- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- A real-time, transient kinetic study of Drosophila melanogaster Dicer-2 elucidates mechanism of termini-dependent cleavage of dsRNA.
R. K. SINGH, M. Jonely, … B. L. Bass·bioRxiv·Sep 29, 2020
- Role of protein dynamics in enthalpy-driven recognition of topologically distinct dsRNAs by dsRBDs
H. Paithankar, J. Chugh·bioRxiv·Dec 4, 2019
- Differential conformational dynamics in two type-A RNA-binding domains drive the double-stranded RNA recognition and binding
F. Parvez, D. Sangpal, … J. Chugh·bioRxiv·Aug 6, 2023
- Identification of new proviral and antiviral factors through the study of the Dicer-2 interactome in vivo during viral infection in Drosophila melanogaster
C. Rousseau, E. Lauret, … C. Meignin·bioRxiv·Dec 21, 2023
- Characterization of conformational dynamics at microsecond timescale in the RNA-binding regions of dsRNA-binding domains
H. Paithankar, J. Chugh·bioRxiv·Dec 5, 2019
- Main constraints for RNAi induced by expressed long dsRNA in mouse cells
Tomáš Demeter, Michaela Vaškovičová, … Petr Svoboda·Life Science AlliancePeer-reviewed·Feb 1, 2019