Recombination Hot Spots and Human Disease Smita M

Recombination Hot Spots and Human Disease Smita M

Downloaded from genome.cshlp.org on September 28, 2021 - Published by Cold Spring Harbor Laboratory Press REVIEW Recombination Hot Spots and Human Disease Smita M. Purandare1 and Pragna I. Patel1–4 Departments of 1Neurology, 2Molecular and Human Genetics and 3Division of Neuroscience, Baylor College of Medicine, Houston, Texas 77030 Recombination between homologous DNA se- phic VNTRs (variable number tandem repeats) or quences occurs in all organisms, and the resultant hypervariable minisatellite DNA, where the size of exchange of information is critical for the survival the repeat unit ranges from 9 to 24 bp. VNTRs have of species. Recombination is an essential cellular been shown to be hot spots for homologous recom- process catalyzed by proteins explicitly expressed bination in human cells (Wahls et al. 1990). Micro- for this purpose. It provides an effective means of satellite DNA consists of small arrays of tandem re- generating genetic diversity that is important for peats (usually 1–4 bp units) that are interspersed evolution. The proteins involved in recombination throughout the genome, in blocks consisting of allow cells to retrieve sequences lost when DNA is <150 bp. damaged by radiation or chemicals, by replacing the In contrast to tandemly repeated DNA, inter- damaged section with an undamaged strand from a spersed repetitive DNA consists of repeat units dis- homologous chromosome. The process of homolo- persed throughout the genome. Based on the repeat gous recombination has also been used to study unit length, two major classes are recognized: short gene function by way of gene knockouts. However, interspersed nuclear elements [(SINES) e.g., the Alu recombination and factors involved in recombina- repeat family] and long interspersed nuclear ele- tion may also be a source of harmful mutations and ments [(LINES) e.g., the LINE-1 or L1 element disease. (Singer 1982)]. The Alu repeat containing a 280-bp Specific DNA sequences are known to mediate repeat unit occurs approximately once every 4 kb in or enhance the rate of recombination in the ge- the human genome. Mispairing between such re- nomes of many organisms. Attempts to identify and peats has been shown to be a frequent cause of de- decipher recombination hot spots have focused on letions and duplications. Breakpoints of disease- determining the influence of various DNA se- causing deletions have been clustered within Alu quences on the rate and type of DNA rearrange- sequences in genes for the low density lipoprotein ments. The human nuclear genome contains a large receptor (LDLR) (Lehrman et al. 1985, 1987), and number of highly repeated DNA sequence families the complement component 1 inhibitor (C1I) (Jelinek and Schmid 1982; Hardman 1986; Vogt (Stoppa-Lyonnet et al. 1991). Such observations 1990), broadly classified as tandemly repeated DNA have suggested a general role for Alu sequences in or interspersed repetitive DNA. Because of their role promoting recombination and recombination-like in mediating disease-causing recombination errors, events. Alu repeats or other dispersed repetitive ele- a brief overview of the various repeats is presented. ments are also thought to have played a role in the Tandemly repeated DNA is characterized by evolution of clustered multigene families by medi- blocks or arrays of tandemly repeated DNA se- ating unequal crossover events that lead to gene du- quences. They are subclassified based on the size of plications. The average length of the L1 element re- the blocks or arrays of tandem repeats into satellite peat unit is 1.4 kb. In addition, there are smaller (0.1 to >2 Mb), minisatellite (0.1–2.0 kb), and mic- repeat sequence families belonging to this class, in- rosatellite (∼150 bp) DNA. Satellite DNA is further cluding the THE-1 (transposable human elements), sub-classified based on the size of the repeat unit MER (medium reiteration), HERV (human endog- within these blocks into types 1 (25–48 bp), 2 and 3 enous retroviruses), and RTLV (retrovirus-like ele- (5 bp), a (alphoid DNA; 171 bp), and b (Sau3A fam- ments) repeats. Members of many of the inter- ily; 68 bp). Minisatellite DNA consists of telomeric spersed repeat families are considered retrotranspos- DNA that has a 6-bp repeat unit, and the polymor- able elements, that is, unstable DNA elements that can migrate to different regions of the genome by transposition via an RNA intermediate. These en- 4Corresponding author. dogenous retroposons are thought to have played E-MAIL [email protected]; FAX (713) 798-8526. an important role in shaping the genomes of verte- 7:773–786 ©1997 by Cold Spring Harbor Laboratory Press ISSN 1054-9803/97 $5.00 GENOME RESEARCH 773 Downloaded from genome.cshlp.org on September 28, 2021 - Published by Cold Spring Harbor Laboratory Press PURANDARE AND PATEL brates by intracellular transposition events and by meiosis (Pentao et al. 1992; Chance et al. 1994) generating hot spots of recombination (Leib-Mosch or intrachromosomally because of either sister chro- and Seifarth 1995). matid exchange during mitosis or DNA slippage The various