High precision registration between zebrafish brain atlases using symmetric diffeomorphic normalization

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Abstract

Atlases provide a framework for information from diverse sources to be spatially mapped and integrated into a common reference space. In particular, brain atlases allow regional annotation of gene expression, cell morphology, connectivity and activity. In larval zebrafish, advances in genetics, imaging and computational methods have enabled the collection of large datasets providing such information on a whole-brain scale. However, datasets from different sources may not be aligned to the same spatial coordinate system, because technical considerations may necessitate use of different reference templates. Two recent brain atlases for larval zebrafish exemplify this problem. The Z-Brain atlas contains information on gene expression, neural activity and neuroanatomical segmentation acquired using immunohistochemical staining of fixed tissue. In contrast, the Zebrafish Brain Browser (ZBB) atlas was constructed from live scans of fluorescent reporter genes in transgenic larvae. Although different reference brains were used, the two atlases included several transgene patterns in common that provided potential 'bridges' for transforming each into the other’s coordinate space. We therefore tested multiple bridging channels and registration algorithms. The symmetric diffeomorphic normalization (SyN) algorithm in ANTs improved the precision of live brain registration while better preserving cell morphology than the previously used B-spline elastic registration algorithm. SyN could also be calibrated to correct for tissue distortion introduced during fixation and permeabilization. Finally, multi-reference channel optimization provided a transformation matrix that enabled Z-Brain and ZBB to be co-aligned with acceptable precision and minimal perturbation of cell and tissue morphology. This study demonstrates the feasibility of integrating whole brain datasets, despite disparate acquisition protocols and reference templates, when sufficient information is present for bridging.

Anatomical abbreviations

ac

anterior commissure

DT

Thalamus

GT

Griseum tectale

Ha

Habenula

Hc

Hypothalamus caudal zone

Hi

Hypothalamus intermediate zone

MO

Medulla oblongata

NXm

Vagus motor neurons

OB

Olfactory bulb

OE

Olfactory epithelium

IO

Inferior olive

LC

Locus coeruleus

MN

Mauthner neuron

MO

Medulla oblongata

Pal

Pallium

pc

posterior commissure

Pr

Pretectum

SR

Superior raphe

Teg

Tegmentum

TeOn

Optic tectum neuropil

TG

Trigeminal ganglion

TL

Torus longitudinalis

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  1. Now published in GigaScience doi: 10.1093/gigascience/gix056

    Gregory D. Marquart , Bethesda, MD 20892Find this author on Google ScholarFind this author on PubMedSearch for this author on this siteKathryn M. Tabor , Bethesda, MD 20892Find this author on Google ScholarFind this author on PubMedSearch for this author on this siteMary Brown , Bethesda, MD 20892Find this author on Google ScholarFind this author on PubMedSearch for this author on this siteHarold A. Burgess , Bethesda, MD 20892Find this author on Google ScholarFind this author on PubMedSearch for this author on this siteORCID record for Harold A. Burgess

    A version of this preprint has been published in the Open Access journal GigaScience (see paper https://doi.org/10.1093/gigascience/gix056 ), where the paper and peer reviews are published openly under a CC-BY 4.0 license.

    These peer reviews were as follows:

    Reviewer 1: http://dx.doi.org/10.5524/REVIEW.100800