Aims: Limited aeration has been demonstrated to cause slowdown in proliferation and delayed budding, resulting eventually in a unique unbudded G2-arrest in the obligate aerobic pathogenic yeast Cryptococcus neoformans. Also, the ability to adapt to decreased oxygen levels during pathogenesis has been identified as a virulence factor in C. neoformans. The aim of this study was to identify and characterize genes that are necessary for the proliferation slowdown and G2-arrest caused by limited aeration.

Methods: Random mutants were prepared and screened for lack of typical slowdown of proliferation under limited aeration. The CNAG_00156.2 gene coding for a zinc-finger transcription factor was identified in mutants showing most distinctive phenotype. Targeted deletion strain and reconstituted strain were prepared to characterize and confirm the gene functions. This gene was also identified in a parallel studies as homologous both to calcineurin responsive (Crz1) and PKC1-dependent (SP1-like) transcription factors.

Results: We have confirmed the role of the cryptococcal homologue of CRZ1/SP1-like transcription factor in cell integrity, and newly demonstrated its role in slowdown of proliferation and survival under reduced aeration, in biofilm formation and in susceptibility to fluconazole.

Conclusions: Our data demonstrate a tight molecular link between slowdown of proliferation during hypoxic adaptation and maintenance of cell integrity in C. neoformans and present a new role for the CRZ1 family of transcription factors in fungi. The exact positioning of this protein in cryptococcal signalling cascades remains to be clarified.

Download full-text PDF

Source
http://dx.doi.org/10.5507/bp.2013.024DOI Listing

Publication Analysis

Top Keywords

slowdown proliferation
16
limited aeration
12
cell integrity
12
biofilm formation
8
pathogenic yeast
8
yeast cryptococcus
8
cryptococcus neoformans
8
transcription factor
8
slowdown
5
proliferation
5

Similar Publications

Proliferating animal cells maintain a stable size distribution over generations despite fluctuations in cell growth and division size. Previously, we showed that cell size control involves both cell size checkpoints, which delay cell cycle progression in small cells, and size-dependent regulation of mass accumulation rates (Ginzberg et al., 2018).

View Article and Find Full Text PDF

Metabolic checkpoints in rheumatoid arthritis.

Semin Arthritis Rheum

November 2024

Department of Medicine, Mayo Clinic Alix School of Medicine, Rochester, MN, 55905, USA; Department of Immunology, Mayo Clinic College of Medicine and Science, Rochester, MN, 55905, USA; Department of Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.

Background: Rheumatoid Arthritis is a systemic autoimmune disease affecting 0.5-1 % of the population. Despite a growing therapeutic armamentarium, RA remains incurable, and many patients suffer significant morbidity over time.

View Article and Find Full Text PDF
Article Synopsis
  • Olduvai protein domains, linked to the NBPF gene family, show significant expansion in humans and correlate with brain size and neuron numbers in primates, as well as human brain variations like microcephaly and macrocephaly.
  • Research indicates that overexpression of the Olduvai gene may lead to downregulation of mitochondrial functions, particularly affecting the electron transport chain and NADH dehydrogenase activity, based on transcriptome and proteome analyses.
  • The findings suggest that this downregulation could slow development processes in primates, especially humans, potentially resulting in an extended neurogenic period that allows for the production of more neurons and a larger brain size.
View Article and Find Full Text PDF

Tumors originating from thyroid follicular cells are the most common endocrine tumors, with rising incidence. Despite a generally good prognosis, up to 20% of patients experience recurrence and persistence, highlighting the need to identify the underlying molecular mechanisms. has been found to be altered in papillary thyroid cancer (PTC).

View Article and Find Full Text PDF

In proliferating bacteria, growth rate is often assumed to be similar between daughter cells. However, most of our knowledge of cell growth derives from studies on symmetrically dividing bacteria. In many α-proteobacteria, asymmetric division is a normal part of the life cycle, with each division producing daughter cells with different sizes and fates.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!