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Genome Res. Jan 1, 2003; 13(1): 37–45.
PMCID: PMC430962

Genome Rearrangements in Mammalian Evolution: Lessons From Human and Mouse Genomes

Abstract

Although analysis of genome rearrangements was pioneered by Dobzhansky and Sturtevant 65 years ago, we still know very little about the rearrangement events that produced the existing varieties of genomic architectures. The genomic sequences of human and mouse provide evidence for a larger number of rearrangements than previously thought and shed some light on previously unknown features of mammalian evolution. In particular, they reveal that a large number of microrearrangements is required to explain the differences in draft human and mouse sequences. Here we describe a new algorithm for constructing synteny blocks, study arrangements of synteny blocks in human and mouse, derive a most parsimonious human–mouse rearrangement scenario, and provide evidence that intrachromosomal rearrangements are more frequent than interchromosomal rearrangements. Our analysis is based on the human–mouse breakpoint graph, which reveals related breakpoints and allows one to find a most parsimonious scenario. Because these graphs provide important insights into rearrangement scenarios, we introduce a new visualization tool that allows one to view breakpoint graphs superimposed with genomic dot-plots.

[Supplemental material is available online at www.genome.org.]

Analysis of genome rearrangements in molecular evolution was pioneered by Dobzhansky and Sturtevant (1938), who published a milestone paper with an evolutionary tree presenting a rearrangement scenario with 17 inversions for the species Drosophila pseudoobscura and Drosophila miranda. Every genome rearrangement study involves solving a combinatorial puzzle to find a series of genome rearrangements to transform one genome into another. Palmer and co-authors (Palmer and Herbon 1988) pioneered studies of the shortest (most parsimonious) rearrangement scenarios and applied this approach to plant mtDNA and cpDNA. Since then, the analysis of the most parsimonious scenarios has become the dominant approach in genome rearrangement studies. For unichromosomal genomes, it usually amounts to analysis of inversions (also known as reversals), which are the most common rearrangement events. The problem of finding the minimum number of reversals to transform one unichromosomal genome into another is known as the “reversal distance problem.” For multichromosomal genomes, the most common rearrangements are reversals, translocations, fusions, and fissions, and the number of such rearrangements in a most parsimonious scenario is known as the “genomic distance” between multichromosomal genomes.

Finding the reversal distance is a difficult combinatorial problem. In the very first computational studies of genome rearrangements, Watterson et al. (1982) and Nadeau and Taylor (1984) introduced the notion of a breakpoint (disruption of gene order) and noticed some correlations between the reversal distance and the number of breakpoints (in fact, Sturtevant and Dobzhansky [1936] implicitly discussed these correlations 65 years ago!). The shortcoming of early genome rearrangement studies is that they considered breakpoints independently without revealing combinatorial dependencies between related breakpoints. The simplest example of related breakpoints are two breakpoints formed by a single reversal. Kececioglu and Sankoff (1995) were the first to recognize the importance of dependencies between breakpoints and to come up with an approximation algorithm for the reversal distance problem. The important result of Bafna and Pevzner (1993, 1996) is the construction of the “breakpoint graph,” which reveals related breakpoints and allows one to find the most parsimonious scenarios.

Based on the concept of the breakpoint graph, Hannenhalli and Pevzner (1995a) developed a polynomial algorithm for the reversal distance problem, that is, for computing a most parsimonious scenario to transform one unichromosomal genome into another. This approach was further extended to the genomic distance problem, that is, finding a most parsimonious scenario for multichromosomal genomes under inversions, translocations, fusions, and fissions of chromosomes (Hannenhalli and Pevzner 1995a; Tesler 2002b). However, these results, although useful, do not yet yield a meaningful estimate of the number of the rearrangement events on the evolutionary path from mouse to human. The problem is that the genomic sequences provide evidence for both microrearrangements (e.g., intrachromosomal rearrangements with a span <1 Mb) and macrorearrangements (e.g., intrachromosomal rearrangements of larger span as well as interchromosomal rearrangements). The existing rearrangement algorithms do not distinguish between these two types of rearrangements. Because some microrearrangements may be caused by fragment assembly errors, mixing microrearrangements and macrorearrangements within one rearrangement scenario may produce a distorted picture greatly influenced by the sequencing errors in draft genomic sequences. Another difficulty is an unreliable assignment of orthologs (false orthologs), which may create an impression of a rearrangement that never happened (Tatusov et al. 1997). The conserved gene order can also be disrupted by recent duplications and insertions (Hardison et al. 1997).

