Skip to main content
Journal cover image

Mechanistic plasticity of sexual reproduction and meiosis in the Candida pathogenic species complex.

Publication ,  Journal Article
Reedy, JL; Floyd, AM; Heitman, J
Published in: Curr Biol
June 9, 2009

BACKGROUND: Candida species are microbial pathogens originally thought to be asexual, but several are now recognized as sexual or parasexual. Candida albicans, the most common fungus infecting humans, is an obligate diploid with a parasexual cycle involving mating, recombination, and genome reduction but no recognized meiosis. Others (C. lusitaniae, C. guilliermondii) are haploid, and their mating produces spores, suggestive of complete meiotic sexual cycles. However, comparative genomic analysis reveals that these species lack key meiotic components, including the recombinase Dmc1 and cofactors (Mei5/Sae3), synaptonemal-complex proteins (Zip1-Zip4/Hop1), and the crossover interference pathway (Msh4/5). RESULTS: Here we elucidate the structure and functions of the mating-type (MAT) locus and establish that C. lusitaniae undergoes meiosis during its sexual cycle. The MAT-encoded a2 (high-mobility group) and alpha1 (alpha domain) factors specify a and alpha cell identity, whereas the a1 homeodomain protein drives meiosis and sporulation and functions without its canonical heterodimeric partner, alpha2. Despite the apparent loss of meiotic genes, C. lusitaniae undergoes meiosis during sexual reproduction involving diploid intermediates, frequent SPO11-dependent recombination, and whole-genome reduction generating haploid progeny. The majority of meiotic progeny are euploid, but approximately one-third are diploid/aneuploid. CONCLUSIONS: The cell identity and meiotic pathways have been substantially rewired, and meiotic generation of both recombinant and aneuploid progeny may expand genetic diversity. These findings inform our understanding of sexual reproduction in pathogenic microbes and the evolutionary plasticity of the meiotic machinery, with implications for the sexual nature of C. albicans and the generation and consequences of aneuploidy in biology and medicine.

Duke Scholars

Altmetric Attention Stats
Dimensions Citation Stats

Published In

Curr Biol

DOI

EISSN

1879-0445

Publication Date

June 9, 2009

Volume

19

Issue

11

Start / End Page

891 / 899

Location

England

Related Subject Headings

  • Transcription Factors
  • Spores, Fungal
  • Reproduction
  • Recombination, Genetic
  • Molecular Sequence Data
  • Meiosis
  • Genome, Fungal
  • Genes, Mating Type, Fungal
  • Esterases
  • Endodeoxyribonucleases
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Reedy, J. L., Floyd, A. M., & Heitman, J. (2009). Mechanistic plasticity of sexual reproduction and meiosis in the Candida pathogenic species complex. Curr Biol, 19(11), 891–899. https://doi.org/10.1016/j.cub.2009.04.058
Reedy, Jennifer L., Anna M. Floyd, and Joseph Heitman. “Mechanistic plasticity of sexual reproduction and meiosis in the Candida pathogenic species complex.Curr Biol 19, no. 11 (June 9, 2009): 891–99. https://doi.org/10.1016/j.cub.2009.04.058.
Reedy JL, Floyd AM, Heitman J. Mechanistic plasticity of sexual reproduction and meiosis in the Candida pathogenic species complex. Curr Biol. 2009 Jun 9;19(11):891–9.
Reedy, Jennifer L., et al. “Mechanistic plasticity of sexual reproduction and meiosis in the Candida pathogenic species complex.Curr Biol, vol. 19, no. 11, June 2009, pp. 891–99. Pubmed, doi:10.1016/j.cub.2009.04.058.
Reedy JL, Floyd AM, Heitman J. Mechanistic plasticity of sexual reproduction and meiosis in the Candida pathogenic species complex. Curr Biol. 2009 Jun 9;19(11):891–899.
Journal cover image

Published In

Curr Biol

DOI

EISSN

1879-0445

Publication Date

June 9, 2009

Volume

19

Issue

11

Start / End Page

891 / 899

Location

England

Related Subject Headings

  • Transcription Factors
  • Spores, Fungal
  • Reproduction
  • Recombination, Genetic
  • Molecular Sequence Data
  • Meiosis
  • Genome, Fungal
  • Genes, Mating Type, Fungal
  • Esterases
  • Endodeoxyribonucleases