Deshpande N, Chopra A, Rangarajan A, Shashidhara L S, Rodrigues V, Krishna S
National Centre for Biological Sciences, TIFR Center, Bangalore 560012, India.
J Biol Chem. 1997 Apr 18;272(16):10664-8. doi: 10.1074/jbc.272.16.10664.
The human transcription enhancer factor-1 (TEF-1) belongs to a family of evolutionarily conserved proteins that have a DNA binding TEA domain. TEF-1 shares a 98% homology with Drosophila scalloped (sd) in the DNA binding domain and a 50% similarity in the activation domain. We have expressed human TEF-1 in Drosophila under the hsp-70 promoter and find that it can substitute for Sd function. The transformants rescue the wingblade defects as well as the lethality of loss-of-function alleles. Observation of reporter activity in the imaginal wing discs of the enhancer-trap alleles suggests that TEF-1 is capable of promoting sd gene regulation. The functional capability of the TEF-1 product was assessed by comparing the extent of rescue by heat shock (hs)-TEF-1 with that of hs-sd. The finding that TEF-1 can function in vivo during wingblade development offers a potent genetic system for the analysis of its function and in the identification of the molecular partners of TEF-1.
人类转录增强因子-1(TEF-1)属于一类进化上保守的蛋白质家族,这些蛋白质具有一个DNA结合TEA结构域。TEF-1在DNA结合结构域与果蝇的扇贝蛋白(sd)有98%的同源性,在激活结构域有50%的相似性。我们已在热休克蛋白-70(hsp-70)启动子控制下在果蝇中表达了人类TEF-1,并发现它可以替代Sd的功能。转化体挽救了翼片缺陷以及功能丧失等位基因的致死性。对增强子陷阱等位基因的成虫翅盘报告基因活性的观察表明,TEF-1能够促进sd基因的调控。通过比较热休克(hs)-TEF-1与hs-sd的挽救程度来评估TEF-1产物的功能能力。TEF-1在翼片发育过程中能在体内发挥作用这一发现,为分析其功能以及鉴定TEF-1的分子伴侣提供了一个有力的遗传系统。