Biochemistry, 4th Edition P92 pps

28.4 How Is DNA Replicated in Eukaryotic Cells? 873 of proteins that interact with Dbp11, leads to the recruitment of DNA polymerase to the replication origins. (The protein acronyms refer to DNA polymerase-binding [Dpb] and proteins encoded by genes that give a lethal phenotype when mutated in Dpb11 mutant strains of yeast [Sld, or synthetic-lethal with Dpb11]. Collectively, these proteins are referred to as the “11-3-2 complex”). The actions of S-CDK and Cdc7-Dbf4 trigger bidirectional DNA replication from each origin, with the two di- verging MCM complexes serving as helicases. Each helicase unwinds the duplex DNA to provide single-stranded templates for the DNA polymerases that follow. Proteins of the Prereplication Complex Are AAA؉ ATPase Family Members Cdc6, the Orc proteins, and MCM proteins are members of the AAA؉ ATPase family, a group of proteins characterized by sequence and structural homology, ATPase activity, and a general function as molecular chaperones. The binding of both ORC and Cdc6 to chromatin in the process of pre-RC assembly is ATP-dependent (Figure 28.12). ORC with ATP bound can bind to origins of replication and recruit Cdc6 and Cdt1 to form a pre-RC in which both ORC and Cdc6 have bound ATP. Cdc6 is required for the recruitment of the MCM proteins, specifically, a complex of MCM2–7 with ATP-dependent helicase activity. To establish the pre-RC, MCM2–7 must be stably associated with the origin, and this stability is achieved fol- lowing ATP hydrolysis, first by Cdc6 and then by ORC. Geminin Provides Another Control Over Replication Initiation Geminin is a protein that provides another level of regulatory control over DNA replication. Geminin inhibits DNA replication by preventing the incorporation of MCM complexes into the pre-RC. Geminin is active during S, G 2 , and M phases, but its destruction during mitosis permits replication initiation in G 1 . Geminin binds to Cdt1, preventing it from recruiting MCM proteins to the pre-RC. Geminin exists as a parallel coiled-coil homodimer. It interacts with Cdt1 in two ways: It has an array of glutamate residues on its surface that interact with positive charges on Cdt1, and an adjacent region on geminin interacts independently with the N-terminal region of Cdt1. Eukaryotic Cells Contain a Number of Different DNA Polymerases At least 19 different DNA polymerases have been described in eukaryotic cells thus far. These various polymerases have been assigned Greek letters in the order of their discovery (Table 28.4 lists the principal ones). Multiple DNA polymerases participate in leading and lagging-strand synthesis, but three—␣, ␦, and ⑀—share the major bur- P P DNA G 1 phase Sld3 Sld2 Cdc45 Cdc45 Cdc45 S-CDK MCM Cdc7-Dbf-4 Cdc6 Cdt1 Origin of replication Dpb11 P P P P S phase P P Sld3 Sld3 Dpb11 Sld2 Sld2 Dpb11 ORC MCM P ORC P FIGURE 28.12 The initiation of DNA replication in eukaryotic cells. Binding of the pre-RC to origins of replication is followed by loading of MCM hexameric helicases, phosphorylation reactions mediated by S-CDK and Cdc7-Dbf4, and the binding of the 11-3-2 complex. The passage of the cell from G 1 to S is defined by these events. DNA polymerases are recruited to the origins of replication, where they can access single-stranded regions of DNA and initiate DNA synthesis. 874 Chapter 28 DNA Metabolism: Replication, Recombination, and Repair den. DNA polymerase ␣ has an associated primase subunit and functions in the initiation of nuclear DNA replication. Given a template, it not only synthesizes an RNA primer of about 10 nucleotides, but it then adds 20 to 30 deoxynucleotides to extend the chain in the 5Ј→3Ј direction. DNA polymerase ␦, a heterotetrameric enzyme, is the principal DNA polymerase in eukaryotic DNA replication. It interacts with PCNA protein (PCNA stands for proliferating cell nuclear antigen). Through its association with PCNA, DNA polymerase ␦ carries out highly processive DNA synthesis. PCNA is the eukaryotic counterpart of the E. coli ␤ 2 -sliding clamp; it clamps DNA polymerase ␦ to the DNA. Like ␤ 2 , PCNA encircles the double helix, but in contrast to the prokaryotic ␤ 2 -sliding clamp, PCNA is a homotrimer, not a homodimer (Figure 28.13). DNA polymerase ⑀ also plays a major role in DNA replication. It has an acidic C-terminal