RNA (ribonucleic acid) is a type of nucleic acid that is involved in the synthesis of proteins and the regulation of gene expression.
RNA is similar in structure to DNA (deoxyribonucleic acid) but has several important differences that allow it to perform its unique functions.
RNA is composed of nucleotides, which are the building blocks of nucleic acids.
Each nucleotide consists of a sugar molecule (ribose in RNA), a nitrogenous base (adenine, guanine, cytosine, or uracil), and a phosphate group.
Unlike DNA, which is double-stranded, RNA is typically single-stranded, although it can form complex secondary and tertiary structures through base pairing interactions within the same molecule or with other molecules.
The nitrogenous bases in RNA can form complementary base pairs with each other through hydrogen bonding.
Adenine (A) pairs with uracil (U), and guanine (G) pairs with cytosine (C).
RNA can form a variety of secondary structures, including hairpin loops, bulges, internal loops, and stem.
Some RNA molecules can form complex three-dimensional structures through interactions between distant parts of the molecule.
In RNA, the nucleotides are joined together by a covalent bond between the 3' hydroxyl group of one nucleotide and the 5' phosphate group of the next nucleotide.
The base pairing interactions in RNA are weaker than in DNA because RNA uses ribose as its sugar instead of deoxyribose, which lacks a hydroxyl (-OH) group at the 2' position.
The presence of this -OH group in RNA makes the sugar more reactive and less stable than deoxyribose.
A forms two hydrogen bonds with U and G forms three hydrogen bonds with C.
RNA synthesis, also known as transcription, begins with the binding of an enzyme called RNA polymerase to a DNA template strand at a specific sequence called the promoter.
The promoter sequence is located upstream of the gene or sequence to be transcribed.
Once RNA polymerase is bound to the DNA template, it unwinds the double helix and starts to synthesise a complementary RNA strand by adding nucleotides one at a time in the 5' to 3' direction.
The RNA molecule grows in length as RNA polymerase moves along the template strand.
RNA polymerase continues to add nucleotides until it reaches a termination sequence that signals the end of the transcription process.
At this point, the newly synthesised RNA molecule is released from the DNA template and RNA polymerase dissociates from the DNA.
The newly synthesised RNA molecule is not immediately functional, and it needs to undergo several processing steps before it can be used by the cell.
In eukaryotic cells, for example, the RNA molecule undergoes capping, splicing, and polyadenylation, which involves the addition of a 5' cap, removal of introns, and addition of a poly(A) tail, respectively.
In eukaryotic cells, a modified nucleotide called the 5' cap is added to the 5' end of the RNA molecule.
RNA molecules can undergo a variety of chemical modifications to their bases, including methylation, pseudouridylation, and deamination.
The cap protects the RNA from degradation and helps it to be recognised by the ribosome during translation.
Splicing involves the removal of introns and the joining of exons.
Eukaryotic mRNAs typically contain a string of adenine nucleotides, called the poly(A) tail, at their 3' end.
The poly(A) tail protects the mRNA from degradation and is involved in the export of the mRNA from the nucleus.
Eukaryotic genes often contain non-coding regions called introns, which are removed from the pre-mRNA by a process called splicing.