Table 2.
Organism or group | No. of pairs of tRNAs with complementary anticodons | No. of pairs with complementary second bases in the acceptors | No. of pairs with noncomplementary second bases in the acceptors |
---|---|---|---|
E. coli (Eubacteria) | 32 | 24 | 8** |
H. volcanii (Archaebacteria) | 29 | 24 | 6** |
S. cerevisiae (Yeast) | 24 | 20 | 4** |
Chloroplasts | 26 | 19 | 7** |
Cytoplasm of plants | 20 | 16 | 4** |
Cytoplasm of animals | 27 | 18 | 9** |
Mitochondria of single cell or fungi | 18 | 12 | 6* |
Mitochondria of plants | 17 | 12 | 5* |
Mitochondria of animal | 17 | 9 | 8* |
Pooled data | 210 | 154 | 56** |
Common consensus (from ref. 6) | 32 | 29 | 3** |
All tRNAs sequence data are retrieved from ref. 7. The table shows that almost ideal dual complementarity represented by common consensus tRNAs diverged in different phyletic pathways. Therefore, consensus tRNAs show a highest index of the dual complementarity. Yet, all groups tested, except for mitochondrial tRNAs, still show significantly nonrandom dual complementarity. Nonrandomness of the dual complementarity was statistically tested using normal approximation to binomial distribution (without continuity correction) and assuming two-tail P values.
Extremely nonrandom (P = 0.0004–0.008). **Significantly nonrandom (P = 0.016–0.04). *Insignificantly nonrandom (P ≥ 0.16).