extension lacking in other DNA polymerases and evidence suggests that this domain is a sensor for DNA damage checkpoint control, halting DNA replication until the damage is repaired. DNA polymerase ␥ is the DNA-replicating enzyme of mitochondria; DNA polymerase ␤ functions in DNA repair. The more recently discovered eukaryotic DNA polymerases (including ␨, ␩, ␫, ␬, and Rev1) are novel in that they are more error-prone, resulting in lower fidelity of DNA replication. Nevertheless, they have the important ability to function in DNA replication and repair when damaged regions of DNA are encountered. Other proteins involved in eukaryotic DNA replication include replication protein A (RPA), an ssDNA-binding protein that is the eukaryotic counterpart of SSB, and replication factor C (RFC). RFC loads the PCNA sliding clamp onto replicating DNA, thus acting as the eukaryotic counterpart of the prokaryotic ␥-complex. 28.5 How Are the Ends of Chromosomes Replicated? Telomeres are the structures at the ends of eukaryotic chromosomes. Telomeres are short (5 to 8 bp), tandemly repeated, G-rich nucleotide sequences that form protective caps 1 to 12 kbp long on the chromosome ends (see Chapter 11). Ver- Subunits Polymerase Localization and Function (mass in kD) Subunit Function DNA polymerase ␣ Nuclear; initiation of nuclear DNA replication DNA polymerase ␦ Nuclear; principal polymerase in leading and lagging strand synthesis; highly processive DNA polymerase ⑀ Nuclear; leading and lagging strand synthesis, sensor of DNA damage checkpoint control DNA polymerase ␥ Mitochondria; mitochondrial DNA replication DNA polymerase ␤ DNA repair TABLE 28.4 Biochemical Properties of the Principal Human DNA Polymerases 180 Catalytic subunit 68 Protein–protein interactions 55 Primase 48 Primase 125 Catalytic subunit 66 Structural 50 Interaction with PCNA 12 Protein–protein interactions 261 Catalytic subunit 59 Multimerization 17 Protein–protein interactions 12 Protein–protein interactions 140 Catalytic subunit 55 Processivity 39 (b) (a) x x FIGURE 28.13 Structure of the human PCNA homotrimer. (a) Ribbon representation of the PCNA trimer (pdb id ϭ 1AXC) with an axial view of a B-form DNA duplex in its center.The molecular mass of each PCNA monomer is 37 kD.(b) Molecular surface of the PCNA trimer-DNA complex. 28.5 How Are the Ends of Chromosomes Replicated? 875 tebrate telomeres have a TTAGGG consensus sequence. Telomeres are necessary for chromosome maintenance and stability. DNA polymerases cannot replicate the extreme 5Ј-ends of chromosomes because these enzymes require a template and a primer and replicate only in the 5Ј→3Ј direction. Thus, lagging strand synthesis at the 3Ј-ends of chromosomes is primed by RNA primase to form Okazaki fragments, but these RNA primers are subsequently removed, resulting in gaps in the progeny 5Ј-terminal strands at each end of the chromosome after each round of replication (“primer gap”; see Figure 28.14). Telomerase is an RNA-dependent DNA polymerase. Telomerase maintains telomere length by restoring telomeres at the 3Ј-ends of chromosomes. The RNA upon which telomerase activity depends is actually part of the enzyme’s structure. That is, telomerase is a ribonucleoprotein, and its RNA component contains a 9- to 30-nucleotide-long region that serves as a template for the synthesis of telomeric repeats at DNA ends. The human telomerase RNA component is 450 nucleotides long; its template sequence is CUAACCCUAA C (base-pairs with TTAGGG). Telomerase uses the 3Ј-end of the DNA as a primer and adds successive TTAGGG (b) Telomerase 5Ј DNA polymerase 5Ј 5Ј Primer gap 3Ј 3Ј 3Ј (a) Primer gap + 3Ј 5Ј 3Ј 5Ј + 3Ј 5Ј ** ** FIGURE 28.14 Telomere replication.