To address these complications, we first describe a new approach to synteny block generation that separates microrearrangements from macrorearrangements. It allows one to study microrearrangements and macrorearrangements separately and to arrive at a new estimate of the number of macrorearrangements that cover ~170 Myr (million years) of evolutionary distance between human and mouse. We also estimate the number of microrearrangements (but it remains to be seen to what extent this estimate is influenced by the fragment assembly errors) on the evolutionary path between mouse and human.

RESULTS

Synteny Blocks

In a pioneering paper, Nadeau and Taylor (1984) introduced the notion of “conserved segments” (i.e., segments with preserved gene orders without disruption by rearrangements) and estimated that there are roughly 180 conserved segments in human and mouse. Later, Copeland et al. (1993), DeBry and Seldin (1996), Waterston et al. (2002), and Gregory et al. (2002) confirmed these estimates. In the past decade, the progress in understanding the evolutionary history of entire genomes was mainly based on comparative genetic maps (O'Brien et al. 1999). However, these estimates suffer from low resolution of comparative maps in certain genomic areas. Present genomic sequences provide evidence that the human and mouse genomes are significantly more rearranged than previously thought. Moreover, they indicate that a large proportion of previously identified conserved segments are not really conserved because there is evidence of multiple microrearrangements in many of them (Mural et al. 2002). These microrearrangements were not visible in the comparative genetic maps that were used for defining ≈180 conserved segments in the past. We study “synteny blocks” instead of conserved segments. Intuitively, the synteny blocks are segments that can be converted into conserved segments by microrearrangements (see the GRIMM-Synteny algorithm below for a formal definition). The synteny blocks do not necessarily represent areas of continuous similarity between two genomes. Instead, they usually consist of short regions of similarity that may be interrupted by dissimilar regions and gaps. Most synteny blocks are subject to microrearrangements within these blocks.

We demonstrate that human and mouse genomes share 281 synteny blocks of size at least 1 Mb (shown in Fig. Fig.1a)1a) and that at least 245 rearrangements of these blocks occurred since the divergence of human and mouse. The positions of these blocks in the human and mouse genomes are given in Supplementary Materials (available online at http://www.genome.org). The largest synteny block in the human genome is 79.6 Mb, and the average block size is 9.6 Mb. The largest synteny block in the mouse genome is 64.8 Mb, and the average block size is 8.5 Mb.

Figure 1.
(a) Human and mouse synteny blocks. Every block corresponds to a rectangle, with a diagonal showing whether the arrangements of anchors in human and mouse (within the synteny block) are the same or reversed. (b) Combining anchors into clusters by the ...

The overall size of syntenic blocks is ~2707 Mb in human and ~2397 Mb in mouse. The breakpoint regions (i.e., intervals between consecutive syntenic blocks) vary and may be as large as 23.2 Mb in human and 6.7 Mb in mouse. The average size of breakpoint regions is 668 kb in human and 458 kb in mouse. The overall size of the breakpoint regions equals 172 Mb in human and 119 MB in mouse (although some of these breakpoint regions may host shorter synteny blocks). There is evidence of at least 3170 microrearrangements (reversals) that happened within the synteny blocks (although many of them may be artifacts of incorrect assemblies). This very high estimate of the number of microrearrangements further confirms the conjecture that microrearrangements are more common than previously thought (Carver and Stubbs 1997; Puttagunta et al. 2000; Thomas et al. 2000; Kumar et al. 2001). In fact, this number does not even include the microrearrangements within synteny blocks shorter than 1 Mb.

