Translational frameshifting or ribosomal frameshifting refers to an alternative process of protein translation. A protein is translated from one end of the mRNA to the other, from the 5' to the 3' end. Normally a protein is translated from a template mRNA with consecutive blocks of 3 nucleotides being read as single amino acids. However, certain organisms may exhibit a change or shift in the ribosomes frame by one or two nucleotides when translating the genetic code. This is deemed translational or ribosomal frameshifting. The process can be programmed by the nucleotide sequence of the mRNA and is sometimes affected by the secondary or tertiary mRNA structure. It has been described mainly in viruses (especially retroviruses), retrotransposons and bacterial insertion elements, and also in some cellular genes.
Proteins are translated unidirectionally by reading tri-nucleotides on the mRNA strand also known as codons. Therefore, a shift of any number of nucleotides that is not divisible by 3 in the reading frame will result in subsequent codons to be read differently. This effectively changes the ribosomal reading frame. For example, the following sentence when read from the beginning makes sense to a reader:
|Start|THE CAT AND THE MAN ARE FAT ... |Start|123 123 123 123 123 123 123 ...
However, changing the reading frame by say shifting the first reading up one letter between the T and H on the first word:
T|Start|HEC ATA NDT HEM ANA REF AT... -|Start|123 123 123 123 123 123 12...
Now the sentence makes absolutely no sense. In the case of a translating ribosome, a frameshift can result in nonsense being created after the frameshift or a completely different protein being created after the frameshift. When referring to translational frameshifting, the latter is always implied, the former being usually a result of a point mutation such as a deletion.
The main distinction between frameshifts resulting from mutation and those resulting from ribosomal frameshifting is that the latter are controlled by various mechanisms found in codons. These mechanisms emerge from the fact that ribosomes do not translate proteins at a steady rate, regardless of the sequence. Certain codons take longer to translate, because there are not equal amounts of tRNA of that particular codon in the cytosol. Due to this lag, there exist in small sections of codons sequences that control the rate of ribosomal frameshifting. Sections of less accessible codons that slow ribosomal transaction are known as "choke points," and sections of easily accessible codons which result in faster ribosomal transaction are "slippery sequences." Slippery sequences can potentially make the reading ribosome "slip" and skip a number of nucleotides (usually only 1) and read a completely different frame hereafter. Choke points reduce the probability of this happening.
This type of frameshifting may be programmed to occur at particular recoding sites and is important in some viruses (e.g. SARS, HIV) and some cellular genes (e.g. prfB a release factor). Its use is primarily for compacting more genetic information into a shorter amount of genetic material.
- Antizyme RNA frameshifting stimulation element
- Coronavirus frameshifting stimulation element
- DnaX ribosomal frameshifting element
- Frameshift mutation
- HIV ribosomal frameshift signal
- Insertion sequence IS1222 ribosomal frameshifting element
- Recode database
- Ribosomal frameshift
- Ribosomal pause
- Slippery sequence
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- Frameshifting,+Ribosomal at the US National Library of Medicine Medical Subject Headings (MeSH)
- Wise2 — aligns a protein against a DNA sequence allowing frameshifts and introns
- FastY — compare a DNA sequence to a protein sequence database, allowing gaps and frameshifts
- Path — tool that compares two frameshift proteins (back-translation principle)
- Recode2 — Database of recoded genes, including those that require programmed Translational frameshift.