The structure of DNA double helix and how it was discovered. Chargaff, Watson and Crick, and Wilkins and Franklin.
Today, the DNA double helix is probably the most iconic of all biological molecules. It's inspired staircases, decorations, pedestrian bridges (like the one in Singapore, shown below), and more.
I have to agree with the architects and designers: the double helix is a beautiful structure, one whose form fits its function in a remarkable way. But the double helix was not always part of our cultural lexicon. In fact, until the 1950s, the structure of DNA remained a mystery.
In this article, we'll briefly explore how the double-helical structure of DNA was discovered through the work of James Watson, Francis Crick, Rosalind Franklin, and other researchers. Then, we'll take a look at the properties of the double helix itself.
The components of DNA
From the work of biochemist Phoebus Levene and others, scientists in Watson and Crick's time knew that DNA was composed of subunits called nucleotides. A nucleotide is made up of a sugar (deoxyribose), a phosphate group, and one of four nitrogenous bases: adenine (A), thymine (T), guanine (G) or cytosine (C).
C and T bases, which have just one ring, are called pyrimidines, while A and G bases, which have two rings, are called purines.
DNA nucleotides assemble in chains linked by covalent bonds, which form between the deoxyribose sugar of one nucleotide and the phosphate group of the next. This arrangement makes an alternating chain of deoxyribose sugar and phosphate groups in the DNA polymer, a structure known as the sugar-phosphate backbone
One other key piece of information related to the structure of DNA came from Austrian biochemist Erwin Chargaff. Chargaff analyzed the DNA of different species, determining its composition of A, T, C, and G bases. He made several key observations:
- A, T, C, and G were not found in equal quantities (as some models at the time would have predicted)
- The amounts of the bases varied among species, but not between individuals of the same species
- The amount of A always equalled the amount of T, and the amount of C always equalled the amount of G (A = T and G = C)
These findings, called Chargaff's rules, turned out to be crucial to Watson and Crick's model of the DNA double helix.
Watson, Crick, and Rosalind Franklin
In the early 1950s, American biologist James Watson and British physicist Francis Crick came up with their famous model of the DNA double helix. They were the first to cross the finish line in this scientific "race," with others such as Linus Pauling (who discovered protein secondary structure) also trying to find the correct model.
Rather than carrying out new experiments in the lab, Watson and Crick mostly collected and analyzed existing pieces of data, putting them together in new and insightful ways. Some of their most crucial clues to DNA's structure came from Rosalind Franklin, a chemist working in the lab of physicist Maurice Wilkins.
Franklin was an expert in a powerful technique for determining the structure of molecules, known as X-ray crystallography. When the crystallized form of a molecule such as DNA is exposed to X-rays, some of the rays are deflected by the atoms in the crystal, forming a diffraction pattern that gives clues about the molecule's structure.
Franklin’s crystallography gave Watson and Crick important clues to the structure of DNA. Some of these came from the famous “image 51,” a remarkably clear and striking X-ray diffraction image of DNA produced by Franklin and her graduate student. (A modern example of the diffraction pattern produced by DNA is shown above.) To Watson, the X-shaped diffraction pattern of Franklin's image immediately suggested a helical, two-stranded structure for DNA.
Watson and Crick brought together data from a number of researchers (including Franklin, Wilkins, Chargaff, and others) to assemble their celebrated model of the 3D structure of DNA. In 1962, James Watson, Francis Crick, and Maurice Wilkins were awarded the Nobel Prize in Medicine. Unfortunately, by then Franklin had died, and Nobel prizes are not awarded posthumously.
Watson and Crick's model of DNA
The structure of DNA, as represented in Watson and Crick's model, is a double-stranded, antiparallel, right-handed helix. The sugar-phosphate backbones of the DNA strands make up the outside of the helix, while the nitrogenous bases are found on the inside and form hydrogen-bonded pairs that hold the DNA strands together.
In the model below, the orange and red atoms mark the phosphates of the sugar-phosphate backbones, while the blue atoms on the interior of the helix belong to the nitrogenous bases.
