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Transcription Termination
Transcription termination of plastid genes has not been adequately studied. Analysis of RNA 3' -ends has revealed sequences with dyad symmetry proximal RNA termini. In E. coli factor independent transcription terminators typically contain a GC-rich region of dyad symmetry followed by an AT--rich stretch that often contains a run of thymidines.

In vitro experiments indicated that DNA sequences with dyad symmetry located at the 3' -end of rbcL do not cause transcription termination. Transcription was terminated with low efficiency by 3' regions of spinach psbA, rrnB and petD. In contrast, trnS and trnH caused termination with high efficiency (80%) although these genes are not followed by regions of dyad symmetry.

These results suggest that the stem loop structures found at RNA 3' -ends may not play a significant role in factor independent transcription termination. Presently available data, on the other hand, does not rule out a role for these sequences in transcript stability.

Transcription from plastid gene promoters is stimulated in vitro when supercoded DNA templates are used instead of relaxed circular or linear templates. Furthermore, DNA conformation affected the relative ratio of transcription of two adjacent promoters (atpB, rbcL) in vitro studies.

Chloroplasts of higher plants contain gyrase and topisomerase I activity which could alter the superhelicity of plastid DNA in vivo. To date, however, no direct test of this possibility in higher plants has been reported. In Chlamydomonas, inhibitors of gyrase, such as novobiocin, change the relative transcription rates of several plastid genes.