Literature DB >> 32950720

The pheromone response module, a mitogen-activated protein kinase pathway implicated in the regulation of fungal development, secondary metabolism and pathogenicity.

Dean Frawley1, Özgür Bayram2.   

Abstract

Mitogen-activated protein kinase (MAPK) pathways are highly conserved from yeast to human and are required for the regulation of a multitude of biological processes in eukaryotes. A pentameric MAPK pathway known as the Fus3 pheromone module was initially characterised in Saccharomyces cerevisiae and was shown to regulate cell fusion and sexual development. Individual orthologous pheromone module genes have since been found to be highly conserved in fungal genomes and have been shown to regulate a diverse array of cellular responses, such as cell growth, asexual and sexual development, secondary metabolite production and pathogenicity. However, information regarding the assembly and structure of orthologous pheromone modules, as well as the mechanisms of signalling and their biological significance is limited, specifically in filamentous fungal species. Recent studies have provided insight on the utilization of the pheromone module as a central signalling hub for the co-ordinated regulation of fungal development and secondary metabolite production. Various proteins of this pathway are also known to regulate reproduction and virulence in a range of plant pathogenic fungi. In this review, we discuss recent findings that help elucidate the structure of the pheromone module pathway in a myriad of fungal species and its implications in the control of fungal growth, development, secondary metabolism and pathogenicity.
Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Fungal development; Fungi; MAP kinases; Pathogenicity; Pheromone module; Secondary metabolism

Year:  2020        PMID: 32950720     DOI: 10.1016/j.fgb.2020.103469

Source DB:  PubMed          Journal:  Fungal Genet Biol        ISSN: 1087-1845            Impact factor:   3.495


  7 in total

1.  Secondary Metabolism Gene Clusters Exhibit Increasingly Dynamic and Differential Expression during Asexual Growth, Conidiation, and Sexual Development in Neurospora crassa.

Authors:  Zheng Wang; Francesc Lopez-Giraldez; Jason Slot; Oded Yarden; Frances Trail; Jeffrey P Townsend
Journal:  mSystems       Date:  2022-05-31       Impact factor: 7.324

2.  MAPK CcSakA of the HOG Pathway Is Involved in Stipe Elongation during Fruiting Body Development in Coprinopsis cinerea.

Authors:  Jing Zhao; Jing Yuan; Yating Chen; Yu Wang; Jing Chen; Jingjing Bi; Linna Lyu; Cigang Yu; Sheng Yuan; Zhonghua Liu
Journal:  J Fungi (Basel)       Date:  2022-05-20

3.  Cdc42-Specific GTPase-Activating Protein Rga1 Squelches Crosstalk between the High-Osmolarity Glycerol (HOG) and Mating Pheromone Response MAPK Pathways.

Authors:  Jesse C Patterson; Louise S Goupil; Jeremy Thorner
Journal:  Biomolecules       Date:  2021-10-17

4.  Transcriptome Analysis Reveals that Exogenous Melatonin Confers Lilium Disease Resistance to Botrytis elliptica.

Authors:  Xuehua Xie; Yu Han; Xi Yuan; Man Zhang; Ping Li; Aiqin Ding; Jia Wang; Tangren Cheng; Qixiang Zhang
Journal:  Front Genet       Date:  2022-06-14       Impact factor: 4.772

5.  Phosphoproteomic and Metabolomic Profiling Uncovers the Roles of CcPmk1 in the Pathogenicity of Cytospora chrysosperma.

Authors:  Lu Yu; Yuchen Yang; Dianguang Xiong; Chengming Tian
Journal:  Microbiol Spectr       Date:  2022-06-23

Review 6.  Post-translational modifications drive secondary metabolite biosynthesis in Aspergillus: a review.

Authors:  Kunlong Yang; Jun Tian; Nancy P Keller
Journal:  Environ Microbiol       Date:  2022-05-30       Impact factor: 5.476

7.  Fus3, as a Critical Kinase in MAPK Cascade, Regulates Aflatoxin Biosynthesis by Controlling the Substrate Supply in Aspergillus flavus, Rather than the Cluster Genes Modulation.

Authors:  Longxue Ma; Xu Li; Fuguo Xing; Junning Ma; Xiaoyun Ma; Yiran Jiang
Journal:  Microbiol Spectr       Date:  2022-02-02
  7 in total

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