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nucleic$53958$ - translation to ολλανδικά
![Swiss]] [[scientist]] [[Friedrich Miescher]] discovered nucleic acid first naming it as nuclein, in 1868. Later, he raised the idea that it could be involved in [[heredity]].<ref>[[Bill Bryson]], ''[[A Short History of Nearly Everything]]'', Broadway Books, 2015.p. 500.</ref>](https://commons.wikimedia.org/wiki/Special:FilePath/Friedrich Miescher.jpg?width=200 "Swiss]] [[scientist]] [[Friedrich Miescher]] discovered nucleic acid first naming it as nuclein, in 1868. Later, he raised the idea that it could be involved in [[heredity]].<ref>[[Bill Bryson]], ''[[A Short History of Nearly Everything]]'', Broadway Books, 2015.p. 500.</ref>")
![ochre]], proteins in blue. The active site is a small segment of rRNA, indicated in red.](https://commons.wikimedia.org/wiki/Special:FilePath/50S-subunit of the ribosome 3CC2.png?width=200 "ochre]], proteins in blue. The active site is a small segment of rRNA, indicated in red.")
![[[Secondary structure]] of a [[telomerase RNA]].](https://commons.wikimedia.org/wiki/Special:FilePath/Ciliate telomerase RNA.JPG?width=200 "[[Secondary structure]] of a [[telomerase RNA]].")
![Structure of a [[hammerhead ribozyme]], a ribozyme that cuts RNA](https://commons.wikimedia.org/wiki/Special:FilePath/Full length hammerhead ribozyme.png?width=200 "Structure of a [[hammerhead ribozyme]], a ribozyme that cuts RNA")
![Watson-Crick base pairs in a [[siRNA]] (hydrogen atoms are not shown)](https://commons.wikimedia.org/wiki/Special:FilePath/Piwi-siRNA-basepairing.png?width=200 "Watson-Crick base pairs in a [[siRNA]] (hydrogen atoms are not shown)")
![A hairpin loop from a pre-mRNA. Highlighted are the [[nucleobase]]s (green) and the ribose-phosphate backbone (blue). This is a single strand of RNA that folds back upon itself.](https://commons.wikimedia.org/wiki/Special:FilePath/Pre-mRNA-1ysv-tubes.png?width=200 "A hairpin loop from a pre-mRNA. Highlighted are the [[nucleobase]]s (green) and the ribose-phosphate backbone (blue). This is a single strand of RNA that folds back upon itself.")
Ορισμός
Βικιπαίδεια
Threose nucleic acid (TNA) is an artificial genetic polymer in which the natural five-carbon ribose sugar found in RNA has been replaced by an unnatural four-carbon threose sugar. Invented by Albert Eschenmoser as part of his quest to explore the chemical etiology of RNA, TNA has become an important synthetic genetic polymer (XNA) due to its ability to efficiently base pair with complementary sequences of DNA and RNA. However, unlike DNA and RNA, TNA is completely refractory to nuclease digestion, making it a promising nucleic acid analog for therapeutic and diagnostic applications.
TNA oligonucleotides were first constructed by automated solid-phase synthesis using phosphoramidite chemistry. Methods for chemically synthesized TNA monomers (phosphoramidites and nucleoside triphosphates) have been heavily optimized to support synthetic biology projects aimed at advancing TNA research. More recently, polymerase engineering efforts have identified TNA polymerases that can copy genetic information back and forth between DNA and TNA. TNA replication occurs through a process that mimics RNA replication. In these systems, TNA is reverse transcribed into DNA, the DNA is amplified by the polymerase chain reaction, and then forward transcribed back into TNA.
The availability of TNA polymerases have enabled the in vitro selection of biologically stable TNA aptamers to both small molecule and protein targets. Such experiments demonstrate that the properties of heredity and evolution are not limited to the natural genetic polymers of DNA and RNA. The high biological stability of TNA relative to other nucleic acid systems that are capable of undergoing Darwinian evolution, suggests that TNA is a strong candidate for the development of next-generation therapeutic aptamers.
The mechanism of TNA synthesis by a laboratory evolved TNA polymerase has been studied using X-ray crystallography to capture the five major steps of nucleotide addition. These structures demonstrate imperfect recognition of the incoming TNA nucleotide triphosphate and support the need for further directed evolution experiments to create TNA polymerases with improved activity. The binary structure of a TNA reverse transcriptase has also been solved by X-ray crystallography, revealing the importance of structural plasticity as a possible mechanism for template recognition.
