Muntean Andrew G, Giannola Diane, Udager Aaron M, Hess Jay L
Department ofPathology, University of Michigan Medical School, Ann Arbor, USA.
Blood. 2008 Dec 1;112(12):4690-3. doi: 10.1182/blood-2008-01-134056. Epub 2008 Sep 16.
Chromosomal translocations involving the mixed lineage leukemia (MLL) gene are associated with aggressive acute lymphoid and myeloid leukemias. These translocations are restricted to an 8.3-kb breakpoint region resulting in fusion of amino terminal MLL sequences in frame to 1 of more than 60 different translocation partners. The translocations consistently delete the plant homeodomain (PHD) fingers and more carboxyl terminal MLL sequences. The function of the PHD fingers is obscure and their specific role in transformation has not been explored. Here we show that inclusion of the PHD fingers in the MLL fusion protein MLL-AF9 blocked immortalization of hematopoietic progenitors. Inclusion of 2 or more PHD fingers reduced association with the Hoxa9 locus and suppressed Hoxa9 up-regulation in hematopoietic progenitors. These data provide an explanation for why MLL translocation breakpoints exclude the PHD fingers and suggest a possible role for these domains in regulating the function of wild-type MLL.
涉及混合谱系白血病(MLL)基因的染色体易位与侵袭性急性淋巴细胞白血病和髓细胞白血病相关。这些易位局限于一个8.3kb的断点区域,导致MLL氨基末端序列与60多种不同易位伙伴中的1种框内融合。这些易位始终会删除植物同源结构域(PHD)指状结构和更多的羧基末端MLL序列。PHD指状结构的功能尚不清楚,其在转化中的具体作用也未被探究。在此我们表明,在MLL融合蛋白MLL-AF9中包含PHD指状结构会阻止造血祖细胞的永生化。包含2个或更多PHD指状结构会减少与Hoxa9基因座的结合,并抑制造血祖细胞中Hoxa9的上调。这些数据解释了为什么MLL易位断点会排除PHD指状结构,并提示这些结构域在调节野生型MLL功能中可能发挥的作用。