Challenging artificial genetic systems: thymidine analogs with 5-position sulfur functionality

被引:58
作者
Held, HA
Benner, SA
机构
[1] Univ Florida, Dept Chem, Gainesville, FL 32611 USA
[2] Univ Florida, Dept Anat & Cell Biol, Gainesville, FL 32611 USA
关键词
D O I
10.1093/nar/gkf500
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
Eight different polymerases, chosen from evolutionary families A (Taq, Tfl, HotTub and Tth) and B (Pfu, Pwo, Vent and Deep Vent), were examined for their ability to incorporate 5-position modified 2'-deoxyuridine derivatives that carry a protected thiol group appended via different linkers containing either three or four carbon atoms. This represents the first attempt to incorporate the thiol functionality into DNA via enzymatic synthesis. Each polymerase-substrate combination was evaluated using a hierarchy of increasingly more difficult challenges, starting with incorporation of a single derivative, proceeding to incorporation of two derivatives at adjacent sites and non-adjacent sites, then examining the ability of the polymerase to accept the derivative within the template, and concluding with a challenge involving PCR. The evaluation of thiol-bearing 2'-deoxyuridine derivatives was then extended to consider their chemical stabilities. Stability was found to be less than satisfactory when the thiol functionality has a 'propargylic' relationship to the unsaturation in the linker. The best polymerase-appendage combination used the polymerase from Pyrococcus woesei (Pwo) and the 5'-tBu-SS-CH2-CH2-Cequivalent toC- linker. This pair supported PCR amplification and therefore should have value in artificial in vitro selection experiments. Indeed, we discovered that Pwo and Pfu preferred the derivative triphosphate over TTP, the natural substrate, in competition studies. These studies confirm an earlier suggestion that membership of an evolutionary family of polymerases is a partial predictor of the ability of the polymerase to accept 5-modified 2'-deoxyuridines. Considerable differences are displayed by different members within a polymerase family, however. This remains curious, as the ability of the polymerase to replicate natural DNA with high fidelity and its propensity to exclude unnatural analogs are presumed to be correlated.
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页码:3857 / 3869
页数:13
相关论文
共 34 条
[21]   Structure and dynamics of disulfide cross-linked DNA triple helices [J].
Osborne, SE ;
Cain, RJ ;
Glick, GD .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1997, 119 (06) :1171-1182
[22]   Expanding the catalytic repertoire of nucleic acid catalysts:: Simultaneous incorporation of two modified deoxyribonucleoside triphosphates bearing ammonium and imidazolyl functionalities. [J].
Perrin, DM ;
Garestier, T ;
Hélène, C .
NUCLEOSIDES & NUCLEOTIDES, 1999, 18 (03) :377-391
[23]   ENZYMATIC INCORPORATION OF A NEW BASE PAIR INTO DNA AND RNA EXTENDS THE GENETIC ALPHABET [J].
PICCIRILLI, JA ;
KRAUCH, T ;
MORONEY, SE ;
BENNER, SA .
NATURE, 1990, 343 (6253) :33-37
[24]   A SYSTEM FOR RAPID DNA SEQUENCING WITH FLUORESCENT CHAIN-TERMINATING DIDEOXYNUCLEOTIDES [J].
PROBER, JM ;
TRAINOR, GL ;
DAM, RJ ;
HOBBS, FW ;
ROBERTSON, CW ;
ZAGURSKY, RJ ;
COCUZZA, AJ ;
JENSEN, MA ;
BAUMEISTER, K .
SCIENCE, 1987, 238 (4825) :336-341
[25]   NUCLEIC-ACID RELATED-COMPOUNDS .39. EFFICIENT CONVERSION OF 5-IODO TO 5-ALKYNYL AND DERIVED 5-SUBSTITUTED URACIL BASES AND NUCLEOSIDES [J].
ROBINS, MJ ;
BARR, PJ .
JOURNAL OF ORGANIC CHEMISTRY, 1983, 48 (11) :1854-1862
[26]   Crystal structure of a pol α family DNA polymerase from the hyperthermophilic archaeon Thermococcus sp. 9°N-7 [J].
Rodriguez, AC ;
Park, HW ;
Mao, C ;
Beese, LS .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 299 (02) :447-462
[27]  
Sakthivel K, 1998, ANGEW CHEM INT EDIT, V37, P2872, DOI 10.1002/(SICI)1521-3773(19981102)37:20<2872::AID-ANIE2872>3.0.CO
[28]  
2-5
[29]   ENZYMATIC INCORPORATION OF A NEW BASE PAIR INTO DNA AND RNA [J].
SWITZER, C ;
MORONEY, SE ;
BENNER, SA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1989, 111 (21) :8322-8323
[30]   RNA-catalysed carbon-carbon bond formation [J].
Tarasow, TM ;
Tarasow, SL ;
Eaton, BE .
NATURE, 1997, 389 (6646) :54-57