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鉴定逆转录转座所需的最小Alu结构域。

Identification of a minimal Alu domain required for retrotransposition.

作者信息

Moldovan John B, Yin John, Moran John V

机构信息

Department of Human Genetics, University of Michigan Medical School, Ann Arbor, MI 48109, United States.

Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI 48109, United States.

出版信息

Nucleic Acids Res. 2025 Jun 20;53(12). doi: 10.1093/nar/gkaf526.

Abstract

Alu elements are primate-specific retrotransposons that comprise ∼11% of human DNA. Alu sequences contain an internal RNA polymerase III promoter, and the resultant Alu RNA transcripts mobilize by a replicative process termed retrotransposition, which requires the long interspersed element-1 open reading frame 2-encoded protein (ORF2p). Here, we used HeLa cell-based retrotransposition assays to define a minimal Alu domain necessary for retrotransposition. We demonstrate that Alu transcripts expressed from a cytomegalovirus (CMV) RNA polymerase II promoter can efficiently undergo retrotransposition. The use of an external CMV promoter to express Alu RNA allowed us to construct separation-of-function mutations to examine the effects of large deletions within the Alu sequence on retrotransposition. Deletion mutagenesis demonstrated that a 46-nucleotide (nt) domain located at the 5' end of the Alu RNA transcript is necessary for retrotransposition. Consistent with current models, the 46-nt 5' Alu domain associates with SRP9/14 in HeLa-HA cell extracts and can promote retrotransposition in HeLa-HA cells. We propose that the 46-nt 5' Alu domain forms a discrete structure that allows for SRP9/14 binding and ribosomal association, thereby allowing the Alu poly(A) tract to compete with the L1 poly(A) tail for ORF2p RNA binding to mediate its retrotransposition.

摘要

Alu元件是灵长类特有的逆转座子,约占人类DNA的11%。Alu序列包含一个内部RNA聚合酶III启动子,由此产生的Alu RNA转录本通过一种称为逆转座的复制过程进行移动,这需要由长散在元件1开放阅读框2编码的蛋白质(ORF2p)。在这里,我们使用基于HeLa细胞的逆转座分析来确定逆转座所需的最小Alu结构域。我们证明,从巨细胞病毒(CMV)RNA聚合酶II启动子表达的Alu转录本可以有效地进行逆转座。使用外部CMV启动子来表达Alu RNA使我们能够构建功能分离突变体,以检查Alu序列内大的缺失对逆转座的影响。缺失诱变表明,位于Alu RNA转录本5'端的一个46个核苷酸(nt)的结构域是逆转座所必需的。与当前模型一致,46-nt 5' Alu结构域在HeLa-HA细胞提取物中与SRP9/14结合,并可促进HeLa-HA细胞中的逆转座。我们提出,46-nt 5' Alu结构域形成一个离散的结构,允许SRP9/14结合和核糖体结合,从而使Alu poly(A)尾能够与L1 poly(A)尾竞争ORF2p RNA结合,以介导其逆转座。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55fc/12199147/9991ed02e3d2/gkaf526figgra1.jpg

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