What Is Protein Coding and How Does It Work?
Explore the biological process of converting genetic instructions into proteins, the essential molecules that carry out nearly all cellular functions.
Explore the biological process of converting genetic instructions into proteins, the essential molecules that carry out nearly all cellular functions.
Protein coding is the process cells use to translate the nucleotide language of DNA into the amino-acid language of proteins. These resulting proteins are responsible for countless tasks in all living things, from providing structural support to catalyzing biochemical reactions. This process explains how the instructions encoded in genes are expressed to create the functional molecules that sustain life.
The instructions for building every protein are stored within an organism’s deoxyribonucleic acid, or DNA. Specific segments of DNA that hold the instructions for a single protein are known as protein-coding genes. While much of an organism’s DNA is non-coding, these specific genes contain the precise order of chemical bases that dictate a protein’s structure. In plants and animals, this DNA blueprint is housed within a cellular compartment called the nucleus.
Each protein-coding gene is structured with distinct regions. A “promoter” sequence at the beginning of the gene acts as a binding site and signals where to start reading. The main part of the gene, the coding region, contains the actual sequence that will be translated. This region begins with a specific “start” codon, typically a three-nucleotide sequence of ATG in the DNA, which marks the precise point to begin protein assembly.
The end of the genetic instructions is marked by one of three “stop” codons, which signal that the protein is complete. The entire stretch of DNA from the start codon to the stop codon is known as an open reading frame. This arrangement ensures the cell can accurately process the genetic information to produce a specific protein.
The first step in protein coding is transcription, where genetic information from a gene is copied into a molecule called messenger RNA (mRNA). This process begins when an enzyme, RNA polymerase, binds to the gene’s promoter region, causing the DNA double helix to unwind. The unwinding exposes one of the two DNA strands, which serves as a template for creating the mRNA molecule.
As RNA polymerase moves along the DNA template, it synthesizes a complementary strand of RNA. This synthesis follows specific base-pairing rules:
The enzyme adds the corresponding RNA nucleotides one by one, forming a single strand of mRNA that copies the gene’s instructions.
When the RNA polymerase reaches a “terminator” sequence at the end of the gene, it stops adding nucleotides and the new mRNA strand detaches. In eukaryotic cells, this mRNA molecule often undergoes processing, which includes removing non-coding regions called introns. The mature mRNA molecule then exits the nucleus, carrying the instructions into the cytoplasm for the next stage.
Translation is the second phase of protein coding, where the message carried by the mRNA is decoded to build a protein. This process occurs in the cytoplasm on molecular machines called ribosomes. A ribosome attaches to the mRNA molecule and moves along its sequence, reading the instructions.
The genetic code on the mRNA is read in groups of three nucleotides called codons, and each codon specifies a particular amino acid. To deliver the correct amino acids, the cell uses transfer RNA (tRNA). Each tRNA molecule has a three-nucleotide sequence called an anticodon that is complementary to an mRNA codon and carries the corresponding amino acid.
The process starts when the ribosome encounters the “start” codon on the mRNA. A tRNA molecule with the matching anticodon binds to this codon, bringing the first amino acid into position. The ribosome then moves to the next codon, and another tRNA arrives with the second amino acid. The ribosome catalyzes the formation of a peptide bond between the two amino acids.
This cycle continues as the ribosome moves along the mRNA, elongating the growing chain of amino acids, known as a polypeptide. The process concludes when the ribosome reaches a “stop” codon, for which there is no corresponding tRNA. The completed polypeptide chain is then released from the ribosome and folds into its three-dimensional shape to become a functional protein.
Proper protein coding is necessary for the health and function of all living organisms. The proteins produced perform a wide variety of roles. For example, enzymes catalyze biochemical reactions, and structural proteins like collagen provide support to tissues. Other proteins function in transport, like hemoglobin carrying oxygen, or in defense, such as antibodies that fight pathogens.
When errors occur in the protein coding process, the consequences can be serious. Mistakes in the DNA sequence, known as mutations, can lead to the production of faulty or non-functional proteins. For instance, a single base change in the gene for hemoglobin can cause sickle cell anemia, a disease where red blood cells become misshapen. Similarly, errors can cause proteins to misfold, leading to clumps associated with neurodegenerative diseases like Alzheimer’s and Parkinson’s.
Understanding protein coding has direct applications in medicine and biotechnology. Knowing how specific proteins are made allows scientists to develop drugs that target proteins involved in disease. This knowledge is also the basis for understanding genetic disorders and developing gene therapies. Biotechnology also uses this process to produce therapeutic proteins, like insulin, by inserting human genes into bacteria or yeast.