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一个新的与Pbx相关的同源框基因家族的鉴定。

Identification of a new family of Pbx-related homeobox genes.

作者信息

Nakamura T, Jenkins N A, Copeland N G

机构信息

ABL-Basic Research Program, NCI-Frederick Cancer Research and Development Center, Frederick, Maryland 21702, USA.

出版信息

Oncogene. 1996 Nov 21;13(10):2235-42.

PMID:8950991
Abstract

The expression of Meis1 (a novel Pbx-related homeobox gene) and either Hoxa7 or Hoxa9 are coactivated by retroviral integration in BXH2 murine myeloid leukemias (T Nakamura, DA Largaespada, JD Shaughnessy Jr, NA Jenkins and NG Copeland (1996) Nature Genet. 12: 149-153). As Pbx proteins are Hox cofactors, which cooperatively bind DNA with Hox proteins to modulate the otherwise similar DNA bind specificities of Hox proteins, these results suggested that Meis1 may function as a cofactor for Hoxa7 and Hoxa9 in the induction of murine myeloid leukemias. By DNA cross-hybridization we have identified two Meis1-related genes, Meis2 and Meis3. Sequence analysis revealed extensive amino acid similarity among the three Meis proteins both within and outside of the homeodomain. Phylogenetic analysis showed that the Meis genes belong to a distinct family of Pbx-related genes. Chromosome mapping studies indicated that Meis2 and Meis3 are unlinked to Meis1 and map to mouse chromosome 2 and 7, respectively. The Meis genes displayed distinct but overlapping patterns of expression in normal tissues and were expressed in some cases of murine myeloid leukemia. The identification of two additional Meis genes identifies a new family of potential Hox cofactors as well as two new potential disease genes.

摘要

Meis1(一种新的与Pbx相关的同源框基因)以及Hoxa7或Hoxa9的表达在BXH2小鼠髓性白血病中通过逆转录病毒整合而被共同激活(T·中村、DA·拉加埃斯帕达、JD·肖纳西二世、NA·詹金斯和NG·科普兰(1996年)《自然遗传学》12: 149 - 153)。由于Pbx蛋白是Hox辅因子,它们与Hox蛋白协同结合DNA以调节Hox蛋白原本相似的DNA结合特异性,这些结果表明Meis1在小鼠髓性白血病的诱导中可能作为Hoxa7和Hoxa9的辅因子发挥作用。通过DNA交叉杂交,我们鉴定出了两个与Meis1相关的基因,Meis2和Meis3。序列分析揭示了这三种Meis蛋白在同源结构域内外都有广泛的氨基酸相似性。系统发育分析表明,Meis基因属于一个与Pbx相关的独特基因家族。染色体定位研究表明,Meis2和Meis3与Meis1不连锁,分别定位于小鼠染色体2和7。Meis基因在正常组织中表现出不同但重叠的表达模式,并且在一些小鼠髓性白血病病例中也有表达。另外两个Meis基因的鉴定确定了一个潜在的Hox辅因子新家族以及两个新的潜在疾病基因。

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