Developmentally regulated genes drive phylogenomic splits in ovule evolution

The evolution of seeds transformed life on earth and is responsible for our most important food crops. Gymnosperms, the oldest living seed plants, are an untapped genomic reservoir for genes involved in seed evolution. To tap this resource, we assemble deep transcriptomes of 14 gymnosperms, four angiosperms, and two ferns and identified 22,429 phylogenetically informative ortholog groups. We observe that genes differentially expressed in ovules or leaves provide the majority of phylogenomic support for the evolutionary splits between 1) seed and non-seed plants; 2) gymnosperms and angiosperms; and/or 3) within gymnosperms (conifers vs. "ancient" gymnosperms). Our gymnosperm data identifies unreported candidate ovule regulated genes in Arabidopsis. Moreover, prior knowledge from Arabidopsis helps uncover 4,076 candidate ovule genes that influence these evolutionary splits. We validate the expression of candidate ovule genes in gymnosperm-specific ovule structures. Our work provides a resource for seed gene discovery, conservation, and crop improvement.

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Journal
Nature Communications
Published
2025-11-13
DOI
https://doi.org/10.1038/s41467-025-65399-3
Primary Topic
Plant Molecular Biology Research
Type
article
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article

Developmentally regulated genes drive phylogenomic splits in ovule evolution

Gil Eshel, Gloria M. Coruzzi, Lisa DeGironimo, Dennis Wm. Stevenson et al.
Nature Communications
Plant Molecular Biology Research
article

Developmentally regulated genes drive phylogenomic splits in ovule evolution

Gil Eshel, Gloria M. Coruzzi, Lisa DeGironimo, Dennis Wm. Stevenson, Barbara A. Ambrose, Kranthi Varala, Manpreet S. Katari, Damon P. Little, Veronica M. Sondervan, Sebastiano Nigris, W. Richard McCombie, Tim L. Jeffers, Cecilia Zumajo‐Cardona, Samantha Frangos, Tynisha L. Smalls
article en

Abstract

The evolution of seeds transformed life on earth and is responsible for our most important food crops. Gymnosperms, the oldest living seed plants, are an untapped genomic reservoir for genes involved in seed evolution. To tap this resource, we assemble deep transcriptomes of 14 gymnosperms, four angiosperms, and two ferns and identified 22,429 phylogenetically informative ortholog groups. We observe that genes differentially expressed in ovules or leaves provide the majority of phylogenomic support for the evolutionary splits between 1) seed and non-seed plants; 2) gymnosperms and angiosperms; and/or 3) within gymnosperms (conifers vs. "ancient" gymnosperms). Our gymnosperm data identifies unreported candidate ovule regulated genes in Arabidopsis. Moreover, prior knowledge from Arabidopsis helps uncover 4,076 candidate ovule genes that influence these evolutionary splits. We validate the expression of candidate ovule genes in gymnosperm-specific ovule structures. Our work provides a resource for seed gene discovery, conservation, and crop improvement.

Nature CommunicationsVol. 16(1)
University of Padua (IT), Purdue University West Lafayette (US), Cold Spring Harbor Laboratory (US), New York Botanical Garden (US), New York University (US)
Openalex Percentile: Top 75%
Plant Molecular Biology Research
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