(a) In replication of the lagging strand, short RNA primers are added (pink) and extended by DNA polymerase.When the RNA primer at the 5Ј-end of each strand is removed, there is no nucleotide sequence to read in the next round of DNA replication.The result is a gap (primer gap) at the 5Ј-end of each strand (only one end of a chromosome is shown in this figure). (b) Asterisks indicate sequences at the 3Ј-end that cannot be copied by conventional DNA replication. Synthesis of telomeric DNA by telomerase extends the 5Ј-ends of DNA strands, allowing the strands to be copied by normal DNA replication. HUMAN BIOCHEMISTRY Telomeres—A Timely End to Chromosomes? Mammalian cells in culture undergo only 50 or so cell divisions be- fore they die. Somatic cells are known to lack telomerase activity, and thus, they inevitably lose bits of their telomeres with each cell division. Telomerase activity is missing because the telomerase– reverse transcriptase gene (the TRT gene) is switched off. This fact has led to a telomere theory of cell aging, which suggests that cells senesce and die when their telomeres are gone. In support of this notion, a team of biologists headed by Calvin B. Harley at Geron Corporation used recombinant DNA techniques to express the catalytic subunit of human telomerase in skin cells in culture and ob- served that such cells divide 40 times more after cells lacking this treatment have become senescent. These results, although contro- versial, may have relevance to the aging process. 876 Chapter 28 DNA Metabolism: Replication, Recombination, and Repair repeats to it, employing its RNA as template over and over again (Figure 28.14, see also the figure in the Chapter 11 Human Biochemistry box Telomeres and Tumors). 28.6 How Are RNA Genomes Replicated? Many viruses have genomes composed of RNA, not DNA. How then is the information in these RNA genomes replicated? In 1964, Howard Temin noted that in- hibitors of DNA synthesis prevented infection of cells in culture by RNA tumor viruses such as avian sarcoma virus. On the basis of this observation, Temin proposed that DNA is an intermediate in the replication of such viruses; that is, an RNA tumor virus can use viral RNA as the template for DNA synthesis. RNA viral chromosome⎯⎯→DNA intermediate⎯⎯→RNA viral chromosome In 1970, Temin and David Baltimore independently discovered a viral enzyme capable of mediating such a process, namely, an RNA-directed DNA polymerase or, as it is usually called, reverse transcriptase. All RNA tumor viruses contain such an enzyme within their virions (viral particles). RNA viruses that replicate their RNA genomes via a DNA intermediate are classified as retroviruses. Like other DNA and RNA polymerases, reverse transcriptase synthesizes polynu- cleotides in the 5Ј→3Ј direction, and like all DNA polymerases, reverse transcriptase requires a primer. Interestingly, the primer is a specific tRNA molecule captured by the virion from the host cell in which it was produced. The 3Ј-end of the tRNA is base- paired with the viral RNA template at the site where DNA synthesis initiates, and its free 3Ј-OH accepts the initial deoxynucleotide once transcription commences. Re- verse transcriptase then transcribes the RNA template into a complementary DNA (cDNA) strand to form a double-stranded DNAϺRNA hybrid. The Enzymatic Activities of Reverse Transcriptases Reverse transcriptases possess three enzymatic activities, all of which are essential to viral replication: 1. RNA-directed DNA polymerase activity, for which the enzyme is named (see Figure 12.10). 2. RNase H activity. Recall that RNase H is a nuclease that specifically degrades RNA chains in DNAϺRNA hybrids (see Figure 12.10). The RNase H function of reverse transcriptase is an exonuclease activity that degrades the template genomic RNA and also removes the priming tRNA after DNA synthesis is completed. 3. DNA-directed DNA polymerase activity. This activity replicates the ssDNA remaining after RNase H degradation of the viral genome, yielding a DNA duplex. This DNA duplex directs the remainder of the viral infection process or becomes integrated into A DEEPER LOOK RNA as Genetic Material Whereas the genetic material of cells is dsDNA, virtually all plant viruses, several bacteriophages, and many animal viruses have genomes consisting of RNA. In most cases, this RNA is single stranded. Viruses with single-stranded genomes use the single strand as a template for synthesis of a complementary strand, which can then serve as template in replicating the original strand. Retroviruses are an interesting group of eukaryotic viruses with single-stranded RNA genomes that replicate through a dsDNA intermediate. Furthermore, the life cycle of retroviruses includes an obligatory step in which the dsDNA is inserted into the host cell genome in a transposition event. Retroviruses are responsible for many diseases, including tumors and other disorders. HIV-1, the human immunodeficiency virus that causes AIDS, is a retrovirus. 