4.7 Article

Discovering the DNA-Binding Consensus of the Thermus thermophilus HB8 Transcriptional Regulator TTHA1359

期刊

出版社

MDPI
DOI: 10.3390/ijms221810042

关键词

bioinformatics; biolayer interferometry (BLI); electrophoretic mobility shift assay (EMSA); extremophile; protein-DNA binding; type IIS restriction endonuclease

资金

  1. US National Science Foundation [1714778, 2041202]
  2. Kennesaw State University Foundation
  3. Direct For Biological Sciences
  4. Div Of Molecular and Cellular Bioscience [1714778] Funding Source: National Science Foundation
  5. Div Of Molecular and Cellular Bioscience
  6. Direct For Biological Sciences [2041202] Funding Source: National Science Foundation

向作者/读者索取更多资源

Transcription regulatory proteins, also known as transcription factors, act as molecular switches modulating gene expression at the transcription initiation stage. This study applied a reverse-genetic methodology to analyze the DNA-binding consensus sequence of TTHA1359 and identified regulatory binding sites within the T. thermophilus HB8 genome.
Transcription regulatory proteins, also known as transcription factors, function as molecular switches modulating the first step in gene expression, transcription initiation. Cyclic-AMP receptor proteins (CRPs) and fumarate and nitrate reduction regulators (FNRs) compose the CRP/FNR superfamily of transcription factors, regulating gene expression in response to a spectrum of stimuli. In the present work, a reverse-genetic methodology was applied to the study of TTHA1359, one of four CRP/FNR superfamily transcription factors in the model organism Thermus thermophilus HB8. Restriction Endonuclease Protection, Selection, and Amplification (REPSA) followed by next-generation sequencing techniques and bioinformatic motif discovery allowed identification of a DNA-binding consensus for TTHA1359, 5 '-AWTGTRA(N)(6)TYACAWT-3 ', which TTHA1359 binds to with high affinity. By bioinformatically mapping the consensus to the T. thermophilus HB8 genome, several potential regulatory TTHA1359-binding sites were identified and validated in vitro. The findings contribute to the knowledge of TTHA1359 regulatory activity within T. thermophilus HB8 and demonstrate the effectiveness of a reverse-genetic methodology in the study of putative transcription factors.

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