Literature DB >> 15590816

FoSTUA, encoding a basic helix-loop-helix protein, differentially regulates development of three kinds of asexual spores, macroconidia, microconidia, and chlamydospores, in the fungal plant pathogen Fusarium oxysporum.

Toshiaki Ohara1, Takashi Tsuge.   

Abstract

The soil-borne fungus Fusarium oxysporum causes vascular wilt of a wide variety of plant species. F. oxysporum produces three kinds of asexual spores, macroconidia, microconidia, and chlamydospores. Falcate macroconidia are formed generally from terminal phialides on conidiophores and rarely from intercalary phialides on hyphae. Ellipsoidal microconidia are formed from intercalary phialides on hyphae. Globose chlamydospores with thick walls are developed by the modification of hyphal and conidial cells. Here we describe FoSTUA of F. oxysporum, which differentially regulates the development of macroconidia, microconidia, and chlamydospores. FoSTUA encodes a basic helix-loop-helix protein with similarity to Aspergillus nidulans StuA, which has been identified as a transcriptional regulator controlling conidiation. Nuclear localization of FoStuA was verified by using strains expressing FoStuA-green fluorescent protein fusions. The FoSTUA-targeted mutants exhibited normal microconidium formation in cultures. However, the mutants lacked conidiophores and produced macroconidia at low frequencies only from intercalary phialides. Thus, FoSTUA appears to be necessary to induce conidiophore differentiation. In contrast, chlamydospore formation was dramatically promoted in the mutants. These data demonstrate that FoStuA is a positive regulator and a negative regulator for the development of macroconidia and chlamydospores, respectively, and is dispensable for microconidium formation in cultures. The disease-causing ability of F. oxysporum was not affected by mutations in FoSTUA. However, the mutants produced markedly fewer macroconidia and microconidia in infected plants than the wild type. These results suggest that FoSTUA also has an important role for microconidium formation specifically in infected plants.

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Year:  2004        PMID: 15590816      PMCID: PMC539018          DOI: 10.1128/EC.3.6.1412-1422.2004

Source DB:  PubMed          Journal:  Eukaryot Cell        ISSN: 1535-9786


  45 in total

1.  Aspergillus asexual reproduction and sexual reproduction are differentially affected by transcriptional and translational mechanisms regulating stunted gene expression.

Authors:  J Wu; B L Miller
Journal:  Mol Cell Biol       Date:  1997-10       Impact factor: 4.272

2.  Isolation and physical characterization of three essential conidiation genes from Aspergillus nidulans.

Authors:  M T Boylan; P M Mirabito; C E Willett; C R Zimmerman; W E Timberlake
Journal:  Mol Cell Biol       Date:  1987-09       Impact factor: 4.272

3.  Alterations in superoxide dismutase and catalase in Fusarium oxysporum during starvation-induced differentiation.

Authors:  Y Kono; H Yamamoto; M Takeuchi; H Komada
Journal:  Biochim Biophys Acta       Date:  1995-07-20

4.  Efg1p, an essential regulator of morphogenesis of the human pathogen Candida albicans, is a member of a conserved class of bHLH proteins regulating morphogenetic processes in fungi.

Authors:  V R Stoldt; A Sonneborn; C E Leuker; J F Ernst
Journal:  EMBO J       Date:  1997-04-15       Impact factor: 11.598

5.  Asm-1+, a Neurospora crassa gene related to transcriptional regulators of fungal development.

Authors:  R Aramayo; Y Peleg; R Addison; R Metzenberg
Journal:  Genetics       Date:  1996-11       Impact factor: 4.562

Review 6.  Asexual sporulation in Aspergillus nidulans.

Authors:  T H Adams; J K Wieser; J H Yu
Journal:  Microbiol Mol Biol Rev       Date:  1998-03       Impact factor: 11.056

7.  Factors affecting spore formation in a Candida albicans strain.

Authors:  M Montazeri; H G Hedrick
Journal:  Appl Environ Microbiol       Date:  1984-06       Impact factor: 4.792

8.  Gene cluster involved in melanin biosynthesis of the filamentous fungus Alternaria alternata.

Authors:  N Kimura; T Tsuge
Journal:  J Bacteriol       Date:  1993-07       Impact factor: 3.490

9.  Tfo1: an Ac-like transposon from the plant pathogenic fungus Fusarium oxysporum.

Authors:  M Okuda; K Ikeda; F Namiki; K Nishi; T Tsuge
Journal:  Mol Gen Genet       Date:  1998-06

10.  Interactions of three sequentially expressed genes control temporal and spatial specificity in Aspergillus development.

