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

被引:19
|
作者
Hu, Haiyang [1 ,2 ]
Liu, Jian-Mei [3 ,4 ]
Hu, Zhenyu [3 ,4 ]
Jiang, Xi [2 ]
Yang, Xiaode [2 ,5 ]
Li, Jiangxia [3 ,4 ]
Zhang, Yao [3 ,4 ]
Yu, Haijing [3 ,4 ]
Khaitovich, Philipp [6 ,7 ,8 ,9 ,10 ]
机构
[1] China Pharmaceut Univ, Sch Life Sci & Technol, Nanjing, Jiangsu, Peoples R China
[2] CAS MPG Partner Inst Computat Biol, CAS Key Lab Computat Biol, Shanghai, Peoples R China
[3] Yunnan Univ, Sch Life Sci, State Key Lab Nat Resource Conservat & Utilizat, Kunming, Yunnan, Peoples R China
[4] Yunnan Univ, Sch Life Sci, Ctr Life Sci, Kunming, Yunnan, Peoples R China
[5] Univ Chinese Acad Sci, Beijing, Peoples R China
[6] Skolkovo Inst Sci & Technol, Skolkovo, Russia
[7] Chinese Acad Sci, Ctr Excellence Anim Evolut & Genet, Kunming, Yunnan, Peoples R China
[8] CAS MPG Partner Inst Computat Biol, Comparat Biol Grp, Shanghai, Peoples R China
[9] Max Planck Inst Evolutionary Anthropol, Leipzig, Germany
[10] ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai, Peoples R China
基金
俄罗斯科学基金会; 中国国家自然科学基金;
关键词
microRNA sponge; young noncoding RNA; co-evolution; tumorigenesis; LONG NONCODING RNAS; MICRORNA TARGET SITES; GENE-EXPRESSION; MESSENGER-RNAS; CIRCULAR RNAS; DATABASE; EVOLUTION; ANNOTATION; PREDICTION; EFFICIENT;
D O I
10.1093/molbev/msy022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1063 / 1077
页数:15
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