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RNA Primers and Editing

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The importance of the editing functions in lowering the number of mistakes during replication may explain why DNA replication is primed by RNA rather than by DNA. When the replication of a DNA chain has just initiated, the helix may be too short for distortions in its structure to be easily recognized by the editing proteins. The mistakes may then go uncorrected. However, if the first nucleotides inserted in a growing chain are ribonucleotides rather than deoxynucleotides, an RNA primer is synthesized rather than a DNA primer. The RNA primer can be removed and resynthesized as DNA by using preexisting upstream DNA as a primer. Under these conditions, a distortion in the helix can be detected by the editing functions, and mistakes are avoided.

Another important system that safeguards the fidelity of the replication process is responsible for fixing mismatches after the growing DNA strand leaves the polymerase. In E. coli and its closest relatives, this process is guided by methylation and is termed methyl-directed mismatch repair. Related mismatch repair systems are used across all three domains of life, but the use of methylation signals is not widespread. The methyl-directed mismatch repair system is discussed in chapter 10.

Snyder and Champness Molecular Genetics of Bacteria

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