Most humans have nearly the same complement of genes, all of which have come from our primate ancestors (Salzberg, 2017). On the other hand, even closely related strains of the bacterium Escherichia coli can differ by hundreds of genes (Touchon et al., 2009) despite having a much smaller genome. These genes have been acquired via a process called horizontal gene transfer (HGT), which is an important driver of adaptation, as it allows bacteria and other prokaryotes to gain the genes they need in order to thrive in certain environments (Koonin et al., 2001). Moreover, this exchanging of genes has resulted in many genetic elements in prokaryotes becoming highly mobile, making it easier for DNA to be transferred to a diverse range of hosts.
HGT has also been observed in animals, plants and other eukaryotes (Husnik and McCutcheon, 2018), but its role in determining genome composition and facilitating adaptation in these species remains unclear (Ku and Martin, 2016). Now, in eLife, Andreas Weber and co-workers at Heinrich Heine University, Arizona State University and Rutgers University – including Alessandro Rossoni as first author – report evidence for HGT between prokaryotes and the red alga Cyanidiales (Rossoni et al., 2019). These are remarkable single-cell organisms that can perform photosynthesis at temperatures up to 56°C, and can live in extreme environments such as hot springs and acid rivers (Schönknecht et al., 2013). Cyanidiales can also be used to investigate HGT over geological timescales because they share a common ancestor that dates back 800 million years to a time before animals had even evolved.
Based on an analysis of ten new and three previously reported Cyanidiales genomes, Rossoni et al. found that 1% of genes had been obtained via HGT. Moreover, many of these genes coded for proteins that were needed to survive in extreme environments (such as proteins involved in detoxifying heavy metals like arsenic or mercury, or removing free radicals; Figure 1). Additionally, prokaryotes adapted to the same extreme environment as Cyanidiales were commonly identified as the source of these genes. It seems likely, therefore, that HGT influenced the evolution of Cyanidiales, especially because the criterion used to detect HGT was conservative and the study did not attempt to detect gene transfer from other eukaryotes.
The evolutionary trajectory of the red algae Cyanidiales is shown from top to bottom. Rossini et al. investigated genetic changes that took place before and after the Cambrian explosion 541 million …
Comparing the new Cyanidiales genes to genes found in present-day bacteria and archaea databases did not yield any recent examples of HGT. This absence of recent events is unsurprising, as Rossoni et al. estimated that Cyanidiales acquire just one gene via HGT every 14.6 million years – the same amount of time it took for humans to diverge from the orangutan. Such a low rate makes finding a fresh transfer in a small number of genomes unlikely. Instead, the majority of HGT candidate genes found by Rossoni et al. have acquired introns (non-protein coding segments of DNA), and then persisted over hundreds of millions of years.
Despite there being evidence to show HGT occurred, it still remains unclear how these transfers took place. The best-studied mechanisms by which eukaryotes acquire DNA from other organisms are sexual reproduction and by transferring DNA from symbionts (biological organisms that live cooperatively with other organisms). However, meiotic sex only occurs between closely related species, and therefore cannot explain how Cyanidiales appear to have gained DNA from such a diverse range of prokaryotes: moreover, the evolution of symbiotic transfer is uncommon in most taxonomic groups. Instead DNA was more likely obtained via viral infection or plasmids (circular molecules of double stranded DNA) being transferred between prokaryotes and eukaryotes (Heinemann and Sprague, 1989). Indeed, a recent study has shown that many eukaryotes, including red algae, can acquire plasmids carrying genes derived from plants, viruses and bacteria (Lee et al., 2016).
The work of Rossoni et al. suggests that, in terms of gene content evolution, Cyanidiales are more similar to humans than to E. coli, which is consistent with previous qualitive comparisons of HGT patterns in eukaryotes and prokaryotes (Ku and Martin, 2016). However, a number of mysteries still remain. For example, what are the most common modes of plasmid transmission in Cyanidiales? How do plasmids maintain themselves in populations? How often do they jump between species, and how far do they jump? To answer these questions we should first observe what is happening all around us today (Popa et al., 2017) and, if possible, study events that occur more frequently than once every 14.6 million years.
© 2019, Kobras and Falush
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Gene duplication drives evolution by providing raw material for proteins with novel functions. An influential hypothesis by Ohno (1970) posits that gene duplication helps genes tolerate new mutations and thus facilitates the evolution of new phenotypes. Competing hypotheses argue that deleterious mutations will usually inactivate gene duplicates too rapidly for Ohno’s hypothesis to work. We experimentally tested Ohno’s hypothesis by evolving one or exactly two copies of a gene encoding a fluorescent protein in Escherichia coli through several rounds of mutation and selection. We analyzed the genotypic and phenotypic evolutionary dynamics of the evolving populations through high-throughput DNA sequencing, biochemical assays, and engineering of selected variants. In support of Ohno’s hypothesis, populations carrying two gene copies displayed higher mutational robustness than those carrying a single gene copy. Consequently, the double-copy populations experienced relaxed purifying selection, evolved higher phenotypic and genetic diversity, carried more mutations and accumulated combinations of key beneficial mutations earlier. However, their phenotypic evolution was not accelerated, possibly because one gene copy rapidly became inactivated by deleterious mutations. Our work provides an experimental platform to test models of evolution by gene duplication, and it supports alternatives to Ohno’s hypothesis that point to the importance of gene dosage.
Maintenance of rod-shape in bacterial cells depends on the actin-like protein MreB. Deletion of mreB from Pseudomonas fluorescens SBW25 results in viable spherical cells of variable volume and reduced fitness. Using a combination of time-resolved microscopy and biochemical assay of peptidoglycan synthesis, we show that reduced fitness is a consequence of perturbed cell size homeostasis that arises primarily from differential growth of daughter cells. A 1000-generation selection experiment resulted in rapid restoration of fitness with derived cells retaining spherical shape. Mutations in the peptidoglycan synthesis protein Pbp1A were identified as the main route for evolutionary rescue with genetic reconstructions demonstrating causality. Compensatory pbp1A mutations that targeted transpeptidase activity enhanced homogeneity of cell wall synthesis on lateral surfaces and restored cell size homeostasis. Mechanistic explanations require enhanced understanding of why deletion of mreB causes heterogeneity in cell wall synthesis. We conclude by presenting two testable hypotheses, one of which posits that heterogeneity stems from non-functional cell wall synthesis machinery, while the second posits that the machinery is functional, albeit stalled. Overall, our data provide support for the second hypothesis and draw attention to the importance of balance between transpeptidase and glycosyltransferase functions of peptidoglycan building enzymes for cell shape determination.