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Segmental duplications: an 'expanding' role in genomic instability and disease
Author: B. S. Emanuel
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"Several genetic disorders have been classified as seg- mental aneusomy syndromes, which are disorders that result from inappropriate dosage for crucial genes in a genomic segment. This definition applies when the dosage imbalance occurs by structural (deletion or duplication) or functional mechanisms (by IMPRINTING defects or UNIPARENTAL DISOMY). Recently, it is increasingly clear that a significant proportion of segmental aneu- somy arises from the genomic restructuring caused by aberrant recombination that occurs at region- or chro- mosome-specific low-copy repeats, also known as seg- mental duplications 1?4 . The cytogenetic alterations mediated by segmental duplications include deletions, interstitial duplications, translocations, inversions and the formation of small marker chromosomes. These rearrangements can give rise to an altered copy number of a gene(s) or, alternatively, might disrupt the integrity of a single gene. Because a change at the genomic level is involved, these disorders have been referred to as genomic disorders 2 . Segmental duplications represent a new class of repet- itive DNA element that has recently been identified in the human genome. Segmental duplications have resulted from the duplication of large segments of genomic DNA that range in size from 1 to 400 kb (REFS 4,5) and can be divided into two classes ? interchromosomal and intra- chromosomal. The interchromosomal class is duplicated on non-homologous chromosomes, and many members of this class localize to the pericentromeric and sub- telomeric regions of human chromosomes 6?10 . The intra- chromosomal duplications, also referred to as region- or chromosome-specific low-copy repeats, are typically found on a single chromosome or in a single chromoso- mal band 1?3 . Recent evidence has implicated many of these intrachromosomal segmental duplications in the aetiology of the chromosomal rearrangements associated with genomic disorders 1?3,11,12 . There seems to be a signif- icant bias for genomic rearrangements that are mediated by intrachromosomal segmental duplications to be near centromeres and telomeres (FIG. 1). This has led to the suggestion that the pericentromeric and subtelomeric regions of chromosomes are more permissive to the gen- eration and expansion of segmental duplications 3 . Furthermore, the processes responsible for the genera- tion of segmental duplication and for disease-causing genomic rearrangements have been proposed to be mol- ecularly interrelated 3 .However,a direct connection between these two processes has not yet been established. Although they seem to localize near centromeres and telomeres, intrachromosomal segmental duplications are more distant from centromeres and telomeres than are the pericentromeric and subtelomeric interchromoso- mal segmental duplications 3,6?10 . Also, not all intrachro- mosomal segmental duplications, or the genomic SEGMENTAL DUPLICATIONS: AN ?EXPANDING? ROLE IN GENOMIC INSTABILITY AND DISEASE Beverly S. Emanuel* ? and Tamim H. Shaikh* The knowledge that specific genetic diseases are caused by recurrent chromosomal aberrations has indicated that genomic instability might be directly related to the structure of the regions involved. The sequencing of the human genome has directed significant attention towards understanding the molecular basis of such recombination ?hot spots?. Segmental duplications have emerged as a significant factor in the aetiology of disorders that are caused by abnormal gene dosage. These observations bring us closer to understanding the mechanisms and consequences of genomic rearrangement. IMPRINTING A genetic mechanism by which genes are selectively expressed from the maternal or paternal homologue of a chromosome. UNIPARENTAL DISOMY A condition whereby an individual or embryo carries two chromosomes inherited from the same parent. NATURE REVIEWS | GENETICS VOLUME 2 | OCTOBER 2001 | 791 *Division of Human Genetics and Molecular Biology, 1002 Abramson Research Center, The Children?s Hospital of Philadelphia, 3516 Civic Center Blvd, Philadelphia, Pennsylvania 19104, USA. ? Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA. e-mails: beverly @mail.med.upenn.edu, shaikh@email.chop.edu REVIEWS � 2001 Macmillan Magazines Ltd 792 | OCTOBER 2001 | VOLUME 2 www.nature.com/reviews/genetics REVIEWS Misalignment, followed by recombination between non-allelic segmental duplications on homologous chromosomes, has been proposed to give rise to many genomic disorders, some of which are listed in TABLE 1. These disorders include Charcot?Marie?Tooth disease type 1A (CMT1A)/hereditary neuropathy with liability rearrangements they mediate, are near centromeres and telomeres 1?3 . In this review, we describe the genomic organization of several clinically relevant intrachromoso- mal segmental duplications, the chromosomal abnor- malities generated by them and the mechanisms by which they arise. STENOSIS The blocking of a blood vessel that can be cleared by mechanical disruption. ab c e 3 Mb (85?90%) 1.5 Mb (8%) 2 Mb (2%) DGS/VCFS 22q11 CES BP t(11 ; 22) BP CES BP 22 1.5 Mb CMT1A/HNPP 17p12 17q11 PMP22 17p11 