Insights into cephalochordate genome and gene evolution from the early-diverging amphioxus <i>Asymmetron lucayanum</i>

Y Yifan Ren (State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Department of Experimental Research, Sun Yat-sen University Cancer Center) Z Zepu Miao (State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Department of Experimental Research, Sun Yat-sen University Cancer Center) C Che-Yi Lin (Institute of Cellular and Organismic Biology, Academia Sinica) L Ludong Yang (State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Department of Experimental Research, Sun Yat-sen University Cancer Center) H Huihui Li (CAS Key Laboratory of Nanosystem and Hierarchical Fabrication) L Linda Z. Holland (Marine Biology Research Division, Scripps Institution of Oceanography, University of California San Diego) S Sung-Jin Cho (Department of Biological Sciences and Biotechnology, Chungbuk National University) J Jr-Kai Yu (Institute of Cellular and Organismic Biology, Academia Sinica) J Jia-Xing Yue

Abstract

Cephalochordates (amphioxus or lancelet) are considered as living proxies for ancestral chordates due to their key phylogenetic position and slow evolutionary rate. The genomes of living amphioxus thus can help to reveal the genetic basis shaping the evolutionary transition from nonvertebrate animals to vertebrates. To gain a comprehensive understanding of the genome architecture in amphioxus, we generated a chromosome-anchored genome assembly for Asymmetron lucayanum , representing the earliest diverging cephalochordate genus. We show that Asymmetron has an enlarged genome compared to those of the other four cephalochordate genomes decoded so far (all in the genus Branchiostoma ), caused by pervasive expansions of intergenic transposable elements (TEs). Nevertheless, both macrosynteny and microsynteny remain highly conserved between Asymmetron and Branchiostoma , enabling reconstruction of the ancestral genomic architecture of the cephalochordate lineage for tracing genome evolutionary processes during deuterostome and chordate diversification. Integration of developmental transcriptomic data further reveals that selective constraints on cotranscriptional regulation underline the maintenance of the conserved microsynteny blocks among cephalochordate species. We also examine the evolutionary history of the Hox cluster in cephalochordates and vertebrates, and identify species-specific inversions and TE invasions at this locus in both Asymmetron and Branchiostoma . Finally, we survey key molecular building blocks underlying both innate and adaptive immunity (e.g., TLR , NLR , MHC, and RAG ) and uncover their evolutionary dynamics and plausible ancestry in chordates. Taken together, our findings illuminate the genome and gene evolution of cephalochordates and provide valuable resources for understanding the early evolution of chordates and the origin of vertebrates.

Article Details

Volume / Issue Vol. 123, Issue 12
Published March 24, 2026
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (9)

Y

Yifan Ren

State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Department of Experimental Research, Sun Yat-sen University Cancer Center

Z

Zepu Miao

State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Department of Experimental Research, Sun Yat-sen University Cancer Center

C

Che-Yi Lin

Institute of Cellular and Organismic Biology, Academia Sinica

L

Ludong Yang

State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Department of Experimental Research, Sun Yat-sen University Cancer Center

H

Huihui Li

CAS Key Laboratory of Nanosystem and Hierarchical Fabrication

L

Linda Z. Holland

Marine Biology Research Division, Scripps Institution of Oceanography, University of California San Diego

S

Sung-Jin Cho

Department of Biological Sciences and Biotechnology, Chungbuk National University

J

Jr-Kai Yu

Institute of Cellular and Organismic Biology, Academia Sinica

J

Jia-Xing Yue