RT Journal Article SR Electronic T1 AURTHO: autoregulation as facilitator of cis-acting element discovery of orthologous transcription factors JF bioRxiv FD Cold Spring Harbor Laboratory SP 2022.04.06.487287 DO 10.1101/2022.04.06.487287 A1 Anderssen, Sinaeda A1 Naômé, Aymeric A1 Jadot, Cédric A1 Brans, Alain A1 Tocquin, Pierre A1 Rigali, Sébastien YR 2022 UL http://biorxiv.org/content/early/2022/04/10/2022.04.06.487287.abstract AB Transcriptional regulation is key in bacteria for providing an adequate response in time and space to changing environmental conditions. However, despite decades of research, the binding sites and therefore the target genes and the function of most transcription factors (TFs) remain unknown. Filling this gap in knowledge through conventional methods represents a colossal task which we demonstrate here can be significantly facilitated by a widespread feature in transcriptional control: the autoregulation of TFs implying that the yet unknown transcription factor binding site (TFBS) is neighbouring the TF itself. In this work, we describe the “AURTHO” methodology (AUtoregulation of oRTHOlogous transcription factors), consisting of analyzing upstream regions of orthologous TFs in order to uncover their associated TFBSs. AURTHO enabled the de novo identification of novel TFBSs with an unprecedented improvement in terms of quantity and reliability. DNA-protein interaction studies on a selection of candidate cis-acting elements yielded an >90% success rate, demonstrating the efficacy of AURTHO at highlighting true TF-TFBS couples and confirming the identification in a near future of a plethora of TFBSs across all bacterial species.Key pointsTranscription factor (TF) autoregulation implies that their binding site (TFBS) is in their close vicinityWe developed and assessed the AURTHO methodology (AUtoregulation of oRTHOlogous TFs) for TFBS discoveryOur results shows that AURTHO greatly facilitates the identification of highly reliable novel TFBSsCompeting Interest StatementThe authors have declared no competing interest.