Transcriptional sequencing: A method for DNA sequencing using RNA polymerase

被引:32
作者
Sasaki, N
Izawa, M
Watahiki, M
Ozawa, K
Tanaka, T
Yoneda, Y
Matsuura, S
Carninci, P
Muramatsu, M
Okazaki, Y
Hayashizaki, Y
机构
[1] Inst Phys & Chem Res, Tsukuba Life Sci Ctr, Genome Sci Lab, Ibaraki, Osaka 305, Japan
[2] Nippon Gene Co Ltd, Res & Dev, Toyama 930, Japan
[3] Wako Pure Chem Ind Ltd, Osaka Res Labs, Amagasaki, Hyogo 661, Japan
关键词
D O I
10.1073/pnas.95.7.3455
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have developed a sequencing method based on the RNA polymerase chain termination reaction with rhodamine dye attached to 3'-deoxynucleoside triphosphate (3'-dNTP). This method enables us to conduct a rapid isothermal sequencing reaction in <30 min, to reduce the amount of template required, and to do PCR direct sequencing without the elimination of primers and 2'-dNTP, which disturbs the Sanger sequencing reaction. An accurate and longer read length was made possible by newly designed four-color dye-3'-dNTPs and mutated RNA polymerase with an improved incorporation rate of 3'-dNTP. This method should be useful for large-scale sequencing in genome projects and clinical diagnosis.
引用
收藏
页码:3455 / 3460
页数:6
相关论文
共 24 条
[1]   TRANSCRIPTION FROM BACTERIOPHAGE-T7 AND SP6 RNA-POLYMERASE PROMOTERS IN THE PRESENCE OF 3'-DEOXYRIBONUCLEOSIDE 5'-TRIPHOSPHATE CHAIN TERMINATORS [J].
AXELROD, VD ;
KRAMER, FR .
BIOCHEMISTRY, 1985, 24 (21) :5716-5723
[2]   Microfabrication technologies for integrated nucleic acid analysis [J].
Burke, DT ;
Burns, MA ;
Mastrangelo, C .
GENOME RESEARCH, 1997, 7 (03) :189-197
[3]  
CUNNINGHAM PR, 1990, BIOTECHNIQUES, V9, P713
[4]   HOW IS THE HUMAN GENOME PROJECT DOING, AND WHAT HAVE WE LEARNED SO FAR [J].
GUYER, MS ;
COLLINS, FS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (24) :10841-10848
[5]  
HAYASHIZAKI Y, 1985, FEBS LETT, V188, P394, DOI 10.1016/0014-5793(85)80409-9
[6]   ENGINEERING HYBRID GENES WITHOUT THE USE OF RESTRICTION ENZYMES - GENE-SPLICING BY OVERLAP EXTENSION [J].
HORTON, RM ;
HUNT, HD ;
HO, SN ;
PULLEN, JK ;
PEASE, LR .
GENE, 1989, 77 (01) :61-68
[7]   DNA SEQUENCING USING CAPILLARY ARRAY ELECTROPHORESIS [J].
HUANG, XHC ;
QUESADA, MA ;
MATHIES, RA .
ANALYTICAL CHEMISTRY, 1992, 64 (18) :2149-2154
[8]   DNA SEQUENCING WITH THERMUS-AQUATICUS DNA-POLYMERASE AND DIRECT SEQUENCING OF POLYMERASE CHAIN REACTION-AMPLIFIED DNA [J].
INNIS, MA ;
MYAMBO, KB ;
GELFAND, DH ;
BROW, MAD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (24) :9436-9440
[9]   IDENTIFICATION OF A REGION OF THE BACTERIOPHAGE T3 AND T7 RNA-POLYMERASES THAT DETERMINES PROMOTER SPECIFICITY [J].
JOHO, KE ;
GROSS, LB ;
MCGRAW, NJ ;
RASKIN, C ;
MCALLISTER, WT .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (01) :31-39
[10]   FLUORESCENCE ENERGY-TRANSFER DYE-LABELED PRIMERS FOR DNA-SEQUENCING AND ANALYSIS [J].
JU, JY ;
RUAN, CC ;
FULLER, CW ;
GLAZER, AN ;
MATHIES, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (10) :4347-4351