Departamento de Bioquímica y Biología Estructural, Instituto de Fisiología Celular, Universidad Nacional Autónoma de México, Apartado postal 70-242, 04510 Mexico City, Mexico.
División de Biología Molecular, IPICYT, Camino a la Presa San José No 2055, Lomas Cuarta Sección 78216, San Luis Potosí, Mexico.
Microbiology (Reading). 2011 Mar;157(Pt 3):879-889. doi: 10.1099/mic.0.044974-0. Epub 2010 Nov 4.
The transcriptional activation response relies on a repertoire of transcriptional activators, which decipher regulatory information through their specific binding to cognate sequences, and their capacity to selectively recruit the components that constitute a given transcriptional complex. We have addressed the possibility of achieving novel transcriptional responses by the construction of a new transcriptional regulator--the Hap2-3-5-Gln3 hybrid modulator--harbouring the HAP complex polypeptides that constitute the DNA-binding domain (Hap2-3-5) and the Gln3 activation domain, which usually act in an uncombined fashion. The results presented in this paper show that transcriptional activation of GDH1 and ASN1 under repressive nitrogen conditions is achieved through the action of the novel Hap2-3-5-Gln3 transcriptional regulator. We propose that the combination of the Hap DNA-binding and Gln3 activation domains results in a hybrid modulator that elicits a novel transcriptional response not evoked when these modulators act independently.
转录激活反应依赖于一系列转录激活因子,这些转录激活因子通过其特异性结合同源序列来解读调控信息,并通过选择性招募构成特定转录复合物的成分来发挥作用。我们通过构建一种新型转录调节剂——Hap2-3-5-Gln3 混合调节剂,探讨了实现新的转录反应的可能性,该调节剂包含构成 DNA 结合域(Hap2-3-5)和 Gln3 激活域的 HAP 复合物多肽,通常以未结合的形式发挥作用。本文的研究结果表明,新型 Hap2-3-5-Gln3 转录调节剂的作用实现了在抑制性氮条件下 GDH1 和 ASN1 的转录激活。我们提出,Hap DNA 结合域和 Gln3 激活域的组合产生了一种混合调节剂,引起了一种新的转录反应,而当这些调节剂独立作用时不会引起这种反应。