From Local Alignments to Synteny Blocks

Given two genomic sequences, how one can construct synteny blocks? False ortholog assignments and microrearrangements make it nontrivial to find the analogs of synteny blocks (conserved gene clusters) even in shorter bacterial genomes (Fujibuchi et al. 2000; Lathe et al. 2000; Wolf et al. 2001; Rogozin et al. 2002). In addition, human–mouse sequence similarities in noncoding regions (Koop and Hood 1994; Thomas et al. 2000) may further complicate ortholog assignments and make it difficult to apply the methods developed in bacterial genomics to construction of human–mouse synteny blocks.

Sankoff and Blanchette (1997) were the first to come up with an algorithm for synteny block generation. However, their approach was mainly intended for comparative mapping data. Below we describe a different approach that is geared toward genomic sequences. To construct the human–mouse synteny blocks, we start with bidirectional best local similarities (also called anchors) between human and mouse genomic sequences (Tatusov et al. 1997; Mural et al. 2002). Several software tools have recently become available to generate such anchors for entire mammalian genomes (Mayor et al. 2000; Schwartz et al. 2000; Kent 2002; Ma et al. 2002). We assume that a set of nonoverlapping anchors (local alignments between two genomes) is given and the goal is to construct the synteny blocks based on these anchors. We study the same versions of draft human and mouse sequences and the same set of anchors that were used in Waterston et al. (2002). This set of anchors was provided by Michael Kamal at the Whitehead Institute and was generated by PatternHunter (Ma et al. 2002). The set consists of 558,678 anchors with alignment lengths ranging from 40–9647 nt (the mean is 340). We emphasize that these anchors do not necessarily represent similarities within human and mouse genes but may also represent similarities between noncoding regions. This is a departure from the previous “gene order comparison” approach of genome rearrangement studies. It allows us to bypass the difficult issues of gene annotation and ortholog identification, which are not necessary for genome rearrangement studies. This approach may miss similarities between some genes at evolutionary distances where protein similarity still exists but DNA similarity has faded away. However, this is not a serious concern for the rather similar human and mouse genomes. Moreover, our approach can be generalized to handle both DNA and protein similarities in a unified framework.

We assume that human and mouse chromosomes are concatenated to form a single coordinate system. An anchor that starts at position h in the human genome and at position m in the mouse genome is described by its starting point (h,m) in two dimensions (2D). We remark that in reality the anchors are not points (h,m) but diagonals in 2D described by the coordinates (h,m) of an alignment start and the length of the alignment. Such a coordinate system is shown in Figure Figure1a,1a, with chromosomes dividing the plane into rectangles. We define the distance between two points (h1,m1) and (h2,m2) from the same chromosome pair (the same rectangle) as the Manhattan distance |h2  h1| + |m2  m1|. The distance between points from different chromosome pairs is defined as infinity. The distance between two anchors is defined as the distance between their closest ends.

Although the number of anchors may be very large (hundreds of thousands), one still can apply fast genome rearrangement algorithms (Tesler 2002b) to find a most parsimonious scenario to transform the order of anchors in human into an order of anchors in mouse. However, this scenario will likely be unrealistic because many anchors may correspond to false orthologs. Therefore, a technique to filter out false orthologs (even at the expense of filtering some real orthologs) is needed. False orthologs will often look like isolated points (or “small clusters”) in a genomic dot-plot, whereas synteny blocks will be formed from clusters consisting of a larger number of points. Figure Figure2a2a presents the genomic dot-plots for anchors from the X chromosomes (a blowup of the X–X rectangle from Fig. Fig.1a).1a). A brief look at Figure Figure2a2a reveals 16 clusters (Fig. (Fig.2b).2b). Figure Figure2c2c presents rectified clusters that ignore the details of the internal anchor arrangements in the clusters and represent every cluster as a diagonal. These rectified clusters are further combined into diagonals that correspond to 11 synteny blocks (Fig. (Fig.2d).2d). Although the synteny blocks in Figure Figure2d2d differ in size, the sizes of synteny blocks are irrelevant for genome rearrangement algorithms. Figure Figure2e2e is a symbolic representation of synteny blocks as units of the same size, used in the construction of the breakpoint graph.

