Levanon D, Negreanu V, Bernstein Y, Bar-Am I, Avivi L, Groner Y
Department of Molecular Genetics and Virology, Weizmann Institute of Science, Rehovot, Israel.
Genomics. 1994 Sep 15;23(2):425-32. doi: 10.1006/geno.1994.1519.
cDNAs corresponding to three human runt domain containing genes, AML1, AML2, and AML3, were isolated and characterized. In addition to homology in the highly conserved runt domain, extensive sequence similarities were also observed in other parts of the proteins. All three carried an identical, putative ATP binding site -GRSGRGKS-, and their C-terminal halves were particularly rich in proline and serine residues. While AML1 cDNAs were cloned by others, AML2 represents a new member, not previously described, of the runt domain gene family, and AML3 was identified as the human homologue of mouse PEB-P2 alpha A. The chromosomal location of AML1 to chromosome 21q22 was confirmed, while AML2 and AML3 were mapped to chromosome regions 1p36 and 6p21, respectively. Analysis of AML1 and AML2 expression in hematopoietic cell lines revealed a distinct pattern of expression.
分离并鉴定了与三种含人类 runt 结构域基因 AML1、AML2 和 AML3 相对应的 cDNA。除了在高度保守的 runt 结构域具有同源性外,在蛋白质的其他部分也观察到广泛的序列相似性。所有三种基因都带有一个相同的假定 ATP 结合位点 -GRSGRGKS-,并且它们的 C 末端富含脯氨酸和丝氨酸残基。虽然 AML1 的 cDNA 已被其他人克隆,但 AML2 代表了 runt 结构域基因家族中一个先前未描述的新成员,而 AML3 被鉴定为小鼠 PEB-P2αA 的人类同源物。AML1 定位于染色体 21q22 这一染色体定位得到了证实,而 AML2 和 AML3 分别定位于染色体区域 1p36 和 6p21。对造血细胞系中 AML1 和 AML2 表达的分析揭示了一种独特的表达模式。