Bidirectional PCR amplification of specific alleles
AssigneeCity of Hope
InventorsQiang Liu, Steve S. Sommer
Life of this patent
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Abstract
Bi-directional polymerase chain reaction (PCR) amplification of specific alleles (Bi-PASA). Two outer primers (P and Q) and two inner primers (A and B) are used. A and B are each specific for different alleles. In heterozygotes, three segments are amplified: a segment of size AQ resulting from one allele, another segment of size PB resulting from the second allele, and a combined segment of size PQ. In homozygotes, segment PQ and either segments AQ or PB amplify.
Claims13
A method for conducting a bi-directional PCR amplification of specific alleles which comprises subjecting DNA which may contain one or both of first and second alleles to a single one tube PCR under a thermal cycling condition utilizing an outer pair of primers P and Q and an inner pair of primers A and B, where
- Q is complementary to the sense strand of both alleles in a region downstream of the sequence difference X which distinguishes the alleles and P is complementary to the anti-sense strand of both alleles in a region upstream of X;
- B has a region at its 3′ end which is complementary to the sense strand of the first allele and A has a region at its 3′ end which is complementary to the antisense strand of the second allele, each of A and B also has a non-complementary G+C-rich tail at its 5′ end, and X occurs at or near the 3′ end of each of A and B, whereby A and B are in two directions with partially overlapped 3′ ends;
- whereby DNA which is heterozygous with respect to the two alleles results in simultaneous amplification of three overlapping sequences, PQ, PB and AQ, DNA which is homozygous with respect to the first allele results in simultaneous amplification of two overlapping sequences, PQ and PB, and DNA which is homozygous with respect to the second allele results in simultaneous amplification of two overlapping sequences, PQ and AQ, where PQ, PB and AQ, respectively, stand for the sequences extending from P to Q inclusive, from P to B inclusive, and from A to Q inclusive, wherein the method is conducted at a substantially constant annealing temperature in the range of about 50-65° C. and with a ratio of concentrations of the outer and inner primers in the PCR mixture in the range of about 1:1 to 1:6.
A method for conducting a bi-directional PCR amplification of specific alleles in DNA which may contain one or both of first and second alleles, one of which is a mutant allele containing a point mutation X and one of which is a wild type allele, which comprises subjecting the DNA to a single one-tube PCR under a thermal cycling condition utilizing an outer pair of primers P and Q and an inner pair of primers A and B, where
- Q is complementary to the sense strand of both alleles in a region downstream of X and P is complementary to the anti-sense strand of both alleles in a region upstream of X;
- B has a region at its 3′ end which is complementary to the sense strand of the first allele and A has a region at its 3′ end which is complementary to the antisense strand of the second allele, each of A and B also has a non-complementary G+C-rich tail at its 5′ end, and X occurs at or near the 3′ end of each of A and B, whereby A and B are in two directions with partially overlapped 3′ ends;
- whereby DNA which is heterozygous with respect to the two alleles results in simultaneous amplification of three overlapping segments, PQ, PB and AQ, DNA which is homozygous with respect to the first allele results in simultaneous amplification of two overlapping segments, PQ and PB, and DNA which is homozygous with respect to the second allele results in simultaneous amplification of two overlapping segments, PQ and AQ, where PQ, PB and AQ, respectively, stand for the segments extending from P to Q inclusive, from P to B inclusive, and from A to Q inclusive, wherein the method is conducted at a substantially constant annealing temperature in the range of about 50-65° C. and with a ratio of concentrations of the outer and inner primers in the PCR mixture in the range of about 1:1 to 1:6.
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