Suppr超能文献

在一例伴有t(3;11)(q29q13;p15)del(3)(q29)易位的急性T淋巴细胞/髓细胞白血病中鉴定出一种新的融合基因NUP98-IQCG。

A new fusion gene NUP98-IQCG identified in an acute T-lymphoid/myeloid leukemia with a t(3;11)(q29q13;p15)del(3)(q29) translocation.

作者信息

Pan Q, Zhu Y-J, Gu B-W, Cai X, Bai X-T, Yun H-Y, Zhu J, Chen B, Weng L, Chen Z, Xue Y-Q, Chen S-J

机构信息

State Key Lab for Medical Genomics, Shanghai Institute of Hematology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, PR China.

出版信息

Oncogene. 2008 May 29;27(24):3414-23. doi: 10.1038/sj.onc.1210999. Epub 2007 Dec 17.

Abstract

NUP98 has been involved in multiple recurrent chromosome rearrangements in leukemia. We identified a novel fusion between NUP98 and IQ motif containing G (IQCG) gene from a de novo acute T-lymphoid/myeloid leukemia harboring t(3;11)(q29q13;p15)del(3)(q29). IQCG has two putative coiled-coil domains and one IQ domain. The FG repeat from NUP98 and the coiled-coil domain from IQCG were retained in the fusion protein. We demonstrated that NUP98-IQCG could form homodimer, heterodimerize with NUP98 or IQCG, bind co-activators and/or co-repressors, and show transcriptional activity in vitro. Expression of NUP98-IQCG inhibited 32Dcl3 cell apoptosis induced by Ara-C, and partially blocked granulocyte differentiation induced by G-CSF. Colony-forming assay and serial replating assays indicated that NUP98-IQCG was able to stimulate proliferation, partially block differentiation of hematopoietic stem/progenitor cells but was unable to confer transformation alone. Taken together, our data indicate that newly identified NUP98-IQCG fusion protein may play an essential role in leukemogenesis, but by itself may not be sufficient to induce leukemia.

摘要

核孔蛋白98(NUP98)参与了白血病中多种反复出现的染色体重排。我们从一例患有t(3;11)(q29q13;p15)del(3)(q29)的新发急性T淋巴细胞/髓细胞白血病中鉴定出一种新的NUP98与含IQ模体的G(IQCG)基因的融合。IQCG有两个推定的卷曲螺旋结构域和一个IQ结构域。融合蛋白中保留了来自NUP98的FG重复序列和来自IQCG的卷曲螺旋结构域。我们证明,NUP98-IQCG可形成同二聚体,与NUP98或IQCG异源二聚化,结合共激活因子和/或共抑制因子,并在体外表现出转录活性。NUP98-IQCG的表达抑制了阿糖胞苷诱导的32Dcl3细胞凋亡,并部分阻断了粒细胞集落刺激因子诱导的粒细胞分化。集落形成试验和连续再接种试验表明,NUP98-IQCG能够刺激增殖,部分阻断造血干/祖细胞的分化,但不能单独赋予转化能力。综上所述,我们的数据表明,新鉴定的NUP98-IQCG融合蛋白可能在白血病发生中起重要作用,但仅凭其自身可能不足以诱发白血病。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验