US20050164190A1 - Primers for nucleic acid amplification in detecting housekeeping gene mrna and test method using these primers - Google Patents

Primers for nucleic acid amplification in detecting housekeeping gene mrna and test method using these primers Download PDF

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US20050164190A1
US20050164190A1 US10/504,930 US50493004A US2005164190A1 US 20050164190 A1 US20050164190 A1 US 20050164190A1 US 50493004 A US50493004 A US 50493004A US 2005164190 A1 US2005164190 A1 US 2005164190A1
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Sachiyo Tada
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Sysmex Corp
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    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876—Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
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    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
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    • C12Q1/6851—Quantitative amplification
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    • C12Q2545/00—Reactions characterised by their quantitative nature
    • C12Q2545/10—Reactions characterised by their quantitative nature the purpose being quantitative analysis
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    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/16—Primer sets for multiplex assays
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    • C12Q2600/00—Oligonucleotides characterized by their use
    • C12Q2600/166—Oligonucleotides used as internal standards, controls or normalisation probes

Definitions

  • the present invention relates to primers for nucleic acid amplification to detect a housekeeping gene.
  • nucleic acid amplification methods including polymerase chain reaction method (PCR method: Science, 230:1350-1354, 1985) and NASBA method (Nucleic Acid Sequence Based Amplification method: Nature, 350, 91-92, 1991; Japanese Patent No. 2648802, and Japanese Patent No. 2650159), detection of an infinitesimal amount of nucleic acid present in a biological sample, which has been difficult so far, has become possible, thereby dramatically facilitating genetic analyses.
  • tumor marker protein such as cytokeratin (CK). Due to the recent development of genetic analysis technology, detection of mRNA expression of tumor marker protein has allowed effective diagnosis of tumor (The Hokkaido journal of medical science, vol. 66(2), pp. 135-141, 1991). RT-PCR has allowed detection of CK mRNA expression in excised tissue, and underdiagnosis of tumor metastasis can be prevented to some extent. These nucleic acid amplification methods have been put to practical use in the field of diagnosis of tumor and cancer (Manual of Clinical Laboratory Medicine, 31st ed., Kanehara & Co., Ltd, published on Sep. 20, 1998).
  • the LAMP method is a gene amplification method using multiple primers including those forming a hairpin structure at the ends of the amplified product as the strand displacement reaction proceeds.
  • a dumbbell-like structure with loops at both ends is synthesized from template DNA by using a pair of inner primers (FIP and RIP), a pair of outer primers (F3 and R3 primers) and strand-displacement DNA polymerase.
  • F3 and R3 primers a pair of outer primers
  • strand-displacement DNA polymerase strand-displacement DNA polymerase.
  • the amplified product is composed of a number of repeat structures, each unit of which comprises, within the strand, the complementary regions linked in the inverted direction which are derived from the nucleotide sequences of double-stranded nucleic acids corresponding to the amplified region between the primers.
  • the LAMP method has features that heat denature of double-strands to single-strands is not required and that all the amplification reactions can proceed consecutively at a fixed temperature (Non-patent Documents 1 and 2).
  • the starting structure can be synthesized by adding reverse transcriptase to the composition of the reaction solution for DNA template, and the amplification can be conducted (RT-LAMP method).
  • the LAMP method gives a sufficient amount of amplification product to be detected in about 30 minutes.
  • this method may be applied to the diagnosis of tumor metastasis to lymph nodes for the purpose of prompt determination of the therapeutic strategy, because the time required for detection of nucleic acids is reduced.
  • This method is also promising for application to intraoperative diagnosis, since it can give prompt results.
  • mRNA of a housekeeping gene may be used as an internal control in the sample.
  • Use of the housekeeping gene mRNA as an internal control has the advantage of being able to detect mRNA of the target gene in a relative manner without regard to the extraction efficiency of the target gene mRNA or the cDNA synthesis efficiency.
  • housekeeping gene examples include the gene for ⁇ -actin, a component of the cytoskeleton, and gene for glyceraldehyde-3-phosphate dehydrogenase (hereinafter, referred to as “GAPDH”), a major enzyme in the glycolysis system.
  • GPDH glyceraldehyde-3-phosphate dehydrogenase
  • Action is a protein abundantly found in all the eukaryotic cells. This protein provides a number of structural and regulatory functions, including the role in mitosis, motility and the integrity of the structure of higher eukaryotic cells.
