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Domestic chickens activate a piRNA defense against avian leukosis virus
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PIWI-interacting RNAs (piRNAs) protect the germ line by targeting transposable elements (TEs) through the base-pair complementarity. We do not know how piRNAs co-evolve with TEs in chickens. Here we reported that all active TEs in the chicken germ line are targeted by piRNAs, and as TEs lose their activity, the corresponding piRNAs erode away. We observed de novo piRNA birth as host responds to a recent retroviral invasion. Avian leukosis virus (ALV) has endogenized prior to chicken domestication, remains infectious, and threatens poultry industry. Domestic fowl produce piRNAs targeting ALV from one ALV provirus that was known to render its host ALV resistant. This proviral locus does not produce piRNAs in undomesticated wild chickens. Our findings uncover rapid piRNA evolution reflecting contemporary TE activity, identify a new piRNA acquisition modality by activating a pre-existing genomic locus, and extend piRNA defense roles to include the period when endogenous retroviruses are still infectious.
eLife Sciences Publications, Ltd
Title: Domestic chickens activate a piRNA defense against avian leukosis virus
Description:
PIWI-interacting RNAs (piRNAs) protect the germ line by targeting transposable elements (TEs) through the base-pair complementarity.
We do not know how piRNAs co-evolve with TEs in chickens.
Here we reported that all active TEs in the chicken germ line are targeted by piRNAs, and as TEs lose their activity, the corresponding piRNAs erode away.
We observed de novo piRNA birth as host responds to a recent retroviral invasion.
Avian leukosis virus (ALV) has endogenized prior to chicken domestication, remains infectious, and threatens poultry industry.
Domestic fowl produce piRNAs targeting ALV from one ALV provirus that was known to render its host ALV resistant.
This proviral locus does not produce piRNAs in undomesticated wild chickens.
Our findings uncover rapid piRNA evolution reflecting contemporary TE activity, identify a new piRNA acquisition modality by activating a pre-existing genomic locus, and extend piRNA defense roles to include the period when endogenous retroviruses are still infectious.
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