# Origins of Avian Hyperactive Mitochondria, Genome Compaction, and Air-Sac Physiology in Early Theropods During the Carnian Pluvial Episode

**Authors:** Takumi Satoh

PMC · DOI: 10.3390/jdb14010011 · Journal of Developmental Biology · 2026-03-02

## TL;DR

The paper suggests that early dinosaurs had bird-like traits, such as efficient mitochondria and compact genomes, which helped them thrive in harsh Late Triassic environments.

## Contribution

The study proposes a link between avian-like physiology in early theropods and adaptation to the Carnian Pluvial Episode's harsh climate.

## Key findings

- Early dinosaurs had hyperactive mitochondria and compact genomes, similar to modern birds.
- These traits likely enhanced metabolic efficiency and locomotor performance in harsh environments.
- The air-sac system and small cell size may have contributed to ecological dominance during the CPE.

## Abstract

Extant birds and the earliest dinosaurs may share fundamental metabolic features essential for aerobic exercise, suggesting that the extraordinary physical performance typical of avian species originated when dinosaurs first appeared during the Carnian Pluvial Episode (CPE). This physiological adaptation is complemented by hyperactive mitochondria that exhibit high oxygen consumption and low reactive oxygen species production. Molecular genomics of fossils, the so-called “Jurassic Genome,” indicates that these early dinosaurs possessed compact genomes, 50–60% the size of the human genome, and small cells, implying a highly stringent metabolic regime. We suggest that hyperactive mitochondria, closely associated with compact genomes and small cells, drive theropod adaptation to the hot, dry, and hypoxic environments of the Late Triassic period, ultimately enabling their ecological dominance. Early dinosaurs such as Herrerasaurus are hypothesized to have possessed advanced physiological traits shared with modern birds, including hyperactive mitochondria, compact genomes, small cells, and a developing air-sac system. Collectively, these features most likely may have contributed to exceptional metabolic capacity, locomotor performance, and adaptation to the harsh environment of the CPE.

## Full-text entities

- **Genes:** UCP2 (uncoupling protein 2) [NCBI Gene 7351] {aka BMIQ4, SLC25A8, UCPH}, UCP1 (uncoupling protein 1) [NCBI Gene 7350] {aka SLC25A7, UCP}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, CPE (carboxypeptidase E) [NCBI Gene 1363] {aka BDVS, CPH, IDDHH}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, SERPINE1 (serpin family E member 1) [NCBI Gene 5054] {aka PAI, PAI-1, PAI1, PLANH1}, SLC2A4 (solute carrier family 2 member 4) [NCBI Gene 6517] {aka GLUT4}, RETN (resistin) [NCBI Gene 56729] {aka ADSF, FIZZ3, RENT, RETN1, RSTN, XCP1}, ITLN1 (intelectin 1) [NCBI Gene 55600] {aka HL-1, HL1, INTL, ITLN, LFR, hIntL}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, PPARGC1A (PPARG coactivator 1 alpha) [NCBI Gene 10891] {aka LEM6, PGC-1(alpha), PGC-1alpha, PGC-1v, PGC1, PGC1A}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, INSR (insulin receptor) [NCBI Gene 3643] {aka CD220, HHF5}, GCGR (glucagon receptor) [NCBI Gene 2642] {aka GGR, GL-R, MVAH}
- **Diseases:** Hypoxia (MESH:D000860), hypoxic (MESH:D002534), Insulin resistance (MESH:D007333), injury to (MESH:D014947), Hyperactive Mitochondria (MESH:C564971), Hyperactive (MESH:D006948)
- **Chemicals:** glycogen (MESH:D006003), ROS (MESH:D017382), glucose (MESH:D005947), carbohydrates (MESH:D002241), CO2 (MESH:D002245), ATP (MESH:D000255), oxygen (MESH:D010100), lipids (MESH:D008055), ketone bodies (MESH:D007657)
- **Species:** Anser (geese, genus) [taxon 8842], Canis lupus familiaris (dog, subspecies) [taxon 9615], Chiroptera (bats, order) [taxon 9397], conifers [taxon 3312], Gallus gallus (bantam, species) [taxon 9031], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13026812/full.md

## References

94 references — full list in the complete paper: https://tomesphere.com/paper/PMC13026812/full.md

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Source: https://tomesphere.com/paper/PMC13026812