Raveche Elizabeth S, Salerno Erica, Scaglione Brian J, Manohar Vijaya, Abbasi Fatima, Lin Yi-Chu, Fredrickson Torgny, Landgraf Pablo, Ramachandra Sumant, Huppi Konrad, Toro Jorge R, Zenger Vincent E, Metcalf Robert A, Marti Gerald E
Department of Pathology and Lab Medicine, University of Medicine and Dentistry New Jersey/New Jersey Medical School, Newark, NJ, USA.
Blood. 2007 Jun 15;109(12):5079-86. doi: 10.1182/blood-2007-02-071225. Epub 2007 Mar 9.
New Zealand black (NZB) mice with autoimmune and B lymphoproliferative disease (B-LPD) are a model for human chronic lymphocytic leukemia (CLL). A genomewide linkage scan of the NZB loci associated with lymphoma was conducted in F1 backcrosses of NZB and a control strain, DBA/2. Of 202 mice phenotyped for the presence or absence of LPD, surface maker expression, DNA content, and microsatellite polymorphisms, 74 had disease. The CD5(+), IgM(+), B220(dim), hyperdiploid LPD was linked to 3 loci on chromosomes 14, 18, and 19 that are distinct from previously identified autoimmunity-associated loci. The region of synteny with mouse D14mit160 is the human 13q14 region, associated with human CLL, containing microRNAs mir-15a16-1. DNA sequencing of multiple NZB tissues identified a point mutation in the 3' flanking sequence of the identical microRNA, mir-16-1, and this mutation was not present in other strains, including the nearest neighbor, NZW. Levels of miR-16 were decreased in NZB lymphoid tissue. Exogenous miR-16 delivered to an NZB malignant B-1 cell line resulted in cell-cycle alterations and increased apoptosis. Linkage of the mir-15a/16-1 complex and the development of B-LPD in this spontaneous mouse model suggest that the altered expression of the mir-15a/16-1 is the molecular lesion in CLL.
患有自身免疫性和B淋巴细胞增殖性疾病(B-LPD)的新西兰黑(NZB)小鼠是人类慢性淋巴细胞白血病(CLL)的一种模型。在NZB与对照品系DBA/2的F1回交中,对与淋巴瘤相关的NZB基因座进行了全基因组连锁扫描。在202只针对LPD的存在与否、表面标志物表达、DNA含量和微卫星多态性进行表型分析的小鼠中,有74只患有疾病。CD5(+)、IgM(+)、B220(dim)、超二倍体LPD与14号、18号和19号染色体上的3个基因座相关联,这些基因座与先前确定的自身免疫相关基因座不同。与小鼠D14mit160同线性的区域是人类13q14区域,与人类CLL相关,包含微小RNA mir-15a/16-1。对多个NZB组织进行DNA测序,在相同的微小RNA mir-16-1的3'侧翼序列中发现了一个点突变,并且该突变在包括最近的邻居NZW在内的其他品系中不存在。NZB淋巴组织中miR-16的水平降低。将外源性miR-16导入NZB恶性B-1细胞系会导致细胞周期改变并增加细胞凋亡。在这个自发小鼠模型中,mir-15a/16-1复合体与B-LPD的发生之间的连锁关系表明,mir-15a/16-1表达的改变是CLL中的分子病变。