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酿酒酵母中HYP2基因的染色体定位以及在基因破坏实验中使用脉冲场凝胶电泳检测不规则重组事件

Chromosomal localization of the HYP2-gene in Saccharomyces cerevisiae and use of pulsed-field gel electrophoresis for detection of irregular recombination events in gene disruption experiments.

作者信息

Wöhl T, Baur M, Friedl A A, Lottspeich F

机构信息

Max-Planck-Institut für Biochemie, Martinsried, Germany.

出版信息

Electrophoresis. 1992 Sep-Oct;13(9-10):651-3. doi: 10.1002/elps.11501301136.

Abstract

In the hypusine-containing protein (HP), a specific lysine residue is modified by spermidine to form the unusual amino acid hypusine (4-amino-2-hydroxybutyllysine). The HP has been designated as an eucaryotic translation initiation factor--eIF-5A--because of its stimulating effect in the methionyl-puromycin in vitro assay. Nevertheless, the precise function of this protein remains to be elucidated. In the yeast Saccharomyces cerevisiae two genes, HYP1 and HYP2, coding for two different forms of the HP, are present. The HYP1-gene is identical to the ANB1-gene and has already been localized on chromosome X. However, the chromosomal localization of the HYP2-gene has not been elucidated. By using pulsed-field gel electrophoresis (PFGE) and subsequent Southern blotting, we determined the localization of the HYP2-gene to chromosome V. Furthermore, PFGE was used for the detection of irregular recombination events, such as misintegration or integration into a duplicated gene, and in gene disruption experiments using haploid and diploid yeast cells. The obtained data support the critical role of the HP for cell viability.

摘要

在含hypusine蛋白(HP)中,一个特定的赖氨酸残基被亚精胺修饰,形成异常氨基酸hypusine(4-氨基-2-羟基丁基赖氨酸)。由于其在甲硫氨酰-嘌呤霉素体外测定中的刺激作用,HP已被指定为真核生物翻译起始因子——eIF-5A。然而,这种蛋白质的确切功能仍有待阐明。在酿酒酵母中,存在两个编码两种不同形式HP的基因,即HYP1和HYP2。HYP1基因与ANB1基因相同,且已定位在X染色体上。然而,HYP2基因的染色体定位尚未阐明。通过使用脉冲场凝胶电泳(PFGE)及随后的Southern印迹法,我们确定了HYP2基因位于第五条染色体上。此外,PFGE还用于检测不规则重组事件,如错误整合或整合到重复基因中,以及在使用单倍体和二倍体酵母细胞的基因破坏实验中。所获得的数据支持了HP对细胞活力的关键作用。

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