DNA is often described as the language of life. With just four letters—A, T, G, and C—genomes encode thousands of genes together with the regulatory elements that govern when and how those genes are expressed. Deciphering the information embedded in DNA not only sheds light on the origin of life, but also reveals how organisms adapt to changing environments and provides knowledge essential for synthetic biology and forecasting future evolutionary trajectories.
As gene sequences follow a precise and universal rule to encode proteins, identifying them in genomes has become relatively straightforward. In contrast, regulatory elements are far more variable in length and sequence composition, making them much harder to recognize. As powerful models like AlphaFold have transformed our ability to predict protein structure and function, a major frontier in life science is now the development of computational tools capable of predicting and designing regulatory elements.
Among various regulatory elements, promoters draw particular attention because they control transcription initiation, the very first step in gene expression. To decipher the rules embedded in promoter sequences, Prof. David Chou’s laboratory at National Taiwan University applied high-throughput methods to construct more than 16 million promoter variants and measure their expression levels in E. coli. The resulting dataset was used to train a computational model, which the team then applied to analyze the genomes of 49 phylogenetically distinct species across the domain Bacteria.
This systems biology approach revealed domain-wide conservation of bacterial promoter architecture, with two major findings:
(1) In addition to the well-known “–35” and “–10” elements, bacterial promoters contain a novel and broadly conserved element that specifies the transcription start site. Prof. Chou named this new element “start.”
(2) The “discriminator” element, located immediately downstream of the –10 element, shows striking sequence divergence between the two major bacterial clades, Terrabacteria and Gracilicutes. This divergence reflects a functional difference: many Gracilicutes use discriminator sequences to tune promoter strength according to growth rate, whereas Terrabacteria do not utilize this regulatory mechanism.
Remarkably, the newly identified bacterial start element closely resembles the “initiator” element used by archaea and eukaryotes to define transcription start sites. This cross-domain similarity suggests that the last universal common ancestor may have already used a promoter architecture much like the one observed today, providing new clues to the ancient origin of gene regulation on Earth.
“These findings reshape our understanding of promoter evolution and lay the foundation for engineering and computationally identifying regulatory elements in diverse bacterial genomes,” said Prof. Chou. This study is featured as the cover story of Nucleic Acids Research (Volume 53, Issue 21–22).
To see article on Asia Research News: https://www.asiaresearchnews.com/content/common-evolutionary-origin-promoter-architecture