SMS 5 Mb 17 1.5 Mb NF1 NF1 7q11 E L N 7 WBS 7q11 1.6 Mb 1.9 Mb Xp22 STS X X-linked ichthyosis Haemophilia A Xq28 F 8 E M D500 kb Inversion polymorphism 48 kb d 15q11?q13 4 Mb PWS/AS 15 Figure 1 | Chromosomal rearrangements mediated by segmental duplications. Chromosomes involved in rearrangements mediated by segmental duplications are depicted by ideograms. The chromosomal bands or regions involved in rearrangement are indicated and expanded. Segmental duplications are shown as filled boxes: green boxes indicate those involved in recurrent chromosomal rearrangements, whereas yellow boxes indicate other copies that are rarely, if ever, involved in chromosomal rearrangements. a | On chromosome 22, recurrent deletions associated with DiGeorge and velocardiofacial syndromes (DGS/VCFS) are shown with the frequency of a particular deletion 25 . The proximal and distal breakpoints (BPs) for the marker chromosomes in cat eye syndrome (CES) and the t(11; 22) BP region are also indicated. b | On chromosome 17, the region on 17p12 that is duplicated/deleted in Charcot?Marie?Tooth disease type 1A and hereditary neuropathy with pressure palsies (CMT1A/HNPP) is shown with PMP22 (peripheral myelin protein 22), the gene involved in their aetiology. Also on 17p11 is the region involved in the Smith?Magenis syndrome (SMS) deletions and the reciprocal duplication. On 17q11 is the region involved in neurofibromatosis type 1 (NF1) deletions. c | Three rearrangements of chromosome X include the region on Xp22 that contains the steroid sulfatase (STS) gene, which is deleted in X-linked ichthyosis; the region on Xq28 that contains the factor VIII (F8) gene, which is inverted in haemophilia A; and the region on Xq28 that contains a polymorphic inversion in the vicinity of the emerin (EMD) gene. EMD is involved in Emery?Dreifuss muscular dystrophy. d | The region on chromosome 15q11?q13 that is deleted in Prader?Willi and Angelman syndromes (PWS/AS) is shown with its numerous duplicated HERC2 (hect domain and RLD 2) gene segments. e | On 7q11, the deletion associated with Williams?Beuren syndrome (WBS) is shown with elastin (ELN), the principal gene responsible for the supravalvular aortic STENOSIS of WBS. � 2001 Macmillan Magazines Ltd NATURE REVIEWS | GENETICS VOLUME 2 | OCTOBER 2001 | 793 REVIEWS are 24 kb in size and share 98.7% nucleotide sequence identity 32 . Recent reports indicate that there might be other low-copy repeats near the CMT1A-REPs, but these do not seem to be directly responsible for the rearrange- ments that lead to CMT1A/HNPP 34 . Other simple seg- mental duplications include the S232 elements that mediate the deletions associated with X-linked ICHTHYOSIS 35?37 , the two 11.3-kb inverted repeats on the X chromosome that mediate the inversion in the emerin gene (responsible for Emery?Dreifuss muscular dystro- phy) gene and show >99% sequence identity 38 , and the int22h (intron 22 homologous region) sequence, which mediates the inversion in the factor VIII gene that leads to haemophilia A (FIG. 1) 39,40 . In contrast to these simple structures, segmental duplications that are large and have a complex organi- zation have been shown to mediate chromosomal rearrangements in several genomic disorders. The complex segmental duplications on 22q11 that mediate constitutional rearrangements, including deletions, interstitial duplications, supernumerary marker chro- mosomes, inversions and translocations, have been characterized extensively 5,24,25 . There are differences in the size, content and organization of duplicated mod- ules in each copy of the 22q11 segmental duplica- tion 25,26 . These segmental duplications contain several truncated gene segments or pseudogenes, which include BCRL, HMPLPL (POM121L), GGTL, GGTrelL, V7 rel, E2F6L, KIAA0649L and others 23,25 . A few of the 22q11 duplications also contain potentially recombino- genic sequences, which include palindromic (A+T)- rich repeats (PATRR) and variable-number tandem- repeat sequences 5,25 . The PATRR present in one of the duplication copies on 22q11 has been proposed to cause genomic instability as it has been shown to be directly involved in the constitutional t(11; 22), as well to pressure palsies (HNPP) on chromosome 17p11.2 (REFS 13,14), neurofibromatosis type 1 (NF1) on 17q11.2 (REF. 15), Prader?Willi/Angelman syndromes (PWS/AS) on 15q11?q13 (REFS 16,17), Williams?Beuren syndrome (WBS) on 7q11.23 (REFS 18,19), Smith?Magenis syndrome (SMS)/duplication 17p11.2 on 17p11.2 (REFS 20,21) and several rearrangements associated with 22q11, including DiGeorge and velocardiofacial syndromes (DGS/VCFS) and cat eye syndrome (CES) 22?25 . The genomic instabili- ty that is related to the structure of 22q11.2 was suspect- ed to underlie the numerous nonrandom rearrange- ments that take place in this region long before the genomic sequence of chromosome 22 became avail- able 26 . So far, a total of eight segmental duplications have been identified on chromosome 22q11 (REFS 5,26) (FIG. 1a). Four copies of the segmental duplications in proximal 22q11 have been identified within and flank- ing the DGS/VCFS region and at the end points of the CES duplications 22,23,25,27 . Furthermore, the breakpoint of the only recurrent, non-Robertsonian, CONSTITUTIONAL TRANSLOCATION [t(11; 22)] takes place in one of these duplications 