Prophage proteins alter long noncoding RNA and DNA of developing sperm to induce a paternal-effect lethality.
basic_science · Level V
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- Record sourced from PubMed, PMID 38452081.
- Also identified by DOI 10.1126/science.adk9469 and PMC identifier 11187695.
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Abstract
The extent to which prophage proteins interact with eukaryotic macromolecules is largely unknown. In this work, we show that cytoplasmic incompatibility factor A (CifA) and B (CifB) proteins, encoded by prophage WO of the endosymbiont <i>Wolbachia,</i> alter long noncoding RNA (lncRNA) and DNA during <i>Drosophila</i> sperm development to establish a paternal-effect embryonic lethality known as cytoplasmic incompatibility (CI). CifA is a ribonuclease (RNase) that depletes a spermatocyte lncRNA important for the histone-to-protamine transition of spermiogenesis. Both CifA and CifB are deoxyribonucleases (DNases) that elevate DNA damage in late spermiogenesis. lncRNA knockdown enhances CI, and mutagenesis links lncRNA depletion and subsequent sperm chromatin integrity changes to embryonic DNA damage and CI. Hence, prophage proteins interact with eukaryotic macromolecules during gametogenesis to create a symbiosis that is fundamental to insect evolution and vector control.
Medical subject headings
- Prophages
- RNA, Long Noncoding
- Spermatozoa
- Wolbachia
- Paternal Inheritance
- Viral Proteins
- Drosophila melanogaster
- Bacterial Proteins
- Deoxyribonucleases