Figure 2.
X-chromosome: from local similarities, to synteny blocks, to breakpoint graph, to rearrangement scenario. (a) Dot-plot of anchors. Anchors are enlarged for visibility. (b) Clusters of anchors. (c) Rectified clusters. (d) Synteny blocks. (e) Synteny blocks ...

The above description hides many important details, and in many cases the choice of synteny blocks is less obvious. Below we describe the GRIMM-Synteny algorithm for synteny block generation from a collection of anchors. The algorithm uses the gap threshold G and minimum cluster size C as parameters and works as follows:

GRIMM-Synteny Algorithm

  1. Form an anchor graph whose vertex set is the set of anchors.
  2. Connect vertices in the anchor graph by an edge if the distance between them is smaller than the gap size G.
  3. Determine the connected components of the anchor graph. Each connected component is called a cluster.
  4. Delete “small” clusters (shorter than the minimum cluster size C in length).
  5. Determine the cluster order and signs for each genome.
  6. Output the strips in the resulting cluster order as synteny blocks.

GRIMM-Synteny finds 319 clusters in the human genome that are longer than 1 Mb. In addition to these clusters, we identified a number of smaller clusters; for example, in the human genome there are 36 clusters whose length varies from 0.5 Mb–1 Mb, 21 clusters whose length varies from 250 kb–500 kb, and 774 clusters with lengths from 50 kb–250 kb. However, smaller syntenic block assignments are less reliable because they may be caused by false orthologs and sequencing errors.

Figure Figure1b1b presents examples of some highly rearranged clusters from human Chromosome 18/mouse Chromosome 17 and the corresponding anchor graph. After constructing the cluster graph and deleting small clusters (steps 1–4), one has to determine the cluster order and signs (step 5). We define the span of a cluster in human (mouse) as the interval between its minimum and maximum coordinates in human (mouse). Similarly to Mural et al. (2002) and Gregory et al. (2002), we found that the cluster spans in human often significantly differ from cluster spans in mouse (the span may include gaps and unaligned regions that contribute to these differences). Note that although different clusters are not supposed to overlap in 2D, they often overlap in 1D (i.e., their span intervals may overlap in human or mouse). Therefore, defining the cluster order for intermingled clusters should be done with caution. We compute the center of mass of all anchors forming the cluster and order clusters in human by the coordinates of their centers of masses. We assign the clusters numbers according to their order on the human genome. This lets us read off a cluster order in the mouse genome in terms of these labels.

Signs (orientations) of the resulting clusters are usually well-defined but in some cases are not obvious. The algorithm for sign assignments in GRIMM-Synteny and the theorem justifying this algorithm will be described elsewhere.

The number of clusters found depends on the value of the gap threshold G. Figure Figure1b1b shows clusters in a region of the genome for the gap threshold G = 100 kb. Increasing the gap threshold will typically merge some clusters; in this case, this region forms a single cluster at G = 1 Mb. The human and mouse genomes include some gaps and regions without anchors that may be longer than G. Such regions break a single synteny block into a few clusters. To combine such clusters into a single synteny block, we define the notion of a strip. A strip is a sequence of consecutive signed clusters i1, …, in in the first genome that either appears consecutively in the same way or in the reverse order −in, …, i1 in the other genome. For example, for G = 1 Mb and C = 1 Mb, the number of clusters in the human and mouse genomes is 319 whereas the number of strips (synteny blocks) is 281. Most synteny blocks correspond to a single cluster, but some synteny blocks contain as many as 5 clusters.

On the X-chromosome, comparing Figures Figures2,2, a–b, most discarded material is very small, but there is a region near the red cluster, at human 84.6–88.6 Mb, mouse 94.3–99.7 Mb, which forms three clusters. Each has length <C = 1 Mb in human, so they are discarded. Increasing G or lowering C sufficiently would retain these clusters and possibly merge them with the red cluster. If they were the only addition, the red block would be larger, but the synteny block order in Figure Figure2e2e would not be affected, thus the rearrangement analysis described below would remain the same. If distinct blocks were added, it would affect the rearrangement analysis. The chosen values of G and C result in a classification of the anchor arrangements into microrearrangements, macrorearrangements, and noise. Rearrangements of anchors within a synteny block are called microrearrangements. Rearrangements of the order and orientation of synteny blocks are called macrorearrangements.