  • Six isoforms of actin have been identified in the vertebrates; four of them are of muscle actin (skeletal muscle, cardiac muscle, aortic smooth muscle and stomach smooth muscle actins) and two of them are of nonmuscle actin (cytoplasmic ⁇ - and ⁇ -actin). Muscle actins are tissue-specifically expressed and involved in muscular contraction. In contrast, cytoplasmic actins are found in all the cells in principle and involved in a number of cellular functions. In spite of its diversity, amino acid sequences of the intracellular actin are highly conserved among different actin types and among eukaryotic species.
  • the sequence of the human cytoplasmic ⁇ -actin gene has already been determined and compared with the sequences of ⁇ -actin genes derived from other species (Nakajima-Iijima et al, PNAS 82, pp. 6133-6137 (1985); EP Patent Application No. 0174608; Ponte et al., 1984, Nucleic Acids Res. 12, pp. 1687-1696 (1984)).
  • Primers for amplification of the entire human ⁇ -actin gene are commercially available from Clontech Laboratories, Inc. (Palo Alto, Calif.) under the name MAPPING Amplimershito for ⁇ -actin.
  • Human glyceraldehyde-3-phosphate is one of the important intermediates involved in the glucose metabolism, such as glycolysis and pentose phosphate cycle, and lipogenesis in the living organisms and this substance is widely distributed in the living body.
  • Human glyceraldehyde-3-phosphate dehydrogenase (GAPDH) is also necessary for synthesis of lipids from this substance and this enzyme is also widely distributed in vivo in human.
  • An object of the present invention is to provide primers for nucleic acid amplification to detect mRNA for housekeeping genes, particularly novel primers for amplification of mRNA for the ⁇ -actin and GAPDH genes.
  • the present inventors conducted extensive research review and succeeded in constructing primers for nucleic acid amplification of housekeeping genes.
  • the present invention comprises the following:
  • the primer of the preceding item 1 in which the housekeeping gene is the ⁇ -actin gene and/or GAPDH gene.
  • a primer for nucleic acid amplification to detect ⁇ -actin which comprises an oligonucleotide having a nucleic acid sequence selected from the group consisting of:
  • a primer for nucleic acid amplification to detect ⁇ -actin which comprises an oligonucleotide selected from the group consisting of the sequences set forth as SEQ ID NOs: 10, 14-17 and 29-50.
  • a primer for nucleic acid amplification to detect GAPDH which comprises an oligonucleotide having a nucleic acid sequence selected from the group consisting of:
  • a primer for nucleic acid amplification to detect GAPDH which comprises an oligonucleotide selected from the group consisting of the sequences set forth as SEQ ID NOs: 58, 62-64 and 73-96.
  • a primer set for nucleic acid amplification to detect ⁇ -actin which is featured by selecting at least two primers from the primers for nucleic acid amplification that comprise oligonucleotides having nucleic acid sequences selected from the group consisting of:
  • a primer set for nucleic acid amplification to detect ⁇ -actin which is featured by selecting at least four primers from the primers for nucleic acid amplification that comprise the oligonucleotides of above 8.
  • primer set for nucleic acid amplification claimed in any one of above 8 and 9, which features that at least two primers contained in the primer set recognize each two gene regions in the nucleotide sequence set forth as SEQ ID NO: 1 and/or the complementary sequence thereof.
  • primer set for nucleic acid amplification claimed in any one of above 9 and 10, which features that the primers contained in the primer set recognize at least six gene regions in the nucleotide sequence set forth as SEQ ID NO: 1 and/or the complementary sequence thereof.
  • a primer set comprising a combination of each one primer selected from each of (a) FIP: SEQ ID NOs: 35-42; (b) RIP: SEQ ID NOs: 43-50; (c) F3: SEQ ID NOs: 10 and 14-17 and (d) R3: SEQ ID NOs: 29-32, which categories consist of the primers for nucleic acid amplification to detect ⁇ -actin that comprise the oligonucleotides having the nucleotide sequences set forth as SEQ ID NOs: 10, 14-17, 29-32, 35-42 and 43-50.
  • the primer set claimed in above 12 which further comprises the oligonucleotides having the nucleotide sequences set forth as SEQ ID NOs: 33 and 34.
  • a primer set for nucleic acid amplification to detect GAPDH which is featured by selecting at least two primers from the primers for nucleic acid amplification that comprise the oligonucleotides defined in above 5.
