Phenotypic characterization of low-Cu-responsive transcription factor Mac1 in A. nidulans. Phenotypic characterization of low-Cu-responsive transcription.

Slides:



Advertisements
Similar presentations
W 3.7 kb 4.9 kb M A B W 448 bp M C W bp D M 2185 bp
Advertisements

Phenotypic analysis of spo73∆ mutant.
High efficiency of gene deletion in all tested genetic backgrounds of A. fumigatus. High efficiency of gene deletion in all tested genetic backgrounds.
Cytoplasmic poly-GR/PR inclusions resemble stress granules in vitro.
cuf2Δ and fzr1Δ cells show a defect in meiotic termination.
Decoupling of Nuclear Division Cycles and Cell Size during the Coenocytic Growth of the Ichthyosporean Sphaeroforma arctica  Andrej Ondracka, Omaya Dudin,
ΔsimA yeast cells appear degraded in vivo.
H-NS2 is upregulated in an hns mutant derivative of the strain E
Dibutyryl cAMP does not rescue staurosporine-induced filamentation of a cyr1Δ/cyr1Δ mutant. Dibutyryl cAMP does not rescue staurosporine-induced filamentation.
Colony and microcolony imaging of cargo transport.
Candidates with a PVM localization.
Mutants impaired in N-acetylglucosamine transport and catabolism display morphological and pH neutralization defects within macrophages. Mutants impaired.
Volume 25, Issue 2, Pages (April 2013)
Analysis of GPCR deletion strains.
Synthetic perturbation of DE and DV genes.
Staurosporine-induced filamentation requires Cyr1 and PKA
The ΔsimA strain shows less cellular proliferation during macrophage infection and ruptured yeast cells. The ΔsimA strain shows less cellular proliferation.
The pho4Δ mutant is less virulent than the WT strain in intranasal (A to C) and intravenous (D to F) models of cryptococcosis. The pho4Δ mutant is less.
IVA can localize to and encase the forespore in the absence of VM
Ras1 is a specific target of Ram1.
Characterization of cell stages and morphologies under the culture conditions used in this study. Characterization of cell stages and morphologies under.
Distribution of HHQ, PQS, and NHQ and total counts (TC) in a 200- by 200-μm area of a P. aeruginosa biofilm grown on an ITO-coated glass substrate (A).
Subcellular localization of UUKV, HRTV, and SFTSV NSs
Morphological studies in the hippocampus of sut mice (A) Low-power images of the hippocampus from WT and sut mice. Morphological studies in the hippocampus.
Side-view and apical-view projections of mutant and validation strain biofilms. Side-view and apical-view projections of mutant and validation strain biofilms.
Prenylation and postprocessing enzymes Ram1, Rce1, Ste24, and Ste14 play a role in mating filament formation during C. neoformans sexual development. Prenylation.
Penelope R Chua, G.Shirleen Roeder  Cell 
Localization of PBANKA_ and PBANKA_ during blood and liver stage development. Localization of PBANKA_ and PBANKA_ during blood.
DIA1(R1204X) induces elongated and thick microvilli in HeLa cells
ILK knockdown decreases mTOR signaling in PKD kidneys.
PhoB also translocates to plant nuclei in leaf and crown cells in response to HK activation with exogenous cytokinin. PhoB also translocates to plant nuclei.
Endogenous SMN1 is not recruited to stress granules in HeLa cells after diverse stresses. Endogenous SMN1 is not recruited to stress granules in HeLa cells.
Tapetal mitochondria in wild-type (WT), drp3b, and elm1 mutants.
Ectopic overexpression of WOR3 drives switching to the opaque cell type. Ectopic overexpression of WOR3 drives switching to the opaque cell type. (A) Visualization.
Recruitment of PH-Akt-GFP to the leading edge of the cell during chemotaxis. Recruitment of PH-Akt-GFP to the leading edge of the cell during chemotaxis.
Cell density and secreted enzymes contribute to aggregate invasive growth. Cell density and secreted enzymes contribute to aggregate invasive growth. (A)
Fcp1 CTD phosphatase affects a broad range of transcripts in the +N and -N media. Fcp1 CTD phosphatase affects a broad range of transcripts in the +N and.
Effect of the plastid translation inhibitor Spec on LR development
Fgfr3;4 mutant lungs display an increase in Mfap5, Igf1 and Fbn2 expression. Fgfr3;4 mutant lungs display an increase in Mfap5,Igf1and Fbn2 expression.
Stability of SsbA (A) and GFP (B) proteins in UA159 and ΔclpX strains.
V-ATPase and proteins involved in late endosomal protein sorting are required for efficient utilization of LDs during growth resumption. V-ATPase and proteins.
Prophase nuclear movements in wild-type, rec8 and rec7 mutant cells.
Lysine residues in the cytoplasmic region of TfR are involved in the MARCH8-induced downregulation of TfR. Lysine residues in the cytoplasmic region of.
KIF13A overexpression favors NP distribution to the cell edge and requires KIF13A binding to microtubules. KIF13A overexpressionfavorsNP distribution to.
Loss of Graf results in plasmatocyte overproliferation.
Expression of simA. Expression of simA. (A) Reverse transcriptase PCR (RT-PCR) of simA and a benA loading control performed on RNA isolated from wild-type.
The BRCA1 aggregates exclude large nuclear structures.
Expression of all the GAP genes is under control of the Csy1 sensor and regulated by nitrogen sources. Expression of all the GAP genes is under control.
Nuclear localization of Sfl1.
Susceptibility to hydrogen peroxide.
SAM transport by Gap4 in S. cerevisiae cells.
Pho4 is regulated by the cyclin-dependent kinase Pho85 and responds to phosphate deprivation by translocating to nuclei. Pho4 is regulated by the cyclin-dependent.
Subnuclear localization of HA-tagged EBNA1 protein.
Using CRISPRi to knock down acm2 expression in L. plantarum WCFS1.
miR-9 regulation of Pax6 expression.
Molecular characterization of the key motifs of AnMac1.
Low pH alters Ras1 localization and its activation state, but these changes are not responsible for the effect of pH on morphology. Low pH alters Ras1.
Diaphanous regulates the presynaptic actin cytoskeleton.
Construction and analysis of C. auris hog1Δ cells.
Septin ring formation and chitin-containing septum formation are aberrant in filaments formed in response to staurosporine. Septin ring formation and chitin-containing.
Epigenetic and posttranslational regulation of nitrogen-induced autophagy in M. oryzae. Epigenetic and posttranslational regulation of nitrogen-induced.
Expression of Chx10-cre and phenotypes of Chx10-cre induced Smo ablation. Expression of Chx10-cre and phenotypes of Chx10-cre induced Smo ablation. A–G,
Construction and characterization of YF/NIEV chimera.
dCas9-mediated repression of transcription.
OMVs displaying WT SusG can rescue a strain with a ΔsusG growth phenotype on starch as the carbon source. OMVs displaying WT SusG can rescue a strain with.
Expression of ylxR-containing operon revealed by lacZ and gfp fusion analysis. Expression of ylxR-containing operon revealed by lacZ and gfp fusion analysis.
Low pH represses growth of cells with the hyphal morphology and promotes growth as pseudohyphae. Low pH represses growth of cells with the hyphal morphology.
Expression and functional characterization of Cu transporters CtrA2 and CtrC in A. nidulans. Expression and functional characterization of Cu transporters.
Sfr1 localizes broadly throughout the basal body microtubule scaffold
Impact of the SOS activities on E. coli mutation rates.
Presentation transcript:

