DNA Tranlession Polymerase in Prokaryotic Cells

deoxyribonucleic acid Tranlession Polymerase in Prokaryotic Cellsdesoxyribonucleic acid Tranlession Polymerase in prokaryotic cells History, structures and characterSoheil Malekpourdesoxyribonucleic acid is one of the most important part of the cell that gives cell integrity and character. This part of the cell earth-closet be exposed to assorted kinds of ruins that may put the cells integrity in jeopardy. The only part of the cell that has this ability to be repaired is desoxyribonucleic acid. Basically repairing should be through due to a reason qualified reason. Repairing the otherwise macromolecules are not profitable. For example, if a defective protein forms, the protein can be simply be replaced by another one. But defects in deoxyribonucleic acid can give problem in the whole cell organisms and the character of cell 1. Usually the whole repairing process is happening fast, although there are defects that persist against this process. The repairing process is done by special polymerases and the whole process of DNA repair is called translesion DNA synthesis (TLS) 2.DNA can be vilifyd due to different reasons, much(prenominal) as base modification, elimination or addition of nucleotides, crosslinking of DNA strands and breakage of phosphodiester backbone 1. These reasons can be due to some environmental conditions such as radiation or insertion of certain chemicals in to the body or due to malfunction of polymerases and enzymes in cellular process, such as putting ravish nucleotide in the DNA strand chain 1. Up to now, it is known that there are three translesion DNA polymerases (TLS polymerases) in E. coli and about fifteen polymerases in eukaryotes that can run this process 2.HistoryFor the first time it was in the early 1940s, that it was found agents causing mutational changes such as ionizing and radiation of UV, move with cells and can damage their genome 3. Also it was found that these cells can survive and recover from theses damages 4 and the term DNA repair was found. DNA repair is a biochemical term that defines biological processes during which alterations in the chemistry of DNA (DNA damage) are removed and the integrity of the genome is restored 3.The first DNA repair mechanism to be discovered was enzymatic photo reactivation (EPR) 3. This process is referred to the elimination of cyclobutane pyrimidine, which are generated by UV radiation and can block both DNA replication and transcription, from the genome 4. This reaction can be catalyzed by photoreactivating enzyme in a reaction that needs a visible range light. The second mechanism found was excision repair 3. This mechanism is referred to DNA damages cut out from genome that leaves some gaps in DNA duplex. These gaps are repaired by a non-semiconservative mode of DNA synthesis called repair synthesis 5.By the end of the 1970s, it was known that cells are using various mechanisms for DNA repair process that focus around two basic principles the exci sion of base damage or its direct reversal such as EPR 3. In the mid1970s Miroslav Radman proposed a new hypothesis called SOS hypothesis 5, 6. TheSOS hypothesis proposes an overall response to DNA damage in which thecell cycleis stopped andDNA repairis induced. Genetics experiments demonstrated that main players entangled in damage-induced mutagenesis are lexA, recA along with umuD and umuC 2. LexA cleavage from recA* and also umuD cleavage that form umuD use the selfsame(prenominal) mechanism and is an absolute requirement for SOS mutagenesis. For showing that, E. coli because of its simple structure was used as a influence for translesion DNA synthesis and mutagenesis.Later Harrison Echols proposed another seat and suggested that in order to help the replication process against the lesions it is possible to reduce the fidelity of proteins so when DNA replication process is stopped at a location of unrepaired DNA damage, certain SOS-regu slowd genes can encode proteins that in teract with the hindered replication process in a manner that reduces their fidelity 3. In the late 1980s and early 1990s, it was demonstrated that Echols genes are in fact specialized low-fidelity DNA polymerases that enhance low-fidelity replication across the lesion, the so-called translesion DNA synthesis (TLS) 3. Their extremely reduced fidelity allows the replicative bypass of sites of DNA damage, but with a high chance of combining incorrect nucleotides 5.Early TLS models and PolVBridges and Woodgate were the first ones who defined the function of Umu proteins during UV-induced TLS in 1985 7. According to them, TLS happened in two steps. In the first step Pol III add a nucleotide opposite the first (3) T of a T-T cytidine diphosphate diacylgelycerol (CPD). Bounding a RecA protein to the template proximal to the lesion is a requirement for this step. In the second step, Pol III interacts with UmuDC proteins to incorporate another nucleotide at the second (5) T of the cytidine diphosphate diacylgelycerol (CPD). At least one of these two steps are non-WC, causing a mutation targeted at the site of the CPD 2. compute 1 shows the process schematically.Another model was proposed by Echols and Goodman in 1990 3. In this model they proposed that when Pol III encounters a template lesion, its holoenzymes (Pol III core, beta slue clamp, gamma-clamp-loading analyzable) are completely blocked. This process follows by the assembly of a damage localized nucleoprotein complex involving RecA, UmuC, UmuD, SSB, and Pol III holoenzyme, a mutasome, to copy past a template lesion 2. The fact that RecA* simplifies the cleavage of UmuD to UmuD was used in this model 8. Later, it was demonstrated that it was actually a dimeric UmuD2 that is cleaved to UmuD2 and that next interacts with UmuC to form a stable complex of UmuD2C 9. This complex was named as Pol V in 1999 by Tang et al. 10. It can be said that genome replication done on un alter DNA by Pol III is rapid and erro r-free 11, the TLS process carried out by mutasome is slow and error-prone 2.A key feature of the mutasome model is the assembly of RecA* on ssDNA proximal to the lesion (Fig. 1). When a replication fork encounters a lesion, an uncoupling of leading-and lagging-strand synthesis may ensue. Then, one of the TLS Pols