28?31 , also implicating the segmental dupli- cations in non-homologous interchromosomal recom- bination events. Structure of segmental duplications The segmental duplications that mediate the chromoso- mal rearrangements seen in genomic disorders show various organizational configurations. They can either be simple in structure or contain a complex arrange- ment of duplicated modules. The best-characterized example of a simple segmental duplication is the CMT1A-REP (REP, repeat) (FIG. 1b), which mediates the interstitial duplication or deletion associated with CMT1A or HNPP, respectively 13,32,33 . The two copies of CMT1A-REP that flank the duplicated/deleted region CONSTITUTIONAL TRANSLOCATION A rearrangement between two chromosomes that occurs in the parental germ line or very early in embryonic development, such that every cell in the body contains the translocated chromosomes. ICHTHYOSIS A genetic disorder that causes the patient to have scaly skin. Table 1 | Genomic disorders mediated by segmental duplications Genomic disorder Chromosomal Chromosomal Rearrangement References rearrangement location size (Mb) Charcot?Marie?Tooth disease Interstitial 17p12 1.5 13,14 type 1A (CMT1A) duplication Hereditary neuropathy with Deletion 17p12 1.5 13,14 pressure palsies (HNPP) Smith?Magenis syndrome (SMS) Deletion 17p11.2 5 20 Duplication 17p11.2 Interstitial 17p11.2 5 21 duplication Neurofibromatosis type1 (NF1) Deletion 17q11.2 1.5 15 Prader?Willi syndrome (PWS) Deletion 15q11?15q13 4 16,17 Angelman syndrome (AS) Deletion 15q11?15q13 4 16,17 Inverted duplication 15 Supernumerary 15q11?15q14 4 73?76 (inv dup (15)) marker chromosome Williams?Beuren syndrome (WBS) Deletion 7q11.23 1.6 18,19 DiGeorge and velocardiofacial Deletion 22q11.2 3 23?25 syndromes (DGS/VCFS) Cat eye syndrome (CES) Supernumerary 22q11.2 3 22 marker chromosome X-linked ichthyosis Deletion Xp22 1.9 56?58 Haemophilia A Inversion Xq28 0.5 39,40 � 2001 Macmillan Magazines Ltd 794 | OCTOBER 2001 | VOLUME 2 www.nature.com/reviews/genetics REVIEWS have occurred relatively recently during primate evolu- tion, ~1?25 million years (Myr) ago. This is based on the observations that there are differences in the copy num- ber and location of the duplications on the chromo- somes of representative members of the higher primates 5?9,16,50 . The duplications implicated in the rearrangement that leads to CMT1A ? the CMT1A- REP ? seem to be human and chimpanzee specif- ic 32,34,47,51 . Similarly, the segmental duplications that mediate the rearrangements leading to PWS/AS are esti- mated to have originated ~15?20 Myr ago 16,43 . Comparative mapping of the mouse genome in the region of CONSERVED SYNTENY with human 22q11.2 has shown no evidence for the presence of the segmental duplications 52?55 . By contrast, duplicated sequences that are orthologous to the 22q11 segmental duplications have recently been identified in non-human primates, including great apes, and Old World and New World monkeys 5,25 . Furthermore, there seems to have been a sequential increase in copy number of duplications dur- ing primate evolution 5 . This indicates that the 22q11 seg- mental duplications have originated relatively recently during the evolution of the primate genome and, there- fore, that segmental duplications might have been important in the evolution of the primate genome by rapidly generating genomic diversity between closely related primate species. It is tempting to speculate that the processes responsible for the generation and ?expan- sion? of segmental duplications are continuing and are therefore likely to have contributed to heteromorphism in the normal human population. Segmental-duplication-mediated rearrangements Deletions. In most patients with X-linked ichthyosis, the disorder is caused by a deletion of the steroid sulfatase (STS) gene on Xp 56?58 . Patients with STS deletions and X-linked ichthyosis have breakpoints that cluster in highly homologous sequence elements that flank the STS locus and are separated by 1.9 Mb on the short arm of the X chromosome 35 (FIG. 1c). The common repeat units are small, and the recombination events seem to involve repeats that are in the same orientation on the chromosome 35,36 . So, segmental duplications can lead to deletions through ?slipped pairing? (aberrant pairing between mismatched copies of the segmental duplica- tion) and unequal crossing over in meiosis. Excessive homologous recombination with unequal crossing over has been shown at the deletion end points of several deletion syndromes. WBS is due to a deletion of ~1.6 Mb in 7q11.23, which includes the elastin (ELN) gene 59 (FIG. 1e). It has been shown that there is a high frequency of recombined HAPLOTYPES in the segments that flank the de novo WBS deletions 60?62 . There is evidence that the WBS deletions are related to the presence of segmental duplications at the deletion breakpoints 63,64 . The region of the duplication has been characterized and shown to contain a transcribed gene 18 . Furthermore, the recombination event seen in several unrelated individuals seems to be similar, resulting in a junctional fragment that deletes the functional copy of this gene. as in other translocations that involve chromosome 22 (REFS 30,31,41,42). Other large and complex segmental duplications include those on 