Double-stranded DNA is an antiparallel molecule, meaning that it's composed of two strands that run alongside each other but point in opposite directions. In a double-stranded DNA molecule, the 5' end (phosphate-bearing end) of one strand aligns with the 3' end (hydroxyl-bearing end) of its partner, and vice versa.
In Watson and Crick's model, the two strands of DNA twist around each other to form a right-handed helix. All helices have a handedness, which is a property that describes how their grooves are oriented in space.
The twisting of the DNA double helix and the geometry of the bases creates a wider gap (called the major groove) and a narrower gap (called the minor groove) that run along the length of the molecule, as shown in the figure above. These grooves are important binding sites for proteins that maintain DNA and regulate gene activity.
In Watson and Crick's model, the two strands of the DNA double helix are held together by hydrogen bonds between nitrogenous bases on opposite strands. Each pair of bases lies flat, forming a "rung" on the ladder of the DNA molecule.
Base pairs aren't made up of just any combination of bases. Instead, if there is an A found on one strand, it must be paired with a T on the other (and vice versa). Similarly, an G found on one strand must always have a C for a partner on the opposite strand. These A-T and G-C associations are known as complementary base pairs.
Base pairing explains Chargaff's rules, that is, why the composition of A always equals that of T, and the composition of C equals that of G. Where there is an A in one strand, there must be a T in the other, and the same is true for G and C. Because a large purine (A or G) is always paired with a small pyrimidine (T or C), the diameter of the helix is uniform, coming in at about nanometers.
Although Watson and Crick's original model proposed that there were two hydrogen bonds between the bases of each pair, we know today that G and C form an additional bond (such that A-T pairs form two hydrogen bonds total, while G-C pairs form three).
The impact of the double helix
The structure of DNA unlocked the door to understanding many aspects of DNA's function, such as how it was copied and how the information it carried was used by the cell to make proteins.
As we'll see in upcoming articles and videos, Watson and Crick's model ushered in a new era of discovery in molecular biology. The model and the discoveries that it enabled form the foundations for much of today's cutting-edge research in biology and biomedicine.
Explore outside of Khan Academy
Do you want to learn more about the DNA ladder? Check out this scrollable interactive from LabXchange.
LabXchange is a free online science education platform created at Harvard’s Faculty of Arts and Sciences and supported by the Amgen Foundation.
Want to join the conversation?
- What is a codon and how does it relate to a DNA function and structure ?(15 votes)
- A codon is the name for a group of three subsequent nucleotides in RNA. Since RNA is transcribed from DNA, the DNA sequence will determine the sequence of RNA, the codons, and ultimately what amino acids come together to form a protein. If a DNA sequence (template strand) goes CTTAGG, the corresponding RNA will read GAAUCC. In this sequence there are two codons: GAA followed by UCC, which will code for amino acids.(49 votes)
- well I have 2 doubts:
1) in the second para under the topic 'right hand helix' i couldn't understand as to why DNA is a right handed helix
2) in the second para under the topic 'base pairing' how exactly is the bigger size of purines and small size of pyramidines affecting the bond length?(7 votes)
- As far as the 2nd question is concerned , it is because the double helix should have a uniform diameter all throughout otherwise there might be problems during the supercoiling . Now if , purine is bonded to purine , both being bigger , would end up in a diameter that would be larger than that formed by the 2 pyrimidines and thus the diameter would be uneven . The fact that A will pair T and G with C was found experimentally .(7 votes)
- I want to make sure I have these ideas true!
It may have nothing to do with the article but I found it relevant.
Starting from zero:
We all have 2 copies of chromosomes; one from the mother and the second from the father.
Each chromosome is formed of DNA and proteins ( basically histamin) .
DNA is a double helix; 2 strands, each one has coding areas ( which are 2% and maybe less) and non-coding areas . Within the gene itself there are non-coding sequences which their name is “ introns “.
The non-coding area (outside the gene) of DNA strand has different types of sequences ; satellites and repeated sequencing .
Is that true for now?(5 votes)
- Seems mostly correct.
The one mistake I notice is that I think the word you were looking for was histones (not histamin).
