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Joyner, O.

Publications and source records attributed to Joyner, O..

2 recordsLinked to original sources

De novo genome assemblies of the dwarf honey bee subgenus Micrapis: Apis andreniformis and Apis florea

The Micrapis subgenus, which includes the black dwarf honey bee (Apis andreniformis) and the red dwarf honey bee (Apis florea), remains underrepresented in genomic studies despite its ecological significance. Here, we present high-quality de novo genome assemblies for both species, generated using a hybrid sequencing approach combining Oxford Nanopore Technologies (ONT) long reads with Illumina short reads. The final assemblies are highly contiguous, with contig N50 values of 5.0 Mb (A. andreniformis) and 4.3 Mb (A. florea), representing a major improvement over the previously published A. florea genome. Genome completeness assessments indicate high quality, with BUSCO scores exceeding 98.5% and k-mer analyses supporting base-level accuracy. Repeat annotation revealed a relatively low repetitive sequence content ([~]6%), consistent with other Apis species. Using RNA sequencing data, we annotated 12,232 genes for A. andreniformis and 12,597 genes for A. florea, with >97% completeness in predicted proteomes. These genome assemblies provide a valuable resource for comparative and functional genomic studies, offering new insights into the genetic basis of dwarf honey bee adaptations.

genomics↗

Regulation of interferon signaling by transposon exonization

SummaryInnate immune signaling is essential for clearing pathogens and damaged cells, and must be tightly regulated to avoid excessive inflammation or autoimmunity. Here, we found that the alternative splicing of exons derived from transposable elements is a key mechanism controlling immune signaling in human cells. By analyzing long-read transcriptome datasets, we identified numerous transposon exonization events predicted to generate functional protein variants of immune genes, including the type I interferon receptor IFNAR2. We demonstrated that the transposon-derived isoform of IFNAR2 is more highly expressed than the canonical isoform in almost all tissues, and functions as a decoy receptor that potently inhibits interferon signaling including in cells infected with SARS-CoV-2. Our findings uncover a primate-specific axis controlling interferon signaling and show how a transposon exonization event can be co-opted for immune regulation.

genomics↗