  • a primer set for nucleic acid amplification to detect GAPDH which is featured by selecting at least four primers from the primers for nucleic acid amplification that comprise the oligonucleotides defined in above 5.
  • primer set for nucleic acid amplification claimed in any one of above 14 and 15, which features that at least two primers contained in the primer set recognize each two gene regions in the nucleotide sequence set forth as SEQ ID NO: 51 and/or the complementary sequence thereof.
  • primer set for nucleic acid amplification claimed in any one of above 14 to 16, which features that the primers contained in the primer set recognize at least six gene regions in the nucleotide sequence set forth as SEQ ID NO: 51 and/or the complementary sequence thereof.
  • a primer set comprising a combination of each one primer selected from each of (a) FIP: SEQ ID NOs: 80-87 and (b) RIP: SEQ ID NOs: 88-96, which categories consist of the primers for nucleic acid amplification to detect GAPDH that comprise the oligonucleotides having the nucleotide sequences set forth as SEQ ID NOs: 80-96
  • the primer set claimed above in 18, which further comprises an oligonucleotide having either one of the nucleotide sequences set forth as SEQ ID NO: 58 or SEQ ID NOs: 62-64 and an oligonucleotide having any one of the nucleotide sequences set forth as SEQ ID NOs: 73-77.
  • a primer set for nucleic acid amplification to detect ⁇ -actin which comprises any one of the following primer sets:
  • a primer set for nucleic acid amplification to detect GAPDH which comprises any one of the following primer sets:
  • a method for detecting nucleic acid in which at least one of the primers defined in any one of above 1 to 7 is used.
  • a method for detecting nucleic acid in which at least one of the primer sets defined in any one of above 8 to 23 is used.
  • a system for detecting nucleic acid which uses the nucleic acid detection method defined in above 24 or 25.
  • FIG. 1 shows the sensitivity when the primers for ⁇ -actin of the present invention were used (Example 2).
  • FIG. 2 shows the results of the determination using the primers for ⁇ -actin of the present invention in the culture of LS180 and Raji cells (Example 3).
  • FIG. 3 shows the sensitivity when the primers for GAPDH of the present invention were used (Example 5).
  • FIG. 4 shows the results of the determination using the primers for GAPDH of the present invention in the culture of LS180 and Raji cells (Example 6).
  • the present invention provides a method for nucleic acid amplification of housekeeping genes. More specifically, the present invention provides primers for nucleic acid amplification that are applicable to methods for nucleic acid amplification relating to mRNA for the ⁇ -actin and GAPDH genes.
  • the regions, F3c, F2c and F1c are provided in this sequence from the 3′ end and the regions, R3, R2 and R1, are provided in this sequence from the 5′ end of a target DNA to be amplified, and oligonucleotide chains containing the nucleotide sequences substantially identical or substantially complementary to at least these six regions are selected for designing at least four primers.
  • nucleotide sequences substantially identical to the nucleotide sequence of F2 include, in addition to the nucleotide sequence precisely the same as that of F2, nucleotide sequences that can function as templates to give nucleotide sequences that hybridize to F2 and serve as starting points for synthesis of complementary sequences.
  • sequences identical to a certain sequence include a complementary sequence to a nucleotide sequence capable of hybridizing to the certain sequence.
  • complementary refers to a sequence that can hybridize under stringent conditions and provide a 3′ end that can serve as a starting point for the synthesis of complementary strands.
  • the primers of the present invention have a length sufficient for base pairing with their complementary strands while maintaining the required specificity under the environment given in the different nucleic acid synthesis reactions described below.
  • the primers have 5 to 200 nucleotide length, more preferably, 10 to 50 nucleotide length. Considering that a primer length of at least about five nucleotides is required for recognition by any known polymerase that catalyzes sequence-dependent synthesis of nucleic acids, the length of the portion subjected to hybridization should be more than that.
  • the primers are desired to retain a length of 10 or more nucleotides. On the other hand, it is difficult to prepare excessively long nucleotide sequences by chemical synthesis. Thus, the nucleotide lengths described above are given as a desirable range.
  • template refers to a nucleic acid that serves as a template for synthesis of the complementary strand.
  • complementary strand having a nucleotide sequence complementary to the template has significance as a strand capable of hybridizing to the template, this relationship is ever relative.
  • a strand synthesized as a complementary strand may function as a template in turn. That is, complementary strands may serve as templates.
