生物
亚科
遗传学
YY1年
激活剂(遗传学)
分子生物学
基因
发起人
基因表达
作者
Karabi Saha,Grace Nielsen,Raj Nandani,Yizi Zhang,Lingqi Kong,Ping Ye,Wenfeng An
摘要
Abstract Long interspersed element type 1 (LINE-1, L1) is an active autonomous transposable element in human and mouse genomes. L1 transcription is controlled by an internal RNA polymerase II promoter in the 5′ untranslated region (5′UTR) of a full-length L1. It has been shown that transcription factor YY1 binds to a conserved sequence at the 5′ end of the human L1 5′UTR and primarily dictates where transcription initiates. Putative YY1-binding motifs have been predicted in the 5′UTRs of two distinct mouse L1 subfamilies, Tf and Gf. Using site-directed mutagenesis, in vitro binding and gene knockdown assays, we experimentally tested the role of YY1 in mouse L1 transcription. Our results indicate that Tf, but not Gf subfamily, harbors functional YY1-binding sites in 5′UTR monomers and YY1 functions as a transcriptional activator for the mouse Tf subfamily. Activation of Tf transcription by YY1 during early embryogenesis is also supported by a reanalysis of published zygotic knockdown data. Furthermore, YY1-binding motifs are solely responsible for the synergistic interaction between Tf monomers, consistent with a model wherein distant monomers act as enhancers for mouse L1 transcription. The abundance of YY1-binding sites in Tf elements also raise important implications for gene regulation across the genome.
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