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通过编码含“Glo”型锌指蛋白的GTS1基因的过表达,在酿酒酵母中实现组成型絮凝。

Constitutive flocculation in Saccharomyces cerevisiae through overexpression of the GTS1 gene, coding for a 'Glo'-type Zn-finger-containing protein.

作者信息

Bossier P, Goethals P, Rodrigues-Pousada C

机构信息

Instituto Gulbenkian de Ciência, Laboratório Genética Molecular, Oeiras, Portugal.

出版信息

Yeast. 1997 Jun 30;13(8):717-25. doi: 10.1002/(SICI)1097-0061(19970630)13:8<717::AID-YEA132>3.0.CO;2-2.

Abstract

The product of the cloned GTS1 gene is characterized by structural features found in transcription factors. It contains one Zn-finger motif (CXXCX16CXXC) situated in the N-terminal end with a high degree of homology to the newly identified 'Glo' family of Zn-finger proteins (Ireland et al., 1994, EMBO J. 13, 3812-3821). The C-terminal end of the protein is characterized by poly (Ala-Gln) and poly-Gln stretches. Poly-Gln are part of trans-acting motifs in known transcription factors. Overexpression of the GTS1 gene results in constitutive flocculation. Whole cell electrophoretic mobility and hydrophobicity of GTS1 overexpressing cells was respectively lower and higher relative to control cells. GTS1-induced flocculation is hardly sensitive to mannose in contrast to FLO1-determined flocculation. Overexpression of the GTS1 gene in a flo1 background does not abolish flocculation, suggesting that the FLO1 gene is not linked with the GTS1 gene in a 'flocculation pathway'.

摘要

克隆的GTS1基因的产物具有转录因子中发现的结构特征。它在N末端含有一个锌指基序(CXXCX16CXXC),与新鉴定的锌指蛋白“Glo”家族具有高度同源性(Ireland等人,1994年,《欧洲分子生物学组织杂志》13卷,3812 - 3821页)。该蛋白的C末端以聚(丙氨酸 - 谷氨酰胺)和聚谷氨酰胺延伸为特征。聚谷氨酰胺是已知转录因子中转录激活基序的一部分。GTS1基因的过表达导致组成型絮凝。相对于对照细胞,过表达GTS1的细胞的全细胞电泳迁移率和疏水性分别更低和更高。与FLO1决定的絮凝相反,GTS1诱导的絮凝对甘露糖几乎不敏感。在flo1背景中过表达GTS1基因不会消除絮凝,这表明FLO1基因在“絮凝途径”中与GTS1基因不相关。

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