Wong S, Witte O N
Molecular Biology Institute, University of California, Los Angeles, California, CA 90095-1662, USA.
Oncogene. 2001 Sep 10;20(40):5644-59. doi: 10.1038/sj.onc.1204638.
The Ph chromosome has been genetically linked to CML and ALL. Its chimeric fusion gene product, BCR-ABL, can generate leukemia in mice. This review will discuss selected model systems developed to study BCR-ABL induced leukemia and focuses on what we have learned about the human disease from these models. Five main experimental approaches will be discussed including: (i) Reconstitution of mice with bone marrow cells retrovirally transduced with BCR-ABL; (ii) Transgenic mice expressing BCR-ABL; (iii) Knock-in mice with BCR-ABL expression driven from the endogenous bcr locus; (iv) Development of CML-like disease in mice with loss of function mutations in heterologous genes; and (v) ES in vitro hematopoietic differentiation coupled with regulated BCR-ABL expression.
费城染色体已在基因上与慢性粒细胞白血病和急性淋巴细胞白血病相关联。其嵌合融合基因产物BCR-ABL可在小鼠中引发白血病。本综述将讨论为研究BCR-ABL诱导的白血病而开发的选定模型系统,并重点关注我们从这些模型中对人类疾病的了解。将讨论五种主要的实验方法,包括:(i)用逆转录病毒转导BCR-ABL的骨髓细胞重建小鼠;(ii)表达BCR-ABL的转基因小鼠;(iii)由内源性bcr基因座驱动BCR-ABL表达的基因敲入小鼠;(iv)在异源基因功能丧失突变的小鼠中发展类似慢性粒细胞白血病的疾病;以及(v)体外胚胎干细胞造血分化与受调控的BCR-ABL表达相结合。