Sun Lei, Kerawalla Hoshnuwar, Wu Xian, Lehnert Matthew S, Uckun Fatih M
Department of Molecular Biology, Parker Hughes Cancer Center, Parker Hughes Institute, St Paul, MN 55113, USA.
Leuk Lymphoma. 2002 Apr;43(4):841-9. doi: 10.1080/10428190290016980.
The purpose of the present study was to characterize the human Helios gene products expressed in leukemia cells. A 3.5 kb human Helios cDNA clone was isolated from a human T-cell cDNA library derived from the human T-acute lymphoblastic leukemia (ALL) cell line JURKAT. This cDNA clone had a unique open reading frame (ORF) encoding a novel 304 amino acid (AA) peptide, which was designated as Helios 3. The sequence of the 289 AA C-terminal portion of Helios 3 downstream of V-16 is identical to the corresponding sequence found in Helios 1 and 2 and contains two zinc fingers. By contrast, the 15 AA N-terminal portion of Helios 3 is unique and does not contain the N-terminal zinc finger motifs that are conserved in Helios 1 and 2 as well as other previously identified members of the Ikaros family. Southern blot analysis of genomic DNA fragments of the human Helios gene locus showed that Helios 3 is encoded by the same genomic locus as Helios 1 and 2. The expression of Helios 3 mRNA was not restricted to T-lineage ALL cells or another immunophenotypically distinct subset of leukemias. Helios 3 mRNA was expressed in freshly obtained primary leukemic cells from six of 15 children with newly diagnosed ALL. Helios 3 exhibited a unique protein interaction profile via its N-terminal portion, which may have biological significance in pathogenesis of human leukemias.
本研究的目的是对白血病细胞中表达的人类Helios基因产物进行表征。从源自人T急性淋巴细胞白血病(ALL)细胞系JURKAT的人T细胞cDNA文库中分离出一个3.5 kb的人类Helios cDNA克隆。该cDNA克隆具有一个独特的开放阅读框(ORF),编码一种新的304个氨基酸(AA)的肽,被命名为Helios 3。Helios 3在V - 16下游的289个AA C末端部分的序列与在Helios 1和2中发现的相应序列相同,并且包含两个锌指。相比之下,Helios 3的15个AA N末端部分是独特的,不包含在Helios 1和2以及Ikaros家族其他先前鉴定的成员中保守的N末端锌指基序。对人类Helios基因座的基因组DNA片段进行Southern印迹分析表明,Helios 3与Helios 1和2由相同的基因组位点编码。Helios 3 mRNA的表达不限于T系ALL细胞或白血病的另一个免疫表型不同的亚组。Helios 3 mRNA在15名新诊断ALL儿童中的6名的新鲜获得的原发性白血病细胞中表达。Helios 3通过其N末端部分表现出独特的蛋白质相互作用谱,这可能在人类白血病的发病机制中具有生物学意义。