... the polymerase (DNA- directed), delta interacting protein (POLDIP3) gene as a binding partner of the human ER PDIP46 ⁄ SKAR had been reported to be an interacting partner of the p50 subunit of DNA ... molecular partners of the p50 subunit of DNApolymerase d [23] No further data on this interaction and the possible role of PDIP46 in processes in which this polymerase takes part have been reported ... with no direct influence on the metabolism of pyrimidines Experimental procedures cDNA cloning and DNA constructs cDNAs of the human genes, ER and POLDIP3 (both isoforms) corresponding to their coding...
... with either p140 cDNA (upper panel), p48 cDNA (middle panel), or glyceraldehyde 3-phosphate dehydrogenase (G3PDH) cDNA (lower panel) Ó FEBS 2003 Meiotic expression of Coprinus DNApolymerase a (Eur ... Coprinus DNApolymerase a (Eur J Biochem 270) 2143 Fig Separation of primase activity from pol a-primase complex by phospho–cellulose column chromatography (A) DNApolymerase (circles) and DNA primase ... should be noted that intrinsic DNApolymerase activity in fraction II has quite low processivity for DNA synthesis which is a typical feature for replicative DNA polymerases [1] Taken together...
... level, DnaE and PolC have many features in common Both have a similar polymerase core consisting of ‘palm’, ‘thumb’ and ‘fingers’ domains The polymerase core in both DnaE and PolC is flanked by a polymerase ... major double-stranded DNA binding determinant in the E coli DnaE [12] Crystal structures revealed that this motif binds double-stranded DNA similarly in both PolC [8] and DnaE [6] The b-clamp ... PolC and DnaE The ability to bind single-stranded DNA has indeed been demonstrated for the E coli DnaE OB domain [12,16] The very N-terminal region of PolC and the C-terminal domain of DnaE appear...
... polynucleotide kinase, E coli DNApolymerase I, the Klenow fragment of E coli DNApolymerase I lacking 3¢ to 5¢ exonuclease activity, Taq DNApolymerase and pfu DNApolymerase were from Takara ... DNApolymerase and DNApolymerase I) degrading the product To our surprise, the addition of doxorubincin did not obviously inhibit expansion, but did inhibit the exonuclease activity of DNApolymerase ... Klenow fragment (Fig 3B, lane 2), Sequenase Version 2.0 DNA poly4514 merase (Fig 3C, lane 2), Taq DNApolymerase (Fig 3E, lane 2) and pfu DNApolymerase (Fig 3F, lane 2) The addition of DDI-1A and...
... associates with RNA polymerase II 24 25 26 27 28 29 30 31 32 33 34 35 36 37 (1996) DNApolymerase e may be dispensable for SV40- but not cellular -DNA replication EMBO J 15, 2298 –2305 Pospiech H, ... compilation ª 2006 FEBS 5537 DNApolymerase e associates with RNA polymerase II A K Rytkonen et al ¨ A B C Fig DNApolymerase (Pol) e interacts with hyperphosphorylated RNA polymerase (pol) II (A) Pol ... 2006 FEBS A K Rytkonen et al ¨ A B Fig UV crosslinking of replicative DNA polymerases to nascent DNA or RNA chains (A) DNA polymerases (Pols) a and e, but not Pol d, are photolabelled with radioactive...
... other X-family DNA polymerases, a tree was drawn based on the amino acid sequences of the DNApolymerase domains Ó FEBS 2004 Plant DNApolymerase k (Eur J Biochem 271) 2803 Table DNA polymerization ... eukaryotic DNA polymerases of the X-family Fig DNApolymerase activity of OsPol k protein (A) Multiple amino acid alignment of a portion of the polymerization active site with the other X-family DNA polymerases ... effects of DNApolymerase inhibitors on the DNApolymerase activity of OsPol k Strong inhibition was noted with 2,3-dideoxythymidine-5-triphosphate, a known inhibitor of mammalian DNA polymerases...
... AtPOLK DNApolymerase and displacement of the replicative DNApolymerase [3,11] Despite its important in vivo functions, the role of the C-terminal region of Y-family DNA polymerases during DNA ... amino acids stimulates the DNApolymerase activity and processivity of AtPOLK on different DNA substrates The C-terminally truncated AtPOLK DNApolymerase is not affected in DNA binding We next examined ... C-terminus in AtPOLK DNApolymerase replicative DNA polymerases preferentially insert A opposite 8-oxodG [21], causing G:C fi T:A transversions [31] Insertion preferences among Y-family DNA polymerases...
