| RNA predates proteins but became a viable genetic code only once its bases were tied to amino acid links |
Holds as a claim about the code (the stereochemical theory). Lab RNA can copy itself a little without peptides, so it fails as a claim about heredity. The binding evidence covers about 8 amino acids, and the transfer RNA adapter is still needed for assembly. |
| Once the minimal set-up exists it can be extended easily |
True at the edges (selenocysteine, pyrrolysine, lab-added amino acids), but the core 20 are frozen. |
| The replication system is an immune function and the instigator of gene transfer |
Not supported. Parts of the copying machinery are parasite-derived, and mobile elements are the main instigators. Defence is a leading reason transfer stays open, and it also filters it. |
| Every gene was born of an immune or replication need |
Only in a narrow form. Many genes come from parasite DNA (syncytin, RAG, Arc), but metabolic and structural genes trace to chemistry and energy. |
| Ageing is gene termination |
True for salmon, octopus and annual plants. For most animals ageing is selection neglecting the late years. |
| Amino acids are central, ubiquitous and immutable |
Central and ubiquitous yes. Immutable only after the code froze, since they are modified chemically after construction. |
| Living = motion |
Better as organised, self-maintaining motion that can reproduce. A dormant seed is the same machinery switched off. |