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Lai, M.-W.

Publications and source records attributed to Lai, M.-W..

2 recordsLinked to original sources

Mitochondrial genome reduction and accelerated evolution in planktonic foraminiferans

The evolution of mitochondria provides crucial insights into the diversification of eukaryotes, with complex events of gene losses revealed through comparative analyses of mitochondrial genomes (mitogenomes) across eukaryotic lineages. However, the mitogenomes of many microbial eukaryotes remain underexplored due to challenges in their isolation and cultivation. Particularly understudied are Foraminifera (Rhizaria, SAR), unicellular calcifyers that are widely distributed across global oceans and important paleoenvironmental proxies. Through single-cell genomic sequencing, here we report a 22-kb complete mitogenome of a planktonic foraminiferan from tropical seawater, which is the smallest known to date among all sequenced mitogenomes of Rhizaria, a major lineage of eukaryotes. It contains only six protein-coding genes and fragmented ribosomal RNA genes, and has lost most genes in oxidative phosphorylation and all genes in mitochondrial translation. Such genome reduction is associated with accelerated evolutionary rates and a lower GC content than that of benthic foraminiferan and other rhizarian mitogenomes. These findings highlight the unique trajectory of mitogenome reduction during rhizarian evolution and the use of single-cell approaches for recovering microbial eukaryotic genomes and expanding our understanding of mitochondrial evolution.

genomics↗

Haplotype-aware multiomics unveils the regulatory basis of haplodiplontic life-cycle differentiation in a cosmopolitan marine alga

Gephyrocapsa huxleyi (formerly Emiliania huxleyi), a key coccolithophore alga influencing the global carbon cycle through photosynthesis and calcification, undergoes a haplodiplontic sexual life cycle with a calcifying non-flagellate diploid and a non-calcifying biflagellate haploid stage. To reveal the molecular basis of their morpho-physiological distinctions, we generated chromosome-level genome assemblies and compared the transcriptomes, proteomes, and methylomes for a pair of isogenic haploid and diploid model strains and conducted haplotype-aware analyses of their multiomic features. In addition to calcification and flagella, transcriptomes and proteomes of haploid and diploid cells modulate their differentiation in photosynthesis, sulfatases, DMSP degradation, DNA replication, and endomembrane system and transport. Haploid-diploid differential gene expression can be partially attributable to allelic imbalance (allele-specific expression) in diploid cells. Gene transcript abundance is positively associated with both CG and CHG gene-body DNA methylation, which can be inheritable, allele-specific, and differentiated between life-cycle phases. This multiomic study unravels the regulatory basis of unicellular algal life-cycle differentiation and provides valuable resources for investigating the ecologically important coccolithophore algae.

genomics↗