Caruccio Lorraine, Bettinotti Maria, Director-Myska Alison E, Arthur Diane C, Stroncek David
Department of Transfusion Medicine, Warren G. Magnuson Clinical Center, and the Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.
Transfusion. 2006 Mar;46(3):441-7. doi: 10.1111/j.1537-2995.2006.00741.x.
PRV-1 mRNA is overexpressed by neutrophils from polycythemia vera patients and is homologous to NB1 a gene overexpressed in reactive neutrophilia.
These investigations were designed to confirm searches of genome databases suggesting that PRV-1 and NB1 are alleles of the same gene, CD177, and confirm a pseudogene adjacent to CD177. Methods included polymerase chain reaction (PCR), cloning, sequencing, and fluorescent hybridization studies.
The coding region of PRV-1 was PCR-amplified from human fetal RNA, cloned, and used to screen the RPCI-11 bacterial artificial chromosome (BAC) library. Five BACs were reactive with the PRV-1 probe. PCR analysis of the BACs with primers encompassing PRV-1 exons, containing four known single-nucleotide polymorphisms, followed by sequencing rendered amplicons identical to PRV-1 in all five BACs. Analysis of all five by restriction digestion yielded fragments possible only if both the gene and the pseudogene are present. End sequencing of the BACs localized them to the same chromosome region. G-banding and fluorescence in situ hybridization at the 400- and 850-band levels of resolution mapped one BAC to chromosome band 19q13.2 and sublocalized the BAC to band 19q13.31, respectively.
PRV-1 and NB1 are alleles of the same gene now referred to as CD177. Changes in CD177 expression may be a marker of increased or decreased myelopoiesis and are therefore an effect of, rather than a cause of, myeloproliferative disorders.
真性红细胞增多症患者的中性粒细胞中PRV-1 mRNA过表达,且与反应性中性粒细胞增多症中过表达的NB1基因同源。
这些研究旨在证实对基因组数据库的检索结果,该结果提示PRV-1和NB1是同一基因CD177的等位基因,并证实CD177附近存在一个假基因。方法包括聚合酶链反应(PCR)、克隆、测序及荧光杂交研究。
从人胎儿RNA中PCR扩增出PRV-1的编码区,进行克隆,并用于筛选RPCI-11细菌人工染色体(BAC)文库。5个BAC与PRV-1探针有反应。用包含PRV-1外显子的引物对BAC进行PCR分析,这些外显子含有4个已知单核苷酸多态性,随后测序显示所有5个BAC中的扩增子与PRV-1相同。对所有5个BAC进行限制性消化分析,只有当基因和假基因都存在时才会产生可能的片段。BAC的末端测序将它们定位到同一染色体区域。在400和850条带分辨率水平下进行G显带和荧光原位杂交,分别将一个BAC定位到染色体带19q13.2,并将该BAC亚定位到带19q13.31。
PRV-1和NB1是同一基因的等位基因,现称为CD177。CD177表达的变化可能是骨髓生成增加或减少的标志物,因此是骨髓增殖性疾病的结果而非原因。