Author
Listed:
- Veronica M. Sondervan
(New York University
New York Botanical Garden)
- Gil Eshel
(New York University)
- Kranthi Varala
(Purdue University)
- Samantha Frangos
(New York University
New York Botanical Garden)
- Manpreet S. Katari
(New York University)
- Tim L. Jeffers
(New York University)
- Cecilia Zumajo-Cardona
(New York Botanical Garden
Università degli studi di Padova)
- Sebastiano Nigris
(Università degli studi di Padova
Università degli studi di Padova)
- Lisa DeGironimo
(New York Botanical Garden)
- Tynisha Smalls
(New York Botanical Garden)
- W. Richard McCombie
(Cold Spring Harbor Laboratory)
- Damon P. Little
(New York Botanical Garden)
- Barbara Ambrose
(New York Botanical Garden)
- Dennis Wm. Stevenson
(New York Botanical Garden)
- Gloria M. Coruzzi
(New York University)
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.
Suggested Citation
Veronica M. Sondervan & Gil Eshel & Kranthi Varala & Samantha Frangos & Manpreet S. Katari & Tim L. Jeffers & Cecilia Zumajo-Cardona & Sebastiano Nigris & Lisa DeGironimo & Tynisha Smalls & W. Richard, 2025.
"Developmentally regulated genes drive phylogenomic splits in ovule evolution,"
Nature Communications, Nature, vol. 16(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-65399-3
DOI: 10.1038/s41467-025-65399-3
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