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Biological function in the twilight zone of sequence conservation
© Ponting et al. 2017
- Published: 16 August 2017
Strong DNA conservation among divergent species is an indicator of enduring functionality. With weaker sequence conservation we enter a vast ‘twilight zone’ in which sequence subject to transient or lower constraint cannot be distinguished easily from neutrally evolving, non-functional sequence. Twilight zone functional sequence is illuminated instead by principles of selective constraint and positive selection using genomic data acquired from within a species’ population. Application of these principles reveals that despite being biochemically active, most twilight zone sequence is not functional.
Functionality of most human protein coding, and some non-coding, sequence is clearly implied when it is conserved across diverse mammalian species. This has been a rule-of-thumb by which to infer whether a sequence is functional without the benefit of experimental data. Conservation, however, is not a faithful indicator of functionality. High sequence conservation could reflect a relatively brief period of neutral evolution over which few mutations accumulated. Just because approximately 98% of human DNA is conserved in chimpanzee, for example, this does not imply that this amount of sequence conveys function. Conversely, poor conservation of a sequence does not imply that it is devoid of function. After all, low conservation could also be explained by frequent episodes when rare mutations are brought to high frequency and fixation within a population by positive selection. Thresholding on percentage nucleotide sequence identity thus fails to neatly separate functional from non-functional sequence. This means that as sequence conservation diminishes we drop into a ‘twilight zone’ [1, 2] in which DNA cannot immediately be ascribed as either functional or non-functional. Population genetics principles illuminate the functionality of sequence in the twilight zone. These can be used to assess whether sequence evolution has been constrained, meaning that it exhibits a slower rate of change than predicted by a model of neutral evolution; selective constraint is inferred by considering the degree by which allele frequencies are depressed across extant populations [3–5]. Conversely, functional sequence subject to positive selection exhibits a rate of change greater than seen for neutrally evolving sequence.
Sequence conservation and constraint are not the only benchmark by which to evaluate functionality. High throughput experimental assays are providing genome-wide assessments of functional sequence. Armed with this experimental information, can we now reveal the extent of functional sequence and associated molecular and cellular biology present in the twilight zone of low sequence conservation? Here I review instances where sequence is functional despite its low conservation, focusing principally on our own and other mammalian species. I conclude that population genomics-based approaches to predict function are paramount because, counterintuitively, experiments are not perfect predictors of function.
Has a poorly conserved homologous sequence diverged by weak negative selection or else by positive selection? Answering this question computationally remains a substantial challenge because some approaches are associated with high rates of false positive predictions . The most compelling examples are when candidate positively selected sites are spatially clustered within ligand-binding pockets, such as observed in mouse major urinary proteins  or in major histocompatibility complex class I subunits . As with these two studies, clear-cut instances are often found for proteins involved in reproduction—because of the genetic arms race inherent in sexual selection —or in immunity and host defence . The genetic arms race with viruses, in particular, is predicted to account for nearly a third of all positively selected change occurring in human protein sequence that is conserved across mammals . The evolution of primate and bat poly-ADP-ribose polymerases, for example, appears to have been subject to considerable genetic arms races with unidentified pathogens, resulting in positively selected sites that cluster in three dimensions and in a disordered region of unknown function .
Genes whose variants have been positively selected, including those involved in reproduction and host defence, are often in large families whose numbers are not well conserved between, or even within, species owing to high rates of duplication and/or pseudogenisation [18–20]. Nevertheless, basal mutational rates of duplication and loss are highly variable; hence, in most cases it is difficult to evaluate the contribution made by selection in retaining or purging gene duplicate and gene disruptive alleles in the population . Some examples in human evolution are more compelling because of their ability to link copy number variation with fitness. A higher gene copy number of CCL3L1, which encodes a known ligand for the human immunodeficiency virus (HIV) co-receptor CCR5, for example, is associated with lower susceptibility to HIV and to acquired immunodeficiency syndrome, and even higher copy numbers are observed in chimpanzees . In general, however, despite their high prevalence, with four-times more human nucleotides present in copy number increased regions than in single nucleotide variant sites, copy number gain of human genes appears to be under little or no selection .
To summarise the hallmarks of a rapidly evolving gene, I return to the 2310003L06Rik protein-coding locus (Fig. 1). It is a member of a large multi-gene family (namely SCPP genes) whose genes duplicated and became pseudogenes rapidly over mammalian evolution; it encodes a secreted protein, which means perhaps that it is more likely to be engaged in inter-specific conflict between host and pathogens; this protein’s structure is apparently flexible and disordered, which is less likely to evolve by purifying selection; and, its expression profile is narrowly restricted to few tissues, indeed to only one, the tongue. Nevertheless, in the absence of statistical evidence that this gene has experienced episodes of positive selection, it need only be stated that its evolution has been more rapid than that of most mammalian genes.
lncRNAs are considered to fall into two distinct classes: enhancer-like lncRNAs show no sequence conservation, whereas promoter-like lncRNA exons are modestly conserved (Fig. 3) . Promoter-like lncRNAs are thus the more likely to possess RNA sequence-dependent functions. The more numerous enhancer-like lncRNAs also show poorly conserved transcription, and likely contribute many of the 40% of mouse loci whose transcription fails to be conserved in the rat in the same tissue . In the absence of frequent sequence and transcriptional conservation, and until there is experimental evidence of RNA-dependent function, such enhancer-like lncRNAs will not justify consideration as genes. For promoter-like lncRNAs, RNA sequence-dependent function could be mediated by secondary structure. Nevertheless, there is no support for proposed conserved secondary structures of well-studied lncRNAs, such as HOTAIR, SRA, and Xist, from pairwise covariation in sequence changes .