Authors:  P M Mirabito; T H Adams; W E Timberlake
Journal:  Cell       Date:  1989-06-02       Impact factor: 41.582

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  28 in total

1.  The transcription factor StuA regulates central carbon metabolism, mycotoxin production, and effector gene expression in the wheat pathogen Stagonospora nodorum.

Authors:  Simon V S IpCho; Kar-Chun Tan; Geraldine Koh; Joel Gummer; Richard P Oliver; Robert D Trengove; Peter S Solomon
Journal:  Eukaryot Cell       Date:  2010-05-21

2.  Identification of Conidiogenesis-Associated Genes in Colletotrichum gloeosporioides by Agrobacterium tumefaciens-Mediated Transformation.

Authors:  Jianyuan Wu; Zhirui Ji; Na Wang; Fumei Chi; Chengnan Xu; Zongshan Zhou; Junxiang Zhang
Journal:  Curr Microbiol       Date:  2016-09-01       Impact factor: 2.188

3.  Chlamydospore formation during hyphal growth in Cryptococcus neoformans.

Authors:  Xiaorong Lin; Joseph Heitman
Journal:  Eukaryot Cell       Date:  2005-10

4.  Analogous and Diverse Functions of APSES-Type Transcription Factors in the Morphogenesis of the Entomopathogenic Fungus Metarhizium rileyi.

Authors:  Caiyan Xin; Jinping Zhang; Siji Nian; Guangxi Wang; Zhongkang Wang; Zhangyong Song; Guangwei Ren
Journal:  Appl Environ Microbiol       Date:  2020-04-01       Impact factor: 4.792

5.  FgFlbD regulates hyphal differentiation required for sexual and asexual reproduction in the ascomycete fungus Fusarium graminearum.

Authors:  Hokyoung Son; Myung-Gu Kim; Suhn-Kee Chae; Yin-Won Lee
Journal:  J Microbiol       Date:  2014-10-03       Impact factor: 3.422

6.  The transcriptional regulators SteA and StuA contribute to keratin degradation and sexual reproduction of the dermatophyte Arthroderma benhamiae.

Authors:  Antje Kröber; Sandra Etzrodt; Maria Bach; Michel Monod; Olaf Kniemeyer; Peter Staib; Axel A Brakhage
Journal:  Curr Genet       Date:  2016-05-11       Impact factor: 3.886

7.  Among developmental regulators, StuA but not BrlA is essential for penicillin V production in Penicillium chrysogenum.

Authors:  Claudia Sigl; Hubertus Haas; Thomas Specht; Kristian Pfaller; Hubert Kürnsteiner; Ivo Zadra
Journal:  Appl Environ Microbiol       Date:  2010-12-10       Impact factor: 4.792

8.  The APSES transcription factor Vst1 is a key regulator of development in microsclerotium- and resting mycelium-producing Verticillium species.

Authors:  Jorge L Sarmiento-Villamil; Nicolás E García-Pedrajas; Lourdes Baeza-Montañez; María D García-Pedrajas
Journal:  Mol Plant Pathol       Date:  2017-01-13       Impact factor: 5.663

9.  Molecular characterization and functional analyses of ZtWor1, a transcriptional regulator of the fungal wheat pathogen Zymoseptoria tritici.

Authors:  Amir Mirzadi Gohari; Rahim Mehrabi; Olivier Robert; Ikbal Agah Ince; Sjef Boeren; Martin Schuster; Gero Steinberg; Pierre J G M de Wit; Gert H J Kema
Journal:  Mol Plant Pathol       Date:  2013-12-17       Impact factor: 5.663

10.  The nuclear protein Sge1 of Fusarium oxysporum is required for parasitic growth.

Authors:  Caroline B Michielse; Ringo van Wijk; Linda Reijnen; Erik M M Manders; Sonja Boas; Chantal Olivain; Claude Alabouvette; Martijn Rep
Journal:  PLoS Pathog       Date:  2009-10-23       Impact factor: 6.823

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