17p11.2, which mediate the deletions associated with SMS and its reciprocal interstitial duplication product 20 . They contain at least four genes or pseudogenes 20,21 . The segmental duplications on 15q11?q13 that mediate the PWS/AS-associated dele- tions are also large and complex 16,17 . These are com- posed to a large extent of duplications of the HERC2 (hect (homologous to the E6-AP carboxyl terminus) domain and RLD 2) gene 17,43 . It has been proposed that the HERC2-containing duplications have evolved a complex configuration by a complicated pathway that includes deletions and inversions 44 . Additional complexity in the organization of segmental duplica- tions on 15q has been reported recently. These newly recognized duplications are found not only on 15q11?q13, but also on 15q24 and 15q26 (REF. 45).The three segmental duplications that mediate the dele- tions of 7q11.23 that are associated with WBS, also contain several genes or pseudogenes arranged in complex configurations 46 . Similarly, the segmental duplications that mediate the NF1 deletions, NF1- REPs, are 15?100 kb in size and contain at least four ESTs (expressed sequence tags) and an expressed SH3GL (SH3-domain GRB2-like) pseudogene 15 . Although only a few of the rearrangements that are mediated by segmental duplications have been analysed at the nucleotide level, there is evidence for recombina- tion hot spots in the segmental duplications. The PATRR in one of the 22q11 segmental duplications dis- cussed above has been shown to be a recurrent break- point for the t(11; 22) translocation 30,31,42 . The t(11; 22) breakpoints all localize in the PATRR, directly implicat- ing them in the rearrangement mechanism 30 . In addi- tion to the 22q11 PATRRs, recombination hot spots in segmental duplications on other chromosomes have also been described. The rearrangement breakpoints associated with CMT1A/HNPP seem to localize to a hot spot in the CMT1A-REP on 17p11.2 (REFS 47,48).The breakpoints of 21 out of 23 unrelated HNPP patients were mapped within a 557-bp region, further refining the hot spot within the CMT1A-REP 33 . The presence of a mariner transposon-like element very close to the CMT1A/HNPP breakpoints had led to the suggestion that the mariner-like element was somehow involved in the recombination 33,48 . However, there is no direct evi- dence to support the involvement of a mariner or any other specific sequence in the rearrangements associat- ed with CMT1A/HNPP. In 46% (n = 54) of unrelated patients with the NF1 deletion, the breakpoints in the NF1-REPs were localized within a 2-kb hot spot that contains a ?-like sequence 49 .In Escherichia coli, ?-ele- ments stimulate recombination in nearby sequences. However, there is no direct evidence for the involvement of any particular sequence, including the ?-like sequences, in the NF1 deletion. The segmental duplications that are known seem to be limited to the genomes of primates. Phylogenetic analyses have indicated that most of these duplications CONSERVED SYNTENY The occurrence of genomic collinearity between homologous genes in different organisms. HAPLOTYPE An experimentally determined profile of genetic markers present on a single chromosome of any given individual. � 2001 Macmillan Magazines Ltd NATURE REVIEWS | GENETICS VOLUME 2 | OCTOBER 2001 | 795 REVIEWS The most common rearrangements associated with chromosome 22 are the deletions in 22q11.2 that are associated with DGS/VCFS. A typically deleted region (TDR) of ~3 Mb is observed in ~85?90% of patients with the 22q11.2 deletion (FIGS 1 and 2). So, there seems to be both a typical proximal and a typical distal deletion end point (DEP) 5,25 . In addition, there are two recurrent, variant distal DEPs. Furthermore, four out of the eight regions that contain the 22q11 segmental duplications coincide with the recurrent DEPs 5,24,25 . The direct involvement of these 22q11 segmental duplications in recombined deletion end-point junction fragments has been recently shown by PULSED-FIELD GEL ELECTROPHORESIS 25 . Hypotheses that would explain these findings have been constructed on the basis of the organization and orienta- tion of the blocks of repeats 5,24 . Duplications/deletions. For several distinct clinical disor- ders, for example CMT1A (duplication) and HNPP (deletion), the existence of both reciprocal products of unequal crossovers in 17p has been observed 14 . These autosomal-dominant peripheral neuropathies result from unequal exchange between misaligned CMT1A- REP elements that are separated by 1.5 Mb on 17p12 (REFS 13,14,67) (FIG. 1b). This 1.5-Mb region contains the PMP22 (peripheral myelin protein 22) gene, which seems to be dosage sensitive and is involved in the aetiol- ogy of the phenotype associated with CMT1A/HNPP 68 . A similar model has been shown for the SMS deletion 20 and the reciprocal interstitial duplication of the same region of 17p11.2, leading to a phenotype that is distinct from SMS 21 . This 17p11.2, deletion/duplication is ~5 Mb in most patients but the gene(s) that contribute to SMS and the reciprocal interstitial duplication are still unknown 20,21 (FIG. 1b). Inversions. It has been shown that the local DNA- sequence environment has an important function in intragenic deletions or rearrangements 69 . A notable example of this is the rearrangement ?hot spot? that