Difference between the 2 bases pairs

In summary, the order of the base pairs in DNA affects its stability, RNA has more stability due to its single-stranded nature, and there are chemical consequences of this.
  • #1
scope
61
0
hi,

i wonder if there is any clear chemical difference between the bases pairs CG and AT? is one more reactive than the other one for example? is there any chemical difference that is used? i would be very grateful for any reply!

thanks!
 
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  • #2
G and C form three hydrogen bonds, A and T form two, and they both differ in the display of (partially) charged groups in the grooves.
 
  • #3
wonderful, and what are the chemical consequences for this? more stability for one ? can you tell me anything like this? this seems so fascinating!
 
  • #4
GC pairs are indeed more stable, and the difference in groove display allows specific enzymes to recognise specific DNA sequences, very useful for controlling gene expression.

There are also chemical consequences of the order of the base pairs, e.g. GC repetitions can cause 'slipping' of the DNA replication machinery and thus cause the size of the repetition to vary in subsequent divisions.
 
  • #5
wonderful. but then if they are most stable, maybe CG is more abundant than AT? since stability is related to abundance?
 
  • #6
Well, you must take into account that DNA has to be able to open its strands in order to replicate or produce an mRNA molecule. Therefore, too high stability is detrimental. In organisms living at higher temperatures, there is a bias towards G/C instead of A/T in certain parts of the genetic code.
 
  • #7
wonderful! does the same occur for RNA if we compare CG and AU?
 
  • #8
scope said:
wonderful! does the same occur for RNA if we compare CG and AU?

RNA is more complicated because it normally is "single" stranded. However, it can fold back on itself providing more stability through base-pairing. This can increase the shelf-life of mRNAs or adds the functionality to functional RNAs.

I reckon, if you were to look, you'd find a higher GC content to functional RNAs or mRNAs (particularly in the 5' and 3' NCRs) with long shelf lives. Its also compounded by proteins which bind RNA can increase their longevity.
 
  • #9
This is also valid for RNA/DNA hybrids, as seen in polyA tracts at the end of mRNA molecules. Since these are thermodynamically less stable, the mRNA strand can more easily release from the DNA template. Of course, this has evolved to exert multiple functions throughout time, but it's unofficially generally accepted that this was the original reason for the terminating polyA sequence.
 
  • #10
Helicases, which are a class of enzymes,start splitting the DNA apart during replication at places rich in A-T pairs because they form 2 hydrogen bonds compared to 3 of G-C bonds. Therefore they are easier to break and require less energy.
 

1. What are the 2 base pairs that make up DNA?

The 2 base pairs that make up DNA are adenine (A) paired with thymine (T), and guanine (G) paired with cytosine (C).

2. How do base pairs determine the genetic code?

The sequence of base pairs in DNA determines the genetic code by encoding the instructions for building proteins. Each unique combination of A, T, G, and C forms a codon, and each codon codes for a specific amino acid that makes up a protein.

3. What is the difference between a base pair and a nucleotide?

A base pair is a pair of nitrogenous bases (A-T or G-C) joined by hydrogen bonds, while a nucleotide is a building block of DNA that consists of a sugar, a phosphate group, and a nitrogenous base.

4. How does the structure of base pairs contribute to DNA's stability?

The structure of base pairs, with A always pairing with T and G always pairing with C, allows for the DNA molecule to maintain its shape and stability. The hydrogen bonds between the base pairs also provide strength and stability to the DNA molecule.

5. Can base pairs be changed or mutated?

Yes, base pairs can be changed or mutated, which can lead to genetic variation and potential health implications. Mutations can occur due to errors in DNA replication, exposure to environmental factors, or other genetic factors.

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