Traduction et analyse de mots par intelligence artificielle ChatGPT
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nucleic$53958$ - traduction vers allemand
![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>")
![DNA major and minor grooves. The latter is a binding site for the [[Hoechst stain]] dye 33258.](https://commons.wikimedia.org/wiki/Special:FilePath/DNA-ligand-by-Abalone.png?width=200 "DNA major and minor grooves. The latter is a binding site for the [[Hoechst stain]] dye 33258.")
![animated version]]).](https://commons.wikimedia.org/wiki/Special:FilePath/DNA animation.gif?width=200 "animated version]]).")
![3′]] hydroxyl group (—OH) on the other.](https://commons.wikimedia.org/wiki/Special:FilePath/DNA chemical structure.svg?width=200 "3′]] hydroxyl group (—OH) on the other.")
![lagging strand]]. This enzyme makes discontinuous segments (called [[Okazaki fragment]]s) before [[DNA ligase]] joins them together.](https://commons.wikimedia.org/wiki/Special:FilePath/DNA replication en.svg?width=200 "lagging strand]]. This enzyme makes discontinuous segments (called [[Okazaki fragment]]s) before [[DNA ligase]] joins them together.")
![B]] and [[Z-DNA]]](https://commons.wikimedia.org/wiki/Special:FilePath/Dnaconformations.png?width=200 "B]] and [[Z-DNA]]")
.jpg?width=200 "Impure DNA extracted from an orange")
![Location of eukaryote [[nuclear DNA]] within the chromosomes](https://commons.wikimedia.org/wiki/Special:FilePath/Eukaryote DNA-en.svg?width=200 "Location of eukaryote [[nuclear DNA]] within the chromosomes")
![[[Maclyn McCarty]] (left) shakes hands with [[Francis Crick]] and [[James Watson]], co-originators of the double-helix model based on the X-ray diffraction data and insights of Rosalind Franklin and Raymond Gosling.](https://commons.wikimedia.org/wiki/Special:FilePath/Maclyn McCarty with Francis Crick and James D Watson - 10.1371 journal.pbio.0030341.g001-O.jpg?width=200 "[[Maclyn McCarty]] (left) shakes hands with [[Francis Crick]] and [[James Watson]], co-originators of the double-helix model based on the X-ray diffraction data and insights of Rosalind Franklin and Raymond Gosling.")
![Interaction of DNA (in orange) with [[histone]]s (in blue). These proteins' basic amino acids bind to the acidic phosphate groups on DNA.](https://commons.wikimedia.org/wiki/Special:FilePath/Nucleosome1.png?width=200 "Interaction of DNA (in orange) with [[histone]]s (in blue). These proteins' basic amino acids bind to the acidic phosphate groups on DNA.")
![The Eagle]] [[pub]] commemorating Crick and Watson](https://commons.wikimedia.org/wiki/Special:FilePath/TheEaglePub-Cambridge-BluePlaque.jpg?width=200 "The Eagle]] [[pub]] commemorating Crick and Watson")
Définition
Wikipédia
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.
