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Chromosome-level assembly of the mangrove plant Aegiceras corniculatum genome generated through Illumina, PacBio and Hi-C sequencing technologies
2022-06-16


Dongna Ma, Zejun Guo, Qiansu Ding, Zhizhu Zhao, Zhijun Shen, Mingyue Wei, Changhao Gao, Ludan Zhang, Huan Li, Shan Zhang, Xueyi Zhu, Hai-Lei Zheng*


Molecular Ecology Resources

https://onlinelibrary.wiley.com/doi/epdf/10.1111/1755-0998.13347


Abstract

Aegiceras corniculatum is a major mangrove plant species adapted to waterlogging and saline conditions, grows in the coastal intertidal zone of tropical and subtropical re-gions. Here, we present a chromosome- level genome assembly of A. corniculatum by incorporating PacBio long- read sequencing and Hi-C technology. The results showed that the PacBio draft genome size is 906.63 Mb. Hi-C scaffolding anchored 885.06 Mb contigs (97.62% of draft assembly) onto 24 pseudochromosomes. The contig N50 and scaffold N50 were 7.1 Mb and 37.74 Mb, respectively. Out of 40,727 protein-coding genes predicted in the study, 89% have functional annotations in public databases. We also showed that of the 603.93 Mb repetitive sequences predicted in the assem-bled genome, long terminal repeat retrotransposons constitute 41.52%. The genome evolution analysis showed that the A. corniculatum genome experienced two whole-genome duplication events and shared the ancient γ whole-genome triplication event. A comparative genomic analysis revealed an incidence of expansion in 1,488 gene families associated with essential metabolism and biosynthetic pathways, including photosynthesis, oxidative phosphorylation, phenylalanine, glyoxylate, dicarboxylate metabolism, and DNA replication, which probably constitute adaptation traits that allow the A. corniculatum to survive in the intertidal zone. Also, the systematic char-acterization of genes associated with flavonoid biosynthesis pathway and the AcNHXgene family conducted in this study will provide insight into the adaptation mecha-nism of A. corniculatum to intertidal environments. The high-quality genome reported here can provide historical insights into genomic transformations that support the survival of A. corniculatum under harsh intertidal habitats.


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