Skip to content
Surf Wiki
Save to docs
general/nucleosides

From Surf Wiki (app.surf) — the open knowledge base

Dihydrouridine

Chemical compound

Dihydrouridine

Chemical compound

Dihydrouridine (abbreviated as D, hU, DHU, or UH2) is a pyrimidine nucleoside which is the result of adding two hydrogen atoms to a uridine, making it a fully saturated pyrimidine ring with no remaining double bonds. D is found in tRNA and rRNA molecules as a nucleoside; the corresponding nucleobase is 5,6-dihydrouracil.

Structure of base pair Adenine Dihydrouracil (AD)

Because it is non-planar, D disturbs the stacking interactions in helices and destabilizes the RNA structure. D also stabilizes the C2′-endo sugar conformation, which is more flexible than the C3′-endo conformation; this effect is propagated to the 5′-neighboring residue. Thus, while pseudouridine and 2′-O-methylations stabilize the local RNA structure, D does the opposite.

The tRNAs of organisms that grow at low temperatures (psychrophiles) have high 5,6-dihydrouridine levels (40-70% more on average) which provides the necessary local flexibility of the tRNA at or below the freezing point.

References

References

  1. IUPAC-IUB Commission on Biochemical Nomenclature. (1970). "Abbreviations and symbols for nucleic acids, polynucleotides, and their constituents". [[Biochemistry (journal).
  2. Dalluge JJ. (Mar 15, 1996). "Conformational flexibility in RNA: the role of dihydrouridine". Nucleic Acids Res.
  3. Dalluge JJ. (March 1, 1997). "Posttranscriptional modification of tRNA in psychrophilic bacteria". J Bacteriol.
Info: Wikipedia Source

This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.

Want to explore this topic further?

Ask Mako anything about Dihydrouridine — get instant answers, deeper analysis, and related topics.

Research with Mako

Free with your Surf account

Content sourced from Wikipedia, available under CC BY-SA 4.0.

This content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.

Report