SEQUENCE-SPECIFIC GENE SIGNATURES CAN BE OBTAINED BY PCR WITH SINGLE SPECIFIC PRIMERS AT LOW STRINGENCY

被引:61
作者
PENA, SDJ
BARRETO, G
VAGO, AR
DEMARCO, L
REINACH, FC
NETO, ED
SIMPSON, AJG
机构
[1] UNIV FED MINAS GERAIS,DEPT BIOCHEM,BR-31270901 BELO HORIZONT,MG,BRAZIL
[2] UNIV FED MINAS GERAIS,DEPT PHARMACOL,BR-31270901 BELO HORIZONT,MG,BRAZIL
[3] UNIV SAO PAULO,INST QUIM,DEPT BIOQUIM,BR-01498 SAO PAULO,BRAZIL
[4] FDN OSWALDO CRUZ,CTR PESQUISAS RENE RACHOU,BR-31090002 BELO HORIZONT,MG,BRAZIL
关键词
D O I
10.1073/pnas.91.5.1946
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
Low-stringency single specific primer PCR (LSSP-PCR) is an extremely simple PCR-based technique that detects single or multiple mutations in gene-sized DNA fragments. A purified DNA fragment is subjected to PCR using high concentrations of a single specific oligonucleotide primer, large amounts of Tag polymerase, and a very low annealing temperature. Under these conditions the primer hybridizes specifically to its complementary region and nonspecifically to multiple sites within the fragment, in a sequence-dependent manner, producing a heterogeneous set of reaction products resolvable by electrophoresis. The complex banding pattern obtained is significantly altered by even a single-base change and thus constitutes a unique ''gene signature.'' Therefore LSSP-PCR will have almost unlimited application in all fields of genetics and molecular medicine where rapid and sensitive detection of mutations and sequence variations is important. The usefulness of LSSP-PCR is illustrated by applications in the study of mutants of smooth muscle myosin light chain, analysis of a family with X-linked nephrogenic diabetes insipidus, and identity testing using human mitochondrial DNA.
引用
收藏
页码:1946 / 1949
页数:4
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