首页> 外文期刊>Fungal Genetics and Biology >Deletion of the MED13 and CDK8 subunits of the Mediator improves the phenotype of a long-lived respiratory deficient mutant of Podospora anserina
【24h】

Deletion of the MED13 and CDK8 subunits of the Mediator improves the phenotype of a long-lived respiratory deficient mutant of Podospora anserina

机译:介体的MED13和CDK8亚基的删除改善了Podospora anserina的长寿命呼吸缺陷型突变体的表型。

获取原文
获取原文并翻译 | 示例
       

摘要

chain is viable. This is due to the presence in this organism, as in most filamentous fungi, of an alternative respiratory oxidase (AOX) that provides a bypass to the cytochrome pathway. However mutants lacking a functional cytochrome pathway present multiple phenotypes including poorly colored thin mycelium and slow growth. In a large genetic screen based on the improvement of these phenotypes, we isolated a large number of independent suppressor mutations. Most of them led to the constitutive overexpression of the aox gene. In this study, we characterize a new suppressor mutation that does not affect the production of AOX. It is a loss-of-function mutation in the gene encoding the MED13 subunit of the kinase module of the Mediator complex. Inactivation of the cdk8 gene encoding another subunit of the same module also results in partial suppression of a cytochrome-deficient mutant. Analysis of strains lacking the MED13 or CDK8 subunits points to the importance of these subunits as regulators involved in diverse physiological processes such as growth, longevity and sexual development. Interestingly, transcriptional analyses indicate that in P. anserina, loss of the respiratory cytochrome pathway results in the up-regulation of glycolysis-related genes revealing a new type of retrograde regulation. The loss of MED13 augments the up-regulation of some of these genes. (C) 2015 Elsevier Inc. All rights reserved.
机译:连锁是可行的。这是由于这种微生物(如大多数丝状真菌)中存在另一种呼吸道氧化酶(AOX),它可以绕过细胞色素途径。然而,缺乏功能性细胞色素途径的突变体表现出多种表型,包括色泽较弱的薄菌丝体和缓慢的生长。在基于这些表型改善的大型遗传筛选中,我们分离了大量独立的抑制子突变。它们中的大多数导致aox基因的组成型过表达。在这项研究中,我们表征了一个新的抑制突变,它不会影响AOX的产生。它是编码介体复合物激酶模块MED13亚基的基因中的功能丧失突变。编码相同模块另一个亚基的cdk8基因失活也会导致细胞色素缺乏突变体的部分抑制。对缺乏MED13或CDK8亚基的菌株的分析表明,这些亚基作为参与多种生理过程(如生长,寿命和性发育)的调节剂的重要性。有趣的是,转录分析表明,在P. anserina中,呼吸细胞色素途径的缺失导致糖酵解相关基因的上调,从而揭示了一种新型的逆行调节。 MED13的缺失增强了其中一些基因的上调。 (C)2015 Elsevier Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号