Killian Audrey, Le Meur Nathalie, Sesboüé Richard, Bourguignon Jeannette, Bougeard Gaëlle, Gautherot Julien, Bastard Christian, Frébourg Thierry, Flaman Jean-Michel
Institut National de la Santé et de la Recherche Médicale (INSERM) U 614 - IFRMP, Faculty of Medicine, 22 Boulevard Gambetta, 76183 Rouen Cedex, France.
Oncogene. 2004 Nov 11;23(53):8597-602. doi: 10.1038/sj.onc.1207845.
Since chromosomal instability (CIN) is a hallmark of most cancer cells, it is essential to identify genes whose alteration results into this genetic instability. Using a yeast CIN indicator strain, we show that inactivation of the YMR131c/RRB1 gene, which is involved in early ribosome assembly and whose expression is induced when the spindle checkpoint is activated, alters chromosome segregation and blocks mitosis at the metaphase/anaphase transition. We demonstrate that RRB1 interacts with YPH1 (yeast pescadillo homologue 1) and other members of the Yph1 complex, RPL3, ERB1 and ORC6, involved in ribosome biogenesis and DNA replication. Transient depletion of the human homologues GRWD, Pescadillo, Rpl3, Bop1 and Orc6L resulted in an increase of abnormal mitoses with appearance of binucleate or hyperploid cells, of cells with multipolar spindles and of aberrant metaphase plates. If deregulation of proteins involved in ribosome biogenesis, commonly observed in malignant tumors, could contribute to cancer through an aberrant protein synthesis, our study demonstrates that alteration of proteins linking ribosome biogenesis and DNA replication may directly cause CIN.
由于染色体不稳定性(CIN)是大多数癌细胞的一个标志,因此识别那些其改变会导致这种基因不稳定的基因至关重要。使用一种酵母CIN指示菌株,我们发现YMR131c/RRB1基因的失活会改变染色体分离并在中期/后期转换时阻断有丝分裂,该基因参与早期核糖体组装且其表达在纺锤体检查点激活时被诱导。我们证明RRB1与YPH1(酵母pescadillo同源物1)以及Yph1复合物的其他成员RPL3、ERB1和ORC6相互作用,这些成员参与核糖体生物合成和DNA复制。人同源物GRWD、Pescadillo、Rpl3、Bop1和Orc6L的瞬时缺失导致异常有丝分裂增加,出现双核或超倍体细胞、具有多极纺锤体的细胞以及异常中期板。如果在恶性肿瘤中常见的核糖体生物合成相关蛋白的失调通过异常蛋白质合成可能导致癌症,我们的研究表明连接核糖体生物合成和DNA复制的蛋白质的改变可能直接导致CIN。