has been described for the factor VIII gene associated with ~45% of patients with haemophilia A. A functional ?deletion? that is caused by disruption of the factor VIII gene results from the presence of small segmental dupli- cations that share a high level of sequence identity. These sequences, referred to as int22h, lie within intron 22 of the factor VIII gene; two additional copies are located in the reverse orientation ~500 kb telomeric to the factor VIII gene 39,40 . These sequence elements allow the distal long arm of the X chromosome to bend back on itself during meiosis, such that breakage and reunion causes an inversion that disrupts the factor VIII gene 70 (FIG. 1c). It is interesting that these inversions occur pri- marily in the male germ line, indicating that X-chromo- somal pairing during meiosis in females might inhibit the distal long arm of the X chromosome from dou- bling back on itself and self pairing 71 . Another, perhaps more striking, example comes from the analysis of the genomic region that surrounds the emerin gene on Xq28, which is flanked by two large inverted repeats (FIG. 1c). Characterization of an emerin PWS and AS are most commonly associated with an ~4-Mb deletion of 15q11?q13 [del(15)(q11?q13)] 16,17 (FIGS 1 and 2). There is evidence that both inter- and intrachromosomal rearrangements take place 65,66 : unequal crossovers during recombination, as well as intrachromosomal recombinational exchanges, occur. The chromosome 15 deletion breakpoints cluster in consistent hot spots, and large segmental duplications span the proximal and distal breakpoint regions 17 .NF1 has been reported to be due to a 1.5-Mb deletion that includes the NF1 gene in a minority of patients (2?13%) (FIG. 1). These deletions seem to be mediated by segmental duplications that are referred to as NF1-REPs 15 . PULSED-FIELD GEL ELECTROPHORESIS An electrophoretic technique used to separate large fragments of DNA (>20 kb and up to 10 Mb) on an agarose gel by periodically changing the orientation of the electric field applied to the gel. q11 q13 Critical region Prader?Willi/ Angelman syndromes 22 22 q11.21 q11.23 Critical region DiGeorge/velocardio- facial syndromes q11.2 inv dup (22) q11.2 cat eye syndrome inv dup (15)s q11 q12 small large q11 q12 q13 1515 a bd Deletions c Inverted duplications Figure 2 | Chromosomes 15 and 22: deletions and inverted duplication chromosomes. Ideograms and partial karyotypes are shown. For the deletions, the arrows indicate a | the deletion of chromosome 15q11?13 associated with Prader?Willi and Angelman syndromes, and b | the deletion of 22q11.21?11.23 (bottom) associated with DiGeorge and velocardiofacial syndromes. c | For the inverted duplications, the ideograms and partial karyotypes of two chromosome 15s show the two different sizes of inv dup (15) chromosomes. The smaller inv dup (15), on the left, is not associated with phenotypic abnormalities, whereas the larger inv dup (15), on the right, is associated with an abnormal phenotype (the central two are normal chromosome 15). d | The inv dup (22) (right) is associated with the cat eye syndrome. (Modified with permission from REF. 91.) � 2001 Macmillan Magazines Ltd 796 | OCTOBER 2001 | VOLUME 2 www.nature.com/reviews/genetics REVIEWS Other rearrangements. At the chromosomal level, another class of frequently observed rearrangements consists of translocations. Translocations can be divided into Robertsonian and reciprocal translocations. Robertsonian translocations involve exchanges between the short arms of the ACROCENTRIC chromosomes and seem to be mediated by satellite DNA repeats close to the centromeres 79 . Reciprocal, non-Robertsonian con- stitutional translocations are the result of crossover between two non-homologous chromosomes and most are known to be unique events. So, little is known about the mechanisms or sequences involved in the formation of most reciprocal translocations. The t(11; 22)(q23; q11) is the only known recurrent, non-Robertsonian constitutional translocation in humans. Balanced translocation carriers have no clinical symptoms, and clustered breakpoints have been reported in numerous unrelated families 28,29,31 . The t(11; 22) breakpoint on 22q11 localizes to one of the segmental duplications on 22q11 (REFS 25,28,30,31). Although chromosome 22 has been almost entirely sequenced, the segmental duplication at which the t(11; 22) breakpoint resides still contains a gap 5,25,26 . It has been shown that palindromic (A+T)-rich sequences surround the breakpoints on chromosomes 11 and 22 (REFS 30,31,42). Computer analysis of the DNA sequence that flanks the breakpoints predicts the formation of hairpin or cruciform structures 30 . It is likely that these unstable DNA structures in 22q11 and 11q23 facilitate the recurrent t(11; 22) translocation. Also, the segmen- tal duplication on 22q11 that contains the chromosome 22 breakpoint of the t(11; 22) seems to be a hot spot for other reciprocal translocations. These include a bal- deletion in a patient with Emery?Dreifuss muscular dystrophy showed ? in addition to the gene deletion ? a partial duplication of nearby sequences, recombi- nation between the inverted repeats and an inversion of this region in 33% of normal females 38 . So, in this instance, the inversion represents a benign, population- based