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最近进化的肿瘤抑制因子转录本 TP73-AS1 作为人类特异性 miR-941 的海绵发挥作用。

Recently Evolved Tumor Suppressor Transcript TP73-AS1 Functions as Sponge of Human-Specific miR-941.

机构信息

School of Life Science and Technology, China Pharmaceutical University, Nanjing, China.

CAS Key Laboratory of Computational Biology, CAS-MPG Partner Institute for Computational Biology, Shanghai, China.

出版信息

Mol Biol Evol. 2018 May 1;35(5):1063-1077. doi: 10.1093/molbev/msy022.

DOI:10.1093/molbev/msy022
PMID:29474580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5913670/
Abstract

MicroRNA (miRNA) sponges are vital components of posttranscriptional gene regulation. Yet, only a limited number of miRNA sponges have been identified. Here, we show that the recently evolved noncoding tumor suppressor transcript, antisense RNA to TP73 gene (TP73-AS1), functions as a natural sponge of human-specific miRNA miR-941. We find unusually nine high-affinity miR-941 binding sites clustering within 1 kb region on TP73-AS1, which forms miR-941 sponge region. This sponge region displays increased sequence constraint only in humans, and its formation can be traced to the tandem expansion of a 71-nt-long sequence containing a single miR-941 binding site in old world monkeys. We further confirm TP73-AS1 functions as an efficient miR-941 sponge based on massive transcriptome data analyses, wound-healing assay, and Argonaute protein immunoprecipitation experiments conducted in cell lines. The expression of miR-941 and its sponge correlate inversely across multiple healthy and cancerous tissues, with miR-941 being highly expressed in tumors and preferentially repressing tumor suppressors. Thus, the TP73-AS1 and miR-941 duo represents an unusual case of the extremely rapid evolution of noncoding regulators controlling cell migration, proliferation, and tumorigenesis.

摘要

微小 RNA (miRNA) 海绵是转录后基因调控的重要组成部分。然而,目前已鉴定出的 miRNA 海绵数量有限。在这里,我们展示了最近进化的非编码肿瘤抑制转录本,即 TP73 基因反义 RNA (TP73-AS1),作为人类特异性 miRNA miR-941 的天然海绵。我们发现,在 TP73-AS1 上的 1kb 区域内,有九个异常高亲和力的 miR-941 结合位点聚集在一起,形成了 miR-941 海绵区域。这个海绵区域仅在人类中显示出增加的序列约束,其形成可以追溯到在旧世界猴中,一个包含单个 miR-941 结合位点的 71nt 长序列的串联扩张。我们进一步通过在细胞系中进行的大规模转录组数据分析、伤口愈合测定和 Argonaute 蛋白免疫沉淀实验,证实了 TP73-AS1 作为有效的 miR-941 海绵的功能。miR-941 和其海绵的表达在多种健康和癌症组织中呈负相关,miR-941 在肿瘤中高表达,并优先抑制肿瘤抑制因子。因此,TP73-AS1 和 miR-941 这一对代表了一种非编码调节剂控制细胞迁移、增殖和肿瘤发生的极其快速进化的特殊情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/fa363593f14d/msy022f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/9c9a3c168a57/msy022f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/a58f3051b45e/msy022f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/cf1b04926fd0/msy022f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/b00831524cd8/msy022f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/7e34e94058d3/msy022f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/094ff62c6957/msy022f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/fa363593f14d/msy022f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/9c9a3c168a57/msy022f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/a58f3051b45e/msy022f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/cf1b04926fd0/msy022f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/b00831524cd8/msy022f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/7e34e94058d3/msy022f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/094ff62c6957/msy022f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb38/5913670/fa363593f14d/msy022f7.jpg

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