Search bioRxivSearch

bioRxiv · 10.1101/2021.01.10.426155

Interhemispheric connectivity endures across species: An allometric expose on the corpuscallosum

Abstract

Rilling & Insel have argued that in primates, bigger brains have proportionally fewer anatomical interhemispheric connections, leading to reduced functional connectivity between the hemispheres (1). They based this on a comparison between surface areas of the corpus callosum and cortex rather than estimating connection counts, while leaving out other quantities also dependent on brain size such as callosal fiber density, neuron density, and number of functional areas. We use data from the literature to directly estimate connection counts. First, we estimate callosal fiber density as a function of brain size. We validate this by comparing out-of-sample human data to our functions estimate. We then mine the literature to obtain function estimates for all other quantities, and use them to estimate intra- and interhemispheric white matter connection counts as a function of brain size. The results show a much larger decrease in the scaling of interhemispheric to intrahemispheric connections than previously estimated. However, we hypothesize that raw connection counts are the wrong quantity to be estimating when considering functional connectivity. Instead, we hypothesize that functional connectivity is related to connection counts relative to the number of cortical areas. Accordingly, we estimate inter-area connection counts for intra- and interhemispheric connectivity and find no difference in how they scale with brain size. We find that, on average, an interhemispheric inter-area connection contains 3-8x more connections than an intrahemispheric inter-area connection, regardless of brain size. In doing so, we find that the fiber count of the human corpus callosum has been underestimated by 20%. Significance StatementThere are arguments in the literature that larger brains have proportionally fewer interhemispheric connections. We find that the decrease is even larger than previously estimated. However, we argue that this quantity is the wrong thing to measure: Rather, we should measure functional connectivity between cortical areas. We show that the ratio of interhemispheric and intrahemispheric connectivity between cortical areas is constant across mammalian species. These findings are consistent with a growing literature that suggest interhemispheric connectivity is special across all primate species.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Cipollini, B., Cottrell, G. W.. 2021-01-11. Interhemispheric connectivity endures across species: An allometric expose on the corpuscallosum. https://doi.org/10.1101/2021.01.10.426155

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Geometry of antigenic evolution improves influenza vaccine selection

Anticipating antigenic evolution is essential for selecting effective seasonal influenza A/H3N2 vaccine strains. To this end, we integrated hemagglutination-inhibition and neutralization titers spanning 2002 to 2025 into a unified Bayesian antigenic map. The map resolves twelve antigenic clusters advancing in discrete steps, with several clusters co-circulating in most seasons. In 15 of 21 seasons, the WHO-recommended vaccine belonged to an earlier cluster than the dominant circulating cluster. The direction of each vaccine update relative to recent viral drift predicted vaccine effectiveness one season ahead in out-of-sample forecasts. Antigenic distance, the conventional measure of vaccine-virus match, was weakly associated with effectiveness until update direction was accounted for. Retrospectively ranking candidate strains by predicted effectiveness would have selected a strain predicted to outperform the WHO recommendation in every season, raising mean predicted effectiveness by 10 percentage points.

evolutionary biology

Evolutionary replay of duplicate-gene retention across independent whole-genome duplications

Whole-genome duplications repeatedly expose ancestral gene lineages to the same broad evolutionary outcome-retention or loss of duplicated copies-but it remains unclear whether this history replays similarly across evolutionary scales. We placed duplicate retention in shared hierarchical orthologous-group coordinates and compared percentile ranks defined within each event-wide mapped universe. Three independent angiosperm whole-genome duplications showed reproducible replay (global rank effect T-replay = 0.210, bootstrap 95% confidence interval 0.172-0.248; permutation P = 1/100,001). A plant reference-panel score specified before target outcomes were examined predicted retention after the Apple/Pear duplication ({rho} = 0.169, n = 373). Deep transfer was heterogeneous: the teleost-genome-duplication estimate was positive but unresolved ({rho} = 0.107, n = 151, 95% confidence interval -0.050 to 0.260), whereas transfer to the ancient budding-yeast whole-genome duplication (yeast WGD) was supported ({rho} = 0.280, n = 186). Independently reconstructed animal outcomes also replayed between teleost and Stylommatophora duplications (r = 0.226, n = 146, P = 0.00326), although the effect remained below a prespecified strong-effect threshold. A strict plant-animal comparison was limited to 25 deeply one-to-one lineages and was unresolved (r = 0.033, 95% confidence interval -0.303 to 0.340). Thus, ancestral gene-lineage identity contributes reproducibly to duplicate retention after independent whole-genome duplications, but replay is structured by evolutionary lineage and modified by event-specific history rather than governed by one universal gene-fate ranking.

evolutionary biology

A Hymenoptera-restricted gene mediating ant castes co-opts deeply conserved machinery to control organ size

Lineage-specific genes are widespread and have been implicated as phenotypic innovation inducers, but how they acquire complex developmental functions remains poorly understood. Ant queens and workers develop dramatically different organ sizes from identical genomes under juvenile hormone (JH) control, yet the molecular effectors translating JH signalling into caste-specific organ growth remain unknown. Here we identify torch, a Hymenoptera-restricted gene, as the most consistently gyne-biased and JH-responsive gene across 68 ant species. Knockdown of torch in virgin queens of Monomorium pharaonis produces a worker-like, multi-organ growth-restricted phenotype. Mechanistically, torch harbours an E-box-like motif activated by the JH receptor Gce-Tai and acts as a GA-repeat-binding transcription factor that regulates Hippo signalling, the deeply conserved organ-size control pathway in animals. Expressing torch heterologously in mice and a growth-restricted Drosophila background shows that the gene retained its general growth-promoting activity across more than 700 million years of animal evolution in lineages that lack the gene, establishing that its function is mediated through conserved rather than ant-specific machinery. A lineage-specific gene can therefore acquire complex morphogenetic function by co-opting ancient organ-size circuitry, providing a general route by which novel genes can drive phenotypic innovation.

evolutionary biology