Aug 2026· Molecular biology and evolution· Vol 43· 0 citations· 53 references
Medicine
TL;DR
The results suggest that the cis-regulatory changes act through their influence on the collective assembly/activation of a transcription factor complex and that changes acting through such a mechanism can allow distinct parts of gene expression, such as expression level and dynamics, to separately diverge.
Abstract
Abstract Changes in regulatory sequences controlling the timing and activity of gene products underlie much of natural phenotypic variation. Yet, identifying which divergent sites matter and how they impact gene expression remains challenging. Here, we investigate how transcriptional activity and homeostatic responsiveness of orthologous promoters of the metabolic gene TDH3 evolved among Saccharomyces yeast. We found that promoter expression level increased specifically in the Saccharomyces cerevisiae lineage and that a substantial part of this increase was caused by genetic variants located between the well-characterized, conserved binding sites for two direct transcriptional regulators. These nucleotide changes altered the promoters’ expression levels while leaving the expression dynamics conserved. Further, the effects of these nucleotide changes were only seen in the presence of a third transcription factor, TYE7p, which is known to be recruited by the other transcription factors through protein–protein interactions. These results suggest that the cis-regulatory changes act through their influence on the collective assembly/activation of a transcription factor complex and that changes acting through such a mechanism can allow distinct parts of gene expression, such as expression level and dynamics, to separately diverge.
This Perspective discusses mechanisms enabling long-range enhancer–promoter communication and the potential advantages that distal enhancer positioning might confer on the establishment of developmental gene expression programs.
The genomic regions regulating gene expression are often themselves transcribed into a variety of noncoding RNAs (ncRNAs). However, the regulatory roles of this noncoding transcription remain largely unknown. By using live imaging, we reveal that the sequential transcription of ncRNAs emanating from distinct regulatory...
It is found that BRI1 contains an exonic enhancer (EE), which is essential to establish the spatial BRI1 expression pattern, and its disruption restricts BRI1 expression and impairs BRI1-dependent root growth, linking exon-encoded regulatory information and development.
Raúl Denia-Mondéjar, Paula Brunot-Garau, Xing Ma et al.· bioRxiv· 0 citations
Analysis of genomic and transcriptomic factors contributing to increased replicative age in recombinant yeast populations harboring standing genetic variation suggests that late-life survival is not predominantly governed by background-independent local cis-regulatory interactions, consistent with a polygenic architect...
K. McHugh, Felipe S. Barreto, M. Burke· G3· 0 citations
This work highlights non-canonical transcriptional kinases that could operate alongside and beyond CDKs to modulate transcription by RNAPII, and discusses how these kinases could introduce context-specific CTD modifications that enable transcriptional plasticity, facilitate rapid loci-specific activation, and integrate...
David D. Lowe, A. Shilatifard· Molecules and Cells· 0 citations
It is demonstrated that gene-CRR associations and FI scoring methods exhibit little consensus, highlighting the impact of the choice of a specific CRR-FI score combination in a given analysis and the need for a systematic approach to evaluate several gene-CRR and FI scoring methods in a unified framework.
R. Riudavets-Puig, Denise G. O'Mahony, I. S. Brorson et al.· PLoS Computational Biology· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.