  • each primer selected from the nucleotide sequence of a target DNA constitutes categorized into FIP (forward inner primer), F3 primer (forward outer primer), RIP (reverse inner primer) or R3 primer (reverse outer primer).
  • An FIP is designed to have the nucleotide sequence of the F2 region, which is substantially complementary to the F2c region of the target DNA, at the 3′ end as well as to have a nucleotide sequence substantially identical to the F1c region of the target DNA at the 5′ end.
  • This design allows an intervening sequence independent from the target DNA to lie between F2 and F1c.
  • This target DNA-independent sequence is acceptable if the length is 0-50 nucleotides, preferably 0-40 nucleotide.
  • An F3 primer is designed to have a nucleotide sequence substantially identical to the F3 region, which is substantially complementary to the F3c region of the target DNA.
  • An RIP is designed to have the nucleotide sequence of the R2 region, which is substantially complementary to the R2c region of the target DNA, at the 3′ end as well as to have a nucleotide sequence substantially identical to the R1c region of the target DNA at the 5′ end.
  • RIP allows an intervening sequence independent from the target DNA to lie between R2 and R1c.
  • An R3 primer is designed to have a nucleotide sequence substantially identical to the R3 region, which is substantially complementary to the R3c region of the target DNA.
  • loop-primer refers to the single-stranded portion of the loop at the 5′ end of the dumbbell structure, in particular, it means a primer having a complementary sequence between, for example, the R1 and R2 region or the F1 and F2 region.
  • Use of the loop primer allows the proliferation of the starting point material for DNA synthesis.
  • Such a loop primer is designed to hybridize to the loop region to which FIP or RIP generated during the process of DNA synthesis.
  • sequences at least 5 nucleotides in length, preferably 10-30 nucleotides in length, and more preferably 17-25 nucleotides in length that recognize the DNA region may be selected, with paying attention to the factors including nucleotide composition, GC content, secondary structure and Tm value.
  • Tm values may be obtained using the Nearest Neighbor method.
  • DNA regions with a Tm value of 55-65° C., preferably 58-64° C., and with a GC content of 40-70%, preferably 50-65% may be selected.
  • the primers of the present invention are selected and designed according to the principle described above.
  • the regions of the ⁇ -actin gene selected for the present invention are included in the region of nucleotides 240-1060 of the nucleotide sequence set forth as SEQ ID NO: 1 and/or the complementary region thereof, preferably nucleotides 240-380 or nucleotides 401-1060 and more preferably nucleotides 740-990 of the nucleotide sequence set forth as SEQ ID NO: 1 and/or the complementary region thereof.
  • a primer for detection of ⁇ -actin is an oligonucleotide available as a primer and is selected and designed from the following: 1) an oligonucleotide of at least 5 nucleotides which is included in the region of nucleotides 240-1060, preferably nucleotides 240-380 or nucleotides 401-1060, and more preferably nucleotides 740-990 of the nucleotide sequence set forth as SEQ ID NO: 1 and/or the complementary sequence thereof; 2) an oligonucleotide comprising the nucleotide sequence set forth as any one of SEQ ID NOs: 2-50; 3) an oligonucleotide complementary to any one of the oligonucleotides defined in above 1) or 2); 4) an oligonucleotide capable of hybridizing to the oligonucleotide defined in any one of 1) to 3) under stringent conditions; and 5) an oligonucleotide having the following: 1) an
  • the regions of the GAPDH gene selected for the present invention are included in the region of nucleotides 110-450 of the nucleotide sequence set forth as SEQ ID NO: 51 and/or the complementary region thereof.
  • a primer for GAPDH is an oligonucleotide available as a primer and is selected and designed from the following: 1) an oligonucleotide of at least 5 nucleotides which is included in the region of nucleotides 110-450 of the nucleotide sequence set forth as SEQ ID NO: 51 and/or the complementary sequence thereof; 2) an oligonucleotide comprising the nucleotide sequence set forth as any one of SEQ ID NOs: 52-96; 3) an oligonucleotide complementary to any one of the oligonucleotides defined in above 1) or 2); 4) an oligonucleotide capable of hybridizing to the oligonucleotide defined in any one of 1) to 3) under stringent conditions; and 5) an oligonucleotide having the primer function, comprising the nucleotide sequence of the oligonuceotide defined in any one of above 1) to 4) in which one or more nucleo
  • Oligonucleotides can be produced by any known method, for example, by chemical synthesis. Alternatively, a naturally occurring nucleic acid is cleaved with an agent such as a restriction enzyme to modify or connect the sequence to be constituted with nucleotide sequences as described above. Specifically, oligonucleotides can be synthesized using an oligonucleotide synthesizer (Applied BioSystems; Expedite Model 8909 DNA Synthesizer). Synthesis of mutated oligonucleotides in which one or more nucleotide is substituted, deleted, inserted or added may be performed using any know process.