can replace Pol III on the - clamp and copy the damaged DNA 2. For both leading and lagging strands it be easily seen that RecA* can be assembled on the form of template strand, proximal to lesion. If the lesion occurred in the leading strand, RecA filaments can be formed on a region of ssDNA that is created by DNA unwinding by DnaB helicase downstream from the lesion but if lesions exist in lagging strand ssDNA is acquaint as a result of Okazaki fragment synthesis 2.Schlacher and Goodman 12 showed RecA* act in trans form on a non-template ssDNA strand and this transactivation of PolV by RecA* to perform TLS happens in-vitro. And this lead to the PolV mutasome model of TL S (Fig. 1). Jiang et al. 13 demonstrated this new PolV form as PolV Mut = UmuD2C-RecA-ATP. PolV Mut has this ability to copy both damaged and unmutilated DNA (e.g. performs TLS) when RecA* is not present 2. So, the straight role of RecA* in SOS-mediated TLS is to transfer a RecA molecule from the 3-filament winding with a molecule of ATP to convert into Pol V Mut, that can cross a different number of DNA lesions on its own. (Fig. 1) 2, 14. PolV Mut can have two conformations. One is activated form that can copy DNA, the other one is deactivated form that is unable(p) to copy the DNA. The activation of PolV Mut is depended on the location of RecA-ATP bond to the polymerase subunits UmuD2 and UmuC 13. By representing the RecA* again, the deactivated form of PolV Mut can be activated. In this case, the old RecA-ATP is substituted by a new RecA-ATP from the 3-filament tip 13. This type of switching on and off is unique to this kind of polymerase and has not been seen in other types o f polymerases. This method can be useful specially preventing the undamaged DNA to go under mutation in E.Coli, and give the cell this power to activate Pol V Mut whenever replication fork have stuck at DNA template damage site 2.PolII and PolIV in E.Coli TLSPolII discovered in 197015. At first, it was thought that mutation is non-informative in PolII 16. Pol II has an activity disjointed from UV-irradiated cells that has this ability to replicate past abasic template lesions 2, 17. This polymerase has some responses to UV radiation and this activity derives from that 2. By purification it was proved that the induced lesion-copying protein was Pol II 17. In 1980, Kenyon and pushchair 18 discovered a DNA damage-inducible gene called dinA that can encode PolII. Also, one of the features of PolII is bypassing N2-deoxyguanosine-acetyl aminofluorene (AAF) adducts, this behavior can be error-free and produces 2-frame shift mutations 19. AAF adducts are of family of redolent(p) amides t hat induce frame shift mutations within GpC sequences, such as the NarI sequences 19. These adducts are able to increase the GC dinucleotide loss in NarI sequence (CGCGCC) by 107 propagation when they are bound to the G in middle of sequence 20. PolII and PolV can complement each other, but it does not mean that their activities are functionally needless 21. As Pham et al. 21 mentioned PolV job is to copy UV-damaged DNA in an error-prone manner in TLS. But Pol II is able to copy chromosomal DNA in an error-free replication process.Kenyon and walker also introduced another gene called dinB gene that can be induced by cellular SOS response to DNA damage 18. For many years, the function of this gene was unknown. After some year Ohmori et al. 22 found other gene, dinP gene, in the same section that dinB gene was found and Wagner et al. showed that they are able to encode Y-family DNA PolIV 23. This kind of polymerases like other polymerases used in TLS are not crucial for life. Their role is to bypass certain N2-dG adducts (such as N2-furfuryl-dG) in an error-free manner 2. Kumari et al. demonstrated they can copy past N2-N2-guanine interstrand cross-links in a high fidelity manner 24.Regulation of TLS polymerasesDifferent polymerases have this ability to swing out an extensive range of DNA lesions but this ability may cause in reducing the fidelity during replicating the undamaged DNA. Usually cells have several mechanisms to chink and control the TLS polymerases because except PolII, all of them has this potential to delete errors made when duplicating an undamaged DNA 2.Usually no regulation is needed for PolII. Because it has high fidelity derived by high intrinsic 3-5 exonucleolytic proofreading. On the other hand, the Y-family polymerases such as PolIV and PolV are exo-nuclease deficient and needed to be controlled 2.PolV activity can be regulated by many proteins and many ways. First as said before the UmuD should be activated by UmuD. All UmuD, UmuC an d UmuD proteins are all exposed to degradation by Lon and ClpXP protease. RecA* that forms PolV Mut can interact with UmuD2C complexes and active them. The PolV Mut itself activity can be enhanced by binding to the -clamp 2.As Wagner et al. showed the PolIV activity can be stimulated by protein interaction with RecA, UmuD and -clamp 25.Although the main mechanisms of DNA repair by various polymerases are known now, more studies can be conducted on E.Coli cells to find more enlarge about the regulation and side reactions happening in this process. E.Coli cells as simple cells are an appropriate model to analyze these functions. Jarosz et al. proposed well questions about the future studies on Y-family DNA polymerases 26(1)How do Y-family polymerases gain access to an appropriate primer terminus and how is their action coordinated with that of replicative polymerases?(2)How do proteinprotein interactions regulate the activity of Y-family polymerases?(3)Are there families of cognate lesions for each different Y-family polymerase?(4) Can mutations introduced by Y-family polymerases be corrected by exonucleolytic proofreading in trans?Different polymerases act in different paces after the damaged. For example PolII is induced directly after DNA damage but PolV is induced about 50 min after the damage 21. An area of interest could be study on how they can be regulated to be induced in shorter time.ReferencesHorton, R. H., Moran, L. A., Perry, M. D., Rawn, D. J. and Scrimgeour, G. K. (2006)Principles of biochemistry. 4th edn. United States Pearson Education (US).Goodman, M. F. and Woodgate, R. 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