上海士鋒生物科技有限公司作者
RNA干擾原理圖解
資料類型 | png文件 | 資料大小 | 51812 |
下載次數 | 114 | 資料圖片 | 【點擊查看】 |
上 傳 人 | 上海士鋒生物科技有限公司 | 需要積分 | 0 |
關 鍵 詞 | RNA干擾原理圖解,RNA |
- 【資料簡介】
Long double-stranded RNAs (dsRNAs; typically >200 nt) can be used to silence the expression of target genes in a variety of organisms and cell types (e.g., worms, fruit flies, and plants). Upon introduction, the long dsRNAs enter a cellular pathway that is commonly referred to as the RNA interference (RNAi) pathway. First, the dsRNAs get processed into 20-25 nucleotide (nt) small interfering RNAs (siRNAs) by an RNase III-like enzymecalled Dicer (initiation step). Then, the siRNAs assemble into endoribonuclease-containing complexes known as RNA-induced silencing complexes (RISCs), unwinding in the process. The siRNA strands subsequently guide the RISCs to complementary RNA molecules, where they cleave and destroy the cognate RNA (effecter step). Cleavage of cognate RNA takes place near the middle of the region bound by the siRNA strand.
In mammalian Cells, introduction of long dsRNA (>30 nt) initiates a potent antiviral response, exemplified by nonspecific inhibition of protein synthesis and RNA degradation. The mammalian antiviral response can be bypassed, however, by the introduction or expression of sirnas.
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The Mechanism of RNA Interference (RNAi)
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