» Articles » PMID: 19880755

Organization and Evolutionary Trajectory of the Mating Type (MAT) Locus in Dermatophyte and Dimorphic Fungal Pathogens

Overview
Journal Eukaryot Cell
Specialty Molecular Biology
Date 2009 Nov 3
PMID 19880755
Citations 36
Authors
Affiliations
Soon will be listed here.
Abstract

Sexual reproduction in fungi is governed by a specialized genomic region, the mating type (MAT) locus, whose gene identity, organization, and complexity are diverse. We identified the MAT locus of five dermatophyte fungal pathogens (Microsporum gypseum, Microsporum canis, Trichophyton equinum, Trichophyton rubrum, and Trichophyton tonsurans) and a dimorphic fungus, Paracoccidioides brasiliensis, and performed phylogenetic analyses. The identified MAT locus idiomorphs of M. gypseum control cell type identity in mating assays, and recombinant progeny were produced. Virulence tests in Galleria mellonella larvae suggest the two mating types of M. gypseum may have equivalent virulence. Synteny analysis revealed common features of the MAT locus shared among these five dermatophytes: namely, a small size ( approximately 3 kb) and a novel gene arrangement. The SLA2, COX13, and APN2 genes, which flank the MAT locus in other Ascomycota are instead linked on one side of the dermatophyte MAT locus. In addition, the transcriptional orientations of the APN2 and COX13 genes are reversed compared to the dimorphic fungi Histoplasma capsulatum, Coccidioides immitis, and Coccidioides posadasii. A putative transposable element, pogo, was found to have inserted in the MAT1-2 idiomorph of one P. brasiliensis strain but not others. In conclusion, the evolution of the MAT locus of the dermatophytes and dimorphic fungi from the last common ancestor has been punctuated by both gene acquisition and expansion, and asymmetric gene loss. These studies further support a foundation to develop molecular and genetic tools for dermatophyte and dimorphic human fungal pathogens.

Citing Articles

as an Invertebrate Model for Studying Fungal Infections.

Marena G, Thomaz L, Nosanchuk J, Taborda C J Fungi (Basel). 2025; 11(2).

PMID: 39997451 PMC: 11856299. DOI: 10.3390/jof11020157.


Current Topics in Dermatophyte Classification and Clinical Diagnosis.

Moskaluk A, VandeWoude S Pathogens. 2022; 11(9).

PMID: 36145389 PMC: 9502385. DOI: 10.3390/pathogens11090957.


Genetic Characterization of Clinical Isolates in the United States.

Moskaluk A, Darlington L, Kuhn S, Behzadi E, Gagne R, Kozakiewicz C J Fungi (Basel). 2022; 8(7).

PMID: 35887433 PMC: 9321804. DOI: 10.3390/jof8070676.


Updates in Biology and Genetic Advances in Fungus Manipulation.

Alencar Chaves A, Navarro M, de Barros Y, Silva R, Xander P, Batista W J Fungi (Basel). 2021; 7(2).

PMID: 33557381 PMC: 7915485. DOI: 10.3390/jof7020116.


She Loves Me, She Loves Me Not: On the Dualistic Asexual/Sexual Nature of Dermatophyte Fungi.

Metin B, Heitman J Mycopathologia. 2019; 185(1):87-101.

PMID: 31578669 PMC: 7050418. DOI: 10.1007/s11046-019-00390-3.


References
1.
Kwon-Chung K, Weeks R, LARSH H . Studies on Emmonsiella capsulata (Histoplasma capsulatum). II. Distribution of the two mating types in 13 endemic states of the United States. Am J Epidemiol. 1974; 99(1):44-9. DOI: 10.1093/oxfordjournals.aje.a121583. View

2.
Graser Y, Scott J, Summerbell R . The new species concept in dermatophytes-a polyphasic approach. Mycopathologia. 2008; 166(5-6):239-56. DOI: 10.1007/s11046-008-9099-y. View

3.
Graser Y, de Hoog S, Summerbell R . Dermatophytes: recognizing species of clonal fungi. Med Mycol. 2006; 44(3):199-209. DOI: 10.1080/13693780600606810. View

4.
Kumar S, Tamura K, Nei M . MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment. Brief Bioinform. 2004; 5(2):150-63. DOI: 10.1093/bib/5.2.150. View

5.
Turgeon B, Yoder O . Proposed nomenclature for mating type genes of filamentous ascomycetes. Fungal Genet Biol. 2000; 31(1):1-5. DOI: 10.1006/fgbi.2000.1227. View