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植物中微小却强大的RNA介导的干扰

Small but mighty RNA-mediated interference in plants.

作者信息

Pattanayak Debasis, Agarwal Sandhya, Sumathi S, Chakrabarti Swarup K, Naik Prakash S, Khurana S M Paul

机构信息

Central Potato Research Institute, India.

出版信息

Indian J Exp Biol. 2005 Jan;43(1):7-24.

Abstract

RNA silencing is a conserved phenomenon of regulation of gene expression by small RNAs derived from cleavage of double-stranded RNA (dsRNA). The present review deals with three overlapping modes of small RNA-mediated silencing particularly in plants. In case of post-transcriptional gene silencing (PTGS), Dicer, an endonuclease, cleaves dsRNA to produce approximately 21nt-long small interfering RNAs (siRNAs), which guide RISC, another nuclease complex, to destroy specific target mRNAs based on sequence complementarity with the siRNA. Another class of siRNAs of 25nt-long is also produced from dsRNA by Dicer, different from that generates 21nt-long siRNA. These longer siRNAs are probably involved in systemic silencing during PTGS and guide methylation of both DNA and histone, and induce heterochromatinization and consequent transcriptional repression of the targeted gene. Both siRNA-mediated PTGS and epigenetic modification of the genome are considered as defense mechanisms to protect against invading viruses, transposons or aberrantly expressing transgenes. Regulation of expression of endogenous genes is mediated by another class of 21nt-long small RNAs called microRNAs (miRNA). Genes encoding the miRNAs are present either in the intergenic regions, introns or coding regions of the plant genome. Cleavage of a stem-loop precursor transcript called pre-miRNA, by another class of Dicer generates miRNAs, which in association with nuclease complex similar to RISC, if not identical, either degrade target mRNA or cause translational repression. The applications of RNA silencing in functional genomics and crop improvement are discussed.

摘要

RNA沉默是一种由双链RNA(dsRNA)切割产生的小RNA对基因表达进行调控的保守现象。本综述主要探讨了小RNA介导的沉默的三种重叠模式,特别是在植物中的情况。在转录后基因沉默(PTGS)中,核酸内切酶Dicer切割dsRNA产生约21个核苷酸长的小干扰RNA(siRNA),这些siRNA引导另一种核酸酶复合物RISC,根据与siRNA的序列互补性来破坏特定的靶标mRNA。Dicer还能从dsRNA产生另一类25个核苷酸长的siRNA,这与产生21个核苷酸长siRNA的情况不同。这些较长的siRNA可能参与PTGS过程中的系统性沉默,并引导DNA和组蛋白的甲基化,诱导异染色质化以及随后靶标基因的转录抑制。siRNA介导的PTGS和基因组的表观遗传修饰都被认为是抵御入侵病毒、转座子或异常表达转基因的防御机制。内源性基因表达的调控由另一类21个核苷酸长的小RNA——微小RNA(miRNA)介导。编码miRNA的基因存在于植物基因组的基因间区域、内含子或编码区域。另一类Dicer切割一种称为前体miRNA的茎环前体转录本产生miRNA,这些miRNA与类似于RISC的核酸酶复合物结合(如果不完全相同),要么降解靶标mRNA,要么导致翻译抑制。本文还讨论了RNA沉默在功能基因组学和作物改良中的应用。

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