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Cellular control GapFill
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Not all of the genome consists of , which code for the amino acid sequence of a polypeptide or a functional RNA; some of the genetic information found in eukaryotes does not have a direct coding purpose. Within genes, these sections are known as , while the coding sections are exons.
During eukaryotic , DNA strands separate and act as templates for the formation of complementary molecules. The enzyme facilitates this process by binding to region and joining adjacent nucleotides together in the new strand. The molecule is then spliced to remove the non-coding segments, creating a molecule.
Gene mutations may arise spontaneously or as a result of a fault during DNA replication. They are changes to one or more in a sequence. Some changes can render a resulting polypeptide non-functional and have huge effects on an organism's phenotype - for example, a single base near the start of a sequence can cause a frameshift, so that all the downstream triplets change. If the wrong base is incorporated into a sequence it is known as a ; however, because many amino acids are coded for by more than one triplet, this does not always result in a change in the final amino acid sequence. If the change results in a stop codon being prematurely incorporated into the sequence, this is referred to as a mutation.
Genes are not always expressed, as they can be switched off; can only bind to DNA to initiate transcription if their binding sites are revealed. Transcription can be inhibited or stimulated by environmental factors such as diet and stress levels, which can affect the levels of mitosis and programmed cell death ( ) occurring.
Genes which determine the body plan of an organism and are expressed during development are called genes. They have been discovered in all major animals, plants and fungi, and are highly between species.