Chromatin is composed of DNA plus associated proteins and RNAs. These other molecules organize, fold, protect, and control the DNA.
A major component of chromatin are nucleosomes — a twist of DNA wrapped around an octamer of histones.
Note that the non-coding DNA between genes is very diverse and much of it is composed of many different families of repeated sequences including multiple types of transposons and inserted retroviral genomes.(9 votes)
- Am I understanding this correctly? The amount of the total bases in a cell's DNA is always the same in each organism in a species, but the amount of each type of base (A,T,G, and C) in a cell's DNA can vary between organisms in the same species.
And is the double-helix form of DNA its condensed or decondensed form?
- Not exactly.
The amount of each type of base in a cell's DNA is the same in all cells in the whole organism. Genetic code is the same, but gene expression is different.
What is different is proprotion of AG to CT for each species and defined as a different number (CHargaff's rule).
The condensed form is chromosomes. The double helix is always double helix, regardless of being part of Euchromatin or Heterochromatin.
So, in metaphase, you can only see the condensed form of chromosomes. But you can isolate DNA (extract) by various methods and see t by the naked eye as well.
Hope this helps :D(5 votes)
- Why is adenine a purine base?(4 votes)
- I'm not sure it is the NH2 group which accepts protons most readily to make it a base. I think it could be the nitrogens in the rings, which I think also have lone pairs of electrons that could accept a H+. I think on the other hand the NH2 nitrogens the lone pair electrons are delocaslised so wouldn't make it very basic.(3 votes)
- How can you tell the helix is right handed?(4 votes)
- You can tell if if the helix is right handed or left handed based on the way it twists. Here's a link to an image that shows the difference between a right and a left. Hope this was helpful!
- What are the four different kinds of nitrogen bases?(2 votes)
- The four nitrogenous bases are as follows: Adenine, Thymine, Guanine, and Cytosine.
Cytosine and Thymine are pyrimidines
Adenine and Guanine are purines.
Adenine and Thymine are a complementary pair.
Cytosine and Guanine are a complementary pair.
Hope that helps!(6 votes)
- What do the data show about the make-up from different species? Before concluding that the pattern seen in the data is universal, which other types of organisms should tested? Why?(4 votes)
- What is the difference between DNA and RNA(1 vote)
- I will answer you the way I have answered this question before with other users. I hope it is adequate.
There are several differences. To start, DNA stands for deoxyribonucleic acid, while RNA stands for ribonucleic acid. These names describe the sugar that makes up their backbone--DNA = deoxyribose and RNA = ribose.
Second, while each has four nucleiotide bases, there is one difference. You probably know that DNA has guanine, cytosine, adenine, and thymine, and that guanine links to cytosine and adenine links to thymine. But RNA doesn't have thymine. Instead, it has uracil, a nucleiotide base with a slightly different chemical makeup. Thymine had the chemical formula C5H6N2O2 and uracil is C4H4N2O2. Uracil links to adenine in RNA just like thymine does in DNA
Finally, DNA is double-stranded and forms a double helix structure. RNA is single-stranded and is generally straight. DNA is a complete set of instructions needed for life (unless you're a virus, but that's a whole different story/debate) and RNA is used to copy DNA and to synthesize proteins. I know this is a lot to take in, but there are several videos and articles on Khan Academy to help. Here are a few.
Anyway, this is probably a lot, but I hope it helps!(6 votes)
- What is the order of the nitrogenous bases of the DNA if I have to put up a 3d model?(2 votes)
- There isn't a single order — all combinations along a strand are possible. The only thing that is fixed in DNA is that A pairs with T, and G pairs with C.
The sequence of bases is a very complex code that we are still working to understand. You can think of DNA as being the instructions for building, operating, and maintaining a cell. The order of the letters is used to encode how, when, and where proteins and RNAs are made. This affects every process within that cell and often in neighboring cells as well.
So, for a structural model of DNA the order doesn't actually matter, but if you could pick the sequence associated with something well known like the restriction enzyme EcoRI ...
Does that help?(3 votes)