In molecular biology, a Base pair is defined as two complementary nitrogenous molecules, which are connected by hydrogen bonds. Base pairs can be found in both double-stranded DNA and RNA, in which the bonds between them connect the two strands by making the possible double-stranded structures. Base pairs themselves can be formed from bases that are complementary nitrogen-rich organic compounds called either pyrimidines or purines.
Complementary base pairing is defined as the phenomenon where in the DNA guanine always hydrogen bonds to the cytosine and adenine binds to thymine always.
The Watson crick base pairing, which is the foundation for the helical structure of double-stranded DNA, states that DNA comprises four bases: adenine (A) thymine (T) (adenine thymine) guanine (G), the two pyrimidines cytosine including guanine (C); or adenine thymine guanine cytosine. A bonds only with T and C bonds only with G inside the DNA molecule. In RNA, thymine is replaced by uracil (U). The base-pairing models of Non-Watson-Crick display alternative hydrogen-bonding patterns. A few examples are Hoogsteen base pairs: C-G or A-T analogs.
[Image will be uploaded soon]
Intramolecular base pairs can take place within the single-stranded nucleic acids. Particularly, this is essential in RNA molecules (for example, transfer RNA), where the Watson–Crick base pairs (adenine–uracil and guanine-cytosine) permit the formation of the short double-stranded helices, and also a wide variety of non–Watson–Crick interactions (for example, A–A or G–U) allows the RNAs to fold into a vast range of particular three-dimensional structures.
Additionally, the base-pairing between the messenger RNA (mRNA) and transfer RNA (tRNA) forms the basis for the molecular recognition events, which result in the nucleotide sequence of the mRNA becoming translated into the amino acid sequence of proteins through the genetic code.
Often, the size of either an entire genome or an individual gene of the organism is measured in the base pairs because usually, DNA is double-stranded. Thus, the total base pairs count is equal to the nucleotides count in one of the strands (including the exception of non-coding single-stranded telomeres' regions).
The haploid human genome (23 chromosomes) can be estimated to be nearly 3.2 billion bases long and to have 20,000–25,000 distinct protein-coding genes. In molecular biology, a kilobase (kb) is a unit of measurement equivalent to 1000 base pairs of RNA or DNA. The total DNA pairs or base pairs count on Earth is estimated at 5.0×1037, having a weight of 50 billion tonnes. In comparison, the biosphere's total mass has been expected as much as 4 TTC (trillion tons of carbon).
Hydrogen bonding is given as the chemical interaction, which underlies the base-pairing rules. Only the "right" pairs will produce stability due to an effective geometrical correspondence of both hydrogen bond donors and acceptors. DNA pairs having high GC content is stable compared to the DNA with low GC content. But, contrary to popular belief, the hydrogen bonds do not significantly stabilize the DNA; stabilization is primarily because of stacking interactions.
The bigger nucleobases, guanine and adenine, are the members of the double-ringed chemical structures class known as purines; the smaller nucleobases, thymine, and cytosine (including uracil) are the members of a single-ringed chemical structure's class known as pyrimidines. And, purines are only complementary with the pyrimidines: pairings of pyrimidine-pyrimidine are energetically unfavourable due to the molecules are too far apart for hydrogen bonding that is to be established; purine-purine pairings are energetically unfavourable since the molecules are too close together, resulting in overlap repulsion.
Purine-pyrimidine base-pairing of either GC or AT, or UA (in the RNA) results in the proper duplex structure. The only other purine-pyrimidine pairings would be AC, GT, and UG (in the RNA); these specific pairings are mismatches due to the patterns of hydrogen donors, and acceptors do not correspond. With two hydrogen bonds, the GU pairing does take place fairly often in RNA.
Paired RNA and DNA molecules are relatively stable at room temperature, whereas the two nucleotide strands will separate over a melting point, which is defined by the molecule's length, the mispairing extent (if any), and the GC content. A high GC content results in higher melting temperatures; thus, it is unsurprising that genomes of extremophile organisms like Thermus thermophilus are specifically GC-rich.
