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一种用于检测突变 JAK2 外显子 12 等位基因负担的高灵敏度定量实时 PCR 检测方法。

A highly sensitive quantitative real-time PCR assay for determination of mutant JAK2 exon 12 allele burden.

机构信息

Department of Hematology, Herlev Hospital, Herlev, Denmark.

出版信息

PLoS One. 2012;7(3):e33100. doi: 10.1371/journal.pone.0033100. Epub 2012 Mar 5.

DOI:10.1371/journal.pone.0033100
PMID:22403733
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3293922/
Abstract

Mutations in the Janus kinase 2 (JAK2) gene have become an important identifier for the Philadelphia-chromosome negative chronic myeloproliferative neoplasms. In contrast to the JAK2V617F mutation, the large number of JAK2 exon 12 mutations has challenged the development of quantitative assays. We present a highly sensitive real-time quantitative PCR assay for determination of the mutant allele burden of JAK2 exon 12 mutations. In combination with high resolution melting analysis and sequencing the assay identified six patients carrying previously described JAK2 exon 12 mutations and one novel mutation. Two patients were homozygous with a high mutant allele burden, whereas one of the heterozygous patients had a very low mutant allele burden. The allele burden in the peripheral blood resembled that of the bone marrow, except for the patient with low allele burden. Myeloid and lymphoid cell populations were isolated by cell sorting and quantitative PCR revealed similar mutant allele burdens in CD16+ granulocytes and peripheral blood. The mutations were also detected in B-lymphocytes in half of the patients at a low allele burden. In conclusion, our highly sensitive assay provides an important tool for quantitative monitoring of the mutant allele burden and accordingly also for determining the impact of treatment with interferon-α-2, shown to induce molecular remission in JAK2V617F-positive patients, which may be a future treatment option for JAK2 exon 12-positive patients as well.

摘要

Janus 激酶 2(JAK2)基因突变已成为费城染色体阴性慢性骨髓增殖性肿瘤的重要鉴定标志。与 JAK2V617F 突变不同,大量的 JAK2 外显子 12 突变对定量检测方法的发展提出了挑战。我们提出了一种高度敏感的实时定量 PCR 检测方法,用于确定 JAK2 外显子 12 突变的突变等位基因负担。结合高分辨率熔解分析和测序,该检测方法鉴定了 6 名携带先前描述的 JAK2 外显子 12 突变和 1 种新突变的患者。2 名患者为纯合子,突变等位基因负担高,而 1 名杂合子患者的突变等位基因负担非常低。外周血的等位基因负担与骨髓相似,但低等位基因负担的患者除外。通过细胞分选分离出髓样和淋巴样细胞群,定量 PCR 显示 CD16+粒细胞和外周血中的突变等位基因负担相似。在一半低等位基因负担的患者中,在 B 淋巴细胞中也检测到了这些突变。总之,我们的高敏感检测方法为定量监测突变等位基因负担提供了重要工具,因此也为确定干扰素-α-2 治疗的影响提供了重要工具,干扰素-α-2 已被证明可诱导 JAK2V617F 阳性患者的分子缓解,这也可能成为 JAK2 外显子 12 阳性患者的未来治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef9/3293922/bcbbf15480d3/pone.0033100.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef9/3293922/35751c265983/pone.0033100.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef9/3293922/c3ce6efee44f/pone.0033100.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef9/3293922/0577b306a1b8/pone.0033100.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef9/3293922/a81c6f0074a7/pone.0033100.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef9/3293922/bcbbf15480d3/pone.0033100.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef9/3293922/35751c265983/pone.0033100.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef9/3293922/c3ce6efee44f/pone.0033100.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef9/3293922/0577b306a1b8/pone.0033100.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef9/3293922/a81c6f0074a7/pone.0033100.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ef9/3293922/bcbbf15480d3/pone.0033100.g005.jpg

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