  • an agent such as a restriction enzyme to modify or connect the sequence to be constituted with nucleotide sequences as described above.
  • oligonucleotides can be synthesized using an oligonucleotide synthesizer (Applied BioSystems; Expedite Model 8909 DNA Synthesizer). Synthesis of mutated oligonu
  • site-directed mutagenesis, homologous recombination, primer elongation, or PCR method may be performed according to the methods described in the literature, including Sambrook et al. (ed.), Molecular Cloning; A Laboratory Manual, Second Edition, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989; Masami Muramatsu (ed.), Labo-Manual: Genetic Engineering, MARUZEN Inc., 1988; and Ehrlich, H E. (ed.), PCR Technology; Principle and Applications for DNA amplification, or using any modification of the methods.
  • Ulmer's method (Science (1983) 219: 666) may be used.
  • any conditions commonly known as stringent conditions for hybridization may be selected. Exemplary conditions are as follows: hybridization overnight at 42° C. in a solution containing 50% formamide, 5 ⁇ SSC (150 mM NaCl and 15 mM trisodium citrate), 50 mM sodium phosphate, pH 7.6, 5 ⁇ Denhardt's solution, 10% dextran sulfate and 20 ⁇ g/ml DNA, primary washing in 2 ⁇ SSC with 0.1% SDS at room temperature, followed by secondary washing in 0.1 ⁇ SSC with 0.1% SDS at about 65° C.
  • 5 ⁇ SSC 150 mM NaCl and 15 mM trisodium citrate
  • 50 mM sodium phosphate pH 7.6, 5 ⁇ Denhardt's solution, 10% dextran sulfate and 20 ⁇ g/ml DNA
  • primary washing in 2 ⁇ SSC with 0.1% SDS at room temperature followed by secondary washing in 0.1 ⁇ SSC with 0.1% SDS at about 65° C.
  • the template for the nucleic acid to be amplified in the present invention is mRNA for a housekeeping gene, it is necessary for the primers used to be designed so as not to amplify genomic DNA contained in the specimen.
  • at least one of the primers included in the primer set of the present invention desirably contains a region extending a plurality of exons in, for example, the ⁇ -actin or GAPDH gene.
  • Such design may prevent amplification of the sequences from genomic DNA and allow selective amplification of the sequence from ⁇ -actin or GAPDH mRNA.
  • primers of the present invention to amplify a nucleic acid, at least two primers are combined as a primer set.
  • at least four primers (FIP, F3 primer, RIP and R3 primer) are combined as a primer set.
  • one or more loop primers may be combined and used as a primer set.
  • the RT-LAMP method is a LAMP method in which RNA is used as template.
  • the fundamental idea underlying the LAMP is as described in Patent Document 1.
  • the starting structure for LAMP is synthesized as cDNA is synthesized from template RNA in a solution. Specifically, amplification of target DNA is performed by repeating the following steps 2) to 5) of DNA elongation after the following step 1):
  • FIP binds to a template RNA strand to elongate a DNA strand complementary to the template RNA strand.
  • a reverse transcriptase such as derived from AMV, is used.
  • RIP binds to the DNA strand displaced in above step 2) to elongate a DNA strand.
  • sequences of the both terminal regions of the DNA strand displaced in above step 4) contain complementary sequences to their own DNA strand, and each complementary sequence is hybridized to have a loop structure at both ends.
  • this reaction can be carried out using one enzyme.
  • synthesized DNA strands have complementary sequences within their own sequence, and most of the complementary sequences form base pairs. Utilizing this feature enables detection of the amplified products.
  • a fluorescent duplex intercalator such as ethidium bromide, SYBER GREEN I, or Pico Green
  • increase in the fluorescence intensity is observed in association with the increase of the product.
  • Simultaneous tracing of DNA amplification and increase in fluorescence in a closed system may be possible by monitoring such changes (see Manual of Clinical Laboratory Medicine, 31st ed., p. 1318; JP, 2001-242169-A, hereinafter, refer merely to as “Real-time Method”).
