Post-amplification Klenow fragment treatment alleviates PCR bias caused by partially single-stranded amplicons

被引:26
作者
Egert, M [1 ]
Friedrich, MW [1 ]
机构
[1] Max Planck Inst Terr Microbiol, D-35043 Marburg, Germany
关键词
genetic diversity analyses; molecular fingerprinting; single-stranded amplicons; T-RFLP;
D O I
10.1016/j.mimet.2004.11.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Partially single-stranded amplicons, formed during PCR amplification of single and mixed templates, are a potential source of bias in genetic diversity Studies. The analysis of 16S rRNA gene diversity in mixed template samples by the fingerprinting technique terminal restriction fragment length polymorphism (T-RFLP) analysis can be biased by the occurrence of pseudo-TRFs, i.e., restriction fragments occurring in addition to the expected terminal restriction fragments of single amplicons. This bias originates from PCR products, which are single-stranded at their terminal restriction site. Here we show that treatment of PCR amplicons with Klenow fragment prior to restriction digest and T-RFLP analysis minimized effectively the occurrence of pseudo-T-RFs. Klenow fragment activity filled in bases into the partially single-stranded amplicons and thereby restored the affected amplicons to complete double strands. Our method allowed to improve the assessment of genetic diversity and gene ratios from T-RFLP analysis of an original environmental sample. Since partially single-stranded amplicons might influence many PCR-based techniques, post-amplification treatment with Klenow fragment may be useful for a wide range of applications, which assess the composition of amplicon pools, e.g., the analysis of marker gene diversity in mixed template samples by fingerprinting techniques or the analysis of sequence diversity by cloning. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:69 / 75
页数:7
相关论文
共 18 条
[1]   Terminal restriction fragment length polymorphism monitoring of genes amplified directly from bacterial communities in soils and sediments [J].
Bruce K.D. ;
Hughes M.R. .
Molecular Biotechnology, 2000, 16 (3) :261-269
[2]   GENETIC AND CRYSTALLOGRAPHIC STUDIES OF THE 3',5'-EXONUCLEOLYTIC SITE OF DNA-POLYMERASE-I [J].
DERBYSHIRE, V ;
FREEMONT, PS ;
SANDERSON, MR ;
BEESE, L ;
FRIEDMAN, JM ;
JOYCE, CM ;
STEITZ, TA .
SCIENCE, 1988, 240 (4849) :199-201
[3]   Formation of pseudo-terminal restriction fragments, a PCR-related bias affecting terminal restriction fragment length polymorphism analysis of microbial community structure [J].
Egert, M ;
Friedrich, MW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (05) :2555-2562
[4]   Microbial community structure in midgut and hindgut of the humus-feeding larva of Pachnoda ephippiata (Coleoptera: Scarabaeidae) [J].
Egert, M ;
Wagner, B ;
Lemke, T ;
Brune, A ;
Friedrich, MW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (11) :6659-6668
[5]  
JENSEN MA, 1993, PCR METH APPL, V3, P186
[6]  
Kanagawa T, 2003, J BIOSCI BIOENG, V96, P317, DOI 10.1263/jbb.96.317
[7]  
Kitts C L, 2001, Curr Issues Intest Microbiol, V2, P17
[8]   Evaluation of PCR amplification bias by terminal restriction fragment length polymorphism analysis of small-subunit rRNA and mcrA genes by using defined template mixtures of methanogenic pure cultures and soil DNA extracts [J].
Lueders, T ;
Friedrich, MW .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (01) :320-326
[9]   DNA rehybridization during PCR: The 'C(O)t effect' and its consequences [J].
MathieuDaude, F ;
Welsh, J ;
Vogt, T ;
McClelland, M .
NUCLEIC ACIDS RESEARCH, 1996, 24 (11) :2080-2086
[10]   TYPE-II RESTRICTION ENDONUCLEASES CLEAVE SINGLE-STRANDED DNAS IN GENERAL [J].
NISHIGAKI, K ;
KANEKO, Y ;
WAKUDA, H ;
HUSIMI, Y ;
TANAKA, T .
NUCLEIC ACIDS RESEARCH, 1985, 13 (16) :5747-5760