28.7 How Is the Genetic Information Shuffled by Genetic Recombination? 877 the host chromosome, where it can lie dormant for many years as a provirus. Acti- vation of the provirus restores the infectious state. HIV reverse transcriptase is of great clinical interest because it is the enzyme for replication of the AIDS virus. DNA synthesis by HIV reverse transcriptase is blocked by nucleotide analogs such as AZT and 3TC (Figure 28.15). HIV reverse transcriptase incorporates these analogs into growing DNA chains in place of dTMP (in the case of AZT) or dCMP (in the case of 3TC). Once incorporated, these analogs block further chain elongation because they lack a 3Ј-OH where the next incoming dNTP can be added. HIV reverse transcriptase is error-prone: It incorporates the wrong base at a frequency of 1 per 2000 to 4000 nucleotides polymerized. This high error rate during replication of the HIV genome means that the virus is ever changing, a feature that makes it difficult to devise an effective vaccine. 28.7 How Is the Genetic Information Shuffled by Genetic Recombination? Genetic recombination is the natural process by which genetic information is re- arranged to form new associations. For example, compared to their parents, progeny may have new combinations of traits because of genetic recombination. At the molecular level, genetic recombination is the exchange (or incorporation) of one DNA sequence with (or into) another. When recombination involves reaction between very similar sequences (homologous sequences) of DNA, the process is called homologous recombination. When very different nucleotide sequences recombine, it’s nonhomologous recombination. Transposition—the enzymatic insertion of a transposon (a mobile segment of DNA, see pages 885–886) into a new location in the genome—and nonhomologous recombination (incorporation of a DNA segment whose sequence differs greatly from the DNA at the point of insertion) are two types of recombination that play a significant evolutionary role. Nonhomologous recombination occurs at a low frequency in all cells and serves as a powerful genetic force that reshapes the genomes of all organisms. Homologous recombination involves an exchange of DNA sequences between homologous chromosomes, resulting in the arrangement of genes into new combinations. Homologous recombination is generally used to fix the DNA so that information is not lost. For example, large le- sions in DNA are repaired via recombination of the damaged chromosome with a homologous chromosome. The process underlying homologous recombination is termed general recombination because the enzymatic machinery that mediates the exchange can use essen- tially any pair of homologous DNA sequences as substrates. Homologous recombination occurs in all organisms and is particularly prevalent during the production of gametes (meiosis) in diploid organisms. In higher animals—that is, those with immune systems—recombination also occurs in the DNA of somatic cells responsible for expressing proteins of the immune response, such as the immunoglobulins. This somatic recombination rearranges the immunoglobulin genes, dramatically increas- ing the potential diversity of immunoglobulins available from a fixed amount of genetic information. Homologous recombination can also occur in bacteria. Indeed, even viral chromosomes undergo recombination. For example, if two mutant viral particles simultaneously infect a host cell, a recombination event between the two viral genomes can lead to the formation of a virus chromosome that is wild-type. General Recombination Requires Breakage and Reunion of DNA Strands Recombination occurs by the breakage and reunion of DNA strands so that a phys- ical exchange of parts takes place. Matthew Meselson and J. J. Weigle demonstrated this in 1961 by coinfecting E. coli with two genetically distinct bacteriophage ␭ CH 3 O O O N N H O HH H H H HOCH 2 N N O S H H H H HOCH 2 N N + – NH 2 N (a) (b) FIGURE 28.15 The structures of AZT (3Ј-azido-2Ј,3Ј- dideoxythymidine) and 3TC (2Ј,3Ј-dideoxy-3Ј- thiacytidine). These nucleosides are phosphorylated in vitro to form deoxynucleoside-5’-triphosphate sub- strate analogs for HIV reverse transcriptase. 