Acyclic and dideoxy terminator preferences denote divergent sugar recognition by archaeon and Taq DNA polymerases

被引:66
作者
Gardner, AF [1 ]
Jack, WE [1 ]
机构
[1] New England Biolabs Inc, Beverly, MA 01915 USA
关键词
D O I
10.1093/nar/30.2.605
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The nucleotide-binding site in a variety of DNA polymerases was probed by analyzing incorporation of dideoxy and acyclic chain terminators. Family B archaeon DNA polymerases Vent, Deep Vent, 9degreesN and Pfu incorporated acyclic in preference to dideoxy terminators, while the Family A DNA polymerases Taq and Klenow preferred dideoxy terminators. These divergent biases suggest that significant differences exist in sugar recognition in these two classes of polymerases. Mutants of Vent (A488L) and Taq (F667Y) that increase incorporation of dideoxy terminators maintained the acyclic/ dideoxy bias of the parent enzyme, while more efficiently incorporating both dideoxy and acyclic terminators. The preference of archaeon DNA polymerases for acyclic analogs was exploited in chain terminator DNA sequence and genotype analysis. This technology was additionally aided by identification of specific dye-modified bases that improve terminator incorporation over that of the unmodified terminator. These three enhancing effects, (I) acyclic analogs, (ii) archaeon variants and (iii) specific dyes, appear to act additively and independently to increase terminator incorporation efficiency, collectively enhancing incorporation similar to8000-fold over the wild-type incorporation of dideoxynucleotides. Fluorescent chain terminator DNA sequence traces demonstrate the applicability of these advances in improving terminator incorporation, as required in DNA sequence and genotype determinations.
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页码:605 / 613
页数:9
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共 24 条
  • [1] Slow rate of phosphodiester bond formation accounts for the strong bias that Taq DNA polymerase shows against 2',3'-dideoxynucleotide terminators
    Brandis, JW
    Edwards, SG
    Johnson, KA
    [J]. BIOCHEMISTRY, 1996, 35 (07) : 2189 - 2200
  • [2] Chen XN, 1999, GENOME RES, V9, P492
  • [3] Template-directed dye-terminator incorporation (TDI) assay: A homogeneous DNA diagnostic method based on fluorescence resonance energy transfer
    Chen, XN
    Kwok, PY
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (02) : 347 - 353
  • [4] Simple version of "megaprimer" PCR for site-directed mutagenesis
    Colosimo, A
    Xu, Z
    Novelli, G
    Dallapiccola, B
    Gruenert, DC
    [J]. BIOTECHNIQUES, 1999, 26 (05) : 870 - +
  • [5] Crystal structure of a bacteriophage T7 DNA replication complex at 2.2 Å resolution
    Doublié, S
    Tabor, S
    Long, AM
    Richardson, CC
    Ellenberger, T
    [J]. NATURE, 1998, 391 (6664) : 251 - 258
  • [6] Improving dideoxynucleotide-triphosphate utilisation by the hyper-thermophilic DNA polymerase from the archaeon Pyrococcus furiosus
    Evans, SJ
    Fogg, MJ
    Mamone, A
    Davis, M
    Pearl, LH
    Connolly, BA
    [J]. NUCLEIC ACIDS RESEARCH, 2000, 28 (05) : 1059 - 1066
  • [7] Base-calling of automated sequencer traces using phred.: II.: Error probabilities
    Ewing, B
    Green, P
    [J]. GENOME RESEARCH, 1998, 8 (03): : 186 - 194
  • [8] Structure of the replicating complex of a pol α family DNA polymerase
    Franklin, MC
    Wang, JM
    Steitz, TA
    [J]. CELL, 2001, 105 (05) : 657 - 667
  • [9] Determinants of nucleotide sugar recognition in an archaeon DNA polymerase
    Gardner, AF
    Jack, WE
    [J]. NUCLEIC ACIDS RESEARCH, 1999, 27 (12) : 2545 - 2553
  • [10] Heringa Jaap, 1994, P87