... 54 54 24374933 26987715 23104211 2299 4951 21230123 30248459 23028461 33593407 2299 8318 15677419 2298 6355 34498368 2297 6686 23016368 2296 4979 16125938 2296 8178 2295 9552 17987543 23108152 39 33 30 ... holoenzyme DnaX complex: association of dd¢ with DnaX (4) forms DnaX (3) dd¢ EMBO J 19, 6536–6545 Tsuchihashi, Z & Kornberg, A (1990) Translational frameshifting generates the c subunit of DNApolymerase ... on DNA – a three-point switch underlies primer handoff from primase to the replicative DNApolymerase Cell 96, 153– 163 27 Xiao, H., Crombie, R., Dong, Z., Onrust, R & O’Donnell, M (1993) DNA polymerase...
... origin of DNA replication (B) The JCV system uses JCV TAg and pJC389 DNA with the JCV origin The cell extracts were supplemented with 0.5 and 1.0 DNApolymerase units of the indicated DNApolymerase ... previously, SV40 DNA replication is absolutely dependent upon human DNApolymerase a-primase (Fig 1A, columns 1–5 [26,27]) and more specifically, upon the human p180 subunit as the hybrid DNApolymerase ... Biochem 270) 2033 Fig DNA synthesis products of the SV40 and JCV DNA replication systems Murine FM3A cell extracts depleted of DNApolymerase a-primase were supplemented with 1.0 DNApolymerase units...
... catalytic activities: (a) DNApolymerase activity, which can be both RNA and DNA dependent; and (b) RNase H activity that selectively hydrolyzes the RNA strand of the RNA :DNA hybrid formed during ... TRP229A Tyr188 O O O LEU234A O O NNRTIbp PHE227A O TYR188A Trp 229 PRO236A Trp 229 Pr Tyr181 TYR188A Cys181 VAL106A TRP229A LEU100A C G LEU100A TYR188A K54 TYR318A O Asp110 K54 TYR183A Trp 229 O ... VAL108A Asp186 O O O Asp185 O NNRTIbp Asp185 TYR318A TRP229A Trp 229 TYR188A MET230A Tyr188 O Tyr181 O Trp 229 TYR188A O O O O NNRTIbp TRP229A LEU234A Cys181 LEU100A Br TYR181A B F Asp110 VAL108A...
... ddNTP-sensitive DNApolymerase activity Fig Comparative analysis of the N-terminal heptatide sequence of purified mungbean DNApolymerase with the other X-family DNA polymerases: (A) DNApolymerase ... for dTTP of mungbean DNApolymerase was 0 .29 lm (Fig 4C), close to the value of 0.3 lm of rice DNApolymerase for dTTP [19] and human polymerase b (0.33 lm) for UV-induced DNA damage repair [24] ... DNApolymerase was 2.3 lm (Fig 4D), slightly higher than value for ddTTP of the ddNTP-sensitive DNApolymerase from rice and of human DNApolymerase b (< 2.0 lm), but much less than that of DNA...
... ¨ (1996) DNApolymerase e may be dispensable for SV40- but not cellular -DNA replication EMBO J 15, 2298 –2305 12 Pospiech H & Syvaoja J (2003) DNApolymerase epsi¨ lon – more than a polymerase ... Journal 273 (2006) 298 4–3001 ª 2006 The Authors Journal compilation ª 2006 FEBS 299 1 Human DNA polymerases a, d and e in replication A K Rytkonen et al ¨ Table Distribution of DNA polymerases (pols) ... FEBS Journal 273 (2006) 298 4–3001 ª 2006 The Authors Journal compilation ª 2006 FEBS 299 3 Human DNA polymerases a, d and e in replication A K Rytkonen et al ¨ Fig DNApolymerase (pol) d and pol...