families of repetitive elements are during replication (Krawczak and Cooper 1991). highly relevant to a number of different mecha- Charcot-Marie-Tooth disease type 1A (CMT1A) nisms of mutagenesis in human genes. As discussed and hereditary neuropathy with liability to pressure in the following sections, recombination between palsies (HNPP) are two autosomal dominant periph- such sequences can lead to rearrangements, includ- eral neuropathies resulting from DNA rearrange- ing deletions, duplications, inversions, and fusion ments that are reciprocal products of an unequal genes. crossing-over event between misaligned flanking CMT1A–REP (repeat) elements on chromosome 17p (Chance et al. 1994; Patel and Lupski 1994) (Fig. 1). Deletions and Duplications Caused by Homologous The proximal and distal CMT1A–REP elements are Recombination ∼30 kb in length, extremely AT rich (64% A + T), and display 98% sequence identity (Reiter et al. Hot spots of homologous recombination between 1996). Given the high degree of homology between misaligned repetitive elements have been observed the proximal and distal repeats, a recombination at the duplication and deletion breakpoints in a event can potentially occur anywhere within the number of human genetic diseases. In Escherichia 30-kb region. However, through the detection of coli, direct repeats in close proximity can mediate novel junction fragments from the recombinant efficient RecA-independent intramolecular recom- CMT1A–REP elements in both CMT1A and HNPP bination. A replicational model for DNA recombi- patients, a 1.7-kb recombination hot spot within nation between direct repeats was suggested by Bi the ∼30-kb CMT1A–REP was identified in 75% of and Liu (1996). They pro- posed that misalignment of repeats at the replication fork creates a recombinogenic in- termediate that can be differ- entially processed and that the proposed sister-strand re- combination mediated by di- rect repeats might be a gen- eral mechanism of deletion or duplication of repeated se- quences in prokaryotic and eukaryotic genomes. Large-scale deletions and duplications may be gener- ated by the pairing of nonal- lelic interspersed or tandem repeats, followed by breakage and rejoining of chromatid fragments. Repeat DNA se- quences may predispose to abnormal chromosome pair- ing and unequal crossing- over, with deletions and du- Figure 1 Generation of the CMT1A duplication and HNPP deletion attributable plications representing the re- to unequal crossing-over. The proximal and distal CMT1A–REP elements (boxes) ciprocal products of such flanking the 1.5-Mb region containing the PMP22 gene (vertical line) on two events. Large deletions within different chromosomes are depicted. Unequal crossing-over because of misalign- duplicated regions may occur ment at meiosis between the distal and proximal CMT1A–REP elements results in either interchromosomally two reciprocal recombination products: the CMT1A duplication (3.0 Mb) chro- because of misalignment of mosome with two PMP22 genes and the HNPP deletion (1.5 Mb) with no PMP22 non-sister chromatids during gene. 774 GENOME RESEARCH Downloaded from genome.cshlp.org on September 28, 2021 - Published by Cold Spring Harbor Laboratory Press RECOMBINATION HOT SPOTS AND HUMAN DISEASE CMT1A duplication patients and 84% of HNPP de- P450 enzyme debrisoquine 4-hydroxylase metabo- letion patients examined (Reiter et al. 1996). Se- lizes many different classes of commonly used phar- quence analysis showed there was no particular in- macological drugs. Among Caucasians, 5%–10% are crease in the degree of sequence identity over this classified as poor metabolizers (PM) because of au- 1.7-kb region, and, interestingly, a mariner transpo- tosomal recessive inheritance of two CYP2D6 dele- son-like element (MITE) was identified in the vicin- tion alleles. In these individuals, administration of ity of the hot spot. Three exons were identified in average therapeutic doses results in toxic plasma the repeat, one of which showed homology at the concentrations and adverse drug reactions. In con- amino acid level to the conserved region of several trast, up to 5% demonstrate ultrarapid metabolism insect transposases. Kiyosawa and Chance (1996) (UM) caused by an inherited duplication of func- further investigated the MITE and found that it is tional CYP2D6 genes, thus requiring higher doses of probably nonfunctional, as several stop codons were drugs to maintain desired plasma levels. A 2.8-kb found in its open reading frame. However, it is pos- repeated sequence (CYP–REP), containing an Alu el- sible that this nonfunctional mariner sequence may ement and a tandem 10-bp direct repeat flanks the be a target for a functional form of the transposase active CYP2D6 gene in the wild-type allele. It is protein transcribed from a gene located elsewhere. thought that the CYP2D6 deletion and duplication Northern blot analysis with the distal CMT1A– alleles are reciprocal products, generated by ho- REP, which encompasses the putative transposase, mologous recombination between nonallelic CYP– identified a low-abundance transcript expressed in REP elements.

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