LIGATION-ANCHORED PCR - A SIMPLE AMPLIFICATION TECHNIQUE WITH SINGLE-SIDED SPECIFICITY

被引:190
作者
TROUTT, AB
MCHEYZERWILLIAMS, MG
PULENDRAN, B
NOSSAL, GJV
机构
[1] Howard Hughes Medical Institute, Stanford University Medical Center, Stanford
关键词
IMMUNOGLOBULIN; T-CELL RECEPTOR; CDNA CLONING; GENE TRAP VECTORS; ALTERNATIVE SPLICING;
D O I
10.1073/pnas.89.20.9823
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
A simple, efficient, and sensitive technique has been developed for amplification of cDNAs encoding molecules with 5' regions of unknown sequence. In this ligation-anchored PCR, T4 RNA ligase is used to covalently link an "anchor" oligonucleotide to first-strand cDNAs. These anchored cDNAs are then amplified by using one PCR primer specific for the anchor and another specific for a sequence within the molecule of interest. The anchor oligonucleotide has been especially designed to facilitate subsequent analysis and cloning of the resultant PCR products. This three-stage procedure does not require purification of product between steps and avoids many of the technical difficulties associated with established anchored PCR protocols. The efficacy of ligation-anchored PCR was demonstrated by amplification of a specific IgG1 cDNA; total RNA equivalent to as few as 100 cells yielded the expected PCR product.
引用
收藏
页码:9823 / 9825
页数:3
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