Kiebler, M. | bioRxiv Science

bioRxiv2026

Robust mammalian RNA localization elements are complex and multipartite

The subcellular localization patterns of RNAs are controlled by regulatory elements contained within them. However, for most localized RNAs, the identities of these elements remain unknown. We had previously identified several localization elements that are necessary and sufficient for robust, kinesin-dependent RNA targeting to microtubule plus ends in a variety of cell types. Yet the characteristics of these elements that are critical for function remained unclear. To address this, we systematically created tens of thousands of mutant localization elements and quantified their ability to regulate subcellular RNA localization in neuronal cells. We found that the minimally active size of these localization elements is large, approximately 200 nucleotides. These elements contain multiple important subsequences, with some being completely intolerant of any changes and others being tolerant to a shuffling of nucleotide order but not to changes in nucleotide composition. Using single molecule microscopy, we verified these findings in primary rat neurons. Together, these results demonstrate that highly active mammalian RNA localization elements are large, complex, and multipartite and lay a foundation for further mechanistic studies of their function.

molecular biology↗

bioRxiv2025

Quality-control Normalization of Fluorescence Microscopy Morphometry and Colocalization Measurements for Improved Accuracy and Cross-instrument Reproducibility

Quantitative fluorescence microscopy is more reproducible when instrument performance is measured and incorporated into the analysis. We show that routinely monitored quality-control (QC) metrics like the system resolution and inter-channel co-registration are determinant variables that can be used to normalize common image readouts and thereby separate instrument-induced variation from genuine biological changes. For intra-channel morphometry, a Gaussian approximation of the fluorescence imaging process yields analytical factors that predict how geometric measurements (length, separation distance, area, volume, etc.) inflate and scale with resolution blur due to optical misalignments or natural optical quality variations. We validate this behavior by deliberately perturbing the system resolution and by exploiting the natural resolution differences in three nominally equivalent objective lenses configured to image the exact same synapses in cultured hippocampal neurons, where structural differences subtle by eye nonetheless produced statistically significant shifts in measured synaptic puncta volumes. For dual-channel colocalization (overlap) measurements, we normalize the inter-channel co-registration QC metric by the measured point-spread function (PSF) resolutions (rather than theoretical limits associated with the objective lens) and demonstrate how fluorescent pre/postsynaptic cleft protein overlap signals decay in a predictable, exponential fashion as the PSF-normalized registration error increases, with the decay rate depending on the imaged object relative to the PSF size ratio. Mapped field-of-view gradients in channel registration also explain feature orientation flips/rotations and overlap loss without any underlying biological change. Finally, we outline a simple QC-aware microscope normalization workflow where each image measurement dataset is paired with its session PSFs and local co-registration error to remove instrument bias and optionally re-project the results to a declared reference PSF without altering the raw images. This approach improves image measurement accuracy and cross-instrument comparability of experiments and reframes light microscope QC from a passive certification of instrument health into a practical normalization that links the acquisition state to quantitative outcomes, thus ensuring the reliability and interpretability of morphometric and colocalization data in fluorescence microscopy.

cell biology↗