878 Chapter 28 DNA Metabolism: Replication, Recombination, and Repair strains, one of which had been density-labeled by growth in 13 C- and 15 N-containing media (Figure 28.16). The phage progeny were recovered and separated by CsCl density gradient centrifugation. Phage particles that displayed recombinant genotypes were distributed throughout the gradient while parental (nonrecombinant) genotypes were found within discrete “heavy” and “light” bands in the density gradient. The results showed that recombinant phage contained DNA derived in varying proportions from both parents. The obvious explanation is that these recombinant DNAs arose via the breakage and rejoining of DNA molecules. A second important observation made during this type of experiment was that some of the plaques formed by the phage progeny contained phage of two different genotypes, even though each plaque was caused by a single phage infecting one bacterium. Therefore, some infecting phage chromosomes must have contained a region of heteroduplex DNA, duplex DNA in which a part of each strand is con- tributed by a different parent (Figure 28.17). Homologous Recombination Proceeds According to the Holliday Model In 1964, Robin Holliday proposed a model for homologous recombination that has proved to be correct in its essential features (Figure 28.18). The two homologous DNA duplexes are first juxtaposed so that their sequences are aligned. This process of chromosome pairing is called synapsis (Figure 28.18a). Holliday suggested that recombination begins with the introduction of single-stranded nicks in the DNA at homologous sites on the two paired chromosomes (Figure 28.18b). The two duplexes partially unwind, and the free, single-stranded end of one duplex begins to base-pair with its nearly complementary, single-stranded region along the intact strand in the other duplex, and vice versa (Figure 28.18c). This strand invasion is followed by ligation of the free ends from different duplexes to create a cross- Infect bacteria with a mixture of heavy and light phage Recombination occurs Phage assembly and cell lysis Heavy phage ABC Light phage abc Phage progeny are centrifuged on CsCl gradient Light phage abc Recombinant phage Abc, aBc, abC, etc. Heavy phage ABC ᮤ ANIMATED FIGURE 28.16 Meselson and Weigle’s experiment. Density-labeled,“heavy” phage, symbolized as ABC phage, was used to coinfect bacteria along with “light” phage, the abc phage. The progeny from the infection were collected and subjected to CsCl density gradient centrifugation. Parental-type ABC and abc phage were well separated in the gradient, but recombinant phage (ABc, Abc, aBc, aBC, and so on) were distributed diffusely between the two parental bands because they contained chromosomes constituted from fragments of both “heavy” and “light” DNA. See this figure animated at www.cengage.com/login. +– XX Yy ZZ Heteroduplex DNA (+ and – strands) Semiconservative DNA replication +– XX YY ZZ Progeny phage of 2 different genotypes +– XX yy ZZ FIGURE 28.17 The generation of progeny bacteriophage of two different genotypes from a single phage parti- cle carrying a heteroduplex DNA region within its chromosome.The heteroduplex DNA is composed of one strand that is genotypically XYZ (the ϩ strand), and the other strand that is genotypically XyZ (the Ϫ strand). That is, the genotype of the two parental strands for gene Y is different (one is Y, the other y). 28.7 How Is the Genetic Information Shuffled by Genetic Recombination? 879 stranded intermediate known as a Holliday junction (Figure 28.18d). The cross- stranded junction can now migrate in either direction (branch migration) by unwinding and rewinding of the two duplexes (Figure 28.18e). Branch migration results in strand exchange; heteroduplex regions of varying length are possible. In order for the joint molecule formed by strand exchange to be resolved into two DNA duplex molecules, another pair of nicks must be introduced. Resolution can AZ + – – + az Nicking Strand invasion Ligation Branch migration Arms conceptually bent “up” and “down” AZ az + – + – + – – + + – – + (–) strands cleaved at junction, strands resolved, religated (+) strands cleaved at junction, strands resolved, religated Patch recombinant heteroduplex Splice recombinant heteroduplex (a) (b) (c) (d) (e) (f) (g) (h) N W E S EW cleavage: NS cleavage: ACTIVE FIGURE 28.18 The Holliday model for homologous recombination.The ϩ signs and Ϫ signs label strands of like polarity. For example, assume that the two strands running 5Ј→3Ј as read left to right are labeled ϩ; and the two strands running 3Ј→5Ј as read left to right are labeled Ϫ. Only strands of like polarity exchange DNA during recombination. (See text for detailed description.) Test yourself on the concepts in this figure at www.cengage.com/login. 