From Synteny Blocks to the Breakpoint Graph

We illustrate the notion of the breakpoint graph using the X-chromosome as an example. The signed permutation describing synteny block order on the X-chromosome in mouse is −4, −5, 3, 11, −2, 8, −9, 10, −6, 7, −1. For our goals, we shall use 1, −7, 6, −10, 9, −8, 2, −11, −3, 5, 4 (a “flip” of the entire chromosome). We may transform this permutation into the “identity” permutation representing the human X-chromosome, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, by 7 reversals (Fig. (Fig.2h)2h) via the Hannenhalli–Pevzner algorithm (Hannenhalli and Pevzner 1995b, 1999). This algorithm uses the breakpoint graph (Fig. (Fig.2g)2g) to construct a most parsimonious evolutionary scenario (Fig. (Fig.2h)2h) in polynomial time. We now show a new way to construct the breakpoint graph.

Figure Figure3a3a presents the genomic dot-plot (with added “start” and “end” elements) and the “human” path (shown with solid edges) traversing the synteny blocks in human order. The projection of this path on the human genome is shown below the human axis. Similarly, Figure Figure3b3b presents the same genomic dot-plot and the “mouse” path (shown with dotted edges) traversing the synteny blocks in mouse order. The two-dimensional breakpoint graph is obtained by superimposing these solid and dotted paths (Fig. (Fig.3c)3c) and further deleting the synteny blocks (Fig. (Fig.3d).3d). One can prove that the breakpoint graph is a collection of alternating solid-dotted cycles. Figure Figure3d3d consists of a cycle of length 2 (containing the start vertex), two cycles of length 4, a cycle of length 6, and a cycle of length 8. After constructing the cycles, we usually color the edges so that each cycle has its own color (Fig. (Fig.2g).2g). At this point, we apply the Hannenhalli–Pevzner algorithm to obtain a most parsimonious scenario. Note that the breakpoint graphs in Figures Figures22 and and33 are different because of the X-chromosome flip.

Figure 3.
Construction of the breakpoint graph from synteny blocks. (a) Solid path through human. (b) Dotted path through mouse. (c) Superposition of paths. (d) Remove blocks to obtain cycles.

Hannenhalli and Pevzner (1995a) demonstrated that the cycles and their interleaving structure are the “fossil records” of rearrangement events and showed how to use them for solving reversal distance and genomic distance problems. The 2D representation of breakpoint graphs shown in Figure Figure33 is different from the representation used by Hannenhalli and Pevzner (1995a; they used the 1D projections of this graph shown along the axis in Fig. Fig.3).3). We believe that the 2D breakpoint graph is a better visualization than the 1D one, in addition to being independent of the choice of the axis. Therefore, it provides better geometrical intuition for the Hannenhalli–Pevzner theory.

Because every reversal creates at most two new breakpoints, the reversal distance is at most half the number of the breakpoints in the genome. If there is no breakpoint reuse, then the reversal distance is exactly half the number of breakpoints. Moreover, in this case the real evolutionary scenario is a most parsimonious one, thus implying that the reversal distance equals the real distance in this case. However, the estimate of reversal distance as half the number of breakpoints is inaccurate because it assumes that the breakpoints are not reused in evolution. In most genome rearrangement studies, there are breakpoint reuses (at least at a certain level of synteny block resolution), thus indicating that breakpoint reuse is the rule rather than the exception. For example, Palmer and Herbon (1988) describe an evolutionary scenario with one breakpoint reuse for cabbage and turnip mtDNA, whereas Bafna and Pevzner (1995) describe an evolutionary scenario with four breakpoint reuses in the rearrangement scenario for human and mouse X-chromosomes.

