Translational stop signals are defined in the genetic code as UAA, UAG
and UGA, although the mechanism of their decoding via protein factors
is clearly different from that of the other codons, There are strong
biases in the upstream and downstream nucleotides surrounding stop cod
ons. Experimental tests have shown that termination-signal strength is
strongly influenced by the identity of the nucleotide immediately dow
nstream of the codon (+4), with a correlation between the strength of
this four-base signal and its occurrence at termination sites, The +4
nucleotide and other biases downstream of the stop codon may reflect s
ites of contact between the release factor and the mRNA, whereas upstr
eam biases may be due to coding restrictions, with the release factor
perhaps recognizing the final tRNA and the last two amino acids of the
polypeptide undergoing synthesis. This means that the translational s
top signal is probably larger than the triplet codon, but its exact le
ngth will be clearer when it is known which nucleotides are in direct
contact with the release factor. Ultimately it will be defined exactly
when a crystal structure of the release factor with its recognition s
ubstrate becomes available.