Phenotypic characterization of low-Cu-responsive transcription factor Mac1 in A. nidulans. Phenotypic characterization of low-Cu-responsive transcription factor Mac1 in A. nidulans. (A) Equal numbers of conidia (2 × 104) from the parental wild-type (WT) strain, ΔAnmac1 mutant (ΔAnmac1) strain, and Anmac1-complemented (Anmac1c) strain were spot-inoculated onto MMPDR media supplemented with various concentrations of Cu, as indicated, and cultured at 37°C for 40 h for photography. (B) AnMac1 tagged with GFP (AnMac1-GFP) was ectopically expressed in the ΔAnMac1 mutant. DIC microscopy and DAPI staining were used to visualize the hyphal morphologies and the nuclei, respectively. AnMac1-GFP localized to the nuclear region in A. nidulans. Scale bar = 10 μm. (C) Colony morphologies of the A. nidulans mutant strains (panel 1) grown on MMPDR media (1 μM Cu) at 37°C for 48 h. Closeup views of the center (panel 2) and edge (panel 3) of individual colonies were taken with a stereo microscope (bars represent 100 μm and 20 μm, respectively). Analyses of the conidiophore morphologies of the relevant mutant strains (panel 4) grown on MMPDR media (1 μM Cu) at 37°C for 40 h were performed. Scale bar = 10 μm. Zhendong Cai et al. mSphere 2019; doi:10.1128/mSphere.00670-18