Methods and compositions for the detection of calr mutations in myeloproliferative diseases

Abstract

Provided herein are methods and compositions for the detection of in-frame deletion germline mutations in the CALR gene. Also provided are methods for determining the prognosis of myeloproliferative diseases and the likelihood of developing somatic mutations in genes involved in the JAK-STAT pathway.

1 . A method for detecting an in-frame deletion mutation (Indel) in exon 9 of the calreticulin (CALR) gene comprising:
 performing a nucleic acid detection assay on a patient sample to detect a CALR exon 9 in-frame deletion mutation, wherein the mutation is selected from the group consisting of p.D397_D400>D and p.E405_V409>V,   
       wherein the nucleic acid detection assay comprises using a labeled oligonucleotide probe to detect the in-frame deletion mutation, wherein the labeled oligonucleotide probe comprises from about 10 to 30 consecutive nucleotides of the sequence SEQ ID NO: 1 having the in-frame deletion and overlaps the in-frame deletion site. 
     
     
         2 . The method of  claim 1 , wherein the method comprises nucleic acid amplification. 
     
     
         3 . The method of  claim 1 , wherein the method comprises nucleic acid amplification using a primer pair, comprising a forward primer and a reverse primer that flank the deletion mutation. 
     
     
         4 . The method of  claim 1 , wherein the method comprises polymerase chain reaction (PCR), reverse transcription polymerase chain reaction (RT-PCR), real-time PCR (qPCR), or nested PCR. 
     
     
         5 . (canceled) 
     
     
         6 . (canceled) 
     
     
         7 . The method of  claim 1 , wherein the method comprises sequencing an amplicon comprising all or a portion of CALR exon 9 comprising the deletion. 
     
     
         8 . The method of  claim 7 , wherein the amplicon is detected using a labeled oligonucleotide probe. 
     
     
         9 . The method of  claim 1 , wherein the nucleic acid is DNA, cDNA, genomic DNA, or RNA. 
     
     
         10 . The method of  claim 1 , wherein the patient sample is a blood, serum, plasma, or biopsy sample. 
     
     
         11 . The method of  claim 1 , wherein the patient sample is from a patient that has a myeloproliferative disease or is suspected of having a myeloproliferative disease. 
     
     
         12 . The method of  claim 11 , wherein the myeloproliferative disease is selected from among polycythemia vera, essential thrombocythemia, idiopathic myelofibrosis, and unclassified myeloproliferative disease. 
     
     
         13 . The method of  claim 1 , further comprising detecting one or more additional mutations in one or more additional genes associated with a myeloproliferative disease, wherein the one or more additional genes is a JAK-STAT pathway gene. 
     
     
         14 . The method of  claim 13 , wherein the one or more additional genes is JAK2, MPL, CSFR3R, ASXL1, or ZRSR2. 
     
     
         15 . The method of  claim 13 , wherein the one or more additional mutations is selected from among a mutation in exon 12 or exon 14 of JAK2, exon 10 of MPL or exon 14 or exon 17 CSFR3R. 
     
     
         16 . The method of  claim 13 , wherein the one or more additional mutations is selected from among JAK2 V617F, MPL W515L, CSFR3R A470T, ASXL1 D954fs*26, or ZRSR2 S449_R450du. 
     
     
         17 .- 44 . (canceled)