Foster D C, Sprecher C A, Grant F J, Kramer J M, Kuijper J L, Holly R D, Whitmore T E, Heipel M D, Bell L A, Ching A F
ZymoGenetics Inc., Seattle, WA 98102.
Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):13023-7. doi: 10.1073/pnas.91.26.13023.
Thrombopoietin (TPO), a lineage-specific cytokine affecting the proliferation and maturation of megakaryocytes from committed progenitor cells, is believed to be the major physiological regulator of circulating platelet levels. Recently we have isolated a cDNA encoding a ligand for the murine c-mpl protooncogene and shown it to be TPO. By employing a murine cDNA probe, we have isolated a gene encoding human TPO from a human genomic library. The TPO locus spans over 6 kb and has a structure similar to that of the erythropoietin gene (EPO). Southern blot analysis of human genomic DNA reveals a hybridization pattern consistent with a single gene locus. The locus was mapped by in situ hybridization of metaphase chromosome preparations to chromosome 3q26-27, a site where a number of chromosomal abnormalities associated with thrombocythemia in cases of acute myeloid leukemia have been mapped. A human TPO cDNA was isolated by PCR from kidney mRNA. The cDNA encodes a protein with 80% identity to previously described murine TPO and is capable of initiating a proliferative signal to murine interleukin 3-dependent BaF3 cells expressing the murine or human TPO receptor.
血小板生成素(TPO)是一种影响定向祖细胞来源的巨核细胞增殖和成熟的谱系特异性细胞因子,被认为是循环血小板水平的主要生理调节因子。最近,我们分离出了一种编码小鼠c-mpl原癌基因配体的cDNA,并证明它就是TPO。通过使用小鼠cDNA探针,我们从人类基因组文库中分离出了一个编码人类TPO的基因。TPO基因座跨度超过6 kb,其结构与促红细胞生成素基因(EPO)相似。对人类基因组DNA进行的Southern印迹分析显示出与单基因座一致的杂交模式。通过中期染色体标本的原位杂交将该基因座定位到3号染色体的q26-27区域,该位点已被定位到一些与急性髓性白血病病例中血小板增多症相关的染色体异常。通过PCR从肾脏mRNA中分离出人类TPO cDNA。该cDNA编码的蛋白质与先前描述的小鼠TPO有80%的同源性,并且能够向表达小鼠或人类TPO受体的小鼠白细胞介素3依赖的BaF3细胞发出增殖信号。