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白色念珠菌中一个DNA连接酶编码基因(CaLIG4)的细胞周期调控

Cell cycle regulation of a DNA ligase-encoding gene (CaLIG4) from Candida albicans.

作者信息

Andaluz E, Ciudad A, Rubio Coque J, Calderone R, Larriba G

机构信息

Departamento de Microbiología, Universidad de Extremadura, Avda. de Elvas s/n, 06071 Badajoz, Spain.

出版信息

Yeast. 1999 Sep 15;15(12):1199-210. doi: 10.1002/(SICI)1097-0061(19990915)15:12<1199::AID-YEA447>3.0.CO;2-S.

Abstract

A DNA ligase (CaLIG4) (formerly CaCDC9) of the human pathogen, Candida albicans, has been characterized. The encoded protein displayed a significant similarity to ligase IV from both Saccharomyces cerevisiae and humans. In addition, whereas CaLIG4 did not complement a S. cerevisiae cdc9 mutant, it re-established non-homologous end-joining of DNA double-strand breaks in a S. cerevisiae lig4 deletant. CaLIG4 was assigned to chromosome 2. Several cis-acting effector sequences were identified in the promoter region of the CaLIG4, including the DNA sequence element ACGNG, which is required for periodic transcription of several DNA-replicating genes in S. cerevisiae. The level of transcription of CaLIG4 in C. albicans varies during the yeast cell cycle. Newly formed cells contained basal levels of transcript which increased to a maximum level when cells were in late G(1). Thereafter, levels of transcript dropped as DNA replication was initiated. Our results suggest that CaLIG4 may perform an important role during the mitotic cycle of C. albicans.

摘要

人类病原体白色念珠菌的一种DNA连接酶(CaLIG4)(以前称为CaCDC9)已得到鉴定。编码的蛋白质与酿酒酵母和人类的连接酶IV有显著相似性。此外,虽然CaLIG4不能互补酿酒酵母的cdc9突变体,但它能在酿酒酵母lig4缺失体中重新建立DNA双链断裂的非同源末端连接。CaLIG4定位于2号染色体。在CaLIG4的启动子区域鉴定出几个顺式作用效应序列,包括DNA序列元件ACGNG,这是酿酒酵母中几个DNA复制基因周期性转录所必需的。白色念珠菌中CaLIG4的转录水平在酵母细胞周期中有所变化。新形成的细胞含有基础水平的转录本,当细胞处于G(1)晚期时转录本增加到最大水平。此后,随着DNA复制的开始,转录本水平下降。我们的结果表明,CaLIG4可能在白色念珠菌的有丝分裂周期中发挥重要作用。

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