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Oct 31, 2023 · Genes are composed of DNA arranged on chromosomes. Some genes encode structural or regulatory RNAs. Other genes encode proteins. Replication copies DNA; transcription uses DNA to make complementary RNAs; translation uses mRNAs to make proteins.
- 15.2: The Genetic Code - The Central ... - Biology LibreTexts
The central dogma of molecular biology describes the flow of...
- 15.1: The Genetic Code - Biology LibreTexts
Genes are used to make mRNA by the process of transcription;...
- 15.2: The Genetic Code - The Central ... - Biology LibreTexts
The genetic code is the set of rules used by living cells to translate information encoded within genetic material (DNA or RNA sequences of nucleotide triplets, or codons) into proteins.
Ultimately, one wishes to determine how genes—and the proteins they encode—function in the intact organism. Although it may sound counterintuitive, one of the most direct ways to find out what a gene does is to see what happens to the organism when that gene is missing.
- Bruce Alberts, Alexander Johnson, Julian Lewis, Martin Raff, Keith Roberts, Peter Walter
- 2002
- 2002
Genes encode proteins and proteins dictate cell function. Therefore, the thousands of genes expressed in a particular cell determine what that cell can do.
- Overview
- Introduction
- Overview: Gene expression and the genetic code
- Code crackers: How the genetic code was discovered
- The triplet hypothesis
- Nirenberg, Khorana, and the identification of codons
- Properties of the genetic code
- Types of codons (start, stop, and "normal")
- Reading frame
- One amino acid, many codons
How is the information in an mRNA sequence decoded to make a polypeptide? Learn how groups of three nucleotides, called codons, specify amino acids (as well as start and stop signals for translation).
•In transcription, the DNA sequence of a gene is "rewritten" using RNA nucleotides. In eukaryotes, the RNA must go through additional processing steps to become a messenger RNA, or mRNA.
•In translation, the sequence of nucleotides in the mRNA is "translated" into a sequence of amino acids in a polypeptide (protein or protein subunit).
Cells decode mRNAs by reading their nucleotides in groups of three, called codons. Each codon specifies a particular amino acid, or, in some cases, provides a "stop" signal that ends translation. In addition, the codon AUG has a special role, serving as the start codon where translation begins. The complete set of correspondences between codons and amino acids (or stop signals) is known as the genetic code.
[Codon table]
In the rest of this article, we'll more closely at the genetic code. First, we'll see how it was discovered. Then, we'll look more deeply at its properties, seeing how it can be used to predict the polypeptide encoded by an mRNA.
Have you ever written a secret message to one of your friends? If so, you may have used some kind of code to keep the message hidden. For instance, you may have replaced the letters of the word with numbers or symbols, following a particular set of rules. In order for your friend on the other end to understand the message, he or she would need to know the code and apply the same set of rules, in reverse, to figure out what you had written.
As it turns out, decoding messages is also a key step in gene expression, the process in which information from a gene is used to construct a protein (or other functional product). How are the instructions for building a protein encoded in DNA, and how are they deciphered by the cell? In this article, we'll take a closer look at the genetic code, which allows DNA and RNA nucleotide sequences to be translated into the amino acids they represent.
Genes that provide instructions for proteins are expressed in a two-step process.
•In transcription, the DNA sequence of a gene is "rewritten" using RNA nucleotides. In eukaryotes, the RNA must go through additional processing steps to become a messenger RNA, or mRNA.
•In translation, the sequence of nucleotides in the mRNA is "translated" into a sequence of amino acids in a polypeptide (protein or protein subunit).
Cells decode mRNAs by reading their nucleotides in groups of three, called codons. Each codon specifies a particular amino acid, or, in some cases, provides a "stop" signal that ends translation. In addition, the codon AUG has a special role, serving as the start codon where translation begins. The complete set of correspondences between codons and amino acids (or stop signals) is known as the genetic code.
[Codon table]
In the rest of this article, we'll more closely at the genetic code. First, we'll see how it was discovered. Then, we'll look more deeply at its properties, seeing how it can be used to predict the polypeptide encoded by an mRNA.
To crack the genetic code, researchers needed to figure out how sequences of nucleotides in a DNA or RNA molecule could encode the sequence of amino acids in a polypeptide.
Why was this a tricky problem? In one of the simplest potential codes, each nucleotide in an DNA or RNA molecule might correspond to one amino acid in a polypeptide. However, this code cannot actually work, because there are 20 amino acids commonly found in proteins and just 4 nucleotide bases in DNA or RNA. Thus, researchers knew that the code must involve something more complex than a one-to-one matching of nucleotides and amino acids.
In the mid-1950s, the physicist George Gamow extended this line of thinking to deduce that the genetic code was likely composed of triplets of nucleotides. That is, he proposed that a group of 3 successive nucleotides in a gene might code for one amino acid in a polypeptide.
Gamow's reasoning was that even a doublet code (2 nucleotides per amino acid) would not work, as it would allow for only 16 ordered groups of nucleotides (42 ), too few to account for the 20 standard amino acids used to build proteins. A code based on nucleotide triplets, however, seemed promising: it would provide 64 unique sequences of nucleotides (43 ), more than enough to cover the 20 amino acids.
