Transcription Factor Binding Not So Evolutionarily Conserved

Researchers writing in Science have discovered a remarkable amount of plasticity in how transcription factors, the proteins that bind to DNA to control the activation of genes, maintained their function over 300 million years of evolution. They say that sequence conservation is not the whole story when it comes to maintaining tissue-specific gene regulation.Scientists believe that transcription factors recognize the genes that they regulate by binding to short, sequence-specific lengths of DNA upstream or downstream of their target genes. It was widely assumed that, like the sequences of the genes themselves, these transcription factor binding sites would be highly conserved throughout evolution. However, this turns out not to be the case in mammals.

Researchers writing in Science have discovered a remarkable amount of plasticity in how transcription factors, the proteins that bind to DNA to control the activation of genes, maintained their function over 300 million years of evolution.

They say that sequence conservation is not the whole story when it comes to maintaining tissue-specific gene regulation.

Scientists believe that transcription factors recognize the genes that they regulate by binding to short, sequence-specific lengths of DNA upstream or downstream of their target genes. It was widely assumed that, like the sequences of the genes themselves, these transcription factor binding sites would be highly conserved throughout evolution. However, this turns out not to be the case in mammals.

The new Science study traced the evolution of gene regulation by comparing the binding of evolutionarily conserved transcription factors in the genomes of five vertebrate species – human, dog, mouse, short-tailed opossum and chicken.

In all tested species, the transcription factors CEBPA and HNF4A are master regulators of liver-specific genes. By mapping the binding of CEBPA and HNF4A in the genomes of each species and comparing those maps, they found that in most cases neither the site nor the sequence of the transcription factor binding sites is conserved, yet despite this, these transcription factors still manage to regulate the largely conserved gene expression and function of liver tissue.

"The evolutionary changes in transcription factor binding in the five species have left clues that we can use to explain how function is preserved but not necessarily sequence," said Paul Flicek, a researcher at the European Bioinformatics Institute. "What we have learnt is that although the transcription factors regulate similar target genes in all five species, the binding events underpinning this regulation have not been conserved as the species diverged."

"By studying changes in transcription factor binding, we can understand the evolution of gene regulation," said Duncan Odom from Cancer Research UK Cambridge Research Institute and coauthor on the paper. "Differences in gene regulation are central to explaining differences between species, and gene misregulation is a key causative factor in diseases like cancer."

Citation: Schmidt et al., 'Five-Vertebrate ChIP-seq Reveals the Evolutionary Dynamics of Transcription Factor Binding', Science, April 2010; doi:10.1126/science.1186176

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