Given an evolutionary scenario, we call two breakpoints, B1 and B2, siblings if they are endpoints of a reversal R from this scenario. Two breakpoints are related if there is a series of breakpoints B1,B2,  ,Bn such that every two consecutive breakpoints in this series are siblings. In addition, reconstructing a most parsimonious scenario and identification of related breakpoints are nontrivial tasks, even in the absence of breakpoint reuse. The breakpoint graph reveals related breakpoints and allows one to find the most parsimonious scenarios. In the scenario shown in Figure Figure2h,2h, the breakpoint at the start (flat end) of block 4 is used twice. We emphasize that by reusing breakpoints we do not mean multiple use of exactly the same genomic position as an endpoint of rearrangements, but rather the fact that between synteny blocks, there are regions that host endpoints for multiple rearrangement events.

In contrast to unichromosomal breakpoint graphs (consisting of cycles), the multichromosomal breakpoint graph consists of both cycles and paths (such paths correspond to breaking the cycles at the chromosome endpoints). The breakpoint graph for the entire human and mouse genomes is very complicated (Fig. (Fig.4).4).

Figure 4.
Multichromosomal breakpoint graph of the whole human and mouse genomes. The conventional chromosome order and orientation are not suitable for such graphs; an optimal chromosome order and orientation were determined by the algorithm in Tesler (2002b) ...

From the Breakpoint Graph to Rearrangement Scenarios

A previous analysis of comparative maps of human and mouse X-chromosomes revealed 8 syntenic blocks and postulated a most parsimonious rearrangement scenario with 6 inversions (Bafna and Pevzner 1995). The genomic sequences reveal 11 synteny blocks of 1 Mb and longer and provide evidence for at least 7 inversions (Fig. (Fig.2h).2h). Moreover, there are 177 microrearrangements within the X-chromosome that were beyond the resolution of previous comparative mapping studies (some of them may be artifacts of assembly errors). Two out of 11 synteny blocks on the X-chromosome show evidence of extensive microrearrangements.

These estimates are based on the Hannenhalli and Pevzner (1995a) theorem that expresses the reversal distance between two genomes as n + 1  c + h, where n is the number of synteny blocks, c is the number of cycles in the breakpoint graph, and h is another easily computable combinatorial parameter of the breakpoint graph. Because h equals zero for many biological data sets, n + 1  c is usually a good approximation for reversal distance. For the X-chromosome as depicted in Figure Figure2g,2g, we have n = 11, c = 4, h = 0, and we obtain a reversal distance of 8. However, flipping the whole mouse X-chromosome results in the breakpoint graph of Figure Figure3d,3d, with n = 11, c = 5, h = 0, and reversal distance 7. Flipping a whole chromosome does not count as a rearrangement event, thus the genomic distance on the X-chromosome between human and mouse is 7.

A similar theorem (Hannenhalli and Pevzner 1995b, 1999; Tesler 2002b) holds for multichromosomal genomes, and automatically takes into account whole chromosome flips. We used a fast implementation of the Hannenhalli–Pevzner algorithm (Tesler 2002a) to analyze the human–mouse rearrangement scenario (available via the GRIMM Web server at http://www-cse.ucsd.edu/groups/bioinformatics/GRIMM/index.html). Although the algorithm finds a most parsimonious scenario, the real scenario is not necessarily a most parsimonious one (Blanchette et al. 1996), and the order of rearrangement events within a most parsimonious scenario often remains uncertain. Availability of three or more mammalian genomes could remedy some of these limitations and provide a means to infer the gene order in the mammalian ancestor (Bourque and Pevzner 2002).

The GRIMM algorithm constructs a most parsimonious evolutionary scenario between human and mouse genomes with 245 rearrangements. With at least 245 rearrangements between human and mouse and an estimated 83 Myr (Huchon et al. 2002) of evolution from their common ancestor, we obtain an estimated rate of 1.5 chromosomal rearrangements per Myr, which is higher than the previous estimate of 1.0 (Lander et al. 2001). However, this estimate should not be viewed as typical for mammalian evolution because rodents may have unusually rapid chromosome alterations. The comparative mapping data for cat and cow may soon shed further light on the comparative rates of rearrangements in different branches of the mammalian evolutionary tree.

