Unité Physiologie et Pathologie Moléculaires des Rétrovirus Endogènes et Infectieux, CNRS UMR 9196, Gustave Roussy, Villejuif, F-94805, France;
UMR9196, Université Paris-Sud, Orsay, F-91405, France.
Proc Natl Acad Sci U S A. 2017 Aug 8;114(32):E6642-E6651. doi: 10.1073/pnas.1702204114. Epub 2017 Jul 24.
Capture of retroviral envelope genes is likely to have played a role in the emergence of placental mammals, with evidence for multiple, reiterated, and independent capture events occurring in mammals, and be responsible for the diversity of present day placental structures. Here, we uncover a full-length endogenous retrovirus envelope protein, dubbed HEMO [human endogenous MER34 (medium-reiteration-frequency-family-34) ORF], with unprecedented characteristics, because it is actively shed in the blood circulation in humans via specific cleavage of the precursor envelope protein upstream of the transmembrane domain. At variance with previously identified retroviral envelope genes, its encoding gene is found to be transcribed from a unique CpG-rich promoter not related to a retroviral LTR, with sites of expression including the placenta as well as other tissues and rather unexpectedly, stem cells as well as reprogrammed induced pluripotent stem cells (iPSCs), where the protein can also be detected. We provide evidence that the associated retroviral capture event most probably occurred >100 Mya before the split of Laurasiatheria and Euarchontoglires, with the identified retroviral envelope gene encoding a full-length protein in all simians under purifying selection and with similar shedding capacity. Finally, a comprehensive screen of the expression of the gene discloses high transcript levels in several tumor tissues, such as germ cell, breast, and ovarian tumors, with in the latter case, evidence for a histotype dependence and specific protein expression in clear-cell carcinoma. Altogether, the identified protein could constitute a "stemness marker" of the normal cell and a possible target for immunotherapeutic approaches in tumors.
内源性逆转录病毒包膜基因的捕获很可能在胎盘哺乳动物的出现中发挥了作用,有证据表明,在哺乳动物中发生了多次、重复和独立的捕获事件,并负责了现今胎盘结构的多样性。在这里,我们发现了一种全长的内源性逆转录病毒包膜蛋白,被称为 HEMO(人类内源性 MER34(中重复频率家族 34)ORF),具有前所未有的特征,因为它通过跨膜结构域上游的前体包膜蛋白的特异性切割而在人类血液循环中被主动释放。与以前鉴定的逆转录病毒包膜基因不同,其编码基因被发现是从一个独特的富含 CpG 的启动子转录而来的,该启动子与逆转录病毒 LTR 无关,其表达部位包括胎盘以及其他组织,而且相当出人意料的是,还包括干细胞和重编程的诱导多能干细胞(iPSCs),在这些细胞中也可以检测到该蛋白。我们提供的证据表明,相关的逆转录病毒捕获事件很可能发生在 Laurasiatheria 和 Euarchontoglires 分裂之前的 1 亿多年前,鉴定出的逆转录病毒包膜基因在所有灵长类动物中都编码一个全长蛋白,并受到纯化选择的影响,且具有相似的释放能力。最后,对该基因表达的全面筛选揭示了该基因在几种肿瘤组织中具有高转录水平,如生殖细胞、乳腺和卵巢肿瘤,在后一种情况下,有证据表明存在组织类型依赖性和透明细胞癌中特定的蛋白表达。总之,所鉴定的蛋白可能构成正常细胞的“干性标志物”,并可能成为肿瘤免疫治疗方法的潜在靶点。