  • kit includes various oligonucleotides required as the primers for complementary-strand synthesis or for displacing, an enzyme with reverse transcriptase activity, dNTP substrates for complementary-strand synthesis, DNA polymerase for strand-displacement synthesis of complementary strands, buffer solution to provide suitable conditions for enzymatic reaction, and, if necessary, other reagents for detection of reaction products.
  • the present invention includes primers and primer sets for nucleic acid amplification, and a method for detection of nucleic acid using the primers, reagents used for the nucleic acid detection, and kits for nucleic acid detection and the whole system for nucleic acid detection.
  • F1c Genic regions in the complementary strand of the sequence set forth in SEQ ID NO: 1 343-327 5′-tggccttgggttcagg-3′ (SEQ ID NO: 2) 400-381 5′-cgtacatggctggggtgttg-3′ (SEQ ID NO: 3) 822-803 5′-gatgccacaggactccatgc-3′ (SEQ ID NO: 4) 838-817 5′-tgaaggtagtttcgtggatgcc-3′ (SEQ ID NO: 5) 922-904 5′-cagggtacatggtggtgcc-3′ (SEQ ID NO: 6)
  • F2 Genic regions in the sequence set forth in SEQ ID NO: 1 265-284 5′-accttctacaatgagctgcg-3′ (SEQ ID NO: 7) 341-357 5′-ccaaccgcgagaagatg-3′ (SEQ ID NO: 8) 748-766 5′-attggcaatgagcggttcc-3′ (SEQ ID NO: 9) 750-766 5′-tggcaatgagcggttcc-3′ (SEQ ID NO: 10) 774-790 5′-tgaggcactcttccagc-3′ (SEQ ID NO: 11) 782-799 5′-tcttccagccttccttccccccccccccccccccc-3′ (SEQ ID NO: 12) 851-868 5′-agtgtgacgtggacatcc-3′ (SEQ ID NO: 13)
  • F3 Genic regions in the sequence set forth in SEQ ID NO: 1 240-259 5′-cgacatggagaaaatctggc-3′ (SEQ ID NO: 14) 274-290 5′-aatgagctgcgtgtggc-3′ (SEQ ID NO: 15) 718-734 5′-tacgagctgcctgacgg-3′ (SEQ ID NO: 16) 750-766 5′-tggcaatgagcggttcc-3′ (SEQ ID NO: 10) 818-837 5′-gcatccacgaaactaccttc-3′ (SEQ ID NO: 17)
  • R1c Genic regions in the sequence set forth in SEQ ID NO: 1 346-366 5′-cgcgagaagatgacccagatc-3′ (SEQ ID NO: 18) 402-423 5′-tgctatccaggctgtgctatcc-3′ (SEQ ID NO: 19) 848-868 5′-tgaagtgtgacgtggacatcc-3′ (SEQ ID NO: 20) 857-876 5′-acgtggacatccgcaaagac-3′ (SEQ ID NO: 21) 925-945 5′-attgccgacaggatgcagaag-3′ (SEQ ID NO: 22)
  • R2 Genic regions in the complementary strand of the sequence set forth in SEQ ID NO: 1 414-396 5′-agcctggatagcaacgtac-3′ (SEQ ID NO: 23) 461-444 5′-tccatcacgatgccagtg-3′ (SEQ ID NO: 24) 921-905 5′-agggtacatggtggtgc-3′ (SEQ ID NO: 25) 925-909 5′-tgccagggtacatggtg-3′ (SEQ ID NO: 26) 929-911 5′-gcaatgccagggtacatgg-3′ (SEQ ID NO: 27) 1011-994 5′-gtacttgcgctcaggagg-3′ (SEQ ID NO: 28)
  • R3 Genic regions in the complementary strand of the sequence set forth in SEQ ID NO: 1 454-438 5′-cgatgccagtggtacgg-3′ (SEQ ID NO: 29) 497-480 5′-tagatgggcacagtgtgg-3′ (SEQ ID NO: 30) 947-930 5′-tccttctgcatcctgtcg-3′ (SEQ ID NO: 31) 1059-1043 5′-ctggaaggtggacagcg-3′ (SEQ ID NO: 32)
  • Loop F Genic regions in the complementary strand of the sequence set forth in SEQ ID NO: 1 816-801 5′-acaggactccatgccc-3′ (SEQ ID NO: 33)