variant that is mediated by the presence of dupli- cated sequences. Marker chromosomes. The second most common rearrangement associated with chromosome 15, after the deletions associated with PWS/AS, is the inverted dupli- cation (inv dup (15)), which seems to be the most com- mon marker chromosome in newborns 72 . There are sev- eral types of inv dup (15) marker chromosome, based on their size and rearrangement breakpoints 73?76 (FIG. 2). Most of the inv dup (15) chromosome breakpoints also seem to cluster within the segmental duplications in 15q11?q13 16,73,75,77 . In CES, a BISATELLITED chromosome that results from an inverted duplication of proximal 22q11 is present as a supernumerary chromosome 22 (FIG. 2). The breakpoints of marker chromosomes in CES patients seem to localize to copies of the segmental duplications in 22q11. The more proximal, most com- mon cat eye chromosome (CEC) breakpoint interval corresponds with the proximal DGS/VCFS deletion end- point interval. The more distal duplication breakpoint of the CEC overlaps with the common distal DGS/VCFS deletion. The resultant marker chromosomes have been divided into three categories on the basis of their size and location of the breakpoints 22 . Furthermore, recent detailed sequence analysis has begun to examine the genes that are duplicated in CES 78 . BISATELLITED A chromosome that contains two copies of the satellited acrocentric short arm, often as a result of an inverted duplication. It is usually present as a supernumerary marker chromosome in a cell. ACROCENTRIC This refers to a chromosome the centromere of which lies very close to one end, such that one arm of the chromosome is much larger than the other. ab Centromere Centromere Deletion M1 M2 M3 M2 M1 M2 M3 M4 M1 M2 M3 M4 M1 M1 M4 M1 M4 M2 M3 M2 M3 M2 M3 M4 M3 M4 M1 M4 Duplication + x + Deletion Deleted fragment � Paracentric inversion M1 M4 M3 M2 � Figure 3 | Models for formation of deletions and duplications. Chromosomes are shown as lines. Black and red are used to distinguish the two homologues. Segmental duplications are shown as yellow or green boxes. a | Interchromosomal recombination between the two homologues of a particular chromosome leads to a reciprocal deletion and duplication. b | Intrachromosomal recombination between segmental duplications on the same chromosome leads to either a deletion or a paracentric inversion. (Modified with permission from REF. 5.) � 2001 Macmillan Magazines Ltd NATURE REVIEWS | GENETICS VOLUME 2 | OCTOBER 2001 | 797 REVIEWS between the duplicated modules forming the ?stem? would then lead to the deletion of intervening DNA pre- sent in the ?loop? (FIG. 3b). This mechanism has been used to explain the deletions associated with NF1 (REF. 15),a few deletions associated with HNPP 83 and some dele- tions associated with DGS/VCFS 5,23,25,62 . Another possible outcome of the intrachromosomal misalignment between inverted segmental duplications is a paracentric inversion (FIG. 3b). This mechanism might explain the intrachromosomal inversions observed in the factor VIII gene that lead to haemophilia A 70 , the polymorphic but benign inversion found close to the emerin gene 38 and the inversions that disrupt the iduronate sulfatase (IDS) gene in Hunter syndrome 87 . Inter- and intrachromosomal recombination events have been reported for the standard 3-Mb deletion associated with DGS/VCFS 23,62,86 , as well as for the genomic aberrations that occur in PWS/AS 65,66 and CMT1A/HNPP 83?85 . Furthermore, the existence of indi- viduals that are mosaic for deletions of 22q11 indicates that mitotic instability does occur 88?90 . Interestingly, although the deletions associated with DGS/VCFS are seen frequently, the reciprocal interstitial duplication event is rarely observed 24 . This is presumed to be the result of a mild and/or nonspecific phenotype. Marker chromosomes. The formation of a bisatellited, supernumerary marker chromosome that is mediated by segmental duplications can be explained using one of two possible models. In the first model, interchromoso- mal misalignment occurs between the two homologues of a particular chromosome by virtue of the segmental duplications or modules within them that lie in oppo- site orientation with respect to one another. Recombination between these inverted sequences could anced t(20; 22) 80 , three unbalanced [t(12; 22), t(4; 22), t(17; 22)] 81 and a balanced t(1; 22) 82 . So, it seems that this copy of the 22q11 duplication might contain sequences or secondary structures that are permissive to translocation. Mechanistic models for rearrangements The sequence analysis of segmental duplications has shown 96?99% sequence identity between duplicated copies over their entire length 4 . On the basis of this high level of sequence identity, several models can be pro- posed to explain the chromosomal rearrangements that are mediated by segmental duplications. Deletions, duplications/deletions and inversions. Deletions could be explained using one of two possible models (FIG. 3). In the first model, an interchromosomal misalignment might occur during meiosis I between the two homo- logues of a particular chromosome. This misalignment might be mediated by the segmental duplications, or by modules within them that lie in direct orientation with respect to each