Short tandem target mimics inhibit Chlamydomonas reinhardtii microRNAs

被引:2
|
作者
Sun, Ting [1 ,2 ]
Wang, Yuting [3 ]
Anwar, Muhammad [1 ,2 ]
Lou, Sulin [1 ]
Zeng, Yanfeng [1 ]
Li, Hui [1 ]
Hu, Zhangli [1 ]
机构
[1] Shenzhen Univ, Coll Life Sci & Oceanog, Guangdong Engn Res Ctr Marine Algal Biotechnol, Longhua Innovat Inst Biotechnol,Guangdong Key Lab, Shenzhen 518060, Peoples R China
[2] Shenzhen Univ, Coll Optoelect Engn, Key Lab Optoelect Devices & Syst, Minist Educ & Guangdong Prov, Shenzhen 518060, Peoples R China
[3] Hebei Normal Univ, Coll Life Sci, Shijiazhuang 050024, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
PLANT; BIOGENESIS; EXPRESSION; MECHANISM; GENES; LONG;
D O I
10.1016/j.algal.2020.101824
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Short tandem target mimic (STTM) RNAs contain two non-cleavable microRNA (miRNA) binding sites linked by a spacer and can be used to effectively block the functions of specific miRNAs in animals and plants. However, the application of STTMs in unicellular organisms has not been reported. In this study, we tested different STTMs targeting miRNAs of the microalga Chlamydomonas reinhardtii to verify the feasibility of this approach in a unicellular organism. Three previously identified C. reinhardtii miRNAs (miR906-5p, miR1166.1, and miR1150.3) were used as targets and transgenic algae containing STTMs were constructed. All three STTM constructs induced significantly lower miRNA levels, from 84% lower levels of miR1150.3 to 73% lower levels of miR1166.1 compared with non-transgenic controls. Surprisingly, this effect on miRNA levels was non-specific, independent of its target miRNA sequence and each STTM suppressed all miRNAs tested. This is the first time that the STTM technique has been tested in a lower unicellular organism. The non-specific inhibition of miRNA expression by the STTMs revealed the complexity of miRNA functions in diverse eukaryotic organisms. © 2020 Elsevier B.V.
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页数:6
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