Milatovich A, Travis A, Grosschedl R, Francke U
Department of Genetics, Stanford University Medical School, California 94305-5428.
Genomics. 1991 Dec;11(4):1040-8. doi: 10.1016/0888-7543(91)90030-i.
LEF-1 is a 54-kDa nuclear protein that is expressed specifically in pre-B and T-cells. It binds to a functionally important site in the T-cell receptor alpha enhancer and contributes to maximal enhancer activity. LEF-1 is a member of a family of regulatory proteins that share homology with the high mobility group protein 1 (HMG1). The location of the LEF1 gene on human and mouse chromosomes was determined by Southern blot analysis of DNA from panels of interspecies somatic cell hybrids using a murine cDNA probe. Human-specific DNA fragments were detected in all somatic cell hybrids that retained the human chromosomal region 4cen-q31.2. Fluorescent in situ hybridization with two biotin-labeled overlapping human genomic cosmids revealed a specific hybridization signal at 4q23-q25. The homologous locus in the mouse was mapped to chromosome 3 by Southern analysis of rodent x mouse hybrid cell DNA. This chromosomal location was confirmed by the use of a restriction fragment length polymorphism (RFLP) in recombinant inbred mouse strains. The results of this RFLP analysis indicated that the mouse Lef-1 gene was closely linked to Pmv-39 and Egf and was likely placed between these loci, both of which were previously mapped to distal mouse chromosome 3. Our mapping results did not suggest involvement of this gene in previously mapped genetic disorders or in known neoplasia-associated translocation breakpoints.
淋巴增强因子-1(LEF-1)是一种54千道尔顿的核蛋白,在B细胞前体和T细胞中特异性表达。它与T细胞受体α增强子中一个功能重要的位点结合,并有助于增强子发挥最大活性。LEF-1是一类调节蛋白家族的成员,与高迁移率族蛋白1(HMG1)具有同源性。使用鼠源cDNA探针,通过对种间体细胞杂种DNA进行Southern印迹分析,确定了LEF1基因在人和小鼠染色体上的位置。在所有保留人类染色体区域4cen-q31.2的体细胞杂种中都检测到了人类特异性DNA片段。用两个生物素标记的重叠人类基因组黏粒进行荧光原位杂交,在4q23-q25处显示出特异性杂交信号。通过对啮齿动物×小鼠杂交细胞DNA进行Southern分析,将小鼠中的同源基因座定位到3号染色体上。在重组近交小鼠品系中使用限制性片段长度多态性(RFLP)证实了这一染色体定位。该RFLP分析结果表明,小鼠Lef-1基因与Pmv-39和Egf紧密连锁,可能位于这两个基因座之间,而这两个基因座先前都被定位到小鼠3号染色体的远端。我们的定位结果并未表明该基因参与了先前定位的遗传疾病或已知的肿瘤相关易位断点。