4.3 Article

Variation and Evolution in the Glutamine-Rich Repeat Region of Drosophila Argonaute-2

期刊

G3-GENES GENOMES GENETICS
卷 6, 期 8, 页码 2563-2572

出版社

GENETICS SOCIETY AMERICA
DOI: 10.1534/g3.116.031880

关键词

Argonaute-2; Drosophila melanogaster; RNA interference; repetitive elements

资金

  1. Natural Environmental Research Council Biomolecular Analysis Facility small grant [NBAF 895]
  2. Darwin Trust of Edinburgh
  3. Wellcome Trust strategic award [WT095831]
  4. Natural Environment Research Council [NBAF010002] Funding Source: researchfish
  5. NERC [NBAF010002] Funding Source: UKRI

向作者/读者索取更多资源

RNA interference pathways mediate biological processes through Argonaute-family proteins, which bind small RNAs as guides to silence complementary target nucleic acids. In insects and crustaceans Argonaute-2 silences viral nucleic acids, and therefore acts as a primary effector of innate antiviral immunity. Although the function of the major Argonaute-2 domains, which are conserved across most Argonaute-family proteins, are known, many invertebrate Argonaute-2 homologs contain a glutamine-rich repeat (GRR) region of unknown function at the N-terminus. Here we combine long-read amplicon sequencing of Drosophila Genetic Reference Panel (DGRP) lines with publicly available sequence data from many insect species to show that this region evolves extremely rapidly and is hyper-variable within species. We identify distinct GRR haplotype groups in Drosophila melanogaster, and suggest that one of these haplotype groups has recently risen to high frequency in a North American population. Finally, we use published data from genome-wide association studies of viral resistance in D. melanogaster to test whether GRR haplotypes are associated with survival after virus challenge. We find a marginally significant association with survival after challenge with Drosophila C Virus in the DGRP, but we were unable to replicate this finding using lines from the Drosophila Synthetic Population Resource panel.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.3
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据