Summary: Dozens of genes previously believed to have similar roles across different organisms are actually unique to humans. The genetic codes are for transcription factors, which help control gene activity. The findings may help to explain how humans evolved.
Source: University of Toronto
Researchers at the Donnelly Centre in Toronto have found that dozens of genes, previously thought to have similar roles across different organisms, are in fact unique to humans and could help explain how our species came to exist.
These genes code for a class of proteins known as transcription factors, or TFs, which control gene activity. TFs recognize specific snippets of the DNA code called motifs, and use them as landing sites to bind the DNA and turn genes on or off.
Previous research had suggested that TFs which look similar across different organisms also bind similar motifs, even in species as diverse as fruit flies and humans. But a new study from Professor Timothy Hughes’ lab, at the Donnelly Centre for Cellular and Biomolecular Research, shows that this is not always the case.
Writing in the journal Nature Genetics, the researchers describe a new computational method which allowed them to more accurately predict motif sequences each TF binds in many different species. The findings reveal that some sub-classes of TFs are much more functionally diverse than previously thought.
“Even between closely related species there’s a non-negligible portion of TFs that are likely to bind new sequences,” says Sam Lambert, former graduate student in Hughes’ lab who did most of the work on the paper and has since moved to the University of Cambridge for a postdoctoral stint.
“This means they are likely to have novel functions by regulating different genes, which may be important for species differences,” he says.
Even between chimps and humans, whose genomes are 99 per cent identical, there are dozens of TFs which recognize diverse motifs between the two species in a way that would affect expression of hundreds of different genes.
“We think these molecular differences could be driving some of the differences between chimps and humans,” says Lambert, who won the Jennifer Dorrington Graduate Research Award for outstanding doctoral research at U of T’s Faculty of Medicine.
To reanalyze motif sequences, Lambert developed new software which looks for structural similarities between the TFs’ DNA binding regions that relate to their ability to bind the same or different DNA motifs. If two TFs, from different species, have a similar composition of amino-acids, building blocks of proteins, they probably bind similar motifs. But unlike older methods, which compare these regions as a whole, Lambert’s automatically assigns greater value to those amino-acids– a fraction of the entire region– which directly contact the DNA. In this case, two TFs may look similar overall, but if they differ in the position of these key amino-acids, they are more likely to bind different motifs. When Lambert compared all TFs across different species and matched to all available motif sequence data, he found that many human TFs recognize different sequences–and therefore regulate different genes– than versions of the same proteins in other animals.
The finding contradicts earlier research, which stated that almost all of human and fruit fly TFs bind the same motif sequences, and is a call for caution to scientists hoping to draw insights about human TFs by only studying their counterparts in simpler organisms.
“There is this idea that has persevered, which is that the TFs bind almost identical motifs between humans and fruit flies,” says Hughes, who is also a professor in U of T’s Department of Molecular Genetics and Fellow of the Canadian Institute for Advanced Research. “And while there are many examples where these proteins are functionally conserved, this is by no means to the extent that has been accepted.”
As for TFs that have unique human roles, these belong to the rapidly evolving class of so-called C2H2 zinc finger TFs, named for zinc ion-containing finger-like protrusions, with which they bind the DNA.
Their role remains an open question but it is known that organisms with more diverse TFs also have more cell types, which can come together in novel ways to build more complicated bodies.
Hughes is excited about a tantalizing possibility that some of these zinc finger TFs could be responsible for the unique features of human physiology and anatomy–our immune system and the brain, which are the most complex among animals. Another concerns sexual dimorphism: countless visible, and often less obvious, differences between sexes that guide mate selection–decisions that have an immediate impact on reproductive success, and can also have profound impact on physiology in the long term. The peacock’s tail or facial hair in men are classic examples of such features.
“Almost nobody in human genetics studies the molecular basis of sexual dimorphism, yet these are features that all human beings see in each other and that we are all fascinated with,” says Hughes. “I’m tempted to spend the last half of my career working on this, if I can figure out how to do it!”
Funding: The research was funded by grants from the Canadian Institutes of Health Research, the National Science and Engineering Research Council, and the US National Institutes of Health. Hughes also holds the Billes Chair of Medical Research at the University of Toronto.
University of Toronto
Jovana Drinjakovic – University of Toronto
The image is credited to Sam Lambert.
Original Research: Closed access
“Similarity regression predicts evolution of transcription factor sequence specificity”. Samuel A. Lambert, Ally W. H. Yang, Alexander Sasse, Gwendolyn Cowley, Mihai Albu, Mark X. Caddick, Quaid D. Morris, Matthew T. Weirauch & Timothy R. Hughes.
Nature Genetics. doi:10.1038/s41588-019-0411-1
Similarity regression predicts evolution of transcription factor sequence specificity
Transcription factor (TF) binding specificities (motifs) are essential for the analysis of gene regulation. Accurate prediction of TF motifs is critical, because it is infeasible to assay all TFs in all sequenced eukaryotic genomes. There is ongoing controversy regarding the degree of motif diversification among related species that is, in part, because of uncertainty in motif prediction methods. Here we describe similarity regression, a significantly improved method for predicting motifs, which we use to update and expand the Cis-BP database. Similarity regression inherently quantifies TF motif evolution, and shows that previous claims of near-complete conservation of motifs between human and Drosophila are inflated, with nearly half of the motifs in each species absent from the other, largely due to extensive divergence in C2H2 zinc finger proteins. We conclude that diversification in DNA-binding motifs is pervasive, and present a new tool and updated resource to study TF diversity and gene regulation across eukaryotes.