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Unraveling the Mystery of Larvae Evolution: Insights from Dr. Martín-Zamora
In this enlightening episode, Dr. Martín-Zamora takes listeners on a deep dive into the complex world of larvae evolution and how temporal shifts in trunk formation underpin the diversification of larvae and bilaterian life cycles. Despite larvae's central role in animal evolution scenarios across all major animal lineages, the understanding of how larvae evolved remains elusive. Dr. Martín-Zamora's groundbreaking research seeks to fill this knowledge gap.
Dr. Martín-Zamora presents his study, where chromosome-scale genome sequencing was performed on the annelid Owenia fusiformis, combined with transcriptomic and epigenomic profiling during the life cycles of this species and two other annelids. His research reveals that trunk development in O. fusiformis is postponed to pre-metamorphic stages in the feeding larva, in contrast to the non-feeding larva of Capitella teleta and the directly developing embryo of Dimorphilus gyrociliatus where it begins post-gastrulation.
His findings also highlight that the embryos of O. fusiformis first develop into an enlarged anterior domain, forming larval tissues and the adult head. This is consistent with observations in the so-called 'head larvae' of other bilaterians, showing extensive transcriptomic similarities with the O. fusiformis larva.
Dr. Martín-Zamora posits that the temporal decoupling of head and trunk formation seen in head larvae may have facilitated larval evolution in Bilateria. This new perspective offers an intriguing departure from traditional theories that attribute larva and adult origins to co-option or innovation of gene regulatory programs.
Key Words: Larvae Evolution, Bilaterian Life Cycles, Temporal Shifts, Trunk Formation, Annelids, Owenia fusiformis, Genome Sequencing, Transcriptomic Profiling, Epigenomic Profiling, Head Larvae, Gene Regulatory Programs, Animal Evolution.
Martín-Zamora, F.M., Liang, Y., Guynes, K. et al. Annelid functional genomics reveals the origins of bilaterian life cycles. Nature (2023). https://doi.org/10.1038/s41586-022-05636-7
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By Catarina CunhaIn this enlightening episode, Dr. Martín-Zamora takes listeners on a deep dive into the complex world of larvae evolution and how temporal shifts in trunk formation underpin the diversification of larvae and bilaterian life cycles. Despite larvae's central role in animal evolution scenarios across all major animal lineages, the understanding of how larvae evolved remains elusive. Dr. Martín-Zamora's groundbreaking research seeks to fill this knowledge gap.
Dr. Martín-Zamora presents his study, where chromosome-scale genome sequencing was performed on the annelid Owenia fusiformis, combined with transcriptomic and epigenomic profiling during the life cycles of this species and two other annelids. His research reveals that trunk development in O. fusiformis is postponed to pre-metamorphic stages in the feeding larva, in contrast to the non-feeding larva of Capitella teleta and the directly developing embryo of Dimorphilus gyrociliatus where it begins post-gastrulation.
His findings also highlight that the embryos of O. fusiformis first develop into an enlarged anterior domain, forming larval tissues and the adult head. This is consistent with observations in the so-called 'head larvae' of other bilaterians, showing extensive transcriptomic similarities with the O. fusiformis larva.
Dr. Martín-Zamora posits that the temporal decoupling of head and trunk formation seen in head larvae may have facilitated larval evolution in Bilateria. This new perspective offers an intriguing departure from traditional theories that attribute larva and adult origins to co-option or innovation of gene regulatory programs.
Key Words: Larvae Evolution, Bilaterian Life Cycles, Temporal Shifts, Trunk Formation, Annelids, Owenia fusiformis, Genome Sequencing, Transcriptomic Profiling, Epigenomic Profiling, Head Larvae, Gene Regulatory Programs, Animal Evolution.
Martín-Zamora, F.M., Liang, Y., Guynes, K. et al. Annelid functional genomics reveals the origins of bilaterian life cycles. Nature (2023). https://doi.org/10.1038/s41586-022-05636-7