  • Loop R Genic regions in the sequence set forth in SEQ ID NO: 1 878-895 5′-tgtacgccaacacagtgc-3′ (SEQ ID NO: 34)
  • FIP (connected sequences of a nucleotide sequence of the F1c regions and a nucleotide sequence of the F2 regions)
  • F3 primers (identical to the nucleotide sequences of the F3 regions)
  • R3 primers (identical to the nucleotide sequences of the R3 regions)
  • F1c Genic regions in the complementary strand of the sequence set forth in SEQ ID NO: 51 213-192 5′-tccattgatgacaagcttcccg-3′ (SEQ ID NO: 52) 236-217 5′-tcctggaagatggtgatggg-3′ (SEQ ID NO: 53) 246-228 5′-gggatctcgctcctggaag-3′ (SEQ ID NO: 54) 234-265 5′-acgtactcagcgccagcatc-3′ (SEQ ID NO: 55) 335-316 5′-aaatgagccccagccttctc-3′ (SEQ ID NO: 56)
  • F2 Genic regions in the sequence set forth in SEQ ID NO: 51 152-169 5′-ccacccatggcaaattcc-3′ (SEQ ID NO: 57) 163-180 5′-aaattccatggcaccgtc-3′ (SEQ ID NO: 58) 179-195 5′-tcaaggctgagaacggg-3′ (SEQ ID NO: 59) 217-235 5′-cccatcaccatcttccagg-3′ (SEQ ID NO: 60) 276-293 5′-tgagtacgtcgtggagtc-3′ (SEQ ID NO: 61)
  • F3 Genic regions in the sequence set forth in SEQ ID NO: 51 103-120 5′-gaccccttcattgacctc-3′ (SEQ ID NO: 62) 159-176 5′-tggcaaattccatggcac-3′ (SEQ ID NO: 63) 163-180 5′-aaattccatggcaccgtc-3′ (SEQ ID NO: 58) 227-244 5′-tcttccaggagcgagatc-3′ (SEQ ID NO: 64)
  • R1c Genic regions in the sequence set forth in SEQ ID NO: 51 216-235 5′-tcccatcaccatcttccagg-3′ (SEQ ID NO: 65) 248-268 5′-ccaaaatcaagtggggcgatg-3′ (SEQ ID NO: 66) 254-271 5′-tcaagtggggcgatgctg-3′ (SEQ ID NO: 67) 305-323 5′-tcaccaccatggagaaggc-3′ (SEQ ID NO: 68) 338-354 5′-aggggggagccaaagg-3′ (SEQ ID NO: 69)
  • R2 Genic regions in the complementary strand of the sequence set forth in SEQ ID NO: 51 295-279 5′-tggactccacgacgtac-3′ (SEQ ID NO: 70) 305-289 5′-aagacgccagtggactc-3′ (SEQ ID NO: 71) 310-294 5′-tggtgaagacgccagtg-3′ (SEQ ID NO: 72) 324-308 5′-agccttctccatggtgg-3′ (SEQ ID NO: 73) 327-311 5′-cccagccttctccatgg-3′ (SEQ ID NO: 74) 365-346 5′-gagatgatgacccttttggc-3′ (SEQ ID NO: 75) 399-383 5′-catgacgaacatggggg-3′ (SEQ ID NO: 76)
  • R3 Genic regions in the complementary strand of the sequence set forth in SEQ ID NO: 51 324-308 5′-agccttctccatggtgg-3′ (SEQ ID NO: 73) 365-346 5′-gagatgatgacccttttggc-3′ (SEQ ID NO: 75) 399-383 5′-catgacgaacatggggg-3′ (SEQ ID NO: 76) 445-426 5′-tgctgatgatcttgaggctg-3′ (SEQ ID NO: 77)
  • Loop F Genic regions in the complementary strand of the sequence set forth in SEQ ID NO: 51 227-212 5′-atggtgatgggatttc-3′ (SEQ ID NO: 78)
  • Loop R Genic regions in the sequence set forth in SEQ ID NO: 51 275-293 5′-ctgagtacgtcgtggagtc-3′ (SEQ ID NO: 79)
  • FIP (connected sequences of a nucleotide sequence of the F1c regions and a nucleotide sequence of the F2 regions)
  • R3 (identical to the nucleotide sequences of the RF3 regions)
  • Amplification reaction by RT-LAMP was initiated using the primers for ⁇ -actin listed in Example 2 in the combinations indicated in Table 1. The time required for confirming the amplification was examined.