Conversely, the genome regions need to separate frequently. The promoter regions of frequently transcribed genes, for example, have a low GC content. When developing primers for PCR reactions, GC material, as well as melting temperature, should be taken into account.
[Image will be uploaded soon]
The first figure - a GC base-pair is having three hydrogen bonds, and the second - an AT base pair with two hydrogen bonds. The non-covalent hydrogen bonds between the bases are represented in dashed lines. The relation to both the pentose sugar and the minor groove direction is represented by these unique wiggly lines.
Base pairs can often be used to measure the size of an individual gene within the DNA molecule. The number of nucleotides in one of the strands is equal to the total number of base pairs (each nucleotide has a base pair, a phosphate group, and a deoxyribose sugar). The detailing of base pairs can be complicated with extremely complex genomes.
1. What are the fundamental base pairs found in a DNA molecule?
In a DNA molecule, the four nitrogenous bases form two specific complementary pairs, which are the fundamental building blocks of the double helix structure. These are:
This strict pairing rule, known as complementary base pairing, ensures the structural integrity and accurate replication of DNA.
2. How do the base pairs in RNA differ from those in DNA?
The primary difference in base pairing between RNA and DNA involves one of the pyrimidine bases. While both share Adenine, Guanine, and Cytosine, in RNA, Thymine (T) is replaced by Uracil (U). Therefore, the base pairs in RNA are:
This allows RNA to form temporary double-stranded regions during processes like transcription and translation.
3. What is the precise difference between a nucleotide and a base pair?
A nucleotide is a single structural unit, or monomer, of DNA or RNA. It consists of three components: a nitrogenous base (A, T, C, or G), a pentose sugar (deoxyribose in DNA), and a phosphate group. A base pair, on the other hand, refers to two complementary nucleotides located on opposite strands of a double-stranded DNA molecule that are linked together by hydrogen bonds, such as the A-T pair or the G-C pair.
4. Why does Adenine (A) only pair with Thymine (T) and not with Cytosine (C)?
The specificity of base pairing is determined by the chemical structure of the bases and the hydrogen bonds they can form. Adenine can form exactly two hydrogen bonds with Thymine. Similarly, Guanine can form exactly three hydrogen bonds with Cytosine. A mismatch, like Adenine with Cytosine, would not allow for stable hydrogen bond formation due to the incorrect arrangement of hydrogen bond donors and acceptors, thus destabilising the DNA double helix structure.
5. How many hydrogen bonds are formed between the different base pairs?
The number of hydrogen bonds differs between the two types of base pairs, which affects the stability of the DNA molecule:
Because of this, DNA regions with a high G-C content are more thermally stable than regions with a high A-T content.
6. What are purines and pyrimidines, and why must one always pair with the other?
Purines and pyrimidines are two classes of nitrogenous bases. Purines (Adenine and Guanine) have a double-ring structure, making them larger. Pyrimidines (Cytosine and Thymine) have a single-ring structure, making them smaller. For the DNA double helix to maintain a consistent diameter, a larger purine on one strand must always pair with a smaller pyrimidine on the other. Pairing two purines would be too wide, while pairing two pyrimidines would be too narrow, both of which would distort the helix.
7. What is the 'wobble base pair' phenomenon and in which process is it significant?
A wobble base pair is a non-standard pairing between two nucleotides that does not follow the strict Watson-Crick rules (A-U, G-C). A common example is the pairing of Guanine (G) with Uracil (U). This phenomenon is primarily significant during the process of protein synthesis (translation). It occurs at the third position of an mRNA codon when it pairs with the tRNA anticodon, allowing a single tRNA molecule to recognise multiple codons for the same amino acid, which adds efficiency to the genetic code.
8. How is the concept of a base pair used as a unit of measurement in genetics?
In genetics and molecular biology, the base pair (bp) is used as a standard unit to measure the length of a DNA or RNA molecule. Since DNA is typically double-stranded, counting the number of pairs is a convenient way to quantify its size. Larger segments are measured in kilobases (kb), which is 1,000 base pairs, or megabases (Mb), which is one million base pairs. For example, the size of the human genome is measured as approximately 3.2 billion base pairs.