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Updated: Jan 13, 2026

En face Cryosectioning of Mouse Retina for High-dimensional Spatial Molecular Analysis
Published on: July 8, 2025
Integration of in situ hybridization and scRNA-seq data provides a 2D topographical map of the developing retina
Heer N V Joisher1,2,3, ChangHee Lee1,4, Chaitra Prabhakara1
1Department of Genetics, Blavatnik Institute, Harvard Medical School, United States.
Abstract:
Precise regional patterning is fundamental to tissue organization, yet the spatial logic that governs it remains poorly defined for many tissues. In the vertebrate retina, molecular domains along the dorsoventral and nasotemporal axes provide positional cues for regional specializations such as the high-acuity area (HAA). We combined multiplexed in situ hybridization data with single-cell transcriptomic data to create quantitative two-dimensional maps of developing retinal cells. In the developing chicken retina, this approach resolved sharp expression boundaries of genes involved in patterning, and revealed novel candidates enriched in the anlagen of the HAA. Comparative analysis of chicken, mouse, and human data demonstrated conserved axis-based programs, but distinct fine-scale organization consistent with presence/absence of an HAA. Here, we show that spatial reconstruction from scRNA-seq data, anchored by experimental benchmarks, enables comparative 2D topographic mapping of gene expression across species and provides a generalizable strategy to investigate the spatial logic of molecular organization in developing tissues.

