EIF1AX
Lua error in Module:Infobox_gene at line 53: attempt to index field 'wikibase' (a nil value). Eukaryotic translation initiation factor 1A, X-chromosomal (eIF1A) is a protein that in humans is encoded by the EIF1AX gene.[1][2][3] This gene encodes an essential eukaryotic translation initiation factor. The protein is a component of the 43S pre-initiation complex (PIC), which mediates the recruitment of the small 40S ribosomal subunit to the 5' cap of messenger RNAs.[3]
Function
[edit | edit source]eIF1A is an important part of the translation intiation mechanism. It is located at the A-site of the small ribosomal subunit. During translation initiation, the 43S pre-initiation complex scans along the mRNA in search of a start codon. eIF1A's N-terminal tail interacts with the initiator tRNA and the start codon by extending into the P-site, thereby increasing the fidelity of start codon selection.[4] After the start codon has been selected and eIF1, eIF2, and eIF5 have left the pre-initiation complex, eIF5B is recruited to continue the initiation process. Here, eIF1A interacts with eIF5B such that eIF5B is remodeled into a conformation that allows joining of the large ribosomal subunit.[5] After the joining of the subunit, it is the dissociation of eIF1A that permits eIF5B to rearrange again, placing the tRNA in its final position.[5]
Clinical significance
[edit | edit source]Mutations in this gene have been recurrently seen associated to cases of uveal melanoma with disomy 3.[6] eIF1A is mutated in thyroid cancers.[7]
Interactions
[edit | edit source]EIF1AX has been shown to interact with IPO13.[8]
See also
[edit | edit source]References
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Further reading
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