Mendizabal I, Rios G, Mulet J M, Serrano R, de Larrinoa I F
Departamento de Química Aplicada, Facultad de Ciencias Químicas, San Sebastian, Spain.
FEBS Lett. 1998 Mar 27;425(2):323-8. doi: 10.1016/s0014-5793(98)00249-x.
Four putative yeast transcription factors (Hal6-9p) have been identified which upon overexpression in multicopy plasmids increase sodium and lithium tolerance. This effect is mediated, at least in part, by increased expression of the Enalp Na+/Li+ extrusion pump. Hal6p and Hal7p are bZIP proteins and their gene disruptions affected neither salt tolerance nor ENA1 expression. Hal8p and Hal9p are putative zinc fingers and their gene disruptions decreased both salt tolerance and ENA1 expression. Therefore, Hal8p and Hal9p, but not Hal6p and Hal7p, qualify as transcriptional activators of ENA1 under physiological conditions. Hal8p seems to mediate the calcineurin-dependent part of ENA1 expression.
已鉴定出四种假定的酵母转录因子(Hal6 - 9p),当它们在多拷贝质粒中过表达时,会提高对钠和锂的耐受性。这种效应至少部分是由Enalp钠/锂外排泵表达增加介导的。Hal6p和Hal7p是bZIP蛋白,它们的基因破坏既不影响耐盐性也不影响ENA1表达。Hal8p和Hal9p是假定的锌指蛋白,它们的基因破坏降低了耐盐性和ENA1表达。因此,在生理条件下,Hal8p和Hal9p而非Hal6p和Hal7p可作为ENA1的转录激活因子。Hal8p似乎介导了ENA1表达中依赖钙调神经磷酸酶的部分。