A protocol for high-throughput extraction of DNA from rice leaves

被引:34
作者
Xu, X
Kawasaki, S
Fujimura, T
Wang, CT [1 ]
机构
[1] S Cent Univ Natl, Key Lab Biotechnol Natl Commiss Natl, Coll Life Sci, Wuhan 430074, Peoples R China
[2] Natl Inst Agrobiol Sci, Dept Plant Physiol, Tsukuba, Ibaraki 3058602, Japan
[3] Univ Tsukuba, Lab Plant Genet Engn, Tsukuba, Ibaraki 3058572, Japan
关键词
DNA isolation; map-based cloning; PCR amplification; rice;
D O I
10.1007/BF02772759
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Current DNA isolation methods have limitations between speed and purity in high-throughput molecular genetic analysis such as gene mapping and marker-assisted selection programs. We have optimized a simple and rapid method for isolating high-quality genomic DNA from rice that significantly minimizes time and the use of laboratory materials. One person can process as many as 384 samples in 2 h. The isolated DNA is suitable for polymerase chain reaction-based techniques and is stable for no less than 6 mo of storage at 4 degrees C.
引用
收藏
页码:291 / 295
页数:5
相关论文
共 14 条
[11]   Cereal DNA: A rapid high-throughput extraction method for marker assisted selection [J].
Paris, M ;
Carter, M .
PLANT MOLECULAR BIOLOGY REPORTER, 2000, 18 (04) :357-360
[12]   Forward genetics and map-based cloning approaches [J].
Peters, JL ;
Cnudde, F ;
Gerats, T .
TRENDS IN PLANT SCIENCE, 2003, 8 (10) :484-491
[13]  
STEENKAMP J, 1994, AM J ENOL VITICULT, V45, P102
[14]   A SIMPLE METHOD OF PREPARING PLANT-SAMPLES FOR PCR [J].
WANG, H ;
QI, MQ ;
CUTLER, AJ .
NUCLEIC ACIDS RESEARCH, 1993, 21 (17) :4153-4154