Gamow’s triplet hypothesis seemed logical and was widely accepted. However, it had not been experimentally proven, and researchers still did not know which triplets of nucleotides corresponded to which amino acids.
The cracking of the genetic code began in 1961, with work from the American biochemist Marshall Nirenberg. For the first time, Nirenberg and his colleagues were able to identify specific nucleotide triplets that corresponded to particular amino acids. Their success relied on two experimental innovations:
•A way to make artificial mRNA molecules with specific, known sequences.
•A system to translate mRNAs into polypeptides outside of a cell (a "cell-free" system). Nirenberg's system consisted of cytoplasm from burst E. coli cells, which contains all of the materials needed for translation.
First, Nirenberg synthesized an mRNA molecule consisting only of the nucleotide uracil (called poly-U). When he added poly-U mRNA to the cell-free system, he found that the polypeptides made consisted exclusively of the amino acid phenylalanine. Because the only triplet in poly-U mRNA is UUU, Nirenberg concluded that UUU might code for phenylalanine. Using the same approach, he was able to show that poly-C mRNA was translated into polypeptides made exclusively of the amino acid proline, suggesting that the triplet CCC might code for proline.
Other researchers, such as the biochemist Har Gobind Khorana at University of Wisconsin, extended Nirenberg's experiment by synthesizing artificial mRNAs with more complex sequences. For instance, in one experiment, Khorana generated a poly-UC (UCUCUCUCUC…) mRNA and added it to a cell-free system similar to Nirenberg's. The poly-UC mRNA that it was translated into polypeptides with an alternating pattern of serine and leucine amino acids. These and other results unambiguously confirmed that the genetic code was based on triplets, or codons. Today, we know that serine is encoded by the codon UCU, while leucine is encoded by CUC.
As we saw above, the genetic code is based on triplets of nucleotides called codons, which specify individual amino acids in a polypeptide (or "stop" signals at its end). The codons of an mRNA are “read” one by one inside protein-and-RNA structures called ribosomes, starting at the 5’ end of the gene and moving towards the 3’ end. Let's take a clos...
Translation always begins at a start codon, which has the sequence AUG and encodes the amino acid methionine (Met) in most organisms. Thus, every polypeptide typically starts with methionine, although the initial methionine may be snipped off in later processing steps. A start codon is required to begin translation, but the codon AUG can also appear later in the coding sequence of an an mRNA, where it simply specifies the amino acid methionine.
Once translation has begun at the start codon, the following codons of the mRNA will be read one by one, in the 5' to 3' direction. As each codon is read, the matching amino acid is added to the C-terminus of the polypeptide. Most of the codons in the genetic code specify amino acids and are read during this phase of translation.
[How do you read the codon table?]
Translation continues until a stop codon is reached. There are three stop codons in the genetic code, UAA, UAG, and UGA. Unlike start codons, stop codons don't correspond to an amino acid. Instead, they act as "stop" signals, indicating that the polypeptide is complete and causing it to be released from the ribosome. More nucleotides may appear after the stop codon in the mRNA, but will not be translated as part of the polypeptide.
The start codon is critical because it determines where translation will begin on the mRNA. Most importantly, the position of the start codon determines the reading frame, or how the mRNA sequence is divided up into groups of three nucleotides inside the ribosome. As shown in the diagram below, the same sequence of nucleotides can encode completely different polypeptides depending on the frame in which it's read. The start codon determines which frame is chosen and thus ensures that the correct polypeptide is produced.
To see what reading frame is, it's helpful to consider an analogy using words and letters. The following message makes sense to us because we read it in the correct frame (divide it correctly into groups of three letters): MOM AND DAD ARE MAD. If we shift the reading frame by grouping letters into threes starting one position later, however, we get: OMA NDD ADA REM AD. The frameshift results in a message that no longer makes sense.
As previously mentioned, the genetic code consists of 64 unique codons. But if there are only 20 amino acids, what are the other 44 codons doing? As we saw, a few are stop codons, but most are not. Instead, the genetic code turns out to be a degenerate code, meaning that some amino acids are specified by more than one codon. For example, proline is represented by four different codons (CCU, CCC, CCA, and CCG). If any one of these codons appears in an mRNA, it will cause proline to be added to the polypeptide chain.
Most of the amino acids in the genetic code are encoded by at least two codons. In fact, methionine and tryptophan are the only amino acids specified by a single codon. Importantly, the reverse isn't true: each codon specifies just one amino acid or stop signal. Thus, there's no ambiguity (uncertainty) in the genetic code. A particular codon in an mRNA will always be predictably translated into a particular amino acid or stop signal.
The central dogma of molecular biology describes the flow of genetic information in cells from DNA to messenger RNA (mRNA) to protein. It states that genes specify the sequence of mRNA molecules, which in turn specify the sequence of proteins.
Genes are used to make mRNA by the process of transcription; mRNA is used to synthesize proteins by the process of translation. The genetic code is degenerate because 64 triplet codons in mRNA specify only 20 amino acids and three nonsense codons.