... MA DNApolymerase activity (%) A N Kasai et al 10 Fig (A) Doseresponse curve of SQG Rat DNApolymerase b (0.05 units) was preincubated with the indicated concentrations (0100 mM) of SQG DNApolymerase ... of DNApolymerase beta Correlation with DNA binding and dRP lyase activity J Mol Biol 296 , 2292 53 18 Sawaya MR, Prasad R, Wilson SH, Kraut J & Pelletier H (1997) Crystal structures of human DNA ... SQMG(C18:1)) and NA on the activities of DNApolymerase b, as a function of the DNA template-primer and the nucleotide substrate concentrations Rat DNApolymerase b was 0.05 units Substrate conc...
... with the recovery of > 95% of DNApolymerase a and > 75% of the other DNA polymerases in the extract Standard DNApolymerase activity and inhibition assays Total DNApolymerase activity was assayed ... attached to DNA polymerases was an indicator of the polymerase activity and was measured after SDS/PAGE by autoradiography Separate results are shown in Fig 2C for DNApolymerase e and for DNA polymerases ... the total nuclear DNApolymerase activity in the standard assay Results by SDS/ PAGE and Western blotting with specific antisera against DNA polymerases a and e [13], and DNApolymerase d [14]...
... cisplatin GpG adducts by human DNApolymerase eta Biochemistry 2000, 39:4575-80 Matsuda T, Bebenek K, Masutani C, Hanaoka F, Kunkel TA: Low fidelity DNA synthesis by human DNApolymerase eta Nature 2000, ... translesion DNA synthesis (TLS) [20] These adduct repairs occur primarily through NER [21] TLS is another alternative way to repair these lesions, which is mainly done by DNA polymerases h [22] Polymeraseh(Polh), ... polh in tumor cells and poor Discussion The present study partially revealed the role of DNA polymeraseh as a DNA repair protein in gastric cancer by detecting its expression in four gastric cancer...
... products but the vertebrate DNApolymerase genes contain introns making the DNApolymerase products from the host genomic DNA much larger than from viral genomic DNA The predicted PCR product ... isolates representing the most common DNA viruses of vertebrates that contain DNApolymerase genes: herpesviridae, iridoviridae, poxviridae and adenoviridae The DNApolymerase PCR was performed on ... disease Also, the amino acid sequences of DNApolymerase of many large DNA viruses have been compared to evaluate virus relationships and compared to the DNA polymerases of other organisms to hypothesize...
... origin dependentDNA synthesis, including an origin binding protein, a helicase, a primase, a primase-associated factor, a single-stranded DNA binding protein, a DNA polymerase, and a DNApolymerase ... highly conserved DNApolymerase in open reading frame (ORF) and a DNApolymerase processivity factor in ORF59 [9] KSHV ORF59 binds DNA as a homodimer, interacts with the ORF9 DNApolymerase to strongly ... as well as a region that enhances the processivity of the DNApolymerase [6] Transport of the viral DNApolymerase into the nucleus is dependent on ORF59 [20], which contains a nuclear localization...
... in Y-family DNA polymerases and their implications for polymerase function and lesion bypass DNA Repair (Amst) 2002, 1:343-358 75 Glick E, Vigna KL, Loeb LA: Mutations in human DNApolymerase ... (at least) two substeps, E* · DNA · PPi ® E · DNA · PPi ® E · DNA + PPi, where the transition from the activated E* · DNA · PPi ternary complex to unactivated E · DNA · PPi ternary complex results ... the DNA substrate and PPi Since in the activated E* · DNA · dNTP (or E* · DNA · PPi) complex the Pol has a stronger interaction with DNA substrate and nucleotide than in the unactivated E · DNA...
... cỏc base ca RNA v DNA Cỏc mi ny c tng hp nh hot ng ca mt loi enzyme khỏc, gi l primase Tt c DNA- polymerase u tng hp DNA theo hng t u 5' n u 3' ca DNA Cho n khụng cú enzyme DNA- polymersae no cú ... phỏp gii trỡnh t (sequencing) da vo hot ng ca enzyme DNA- polymerase quỏ trỡnh tng hp DNA, emzym DNA- polymerase xỳc tỏc gn cỏc nucleotide vo mch n DNA ang tng hp v trớ cú cha nhúm -OH t do, gp nucleotide ... Ging 1: sn phm PCR nhõn gen DNA- polymerase ca chng DTVCKN; ging 2: sn phm PCR nhõn gen DNA- polymerase ca chng DTVVXKN cú kớch thc khong 0,5 kb; ging M: thang DNA chun (DNA ca thc khun th c ct bng...