Search bioRxiv⌕ Search

Biology subjects

Ortega Gurrola, A.

Publications and source records attributed to Ortega Gurrola, A..

2 recordsLinked to original sources

A conserved logic for the development of cortical layering in tetrapods

The cerebral cortex is part of the pallium, a brain region conserved across vertebrates yet remarkably diverse in structure and cellular composition. A defining feature of the cerebral cortex is its organization into neuronal layers with distinct gene expression profiles, input-output connectivity, and function. According to prevailing models, the cerebral cortex emerged in ancestral amniotes (mammals and reptiles) following innovations in pallial development that enabled the generation of diverse neuron types and their laminar organization.1-11 However, little is known about pallial development and architecture in amphibians, the sister group of amniotes. Here we show that in the salamander Pleurodeles waltl, the dorsal pallium is organized in distinct superficial and deep layers with neurons that develop following cellular and molecular principles of mammalian corticogenesis. Using birthdating analysis, barcode-based lineage tracing, and single-cell RNA sequencing, we find that radial glia temporal states and intermediate progenitor cells are conserved across species, while neuronal differentiation trajectories are highly evolvable. Neurons generated at different developmental time points occupy different layers and exhibit distinct molecular and projection identities. Thus, temporally-patterned neurogenesis represents an ancient organizing principle of layered pallia, although mammals display an inverted layer order along the radial axis. Together, these findings demonstrate that the core developmental principles underlying cortical layering - including temporal patterning, intermediate progenitors, and laminar organization - predate the origin of amniotes. Our results suggest that the evolutionary expansion of the mammalian neocortex built upon a deeply conserved developmental framework already present in early tetrapods.

developmental biology↗

Adeno-Associated Viral Tools to Trace Neural Development and Connectivity Across Amphibians

The development, evolution, and function of the vertebrate central nervous system (CNS) can be best studied using diverse model organisms. Amphibians, with their unique phylogenetic position at the transition between aquatic and terrestrial lifestyles, are valuable for understanding the origin and evolution of the tetrapod brain and spinal cord. Their metamorphic developmental transitions and unique regenerative abilities also facilitate the discovery of mechanisms for neural circuit remodeling and replacement. The genetic toolkit for amphibians, however, remains limited, with only a few species having sequenced genomes and a small number of transgenic lines available. In mammals, recombinant adeno-associated viral vectors (AAVs) have become a powerful alternative to genome modification for visualizing and perturbing the nervous system. AAVs are DNA viruses that enable neuronal transduction in both developing and adult animals with low toxicity and spatial, temporal, and cell-type specificity. However, AAVs have never been shown to transduce amphibian cells efficiently. To bridge this gap, we established a simple, scalable, and robust strategy to screen AAV serotypes in three distantly-related amphibian species: the frogs Xenopus laevis and Pelophylax bedriagae, and the salamander Pleurodeles waltl, in both developing larval tadpoles and post-metamorphic animals. For each species, we successfully identified at least two AAV serotypes capable of infecting the CNS; however, no pan-amphibian serotype was identified, indicating rapid evolution of AAV tropism. In addition, we developed an AAV-based strategy that targets isochronic cohorts of developing neurons - a critical tool for parsing neural circuit assembly. Finally, to enable visualization and manipulation of neural circuits, we identified AAV variants for retrograde tracing of neuronal projections in adult animals. Our findings expand the toolkit for amphibians to include AAVs, establish a generalizable workflow for AAV screening in non-canonical research organisms, generate testable hypotheses for the evolution of AAV tropism, and lay the foundation for modern cross-species comparisons of vertebrate CNS development, function, and evolution.

neuroscience↗