This document discusses several types of non-coding RNAs including ribosomal RNA, transfer RNA, small nuclear RNA, small nucleolar RNA, microRNA, and short interfering RNA. It provides details on the structure and function of small nuclear RNAs, small nucleolar RNAs, microRNAs, and short interfering RNAs. Small nuclear RNAs help in splicing mRNA precursors. Small nucleolar RNAs guide chemical modifications of other RNAs during ribosome biogenesis. MicroRNAs and short interfering RNAs are both around 21-25 nucleotides long and can repress translation or catalyze destruction of target mRNAs.
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Si RNA
This document discusses several types of non-coding RNAs including ribosomal RNA, transfer RNA, small nuclear RNA, small nucleolar RNA, microRNA, and short interfering RNA. It provides details on the structure and function of small nuclear RNAs, small nucleolar RNAs, microRNAs, and short interfering RNAs. Small nuclear RNAs help in splicing mRNA precursors. Small nucleolar RNAs guide chemical modifications of other RNAs during ribosome biogenesis. MicroRNAs and short interfering RNAs are both around 21-25 nucleotides long and can repress translation or catalyze destruction of target mRNAs.
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Non-coding RNAs
• Ribosomal RNA (rRNA)
• Transfer RNA (tRNA) • Small nuclear RNA (snRNA) • Small nucleolar RNA (snoRNA) • MicroRNA (miRNA) • Short interfering RNA (siRNA) Other non-coding RNAs.
• Small nuclear RNAs (snRNAs) form
part of the spliceosome which cleaves the introns out of mRNA precursors. • There are 5 snRNAs; U1, U2, U4, U5 and you guessed it U6. Other non-coding RNAs.
• These RNA species are between 50 and
200 nucleotides long and complex with proteins to form snRNPs (small nuclear ribonucleoprotein particles..snurps). • These small RNAs contribute to the recognition of splice sites in the mRNA and in catalysing the breaking and joining of the mRNA. snoRNA • snoRNA are small nucleolar RNAs between 60 and 300 nucleotides in length. • RNA editing function • They recognise their target sequence by base pairing and then recruit specialised proteins to perform nucleotide modifications to these RNAs; – 2’ O-ribose methylation, – base deaminations such as adenine to inosine conversions – addition of pseudouridines. snoRNA • These modifications are crucial to ribosome biogenesis. • snoRNAs are derived from introns. • sno RNAs in conjunction with snRNAs have been suggested as regulators for alternative splice sites. • snoRNAs are derived from the introns of pre-mRNA transcripts, suggesting that introns are not “junk” DNA. miRNA and siRNA • microRNA (miRNA) and short interfering RNA (siRNA) are very small RNA molecules, ranging between 21 to 25 nucleotides long. • These are the hot molecules! They are seen as the next anti-viral agents, cures for cancer etc even a replacement for fossil fuels!!! miRNA and siRNA • The 2 species are quite similar, the variations come from their source or origin. • MicroRNA comes from short endogenous hairpin loop structures, synthesised by RNA pol II, often from within introns. • The hairpin structures are cleaved in the nucleus, exported to the cytoplasm and further processed to ~22 nt duplexes. miRNA • It cuts off the hairpin loop and the 65 75 nt pre-miRNAs are exported to the cytoplasm by exportin 5 • It is further processed by another RNase III endonuclease system, Dicer. • The mature miRNA s are ~22 nt duplexes and act usually to repress translation of target mRNA sequences. siRNA • siRNAs are similar but are produced from long double stranded RNA molecules or giant hairpin molecules, often of exogenous origin. • This whole process is thought to be part of the cell’s antiviral defense. siRNA • Researchers can also introduce their own double stranded RNA. • The double stranded molecules are processed by Dicer, the cytoplasmic RNase III endonuclease system. siRNA • The processed interfering RNA (RNAi) can catalyse the destruction of endogenous mRNAs of the same sequence and this process has been used very successfully by scientists to silence genes or knock them down.