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Making sense of centromeres
© BioMed Central Ltd 2004
- Published: 31 August 2004
Comparative analysis of the proteins that bind exclusively at the centromere provides evidence of an evolutionary battle that may make sense of sex.
- Centromere Protein
- Meiotic Drive
- Female Meiosis
- Centromeric Sequence
- Fred Hutchinson Cancer Research
At the pinched waist of each eukaryotic chromosome is a region that is both elusive and enigmatic. Despite considerable effort, and multiple announcements of completed genome sequences, this zone stubbornly refuses to reveal its complete sequence, and what little we know of it at first sight runs counter to standard theories of evolution. The region in question is, of course, the centromere.
To explain this, Henikoff and colleague Harmit Malik proposed a radical theory . Maybe, they suggested, there is a Darwinian competition going on during female meiosis, the process that yields the eggs. A normal cell contains chromosomes in pairs, with one member of that pair coming from the male parent, the other from the female. In female meiosis the two chromosomes first duplicate to make four chromatids, but then three chromatids are effectively thrown away (as 'polar bodies' in mammals, or non-functional 'megaspores' in plants), while lucky number four becomes packaged ready for use in sexual reproduction. It has always been a puzzle that sexual reproduction creates a scenario in which a parent throws its genes into a new individual with only a 50:50 chance that that individual will pass them on. But what if one of the parents built a centromere that made it more likely that its chromatid would win out in meiotic selection? It would now have a 100% chance of launching its genes into the future. If this were to occur, we would expect to see a genetic 'arms race', with individuals within a species competing to create ever more effective centromeres. You'd see this in rapidly evolving centromeric DNA - the very observation that triggered this line of thought.
The idea behind this centromere drive model is that each of the four copies of a chromosome goes to a distinct area of the cell and the spindles might be induced to favor pulling one towards the zone that becomes the egg. "It makes a lot of cell biological sense, the idea that the cellular geometry of the spindles in female meiosis influences the fate of the products - it's a great theory," comments Sullivan. This solution to the paradox creates its own problem, however. Male meiosis produces four sets of chromosomes, but in this case all are used. Any imbalance in the types of centromere could cause problems with division. The hypothesis therefore conjectures that centromeric proteins would need to evolve rapidly to counteract this potential problem.
Excited by the implications of this research, Henikoff's colleagues Paul Talbert and Terri Bryson began searching for evidence. Clearly there was no point in trying to squeeze more data from the DNA of the centromeres: major sequencing projects had already drawn a blank there. The alternative approach, however, was to examine the centromeric proteins. Within the centromere, the usual histone H3 is replaced by a variant, centromeric H3 (CenH3). The obvious starting point was to ask whether there were signs that CenH3 was actively adapting, and to check this out in many different species.
Evolutionary molecular biologists like Caro-Beth Stewart of the University of Albany have shown that you can say whether a protein has evolved adaptively, neutrally, or negatively by measuring the rate of synonymous and nonsynonymous substitutions in the sequence between species . She likens the task to monitoring speeding cars on a freeway. "After looking at the traffic for long enough you can spot the general regular speed limit, but then among the vehicles there will be a car that is going faster. If this is just for a short burst then it will make no overall difference to that car's progress, but if it consistently speeds then it will be statistically different from the rest and the traffic cops are very likely to spot it," she explains.
By the time that Henikoff's team started the current work , they already knew that CenH3 was evolving adaptively in Drosophila and Arabidopsis [4, 5]. They then compared CenH3s in mice and rats. Contrary to expectation, this comparison showed negative selection: in these species, CenH3s were being actively conserved. The same was the case for the Chinese hamster, chimpanzee and human. Switching to plants, they came to the same conclusion: in maize and sugarcane, CenH3 showed overall negative selection.
At this point lesser mortals might have turned tail and torn up their hypothesis. But Henikoff's team remained convinced of their basic premise and instead started to look at other DNA-binding proteins in the centromere. One obvious target was CENP-C, a poorly conserved centromere protein that is less conserved over its entire length than CenH3 but contains a 24 amino-acid motif known as the CENPC motif. Human CENP-C had previously been shown to bind centromeric DNA and to be needed for centromeres to function successfully. The CENP-C protein is bigger than CenH3 and quite possibly makes more contacts with DNA. Although its function is unclear, it does co-localize with CenH3 within the active heart of centromeres. Once again the team started measuring the rate of protein evolution.
Starting with rodents, they found clear evidence that while the CENPC motif was under negative selection, most of the amino-terminal portion of the protein was under positive selection. Similar findings came from humans and chimpanzees, and in the mustard and grass families CENP-C was much more prone to positive selection than was CenH3. "What is particularly exciting is that when we look at organisms where the CenH3 is not adaptively evolving, CENP-C is," says Henikoff. The adaptive evolution of CenH3 in Drosophila is quite possibly due to the fact that it does not have CENP-C. At the same time, Sullivan wonders whether you could now identify which of the 30 or so known centromeric proteins are in contact with the DNA by looking for regions of adaptive evolution alone.
The idea takes a moment to think through. Peter Langridge, CEO and Director of the Australian Centre for Plant Functional Genomes at the University of Adelaide, has views symptomatic of many. Initially less than convinced, he is warming to the idea. He points out that the fertility of a higher eukaryote is largely determined by the ability of the eggs to become fertilized. "Most plants can tolerate 90% male sterility without a real drop in fertility," he notes. "Having read the paper it seems obvious that such a meiotic drive process would exist, and the observation and arguments that the binding of the centromeric proteins controls this process seem logical. The model provides a good explanation for the variation in centromeric sequence and this was an issue that had puzzled me." That said, Langridge found himself thinking about other possible explanations. Could the centromeric sequences and proteins be influencing some other process, such as recombination? Suppressing recombination at the centromere might present a selective advantage to protect some genes from recombination. "If increasing variability in the sequences of the DNA and proteins at the centromere destabilized protein-centromere interactions and thus lowered the recombination rate, could one get the same results as Henikoff's team?" he asks. "This is the great thing about this paper: it got me thinking in all sorts of weird directions," says Langridge. As with all scientific theories, these models require further testing and rigorous scrutiny from the scientific community. Whatever the outcome of that research, Henikoff and colleagues' new results have provided some much-needed insight into the inscrutable centromere.
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