Nucleophosmin protein (NPM) mutants, corresponding gene sequences and uses thereof
View Patent ↗The invention relates to new nucleophosmin protein (NPM) mutants, corresponding gene sequences and relative uses thereof for diagnosis, monitoring of minimal residual disease, prognostic evaluation and therapy of acute myeloid leukaemia (AML).
1. A method comprising
detecting, in a sample of nucleic acids, a nucleic acid that encodes a mutation in exon 12 of a human nucleophosmin (NPM) gene, wherein the nucleic acid encoding the mutation comprises an exon 12 sequence coding for position 288 and/or position 290 of human NPM protein that results in a loss of a tryptophan residue at position 290,
wherein the detecting comprises identifying the nucleic acid encoding the mutation using
(a) oligonucleotide primers in a polymerase chain reaction assay that can amplify the nucleic acid encoding the mutation but cannot amplify a nucleic acid encoding a wild-type NPM, and/or
(b) an oligonucleotide probe that can bind to the nucleic acid encoding the mutation but not to a nucleic acid encoding a wild-type NPM,
wherein
one of the oligonucleotide primers and/or the oligonucleotide probe comprises a sequence that
(1) is identical or fully complementary to a portion of one of SEQ ID NO:57, 60, 61, 62, 63 or 64 comprising at least four nucleotides that are not present in wild-type NPM sequence SEQ ID NO:84, and
(2) hybridizes to SEQ ID NO:57, 60, 61, 62, 63 or 64 or its complement but not SEQ ID NO:84 or its complement.
2. The method of claim 1 , wherein the nucleic acid encoding the mutation comprises an exon 12 sequence coding for positions 288 and 290 of human NPM protein, wherein the mutation in the NPM gene also results in a loss of a tryptophan at amino acid position 288.
3. The method of claim 1 , wherein the nucleic acid encoding the mutation encodes a signal motif of nuclear export (NES) in the C-terminal region of the NPM gene.
4. The method of claim 3 , wherein the NES comprises an amino acid sequence LxxxVxxVxL (SEQ ID NO:1), wherein x can be any amino acid.
5. The method of claim 4 , wherein the LxxxVxxVxL (SEQ ID NO:1) is LCLAVEEVSL (SEQ ID NO:6); LCMAVEEVSL (SEQ ID NO:7); LCVAVEEVSL (SEQ ID NO:8); LSRAVEEVSL (SEQ ID NO:9); LCTAVEEVSL (SEQ ID NO:11); LSQAVEEVSL (SEQ ID NO: 10); LCHAVEEVSL (SEQ ID NO: 12); LCRAVEEVSL (SEQ ID NO: 13); LCRGVEEVSL (SEQ ID NO: 14); LCQAVEEVSL (SEQ ID NO:15); LCAAVEEVSL (SEQ ID NO:16); or LCKAVEEVSL (SEQ ID NO:17).
6. The method of claim 3 , wherein the NES comprises an amino acid sequence) LxxxLxxVxL (SEQ ID NO:2), wherein the LxxxLxxVxL (SEQ ID NO:2) is LWQSLAQVSL (SEQ ID NO:18); LWQSLEKVSL (SEQ ID NO:19); LWQSLSKVSL (SEQ ID NO: 20); or LCTFLEEVSL (SEQ ID NO:21).
7. The method of claim 3 , wherein the NES comprises an amino acid sequence LxxxFxxVxL (SEQ ID NO:3), wherein the LxxxFxxVxL (SEQ ID NO:3) is LWQCFAQVSL (SEQ ID NO:22); LWQCFSKVSL (SEQ ID NO:23); LWQRFQEVSL (SEQ ID NO:24); or LWQDFLNRL (SEQ ID NO:25).
8. The method of claim 3 , wherein the NES comprises an amino acid sequence LxxxMxxVxL (SEQ ID NO:4), wherein the LxxxMxxVxL (SEQ ID NO:4) is LWQSMEEVSL (SEQ ID NO:26) or LWQRMEEVSL (SEQ ID NO:27).
9. The method of claim 3 , wherein the NES comprises an amino acid sequence LWQCCSQVSL (SEQ ID NO:28).
10. The method of claim 1 , wherein the one of the oligonucleotide primers and/or the oligonucleotide probe is identical or fully complementary to an exon 12 sequence coding for positions 288, 289 and 290 of human NPM protein that results in a loss of a tryptophan residue at position 290.
11. The method of claim 1 , wherein the sample is human blood.
12. The method of claim 1 , wherein the nucleic acids are in cells.
13. The method of claim 1 , wherein both oligonucleotide primers and an oligonucleotide probe are used to identify the nucleic acid.
14. The method of claim 13 , wherein the oligonucleotide probe is a hydrolysis probe.
15. The method of claim 1 , wherein the detecting comprises real-time PCR.
16. The method of claim 1 , wherein the sample is from a patient with acute myeloid leukemia.
17. The method of claim 1 , wherein the oligonucleotide primers comprise at least 19 nucleotides identical or complementary to the NPM gene comprising the mutation and/or the oligonucleotide probe comprises at least 17 nucleotides identical or complementary to the NPM gene comprising the mutation.
18. The method of claim 1 , wherein the detecting comprises identifying the nucleic acid encoding the mutation using a hydrolysis probe.
19. The method of claim 1 , wherein at least one of the oligonucleotide primer and/or the oligonucleotide probe comprises a fluorescent substance, biotin, a radioisotope, or a nanoparticle.
20. The method of claim 10 , wherein at least one of the oligonucleotide primer and/or the oligonucleotide probe comprises a fluorescent substance, biotin, a radioisotope, or a nanoparticle.