The human–mouse breakpoint graph provides insights into rearrangements that may have occurred in the course of evolution. Some of these rearrangements are almost “obvious” (they correspond to short cycles in the breakpoint graph), whereas others involve long series of interacting breakpoints. Such complicated rearrangement events are described by long cycles/paths in the breakpoint graph. The longest path in the human–mouse breakpoint graph involves 26 breakpoints. The human–mouse breakpoint graph has 6 other long paths with more than 10 breakpoints.

The analysis of microrearrangements within the synteny blocks demonstrates a large variation in the rate of microrearrangements (reversals) along the genomes. In particular, 41 out of 281 synteny blocks do not show any evidence of microrearrangements, whereas 10 synteny blocks are extremely rearranged (40 or more rearrangements within a block). For example, a long synteny block on human Chromosome 13/mouse Chromosome 8 (nucleotides 101,902,085 to 113,413,125 on human Chromosome 13) consists of 65 regions of local similarity whose order is perfectly conserved in human and mouse. On the other hand, a long synteny block on human Chromosome 18/mouse Chromosome 17 (positions 2,789,316 to 10,083,804 on human Chromosome 18) consists of 143 regions of local similarity and has a large number of microrearrangement breakpoints, indicating that there were at least 85 inversions within this block (Fig. (Fig.1b).1b). The length of this synteny block in mouse is smaller than in human (6.0 Mb vs. 7.3 Mb). Of course, some of the breakpoints within this synteny block may be caused by assembly errors. There is evidence of at least 3170 microrearrangements within all the synteny blocks, some of which may be due to assembly errors.

Every breakpoint defines two synteny blocks A and B that are adjacent in one genome but separated in the second one. We distinguish between unichromosomal breakpoints (A and B belong to the same chromosome in the second genome) and multichromosomal breakpoints (A and B are on different chromosomes). Most breakpoints in the human and mouse genomes are unichromosomal breakpoints, thus indicating that most rearrangements that happened in the course of human–mouse evolution are intrachromosomal inversions. In particular, one can come up with a most parsimonious rearrangement scenario that includes 134 reversals in the human and mouse genomes before any translocations/fusions/fissions happen. After performing these reversals, the number of synteny blocks is reduced from 281 to 144. The breakpoint graph of these human and mouse “preancestors” allows one to infer which pairs of chromosomes were involved in multiple translocations/fusions/fissions. The longest cycle in this graph involves 8 breakpoints located on 8 different chromosomes in human. The resulting rearrangement scenario from the mouse to human preancestor has 15 inversions, 93 translocations, and 3 fissions. The complete scenario from mouse to human has 149 inversions, 93 translocations, and 3 fissions. (There are other combinations of 245 steps consistent with the breakpoint graph; this is the one we found with the most inversions.)

DISCUSSION

Molecular evolution studies are usually based on the analysis of individual genes rather than entire genomes. However, such widespread phenomena as horizontal gene transfer, differential gene loss, and the like, often lead to situations in which evolutionary trees for different genes tell different stories. An alternative approach is to infer the evolutionary history of entire genomes, rather than individual genes, based on the analysis of gene orders. Although this approach is successful in bacterial genomics (for a recent review, see Wolf et al. 2002), its applications in mammalian genomics are somewhat limited owing to incompleteness of gene order data derived from comparative maps. Human and mouse genomic sequences, for the first time, provide a possibility to accurately estimate the extent of rearrangement events. However, the “original synteny” problem (Nadeau and Sankoff 1997) remains unsolved because at least three mammalian gene orders are required to derive the ancestral mammalian karyotype. The ongoing mammalian sequencing projects and recently developed algorithms for reconstructing ancestral gene orders (Bourque and Pevzner 2002) provide hope that the “original synteny” problem will finally be resolved.

Acknowledgments

We are grateful to Ewan Birney, Guillaume Bourque, and Bill Murphy for many helpful suggestions; and to Bernard Moret for providing his group's genome rearrangement programs. We are also indebted to Michael Kamal, Kerstin Linblad-Toh, and Jade Vinson for their advice on synteny blocks and rearrangements in human and mouse genomes.

The publication costs of this article were defrayed in part by payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 USC section 1734 solely to indicate this fact.

Notes

E-MAIL ppevzner/at/cs.ucsd.edu

Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.757503. Article published online before print in December 2002.

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