Transcription is the process by which DNA is copied into RNA. This process is carried out by RNA polymerase, which binds to the DNA and separates the two strands. The RNA polymerase then uses one of the DNA strands as a template to synthesize a complementary RNA strand.

Translation is the process by which RNA is used to synthesize proteins. This process is carried out by ribosomes, which bind to the RNA and read the sequence of codons. Each codon corresponds to a specific amino acid, and the ribosome uses this information to assemble a chain of amino acids into a protein.

The genetic code is the sequence of codons in RNA. A codon is a sequence of three nucleotides that corresponds to a specific amino acid. The genetic code is used to translate RNA into proteins.

A gene is a region of DNA that codes for a protein. Genes are made up of a series of codons, which are sequences of three nucleotides that correspond to specific amino acids. The sequence of codons in a gene determines the sequence of amino acids in the protein that it codes for.

A mutation is a change in the sequence of nucleotides in DNA. Mutations can be caused by a variety of factors, including errors in DNA replication, exposure to radiation, and exposure to chemicals. Mutations can have a variety of effects, including changes in the structure and function of proteins.

The central dogma of molecular biology is the idea that DNA is transcribed into RNA, which is then translated into protein. This process is essential for the synthesis of proteins, which are the building blocks of cells.

RNA polymerase is an enzyme that plays a key role in transcription. It binds to the DNA and separates the two strands. It then uses one of the DNA strands as a template to synthesize a complementary RNA strand. RNA polymerase also proofreads the RNA strand for errors.

Ribosomes are cellular structures that play a key role in translation. They bind to the RNA and read the sequence of codons. They then use the sequence of codons to assemble a chain of amino acids into a protein. Ribosomes also proofread the protein for errors.

Mutations are a source of new genetic variation in a population. They can be beneficial, harmful, or neutral. Beneficial mutations can increase an organism's fitness and help it to survive and reproduce. Harmful mutations can decrease an organism's fitness and make it less likely to survive and reproduce. Neutral mutations have no effect on an organism's fitness. Mutations can drive the process of natural selection, which is the process by which organisms with beneficial traits are more likely to survive and reproduce than organisms with harmful traits.

A gene is a region of DNA that codes for a protein. An allele is a specific variation of that gene. Alleles can differ from each other in their sequence of nucleotides. These differences can lead to differences in the structure and function of the proteins that they code for.

A dominant allele is an allele that is expressed in the phenotype of an organism. This means that the allele is visible in the organism's physical appearance or behavior. A recessive allele is an allele that is not expressed in the phenotype of an organism. This means that the allele is not visible in the organism's physical appearance or behavior.

A heterozygote is an organism that has two different alleles for a gene. This means that the organism has one copy of the dominant allele and one copy of the recessive allele for the gene. Heterozygotes can express both the dominant and recessive traits for the gene.

A homozygote is an organism that has two copies of the same allele for a gene. This means that the organism has two copies of the dominant allele or two copies of the recessive allele for the gene. Homozygotes can only express one trait for the gene.

A genetic disorder is a disorder that is caused by a mutation in a gene. Mutations can change the structure and function of proteins, which can lead to a variety of health problems. Genetic disorders can be inherited from parents or they can occur spontaneously.