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Updated: Aug 6, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
The molecular mechanism of Drosophila restricting telomeric transposons
Cheng-Xian Wang1, Yi-Kang S Rong1, Min Cui1
1Hengyang Medical College, University of South China, Hengyang 421200, China.
Abstract:
Linear chromosomes of eukaryotes are protected by a DNA-protein-RNA structure called telomere. Remarkably and unlike those of most organisms studied, Drosophila telomeric DNA is not composed of a group of short repeats, but three classes of retrotransposons at the chromosome ends. Telomeric transposons in Drosophila on the other hand serves the function of elongating the host chromosomes yet prevent little harm to the host genome as their insertion sites are strictly limited to the telomere. How the Drosophila host achieves such precise regulation is still unclear. The currently known genome-wide repression of transposon expression includes piRNA pathway and the heterochromatin pathway involving H3K9me3. Recent studies have found that Drosophila telomere capping proteins are involved in the specific regulation of telomeric retrotransposons. In this review, we discuss the specific functions of telomere capping proteins in regulating telomeric transposons. By studying how the Drosophila host interacts and regulates telomeric transposons, we hope to shed lights on universal principles in guiding their co-evolution.
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