Courtois G, Bénit L, Mikaeloff Y, Pauchard M, Charon M, Varlet P, Gisselbrecht S
Institut Cochin de Génétique Moléculaire, Institut National de la Santé et de la Recherche Médicale, Université Paris V, Hôpital Cochin, France.
J Virol. 1995 May;69(5):2794-800. doi: 10.1128/JVI.69.5.2794-2800.1995.
The myeloproliferative leukemia retrovirus (MPLV) has the v-mpl cellular sequences transduced in frame with the deleted and rearranged Friend murine leukemia virus env gene. The resulting env-mpl fusion oncogene is responsible for an acute myeloproliferative disorder induced in mice by MPLV. v-mpl is a truncated form of the c-mpl gene which encodes the receptor for thrombopoietin. We investigated the contribution of the Env-Mpl extracellular domain in the constitutive activation of this truncated cytokine receptor and found that the rearrangement of the env sequences in the env-mpl fusion gene was not required for oncogenicity. A pathogenic variant, DEL3MPLV, was generated, which differs from MPLV by the deletions of 22 amino acids of the Env signal peptide, all of the mature Env sequences, and 18 N-terminal amino acids of the v-Mpl extracellular domain. The resulting del3-mpl oncogene product conserves in its extracellular region the first 12 amino acids of the Env signal sequence including a cysteine residue, and 25 amino acids of the v-Mpl. We show here that a mutation converting this cysteine to a glycine completely abolishes del3-mpl oncogenicity and that the del3-mpl oncogene product is constitutively activated by disulfide-linked homodimerization.
骨髓增殖性白血病逆转录病毒(MPLV)具有与缺失和重排的弗氏小鼠白血病病毒env基因框内转导的v-mpl细胞序列。产生的env-mpl融合癌基因导致MPLV在小鼠中诱发急性骨髓增殖性疾病。v-mpl是编码血小板生成素受体的c-mpl基因的截短形式。我们研究了Env-Mpl细胞外结构域在这种截短的细胞因子受体组成性激活中的作用,发现env-mpl融合基因中env序列的重排对于致癌性并非必需。产生了一种致病性变体DEL3MPLV,它与MPLV的不同之处在于Env信号肽缺失22个氨基酸、所有成熟的Env序列以及v-Mpl细胞外结构域的1个N端氨基酸。产生的del3-mpl癌基因产物在其细胞外区域保留了Env信号序列的前12个氨基酸,包括一个半胱氨酸残基,以及v-Mpl的25个氨基酸。我们在此表明,将该半胱氨酸转化为甘氨酸的突变完全消除了del3-mpl的致癌性,并且del3-mpl癌基因产物通过二硫键连接的同源二聚化而组成性激活。