880 Chapter 28 DNA Metabolism: Replication, Recombination, and Repair be represented best if the duplexes are drawn with the chromosome arms bent “up” or “down” to give a planar representation (Figure 28.18f). Nicks then take place, either at E and W, that is, in the Ϫ strands that were originally nicked (see Figure 28.18b), or at N and S, that is, in the ϩ strands (the strands not previously nicked). Duplex resolution is most easily kept straight by remembering that ϩ strands are complementary to Ϫ strands and any resultant duplex must have one of each. Nicks made in the strands originally nicked lead to DNA duplexes in which one strand of each remains intact. Although these duplexes contain heteroduplex regions, they are not recombinant for the markers (AZ, az) that flank the heteroduplex region; such heteroduplexes are called patch recombinants (Figure 28.18g). Nicks introduced into the two strands not previously nicked yield DNA molecules that are both heteroduplex and recombinant for the markers A/a and Z/z; these heteroduplexes are termed splice recombinants (Figure 28.18h). Although this Holliday model ex- plains the outcome of recombination, it provides no mechanistic explanation for the strand exchange reactions and other molecular details of the process. The Enzymes of General Recombination Include RecA, RecBCD, RuvA, RuvB, and RuvC To illustrate recombination mechanisms, we focus on general recombination as it occurs in E. coli. The principal players in the process are the RecBCD enzyme complex, which initiates recombination; the RecA protein, which binds single-stranded DNA, forming a nucleoprotein filament capable of strand invasion and homologous pairing; and the RuvA, RuvB, and RuvC proteins, which drive branch migration and process the Holliday junction into recombinant products. Eukaryotic homologs of these prokaryotic recombination proteins have been identified, indi- cating that the fundamental process of general recombination is conserved across all organisms. The RecBCD Enzyme Complex Unwinds dsDNA and Cleaves Its Single Strands The RecBCD complex is composed of the proteins RecB (140 kD; 1180 amino acids), RecC (130 kD; 1122 amino acids), and RecD (67 kD; 608 amino acids). This multifunctional enzyme complex has both helicase and nuclease activity and initiates recombination by attaching to the end of a DNA duplex (or at a double-stranded break in the DNA) and using its ATP-dependent helicase function to unwind the dsDNA (Figure 28.19a). RecB and RecD are helicases powered by ATP hydrolysis; each con- sumes an ATP per base pair of DNA traversed. The RecD motor is faster than the RecB motor and leads the way. The greater speed of RecD causes the DNA to loop out between RecD and RecB. The RecB subunit contains the nuclease domain. As RecBCD progresses along unwinding the duplex, the RecB nuclease activity cleaves both of the newly formed single strands (although the strand that provided the 3Ј-end at the RecBCD entry site is cut more frequently than the 5Ј-terminal strand [Figure 28.19b]). SSB (and some RecA protein) readily binds to the emerging single strands. Sooner or later, RecBCD encounters a particular nucleotide sequence, a so-called Chi (or ␹) site, characterized by the sequence 5Ј-GCTGGTGG-3Ј. These ␹ sites are re- combinational “hot spots”; 1009 ␹ sites have been identified in the E. coli genome (on average, about one every 4.5 kb of DNA). When a ␹ sequence is encountered by a RecBCD complex approaching its 3Ј-side (the G-3Ј-side), RecBCD cleaves the ␹-bearing DNA strand four to six bases to the 3Ј side of ␹ (Figure 28.19c). RecBCD flips so that the RecB motor leads the way, and the RecBCD complex no longer ex- presses nuclease activity against the 3Ј-terminal strand, but nuclease activity against the 5Ј-terminal strand increases (Figure 28.19d). Resuming its helicase function, RecBCD unwinds the dsDNA, and collectively these processes generate an ssDNA tail bearing a ␹ site at its 3Ј-terminal end. This ssDNA may reach several kilobases in length. RecA protein now binds to the 3Ј-terminal strand to form a nucleoprotein filament (Figure 28.19e). This filament 28.7 How Is the Genetic Information Shuffled by Genetic Recombination? 