RAPID CLONING AND CHARACTERIZATION OF NEW CHROMOSOME-10 DNA MARKERS BY ALU ELEMENT-MEDIATED PCR

被引:88
作者
BROOKSWILSON, AR
GOODFELLOW, PN
POVEY, S
NEVANLINNA, HA
DEJONG, PJ
GOODFELLOW, PJ
机构
[1] IMPERIAL CANC RES FUND,HUMAN MOLEC GENET LAB,LONDON WC2A 3PX,ENGLAND
[2] UNIV LONDON UNIV COLL,MRC,BIOCHEM GENET UNIT,LONDON NW1 2HE,ENGLAND
[3] UNIV HELSINKI,CENT HOSP,DEPT OBSTET & GYNAECOL,SF-00290 HELSINKI 29,FINLAND
[4] UNIV CALIF LAWRENCE LIVERMORE NATL LAB,DIV BIOMED SCI,LIVERMORE,CA 94550
基金
英国医学研究理事会;
关键词
D O I
10.1016/0888-7543(90)90207-B
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Alu element-mediated polymerase chain reaction is a strategy for rapidly cloning and mapping human DNA markers from mixed DNA sources. A novel primer homologous to the 3′ end of the human Alu repeat element provides the basis for preferential synthesis of human DNA fragments from human/rodent somatic cell hybrid DNA template. This approach has been used to isolate a series of new markers from chromosome 10. The Alu element-mediated PCR probes were regionally assigned on chromosome 10 by hybridization to Southern blots of Alu PCR-synthesized DNA derived from somatic cell hybrid template DNA. Alu element-mediated PCR is generally applicable and makes possible the analysis of complex genomes with a speed and sensitivity that has not been previously possible. © 1990.
引用
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页码:614 / 620
页数:7
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