other. Crossing over would lead to recipro- cal deletion and duplication events (FIG. 3a). This mecha- nism has been used to explain the deletions associated with WBS 60?62 and those associated with SMS, as well as the reciprocal interstitial duplication 20,21 , some of the reci- procal interstitial duplications/deletions associated with CMT1A and HNPP 14,83?85 , and some of the deletions asso- ciated with PWS/AS 17,65,66 and DGS/VCFS 5,23,25,62,86 . The formation of deletions can also be explained by intrachromosomal recombination between segmental duplications during mitosis or meiosis. In this model, the segmental duplications, or modules within them, that lie in inverse orientation with respect to one another might form a ?stem?loop? intermediate. Recombination a Bisatellited chromosome Acentric fragment + M4 M1M2M3 M1 M4 M4M3 M3M2 M2 M1 Centromere M1 M2 M3 M4 x + Paracentric inversion b M1 M2 M3 M4 M1 M3 M2 M4 M1 M2 M3 M4 M1 M4 M2 M3 � + Acentric fragment Bisatellited chromosome Inversion loop M2M2M3M3 M1 M4 M1 M4 M1 M1M3 M2 M4 M3 M2 M4 Figure 4 | Models for formation of cat eye syndrome or inv dup (15) marker chromosomes. Chromosomes are shown as lines. Black and red are used to distinguish the two homologues. Segmental duplications are shown as yellow or green boxes. a | Interchromosomal recombination between the two homologues of a particular chromosome, or b | paracentric inversion in one homologue of a chromosome, followed by recombination in an inversion loop, leads to the formation of a bisatellited marker chromosome and an acentric fragment. Both models can be used to explain all three described types of cat eye chromosome and the formation of the inv dup (15) marker chromosome. (Modified with permission from REF. 5.) � 2001 Macmillan Magazines Ltd 798 | OCTOBER 2001 | VOLUME 2 www.nature.com/reviews/genetics REVIEWS and other bisatellited marker chromosomes result from one or a combination of the models proposed for the CES marker chromosome formation. Other rearrangements. The chromosome 22 breakpoint of the recurrent, constitutional t(11; 22) has been local- ized to one of the 22q11 segmental duplications 30 .Many other balanced and unbalanced translocation break- points also cluster in the same region of 22q11. This fur- ther indicates that this region of 22q11 might contain unstable sequences that predispose it to be involved in translocations. The recent cloning and sequencing of the recurrent, constitutional t(11; 22) breakpoint and the identification of PATRRs at the site of the transloca- tion strongly support this hypothesis 30,42 . Analysis of the available sequence indicates the presence of large palin- dromes that flank the t(11; 22) breakpoint regions on both chromosomes. It has been proposed that these palindromic sequences lead to the formation of hairpins or cruciforms at physiological temperature 30,31 .The translocation breakpoints localize to the tips of the hair- pin/cruciform (B.S.E., unpublished data). Because the tip of the hairpin is sensitive to nucleases, the initiating step of the translocation might be a double-stranded break mediated by this hairpin-nicking activity. Recombination between the nicked chromosome 22 and any other chromosome with similar nicks could lead to a translocation between the two chromosomes (FIG. 5). Although the recurrent, constitutional t(11; 22) seems to be mediated by such a mechanism, there could be additional factors that facilitate this particular recombination event 30,42 . Conclusions and future directions Based on the examples discussed above, it is clear that segmental duplications can create genomic instability by predisposing certain chromosomes or chromosomal bands to rearrangements through misalignment and unequal crossing over. The proposed inter- or intra- chromosomal recombination between copies of the seg- mental duplications might result in deletions, interstitial duplications, inversions, translocations and marker chromosomes. An analysis of the draft human genome sequence indicated that up to 5% of the human genome might be comprised of segmental duplications greater than 10 kb in size 4 . As the human genome sequence approaches completion, many more segmental duplica- tions will probably be identified. So, in the future, more instances of segmental duplications will, no doubt, be shown to be responsible for various genomic disorders. We expect these regions of genomic instability to be principal contributors to the burden of cytogenetic abnormalities seen in a clinical setting. Several models, including those presented here, have been proposed for the mechanisms that are involved in chromosomal rearrangements that are mediated by segmental duplications. It is unclear whether there are precise sequences in the complex, segmental duplications that are directly associated with facilitating the rearrangements. Recombination- promoting sequences have been identified in the lead to the formation of a bisatellited chromosome and an ACENTRIC fragment (FIG. 4a). This model can be used to explain all three types of CEC that have been identified 22 . Therefore, if the misalignment and recom- bination occur between the proximal copies of the 22q11 segmental duplication on both homologues (as shown in FIG. 4a), they would give rise to a type I CEC. Alternatively, the symmetrical type II