Fluorescence images of ybx1 mutant neuromasts [incross]
Data files
Jul 07, 2025 version files 75.16 GB
-
README.md
2.07 KB
-
ybx1_mutant.tar
75.16 GB
Abstract
Like the sensory organs of the human inner ear, the lateral-line neuromasts (NMs) of fish such as the zebrafish (Danio rerio) contain mechanosensory hair cells (HCs) that are surrounded by progenitors called supporting cells. Damaged NMs can quickly regenerate new HCs by expressing in the progenitors HC-specific genes such as atoh1a, the master regulator of HC fate. We used the supervised learning algorithm DELAY to infer regenerating NMs’ early gene-regulatory network (GRN) and identify adaptations that promote the rapid regeneration of lateral-line HCs in larval zebrafish. The central hub in the network, Y-box binding protein 1 (ybx1), is highly expressed in HC progenitors and young HCs and can recognize DNA-binding motifs in cyprinids’ candidate regeneration-responsive promoter elements for atoh1a. We showed that NMs from ybx1 mutant zebrafish larvae display consistent, regeneration-specific deficits in HC number and initiate both HC regeneration and atoh1a expression 20 % slower than in siblings. By demonstrating that ybx1 promotes rapid HC regeneration through early atoh1a upregulation, the results support DELAY’s ability to identify key temporal regulators of gene expression.
https://doi.org/10.5061/dryad.v15dv4257
This study is comprised of four datasets as follows:
- Fluorescence images of ybx1 mutant neuromasts [incross] (DOI: 10.5061/dryad.v15dv4257): Neuromasts from wild-type, heterozygous, and homozygous mutant larvae during development and regeneration
- Fluorescence images of ybx1 mutant neuromasts [time course, wt] (DOI: 10.5061/dryad.g1jwstr1z): Time-course images of fixed neuromasts from wild-type larvae
- Fluorescence images of ybx1 mutant neuromasts [time course, het] (DOI: 10.5061/dryad.jh9w0vtn5): Time-course images of fixed neuromasts from heterozygous mutant larvae
- Fluorescence images of ybx1 mutant neuromasts [Ybx1 immunofluorescence] (DOI: 10.5061/dryad.wm37pvn0h): Immunostaining images in neuromasts from wild-type and heterozygous mutant larvae
Description of the data and file structure
This data set contains fluorescence images of fixed neuromasts from inbred ybx1 mutant zebrafish larvae. Each image comprises: 1) an nd
file with parameters, e.g., X/Y resolution; and, 2) a single-channel fluorescence image (excitation = 405 nm; emission = 460 nm), showing nuclear DAPI and apical phalloidin signals.
Files and variables
File: ybx1_mutant.tar
Description: Main directory with sub-directories for each genotype and condition
- Sub-directories are labeled by development (
dev
) or regeneration (regen
) and genotype (wild-type [wt
], heterozygous [het
], or homozygous mutant [mut
])
- Files are labeled with numerical identifiers for unique larvae (
zf
) and neuromast (nm
), generally arranged from anterior to posterior per-larva - Imaging parameters:
Exposure = 500 ms
IllumSetting = iSIM _405_460
MagNA = 1.35
MagRI = 1.406
MagSetting = 100X SiOil
wavelength = 460
Width: 95.128 microns (2068)
Height: 65.504 microns (1424)
Depth: 25.2000 microns (126)
Resolution: 21.7391 pixels per micron
Voxel size: 0.046x0.046x0.2 micron^3
To label HCs, we fixed 3-5 dpf zebrafish trunks with 4% formaldehyde in phosphate-buffered saline (PBS) solution with 0.1 % Tween-20 (0.1 % PBST) for either 1 hr at room temperature or overnight at 4 °C. For inbred ybx1 mutant offspring, we washed trunks for 30 m in fresh 0.1 % PBST, followed by a 1 hr incubation at room temperature in 0.05 % PBST with DAPI (1:200) and Alexa Fluor Plus 405 phalloidin (1:40; Invitrogen, Eugene, USA). We washed trunks once more for 20-30 m in 1X PBS before mounting and imaging at 100X on an Olympus IX83 inverted confocal microscope with a microlens-based super-resolution imaging system (VT-iSIM, VisiTech International).