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The words cistron and gene were coined before the advancing state of biology made it clear to many people that the concepts they refer to, at least in some senses of the word gene, are either equivalent or nearly so. The same historical naming practices are responsible for many of the synonyms in the life sciences.
Multicistronic message is an archaic term for Polycistronic. Monocistronic, bicistronic and tricistronic are also used to describe mRNA with single, double and triple coding areas (exons). Note that the base word cistron is no longer used in genetics, and has been replaced by intron and exon in eukaryotic mRNA. However, the mRNA found in ...
A typical operon. In genetics, an operon is a functioning unit of DNA containing a cluster of genes under the control of a single promoter. [1] The genes are transcribed together into an mRNA strand and either translated together in the cytoplasm, or undergo splicing to create monocistronic mRNAs that are translated separately, i.e. several strands of mRNA that each encode a single gene product.
It can also affect the expression of the gene in which it occurs, if it occurs in a transcribed region. These mutations tend to occur early within the sequence of genes and can be nonsense, frameshift, or insertion mutations. Polar mutations are found only in organisms containing polycistronic mRNA. [1] [2] [3]
In fact, many prokaryotic genes occur in operons, which are a series of genes that work together to code for the same protein or gene product and are controlled by a single promoter. [2] Bacterial RNA polymerase is made up of four subunits and when a fifth subunit attaches, called the sigma factor (σ-factor), the polymerase can recognize ...
A class of regulatory proteins encoded by the TP53 gene in vertebrates which bind DNA and regulate gene expression in order to protect the genome from mutation and block progression through the cell cycle if DNA damage does occur. [4] It is mutated in more than 50% of human cancers, indicating it plays a crucial role in preventing cancer formation.
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When translating a polycistronic mRNA, a 70S ribosome ends translation at a stop codon.It is now shown that instead of immediately splitting into its two halves, the ribosome can "scan" forward until it hits another Shine–Dalgarno sequence and the downstream initiation codon, initiating another translation with the help of IF2 and IF3. [6]