881 is active in pairing and strand invasion with a homologous region in another dsDNA molecule. The RecA Protein Can Bind ssDNA and Then Interact with Duplex DNA The RecA protein, or recombinase, is a multifunctional protein that acts in general recombination (Figure 28.20a). RecA mediates the ATP-dependent DNA strand exchange reaction leading to formation of a Holliday junction (Figure 28.18b–f). In the presence of ATP and ssDNA, RecA forms a right-handed helical filament having (a) (b) (c) (d) (e) 3Ј 3Ј 3Ј 3Ј 5Ј 5Ј 5Ј 5Ј 3Ј 5Ј 3Ј 5Ј 3Ј 5Ј 3Ј 5Ј 3Ј 5Ј 3Ј 5Ј χ 3Ј 5Ј 3Ј 5Ј χ χ χ χ RecBCD SSB RecA RecA Binding of RecBCD to DNA end; unwinding Nonspecific cleavage (3Ј more than 5Ј); SSB, RecA binding χ encounter and cleavage 3Ј to χ Displacement of SSB; preferential binding of RecA; enhanced 5Ј-terminal cleavage Pairing with homologous DNA du p lex and strand invasion χ FIGURE 28.19 Model of RecBCD-dependent initiation of recombination. (a) RecBCD binds to a duplex DNA end, and its helicase activity begins to unwind the DNA double helix.“Rabbit ears”of ssDNA loop out from RecBCD because the rate of DNA unwinding exceeds the rate of ssDNA release by RecBCD. (b) As it unwinds the DNA, SSB (and some RecA) bind to the single-stranded regions; the RecBCD endonuclease activity randomly cleaves the ssDNA, showing a greater tendency to cut the 3Ј-terminal strand rather than the 5Ј-terminal strand. (c) When RecBCD encounters a properly oriented ␹ site, the 3Ј-terminal strand is cleaved just below the 3Ј-end of ␹. (d) RecBCD now directs the binding of RecA to the 3Ј-terminal strand, as RecBCD endonuclease activity now acts more often on the 5Ј-terminal strand. (e) A nucleoprotein filament consisting of RecA-coated 3Ј-strand ssDNA is formed.This nucleoprotein filament is capable of homologous pairing with a dsDNA and strand invasion. (Adapted from Figure 2 in Eggleston, A. K., and West, S. C., 1996. Exchanging partners: recombination in E. coli.Trends in Genetics 12:20–25; and Figure 3 in Eggleston, A. K., and West, S. C., 1997. Recombination initiation: Easy as A, B, C, D ….␹? Current Biology 7:R745–R749.) 882 Chapter 28 DNA Metabolism: Replication, Recombination, and Repair six monomers per turn, with each monomer spanning about three nucleotides of DNA. The RecA nucleoprotein filament serves as a scaffold upon which the events of recombination take place. This filament has a deep spiral groove large enough to en- compass three strands of DNA. Although RecA-bound ssDNA is relatively stretched and underwound, with about 18.5 nucleotides per turn, its local conformation re- sembles B-DNA (Figure 28.20b). Thus, when dsDNA adds to the complex, the ssDNA is poised to search for the sequence homology that leads to strand exchange. Procession of strand separation of dsDNA and the re-pairing into hybrid strands along the DNA duplex initiates branch migration (Figure 28.21b). Branch migration drives the displacement of the homologous DNA strand from the DNA duplex and its replacement with the ssDNA strand, a process known as single-strand assimilation (b) C-term N-term(a) L1 FIGURE 28.20 (a) RecA, a 352-residue, 38-kD protein, with dATP in the ATP-binding site (pdb id ϭ 2ODN). (b) Structure of a fused RecA hexamer with bound ssDNA (as poly(dT) 18 , magenta). Each of the six RecA units is a different color and each has a bound ADP molecule (marine blue).The adenine nucleotide-binding sites lie at the inter- faces between RecA units (pdb id ϭ 3CMU). 5Ј 3Ј 5Ј 3Ј 3Ј 5Ј 3Ј 5Ј 3Ј 5Ј 5Ј 3Ј 5Ј 5Ј 5Ј 3Ј 5Ј 3Ј 5Ј 3Ј 3Ј 5Ј (a) RecA Homologous DNA duplex (b) (c) SSB FIGURE 28.21 Model for homologous recombination as promoted by RecA enzyme.(a) RecA protein (and SSB) aid strand invasion of the 3Ј-ssDNA into a homologous DNA duplex, (b) forming a D-loop. (c) The D-loop strand that has been displaced by strand invasion pairs with its complementary strand in the original duplex to form a Holli- day junction as strand invasion continues.

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