  • Reaction Components dNTPs (GIBCO) 0.4 mM MgSO 4 2 mM Dithiothreitol 5 mM Betaine (Sigma) 640 mM Thermopol buffer (New England BioLabs) AMV reverse transcriptase (Promega) 1.25 U Bst DNA polymerase (New England BioLabs) 16 U Ethidium Bromide 0.125 mg/ml
  • RNA sample containing 20 ng of human total RNA
  • reaction solution containing the above four primers
  • Table 1 shows the time required for confirmation of the amplification of the ⁇ -actin gene for each primer set used in the reaction. The results reveal that for each primer set, it takes 45 minutes at a maximum, within 30 minutes in most cases, to confirm the amplification.
  • a primer set with which the amplification was confirmed in the shortest time was selected from the primer sets for ⁇ -actin used in Experiment 1. This primer set was further combined with loop primers and used for determination of the sensitivity of the RT-LAMP method.
  • F3 and R3 loop primers were further added at a concentration of 5 pmol each to the same components as described in Experiment 1.
  • RNA sample containing 20 ng of human total RNA
  • reaction solution containing the above six primers
  • FIG. 1 The results are shown in FIG. 1 . They show that the larger amount of the mRNA template for ⁇ -actin allowed earlier confirmation of the amplification. The amplification was confirmed within 30 minutes with 0.02 ng of the template, and in approximately 15 minutes with 20 ng of the template.
  • LS180 cells colonic tumor cell line
  • Raji cells Bokitt's lymphoma cell line
  • a cytokeratin-positive LS180 cell solution was diluted with a cytokeratin-negative Raji cell solution, and amplification of ⁇ -actin was examined for different concentrations of LS180 cell solution, thereby examining whether ⁇ -actin is available as a control for data correction in determination of cytokeratin tumor markers.
  • Samples were prepared to adjust the total cell number of LS180 and Raje cells to 8000.
  • the number of LS180 cells was adjusted to 8000, 800, 80, 8 or 0.
  • Amplification reaction by RT-LAMP was initiated using the primers for GAPDH listed in Example 4 in the combinations indicated in Table 3. The time required for confirming the amplification was examined.
  • RT-LAMP was performed as described in Experiment 1. Specifically, two microliters of the RNA sample (containing 20 ng of human total RNA) was added to 23 ⁇ l of the reaction solution containing the above four primers, and heated at 65° C. for one hour.
  • Table 3 shows the time required for confirmation of the amplification of the GAPDH gene for each primer set used in the reaction. The results reveal that for each primer set, it takes 45 minutes at a maximum, within 30 minutes in most cases, to confirm the amplification.
  • a primer set with which the amplification was confirmed in the shortest time was selected from the primer sets for GAPDH used in Experiment 4. This primer set was further combined with loop primers and used for determination of the sensitivity of the RT-LAMP method.
  • FIG. 3 show that the larger amount of the GAPDH mRNA template for ⁇ -actin allowed earlier confirmation of the amplification.
  • the amplification was confirmed within 30 minutes even with 0.02 ng of the template, and in approximately 10 minutes with 20 ng of the template.
  • LS180 cells colonic tumor cell line
  • Raji cells Bokitt's lymphoma cell line
  • a cytokeratin-positive LS180 cell solution was diluted with a cytokeratin-negative Raji cell solution, and amplification of GAPDH was examined for different concentrations of LS180 cell solution, thereby examining whether GAPDH is available as a control for data correction in determination of cytokeratin tumor markers.
  • Samples were prepared to adjust the total cell number of LS180 and Raje cells to 8000.
  • the number of LS180 cells was adjusted to 8000, 800, 80, 8 or 0.
  • the RT-LAMP method was performed as described in Experiment 2. Two microliters of the cell suspension was added to 23 ⁇ l of the reaction solution containing the same six primers as described in Experiment 5, and heated at 65° C. for one hour.
  • primers or primer sets of the present invention in the LAMP method allows for confirmation of amplification of ⁇ -actin or GAPDH within 15 minutes at the earliest.
  • the use of the primers or primer sets of the present invention will reduce the time required for making a diagnosis during the process for diagnosis of metastasis using nucleic acid amplification, thereby enabling reliable diagnosis.

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