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Enhancement of the stability of genetic switches by overlapping upstream regulatory domains
Molecular Networks · Submitted 1 Nov 2003
abstract compiled · 2026-09-23 · no language-model review
The authors' main claim Our results suggest that robustness against biochemical noise can provide a selection pressure that drives operons, that regulate each other, together in the course of evolution.
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The abstract, sentence by sentence
We study genetic switches formed from pairs of mutually repressing operons. The switch stability is characterised by a well defined lifetime which grows sub-exponentially with the number of copies of the most-expressed transcription factor, in the regime accessible by our numerical simulations. The stability can be markedly enhanced by a suitable choice of overlap between the upstream regulatory domains. Our results suggest that robustness against biochemical noise can provide a selection pressure that drives operons, that regulate each other, together in the course of evolution.
background contribution method result interpretation main claim
| # | sentence | role | the authors' own work | states the main conclusion | strength |
|---|---|---|---|---|---|
| s0 | We study genetic switches formed from pairs of mutually repressing operons. | contribution 0.93 | 0.80 | 0.03 | asserted 0.89 |
| s1 | The switch stability is characterised by a well defined lifetime which grows sub-exponentially with the number of copies of the most-expressed transcription factor, in the regime accessible by our numerical simulations. | result 1.00 | 0.90 | 0.10 | asserted 0.99 |
| s2 | The stability can be markedly enhanced by a suitable choice of overlap between the upstream regulatory domains. | result 1.00 | 0.91 | 0.56 | asserted 0.87 |
| s3 | Our results suggest that robustness against biochemical noise can provide a selection pressure that drives operons, that regulate each other, together in the course of evolution. | interpretation 1.00 | 0.41 | 0.52 | hedged possibility 1.00 |
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Original abstract
We study genetic switches formed from pairs of mutually repressing operons. The switch stability is characterised by a well defined lifetime which grows sub-exponentially with the number of copies of the most-expressed transcription factor, in the regime accessible by our numerical simulations. The stability can be markedly enhanced by a suitable choice of overlap between the upstream regulatory domains. Our results suggest that robustness against biochemical noise can provide a selection pressure that drives operons, that regulate each other, together in the course of evolution.
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