Shorter (~22 nucleotide) microRNAs are also often lineage-specific . Placental and marsupial mammals have experienced a net gain of nearly one new microRNA family per million years, over twice the rate observed in birds . Once a new family arises, it can expand rapidly by tandem duplication and lose members by pseudogenisation, as observed for a primate-specific family of 46 microRNAs present on human chromosome 19 . Concomitantly, mRNA targets of these microRNAs can evolve by the gain or loss of binding sites within mRNAs’ 3′ UTRs [39, 40].
Evolution of the mammalian genome is dominated not by conservation and stasis but by tumult and large-scale change . The human genome, for example, is estimated to have lost 22% (700 Mb) of its DNA and gained an equivalent amount over the last 75 million years . Chromosomal gene content—even between closely related species—is rarely conserved. An extreme example of this is the genomes of Indian and Chinese muntjak deer that have dramatically differing numbers of chromosomes (6 and 46, respectively) despite sharing a common ancestor within the last 2 million years .
Most non-conserved sequence lies within the non-functional ~92% of the mammalian genome [4, 44]. Rapid resculpting of mammalian genomes is dominated by lineage-specific insertion and deletion of transposable element (TE) sequence whose debris, together with other repetitive sequence, contribute up to two-thirds of the human genome . Although occasionally it is proposed that a large fraction of TEs are functional , there is no evolutionary or experimental evidence to support this. Conversely, because the locations of insertion or deletion mutations in TEs occur almost exactly as would be expected from random events, the vast majority of TEs appear to be inert , with less than 2% of TE sequence (approximately 20 Mb) bearing the signature of constraint [44, 48]. The exceptions are, nevertheless, of interest: for example, 18 human Alu elements have evidence for being translated ; a handful of syncytin protein-coding genes have their origins in TEs (Fig. 4); and several families of microRNAs have derived from TEs, albeit slowly over evolutionary time [50, 51].
Open chromatin, which contains many protein-binding sites, contributes both the largest amount of functional (area of circles in Fig. 5) and the greatest density (Fig. 5, X-axis) of functional sequence. Nevertheless, such sites, and promoters and enhancers more generally, are poorly conserved across mammals [52–55]. It is estimated that promoters for over 40% of genes have arisen or been lost in either the human or mouse lineage since their last common ancestor . In a comparison of human, mouse, dog, opossum and chicken, most binding events were unique to one of these species . In large part, the rapidity by which proteins’ DNA binding sites are gained and lost is explained by their short length. In a 1-kb segment of human DNA it is predicted that a new 7–8 bp protein-binding motif arises, by neutral evolution, on average every 60,000 years .
Rapid evolution could also reflect higher than average mutation rates. Sequence with a high CpG dinucleotide content, including protein-coding sequence, evolves particularly rapidly owing to a high rate of mutation from the methylated form of CpG to TpG and CpA in germline genomes [58–60]. Sequence lying within the highly recombining regions of the genome also evolves especially rapidly, with one mouse gene experiencing a 100-fold increase due to this phenomenon of biased gene conversion [61, 62]. Functional regions of the non-coding genome can also mutate rapidly due to DNA-bound factors blocking the displacement of error-prone polymerase-α sequence during replication . Identifying sequences under positive selection due to adaptation is thus made more complex because not just the classical neutral model, but also models accounting for these mutational biases, need to be rejected.
On one hand, 80% of the human genome has been annotated by experiment either as being bound by proteins or as being the substrate of enzymatic activity, the majority of which overlaps with the ~67% of the genome that is TE-derived. On the other hand, this is far more than the ~8% of the human genome that shows evolutionary evidence of constraint, and there is evidence that only very few TEs aligned between species’ genomes are constrained (see above). Resolution of this apparent paradox stems from the realisation that many (even the majority of) molecular phenomena in cells are inconsequential in the sense that they are not surveyed effectively by natural selection [64, 65]. These phenomena include non-functional RNA–protein or protein–protein or protein–DNA interactions [66–68]. In the latter case, most interactions between proteins and chromatin have been shown as failing to alter transcription of putative target genes . Current experiments are thus unable to distinguish cleanly between molecular activities that are incidental and those that are consequential, even vital. By contrast, evolutionary approaches can infer function, annotating sequence by the importance attributed to it by natural selection. Whilst problems remain to be overcome [69, 70], such approaches can discern lineage-specific function in sequence that is not conserved among species, and the absence of function in aligned, notionally conserved sequence . Human genome sequencing at the population level is now accelerating [5, 71, 72]. The resulting extensive diversity data will permit the inference of constraint at high resolution and will thus shed light on function and molecular mechanisms. It will also help to overthrow misguided notions that function requires between-species sequence conservation or that function is widespread outside constrained sequence.
The author thanks the MRC, ERC and the Wellcome Trust for funding, and also two anonymous referees, Oscar Bedoya-Reina, Luis Sanchez-Pulido and other group members for very helpful comments.
CPP wrote this article.
The authors declare that they have no competing interests.
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