The bacterial iron sensor IdeR distinguishes DNA sequences by applying stress to non-cognate DNA
- 1Uppsala University
Abstract
The transcription factor IdeR regulates iron homeostasis in many gram-positive bacteria. It primarily functions as a repressor of iron uptake genes by binding to their promoters and blocking RNA polymerase access. IdeR recognizes a highly conserved DNA sequence consisting of four palindromic 5'-C1C2T3A4A5 repeats. For target site recognition, IdeR requires a thymine in position 3 of the repeat and at least one cytosine in the first two positions, while the identity of the bases in positions 4 and 5 is less important. We have previously shown that IdeR recognizes its target sequences through indirect or shape readout, rather than direct interactions with the bases. However, the mechanism of indirect recognition is unknown. Here we employed molecular dynamics simulations, X-ray crystallography, and DNA-binding assays to investigate the thermodynamic principles underlying accurate pyrimidine recognition by IdeR. We found that the recognition helix of IdeR forms a differential dielectric cleft that accommodates the C-H edge of the 5'-C1C2T3 sequence, with a polar pocket for the first two bases and a non-polar pocket for the third. The local dielectric environment of IdeR applies strain to non-cognate DNA, leading to non-productive binding and thereby ensuring the fidelity of target DNA reading.
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BibTeX
@misc{ghosh2026bacterial,
title = {{The bacterial iron sensor IdeR distinguishes DNA sequences by applying stress to non-cognate DNA}},
author = {S. Ghosh and O. Koshla and D. Maurer and S. Tieleman and J. Aqvist and J. J. Griese and P. Satpati},
howpublished = {bioRxiv},
year = {2026},
month = oct,
doi = {10.64898/2026.10.05.756664},
url = {https://www.biorxiv.org/content/10.64898/2026.10.05.756664v1},
note = {CC BY-NC-ND},
}
RIS
TY - UNPB
TI - The bacterial iron sensor IdeR distinguishes DNA sequences by applying stress to non-cognate DNA
AU - S. Ghosh
AU - O. Koshla
AU - D. Maurer
AU - S. Tieleman
AU - J. Aqvist
AU - J. J. Griese
AU - P. Satpati
PY - 2026
DA - 2026/10/05
PB - bioRxiv
DO - 10.64898/2026.10.05.756664
UR - https://www.biorxiv.org/content/10.64898/2026.10.05.756664v1
AB - The transcription factor IdeR regulates iron homeostasis in many gram-positive bacteria. It primarily functions as a repressor of iron uptake genes by binding to their promoters and blocking RNA polymerase access. IdeR recognizes a highly conserved DNA sequence consisting of four palindromic 5'-C1C2T3A4A5 repeats. For target site recognition, IdeR requires a thymine in position 3 of the repeat and at least one cytosine in the first two positions, while the identity of the bases in positions 4 and 5 is less important. We have previously shown that IdeR recognizes its target sequences through indirect or shape readout, rather than direct interactions with the bases. However, the mechanism of indirect recognition is unknown. Here we employed molecular dynamics simulations, X-ray crystallography, and DNA-binding assays to investigate the thermodynamic principles underlying accurate pyrimidine recognition by IdeR. We found that the recognition helix of IdeR forms a differential dielectric cleft that accommodates the C-H edge of the 5'-C1C2T3 sequence, with a polar pocket for the first two bases and a non-polar pocket for the third. The local dielectric environment of IdeR applies strain to non-cognate DNA, leading to non-productive binding and thereby ensuring the fidelity of target DNA reading.
ER -