Tie-Break: Host and Retrotransposons Play tRNA.

Tie-Break: Host and Retrotransposons Play tRNA.
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DOI:
10.1016/j.tcb.2018.05.006
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发表时间:
2018-10
影响因子:
19
通讯作者:
Martienssen R
Martienssen R
中科院分区:
生物学1区
文献类型:
--
作者:
Schorn AJ;Martienssen R

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tRNA片段(tRF)是一类具有多种功能的小调控rna。3 ‘衍生的trf与使用trna的3 ’端启动逆转录的长末端重复(LTR)逆转录元件完全匹配。最近的研究表明,tRFs针对RNA干扰(RNAi)途径的ltr -逆转录病毒和-转座子,并通过阻断逆转录来抑制移动性。ltr -逆转录元件中高度保守的tRNA引物结合位点(PBS)是3 ' - trf识别和阻断在发育和疾病的表观遗传重编程过程中具有转录活性的丰富而多样的ltr -逆转录转座子的独特靶标。3 ' - trf是在未知条件下由全长trna加工而成的,可能保护许多细胞类型。trf作为RNAi、转座子和基因组稳定性之间的古老联系而出现。
tRNA fragments (tRF) are a class of small, regulatory RNAs with diverse functions. 3’-derived tRFs perfectly match long terminal repeat (LTR)-retroelements which use the 3’-end of tRNAs to prime reverse transcription. Recent work has shown that tRFs target LTR-retroviruses and -transposons for the RNA interference (RNAi) pathway and also inhibit mobility by blocking reverse transcription. The highly conserved tRNA primer binding site (PBS) in LTR-retroelements is a unique target for 3’-tRFs to recognize and block abundant but diverse LTR-retrotransposons that become transcriptionally active during epigenetic reprogramming in development and disease. 3’-tRFs are processed from full-length tRNAs under yet unknown conditions and potentially protect many cell types. tRFs appear as an ancient link between RNAi, transposons, and genome stability.
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