Bias in Template-to-Product Ratios in Multitemplate PCR

@article{citeulike:2754507, abstract = {Bias introduced by the simultaneous amplification of specific genes from complex mixtures of templates remains poorly understood. To explore potential causes and the extent of bias in PCR amplification of 16S ribosomal DNAs (rDNAs), genomic DNAs of two closely and one distantly related bacterial species were mixed and amplified with universal, degenerate primers. Quantification and comparison of template and product ratios showed that there was considerable and reproducible overamplification of specific templates. Variability between replicates also contributed to the observed bias but in a comparatively minor way. Based on these initial observations, template dosage and differences in binding energies of permutations of the degenerate, universal primers were tested as two likely causes of this template-specific bias by using 16S rDNA templates modified by site-directed mutagenesis. When mixtures of mutagenized templates containing AT- and GC-rich priming sites were used, templates containing the GC-rich permutation amplified with higher efficiency, indicating that different primer binding energies may to a large extent be responsible for overamplification. In contrast, gene copy number was found to be an unlikely cause of the observed bias. Similarly, amplification from DNA extracted from a natural community to which different amounts of genomic DNA of a single bacterial species were added did not affect relative product ratios. Bias was reduced considerably by using high template concentrations, by performing fewer cycles, and by mixing replicate reaction preparations.}, author = {Polz, Martin F. and Cavanaugh, Colleen M. }, citeulike-article-id = {2754507}, journal = {Appl. Environ. Microbiol.}, keywords = {pcr, pcr\_bias}, month = {October}, number = {10}, pages = {3724--3730}, posted-at = {2008-05-04 22:02:26}, priority = {2}, title = {Bias in Template-to-Product Ratios in Multitemplate PCR}, url = {http://aem.asm.org/cgi/content/abstract/64/10/3724}, volume = {64}, year = {1998} }

TY - JOUR ID - citeulike:2754507 L3 - citeulike-article-id:2754507 TI - Bias in Template-to-Product Ratios in Multitemplate PCR JF - Appl. Environ. Microbiol. VL - 64 IS - 10 SP - 3724 EP - 3730 N2 - Bias introduced by the simultaneous amplification of specific genes from complex mixtures of templates remains poorly understood. To explore potential causes and the extent of bias in PCR amplification of 16S ribosomal DNAs (rDNAs), genomic DNAs of two closely and one distantly related bacterial species were mixed and amplified with universal, degenerate primers. Quantification and comparison of template and product ratios showed that there was considerable and reproducible overamplification of specific templates. Variability between replicates also contributed to the observed bias but in a comparatively minor way. Based on these initial observations, template dosage and differences in binding energies of permutations of the degenerate, universal primers were tested as two likely causes of this template-specific bias by using 16S rDNA templates modified by site-directed mutagenesis. When mixtures of mutagenized templates containing AT- and GC-rich priming sites were used, templates containing the GC-rich permutation amplified with higher efficiency, indicating that different primer binding energies may to a large extent be responsible for overamplification. In contrast, gene copy number was found to be an unlikely cause of the observed bias. Similarly, amplification from DNA extracted from a natural community to which different amounts of genomic DNA of a single bacterial species were added did not affect relative product ratios. Bias was reduced considerably by using high template concentrations, by performing fewer cycles, and by mixing replicate reaction preparations. KW - pcr KW - pcr_bias AU - Polz, Martin AU - Cavanaugh, Colleen PY - 1998/10/01/ UR - http://aem.asm.org/cgi/content/abstract/64/10/3724 ER -