Suppr超能文献

LAZ3是一种新的锌指编码基因,在人类淋巴瘤中因3号染色体q27区域反复发生的易位而被破坏。

LAZ3, a novel zinc-finger encoding gene, is disrupted by recurring chromosome 3q27 translocations in human lymphomas.

作者信息

Kerckaert J P, Deweindt C, Tilly H, Quief S, Lecocq G, Bastard C

机构信息

Unité 124 INSERM, Institut de Recherches sur le Cancer de Lille, France.

出版信息

Nat Genet. 1993 Sep;5(1):66-70. doi: 10.1038/ng0993-66.

Abstract

We have shown previously that chromosomal translocations involving chromosome 3q27 and immunoglobulin gene regions are the third most common specific translocations in non-Hodgkin's lymphoma (NHL). We now report the isolation of a gene that is disrupted in two cases by t(3;14) and t(3;4) translocations. The gene (LAZ3) encodes a 79 kDa protein containing six zinc-finger motifs and sharing amino-terminal homology with several transcription factors including the Drosophila tramtrack and Broad-complex genes, both of which are developmental transcription regulators. LAZ3 is transcribed as a 3.8 kb message predominantly in normal adult skeletal muscle and in several NHL carrying 3q27 chromosomal defects. We suggest that it may act as a transcription regulator and play an important role in lymphomagenesis.

摘要

我们先前已表明,涉及3号染色体q27区和免疫球蛋白基因区域的染色体易位是非霍奇金淋巴瘤(NHL)中第三常见的特异性易位。我们现在报告分离出一个基因,该基因在两例病例中因t(3;14)和t(3;4)易位而被破坏。该基因(LAZ3)编码一种79 kDa的蛋白质,含有六个锌指基序,并且在氨基末端与几种转录因子具有同源性,包括果蝇的tramtrack基因和Broad-complex基因,这两个基因都是发育转录调节因子。LAZ3转录生成一条3.8 kb的信使RNA,主要在正常成人骨骼肌以及一些携带3号染色体q27染色体缺陷的NHL中表达。我们认为它可能作为一种转录调节因子,并在淋巴瘤发生中起重要作用。

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