USE OF DEOXYINOSINE-CONTAINING PRIMERS VS DEGENERATE PRIMERS FOR POLYMERASE CHAIN-REACTION BASED ON AMBIGUOUS SEQUENCE INFORMATION

被引:33
作者
ROSSOLINI, GM
CRESTI, S
INGIANNI, A
CATTANI, P
RICCIO, ML
SATTA, G
机构
[1] UNIV CAGLIARI, IST MED INTERNA, I-09100 CAGLIARI, ITALY
[2] UNIV CATTOLICA SACRO CUORE, IST MICROBIOL, I-00168 ROME, ITALY
关键词
POLYMERASE CHAIN REACTION; DEOXYINOSINE-CONTAINING PRIMERS; DEGENERATE PRIMERS; AMBIGUOUS SEQUENCE INFORMATION; HUMAN PAPILLOMAVIRUSES;
D O I
10.1006/mcpr.1994.1013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The performance of oligonucleotide primers containing deoxyinosine (dI) at all ambiguous positions for polymerase chain reaction, based on ambiguous sequence information derived either from compilations of consensus nucleotide sequences or from amino acid sequences, has been evaluated in two model systems represented respectively by amplification of conserved genomic regions from different types of human papillomavirus and by amplification of a region of the human lysozyme cDNA on the basis of the protein amino acid sequence. In both instances the dI-containing primers obtained the expected amplification products. When using short primers or primers with very high dI contents, however, peculiar reaction conditions had to be adopted to obtain successful amplification and, in the latter case, performance remained suboptimal. Comparison of results with those obtained using corresponding degenerate primers showed that the use of dI-containing primers can be advantageous in terms of both specificity and yield of the amplification product. Sequence analysis of amplification products showed that dG residues are always found at positions corresponding to the dI residues of the primers. © 1994 Academic Press, Limited.
引用
收藏
页码:91 / 98
页数:8
相关论文
共 32 条
[1]  
Baker C.C., 1987, PAPOVAVIRIDAE, V2, P321
[2]   USE OF INOSINE-CONTAINING OLIGONUCLEOTIDE PRIMERS FOR ENZYMATIC AMPLIFICATION OF DIFFERENT ALLELES OF THE GENE CODING FOR HEAT-STABLE TOXIN TYPE-I OF ENTEROTOXIGENIC ESCHERICHIA-COLI [J].
CANDRIAN, U ;
FURRER, B ;
HOFELEIN, C ;
LUTHY, J .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1991, 57 (04) :955-961
[3]   IMPROVED DETECTION OF HIV-1 ENVELOPE SEQUENCES USING OPTIMIZED PCR AND INOSINE-SUBSTITUTED PRIMERS [J].
CASSOL, S ;
SALAS, T ;
LAPOINTE, N ;
ARELLA, M ;
RUDNIK, J ;
OSHAUGHNESSY, M .
MOLECULAR AND CELLULAR PROBES, 1991, 5 (02) :157-160
[4]  
CHING LP, 1988, P NATIONAL ACADEMY S, V85, P6227
[5]   NUCLEOTIDE-SEQUENCE AND COMPARATIVE-ANALYSIS OF THE HUMAN PAPILLOMAVIRUS TYPE-18 GENOME - PHYLOGENY OF PAPILLOMAVIRUSES AND REPEATED STRUCTURE OF THE E6 AND E7 GENE-PRODUCTS [J].
COLE, ST ;
DANOS, O .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 193 (04) :599-608
[6]   THE NUCLEOTIDE-SEQUENCE AND GENOME ORGANIZATION OF HUMAN PAPILLOMA-VIRUS TYPE-11 [J].
DARMANN, K ;
SCHWARZ, E ;
GISSMANN, L ;
HAUSEN, HZ .
VIROLOGY, 1986, 151 (01) :124-130
[7]   HETEROGENEITY OF THE HUMAN PAPILLOMAVIRUS GROUP [J].
DEVILLIERS, EM .
JOURNAL OF VIROLOGY, 1989, 63 (11) :4898-4903
[8]   DETECTION OF RAS POINT MUTATIONS BY POLYMERASE CHAIN-REACTION USING MUTATION-SPECIFIC, INOSINE-CONTAINING OLIGONUCLEOTIDE PRIMERS [J].
EHLEN, T ;
DUBEAU, L .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 160 (02) :441-447
[9]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[10]   GENERATION OF DNA PROBES FOR PEPTIDES WITH HIGHLY DEGENERATE CODONS USING MIXED PRIMER PCR [J].
GIRGIS, SI ;
ALEVIZAKI, M ;
DENNY, P ;
FERRIER, GJM ;
LEGON, S .
NUCLEIC ACIDS RESEARCH, 1988, 16 (21) :10371-10371