Radioimager quantification of oligonucleotide hybridization with DNA immobilized on transfer membrane: Application to the identification of related sequences

被引:9
作者
Vernier, P [1 ]
Mastrippolito, R [1 ]
Helin, C [1 ]
Bendali, M [1 ]
Mallet, J [1 ]
Tricoire, H [1 ]
机构
[1] INST PHYS NUCL,F-91406 ORSAY,FRANCE
关键词
NUCLEIC-ACIDS; RECEPTOR; PROBES;
D O I
10.1006/abio.1996.0085
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The radioimager scintillating optical fiber imager was used to quantify the hybridization parameters of a 35-mer oligonucleotide probe with target DNAs immobilized on transfer membranes. The amount of the immobilized target DNA remaining accessible to hybridization (R(t)) was shown to be about 4% of the spotted DNA. The time course of the hybridization of a target DNA reacting with an excess of full-match probe exhibited a first-order kinetics, in which rate constant k was the highest for the hybridization temperature close to the calculated T-m. The effect of temperature on the hybridization kinetics of the probe sharing 37 to 100% identity with the immobilized target DNA was assessed: A significant fall of both the rate constant k and R(t) values at the plateau was observed when the identity shared by the target DNA and the probe decreased from 100 to 71%. The highest k and R(t) values were also obtained for temperatures closest to the calculated T-m. A good estimate of the degree of sequence identity may be calculated from the corresponding hybridization signals. Washing procedure did not improve the discrimination between related sequences, except for closely similar sequences. Practical conclusions for the detection of sequences belonging to gene families are presented. (C) 1996 Academic Press, Inc.
引用
收藏
页码:11 / 19
页数:9
相关论文
共 17 条
[1]  
Anderson M.L.M., 1985, NUCL ACID HYBRIDISAT, P73
[2]   REDUCTION IN RATE OF DNA REASSOCIATION BY SEQUENCE DIVERGENCE [J].
BONNER, TI ;
BRENNER, DJ ;
NEUFELD, BR ;
BRITTEN, RJ .
JOURNAL OF MOLECULAR BIOLOGY, 1973, 81 (02) :123-135
[3]  
Britten R J, 1974, Methods Enzymol, V29, P363
[4]   THE DOPAMINE-D2 RECEPTOR - 2 MOLECULAR-FORMS GENERATED BY ALTERNATIVE SPLICING [J].
DALTOSO, R ;
SOMMER, B ;
EWERT, M ;
HERB, A ;
PRITCHETT, DB ;
BACH, A ;
SHIVERS, BD ;
SEEBURG, PH .
EMBO JOURNAL, 1989, 8 (13) :4025-4034
[5]   SEQUENCE OF 2 MESSENGER-RNAS ENCODING ACTIVE-RAT TRYPTOPHAN-HYDROXYLASE [J].
DARMON, MC ;
GUIBERT, B ;
LEVIEL, V ;
EHRET, M ;
MAITRE, M ;
MALLET, J .
JOURNAL OF NEUROCHEMISTRY, 1988, 51 (01) :312-316
[6]   THE GENOMIC CLONE G-21 WHICH RESEMBLES A BETA-ADRENERGIC-RECEPTOR SEQUENCE ENCODES THE 5-HT1A RECEPTOR [J].
FARGIN, A ;
RAYMOND, JR ;
LOHSE, MJ ;
KOBILKA, BK ;
CARON, MG ;
LEFKOWITZ, RJ .
NATURE, 1988, 335 (6188) :358-360
[7]   A QUANTITATIVE ASSAY FOR DNA-RNA HYBRIDS WITH DNA IMMOBILIZED ON A MEMBRANE [J].
GILLESPIE, D ;
SPIEGELMAN, S .
JOURNAL OF MOLECULAR BIOLOGY, 1965, 12 (03) :829-+
[8]   HYBRIDIZATION PROPERTIES OF IMMOBILIZED NUCLEIC-ACIDS [J].
GINGERAS, TR ;
KWOH, DY ;
DAVIS, GR .
NUCLEIC ACIDS RESEARCH, 1987, 15 (13) :5373-5390
[9]   ALTERNATIVE SPLICING DIRECTS THE EXPRESSION OF 2 D2 DOPAMINE RECEPTOR ISOFORMS [J].
GIROS, B ;
SOKOLOFF, P ;
MARTRES, MP ;
RIOU, JF ;
EMORINE, LJ ;
SCHWARTZ, JC .
NATURE, 1989, 342 (6252) :923-926
[10]   CDNA FOR THE HUMAN BETA-2-ADRENERGIC RECEPTOR - A PROTEIN WITH MULTIPLE MEMBRANE-SPANNING DOMAINS AND ENCODED BY A GENE WHOSE CHROMOSOMAL LOCATION IS SHARED WITH THAT OF THE RECEPTOR FOR PLATELET-DERIVED GROWTH-FACTOR [J].
KOBILKA, BK ;
DIXON, RAF ;
FRIELLE, T ;
DOHLMAN, HG ;
BOLANOWSKI, MA ;
SIGAL, IS ;
YANGFENG, TL ;
FRANCKE, U ;
CARON, MG ;
LEFKOWITZ, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (01) :46-50