CEC would result from a misalignment and recombination between the distal copies of the 22q11 segmental duplication (green boxes in FIG. 4a). Finally, misalignment and recombina- tion between any one proximal (yellow box) and any one distal (green box) copy of the segmental duplica- tion would result in the formation of an asymmetrical type II CEC. In the second model, intrachromosomal recombi- nation ? facilitated by the segmental duplications during mitosis or meiosis ? could first lead to a PARACENTRIC INVERSION (FIG. 4b) in one of the homologues of a particular chromosome. Subsequently, a single crossover event between paired homologues within the inversion loop could lead to the formation of the duplication/deficiency CES marker chromosome and an acentric fragment (FIG. 4b). This model might explain the formation of some of the asymmetrical CES chromosomes 22 . It is likely that the inv dup (15) ACENTRIC A chromosome or chromosomal fragment that lacks a centromere. PARACENTRIC INVERSION An inversion of a chromosomal segment that does not contain the centromere. a b c Nicks created by nuclease Centromere Chromosome 22q11 cen tel M4M3 M3 M3 M2 M2 cen tel Translocation der (22) der ('N') M2 M2 N2 N2 N1 N1 M3 M3 + Chromosome 'N' cen tel M2 M3 M2 M3 N1 N2 N1 N2 M2M1 Figure 5 | Model for translocations in 22q11. a | The segmental duplication to which the translocation breakpoint localizes is shown as a green box. Other segmental duplications are shown as grey boxes. b | An expanded view of the region that contains the translocation breakpoint region is shown. The centromeric (cen) and telomeric (tel) ends are indicated. The palindromic sequences (green lines) are predicted to form a hairpin/cruciform structure on chromosome 22. The tips of the cruciforms could be prone to nicking by nucleases. c | A chromosome 22 with double-stranded breaks within the palindrome could recombine with another chromosome (chromosome ?N?) that has similar double-stranded breaks. This would lead to a translocation between chromosome 22 and chromosome ?N? and result in the formation of two derivative (der) chromosomes: der (22) and der (?N?). Most often the ?N? is chromosome 11. (Modified with permission from REF. 5.) � 2001 Macmillan Magazines Ltd NATURE REVIEWS | GENETICS VOLUME 2 | OCTOBER 2001 | 799 REVIEWS genome have been identified and sequenced, very little is known about their formation and amplification in the genome. Furthermore, the extent that these segmental duplications contribute to normal human variation is not known. To better understand segmental duplica- tions and their effect on human disease, future efforts will need to be aimed at elucidating the mechanisms that are involved in their formation and spread in the human genome. It should also be interesting to deter- mine whether segmental duplications have amplified during recent human evolution, which might have resulted in genomic variability in the human popula- tion. Such a finding should help to assess the involve- ment of segmental duplications in creating genetic vari- ation that could lead to the genomic instability that is associated with human genetic disorders. 22q11 segmental duplications 5,25,30 , CMT1A-REP 47,48 and NF1-REP 49 . Based on the example of t(11; 22), it is likely that the unstable, recombination-susceptible sequences present at the breakpoints might lead to double-stranded breaks, which in turn promote the observed chromosomal rearrangements. Further investigation of the precise breakpoints in several indi- viduals with each type of genomic disorder will shed additional light on the mechanism of such recombina- tion and rearrangement events. Genetic change, besides being a principal driving force for evolution, is also a source of human disorders. Segmental duplications represent an under-appreciated source of genetic change owing to their ability to act as substrates for aberrant genomic rearrangements. 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Genet. 75, 288?291 (1998). 90. Anguiano, A. et al. Report of a case with manifestations of DiGeorge/velocardiofacial syndrome (VCFS) and microdeletion 22q11.2 mosaicism. Am. J. Hum. Genet. 67, S142 (2000). 91. Spinner, N. B. & Emanuel, B. S. in Principles and Practice of Medical Genetics Vol. 1 (eds Rimoin, D. L., Conner, J. M., Pyeritz, R. E. & Emery, A. E. H.) 999?1025 (Churchill Livingstone, 1996). Acknowledgements The authors acknowledge support for their efforts from the National Institutes of Health. B.S.E. gratefully acknowledges the support provided by the Charles E. H. Upham chair in Pediatrics. T.H.S. is partially supported by funds from the Florence R. C. Murray Foundation. Online links DATABASES The following terms in this article are linked online to: LocusLink: http://www.ncbi.nlm.nih.gov/LocusLink/ ELN | emerin | HERC2 | IDS | NF1 | PMP22 | STS OMIM: http://www.ncbi.nlm.nih.gov/Omim/ Angelman syndrome | cat eye syndrome | Charcot?Marie?Tooth disease type 1A | DiGeorge syndrome | Emery?Dreifuss muscular dystrophy | haemophilia A | hereditary neuropathy with liability to pressure palsies | Hunter syndrome | neurofibromatosis type 1 | Prader?Willi syndrome | Smith?Magenis syndrome | velocardiofacial syndrome | Williams?Beuren syndrome � 2001 Macmillan Magazines Ltd "
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