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Links from GEO DataSets

Items: 10

1.

Magnaporthe oryzae Auxiliary Activity Protein MoAa91 Functions as Chitin-Binding Protein To Induce Appressorium Formation on Artificial Inductive Surfaces and Suppress Plant Immunity

(Submitter supplied) Here, we performed comparative transcriptomic studies of ΔMorgs mutant and wild-type strains and found that M. oryzae Aa91 (MoAa91), a homolog of the auxiliary activity family 9 protein (Aa9), was required for surface recognition of M. oryzae. We found that MoAA91 was regulated by the MoMsn2 transcription factor and that its disruption resulted in defects in both appressorium formation on the artificial inductive surface and full virulence of the pathogen. more...
Organism:
Pyricularia oryzae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26294
60 Samples
Download data: GTF, TXT
Series
Accession:
GSE128219
ID:
200128219
2.

RNA-Seq Analysis of VRF1-dependent Genes in the appressoria of Magnaporthe oryzae 70-15

(Submitter supplied) Purpose: The goals of this study are to find out the genes regulated directly or indirectly by C2H2 transcription factors Vrf1 by RNA-seq in the rice blast fungus Magnaporthe oryzae Methods: Appressorial mRNAs of the wild type strain 70-15 and Δvrf1 conidia incubated in H2O on plastic membranes at 28˚C for 5 h, in triplicate independently for each strain, were extracted and isolated by RNeasy Plant mini kit (QIAGEN) and AMPure XP beads (Beckman). more...
Organism:
Pyricularia oryzae 70-15
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21479
6 Samples
Download data: TXT
Series
Accession:
GSE78058
ID:
200078058
3.

RNA-seq Analysis of VRF1 and VRF2-dependent Genes in the mycelia of Magnaporthe oryzae 70-15

(Submitter supplied) Purpose: The goals of this study are to find out the genes regulated directly or indirectly by C2H2 transcription factors Vrf1 and Vrf2 by RNA-seq and to evaluate the similarities and differences in gene regulation mechanisms of Vrf1 and Vrf2 in the rice blast fungus Methods: Mycelial mRNAs of the wild type strain 70-15, Δvrf1 and Δvrf2 incubated in H2O at 25˚C for 4 h, in triplicate independently for each strain, were extracted and isolated by RNeasy Plant mini kit (QIAGEN) and AMPure XP beads (Beckman). more...
Organism:
Pyricularia oryzae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18618
9 Samples
Download data: TXT
Series
Accession:
GSE61020
ID:
200061020
4.

Comparison of transcript abundance in mycelium from the rice blast fungus Magnaporthe oryzae grown in rich medium and in minimal medium using RNA-Seq

(Submitter supplied) Mycelium from the rice blast fungus Magnaporthe oryzae was grown in both rich medium and under nutrient limiting conditions. Genes were identified that were more highly expressed in one condition as compared to the other.
Organism:
Pyricularia oryzae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13743
2 Samples
Download data: TXT
Series
Accession:
GSE30327
ID:
200030327
5.

Comparison of transcript abundance in mycelium from the rice blast fungus Magnaporthe oryzae grown in rich medium and in minimal medium using HT-SuperSAGE.

(Submitter supplied) Mycelium from the rice blast fungus Magnaporthe oryzae was grown in both rich medium and under nutrient limiting conditions. Genes were identified that were more highly expressed in one condition as compared to the other.
Organism:
Pyricularia oryzae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13743
6 Samples
Download data: TXT
Series
Accession:
GSE30256
ID:
200030256
6.

Analysis of transcript abundance during appressorium formation in the rice blast fungus Magnaporthe oryzae using HT-SuperSAGE.

(Submitter supplied) The rice-blast fungus Magnaporthe oryzae is disseminated using a three-celled spore or conidium. Upon landing on the surface of a rice leaf, the conidium germinates and forms a specialised structure for entry into the host plant - the appressorium. In this study we have followed gene expression thoughout germination of the conidium and formation of the appressorium to identify genes that may be important for appressorium function. more...
Organism:
Pyricularia oryzae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL13743
12 Samples
Download data: TXT
Series
Accession:
GSE30069
ID:
200030069
7.

RNA-seq Analysis of MoRFX1-dependent Genes in Magnaporthe oryzae 70-15

(Submitter supplied) Purpose: The goals of this study are to find out the genes regulated directly or indirectly by the regulatory factor X protein MoRfx1 by RNA-seq in the rice blast fungus Methods: Mycelial mRNAs of the wild type strain 70-15, ΔMorfx1 incubated in H2O at 25˚C for 4 h, in triplicate independently for each strain, were extracted and isolated by RNeasy Plant mini kit (QIAGEN) and AMPure XP beads (Beckman). more...
Organism:
Pyricularia oryzae
Type:
Expression profiling by high throughput sequencing
Platform:
GPL18618
6 Samples
Download data: TXT
Series
Accession:
GSE65296
ID:
200065296
8.

Peroxisome dynamics determines host-derived ROS accumulation and infectious growth of the rice blast fungus

(Submitter supplied) To investigate the underlying mechanisms that which genes involving in M. oryzae peroxisome dynamics in response to oxidative stress.
Organism:
Pyricularia oryzae; Oryza sativa
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL32309 GPL33328
6 Samples
Download data: XLS
Series
Accession:
GSE229299
ID:
200229299
9.

chip-seq for MoIug4 in rice

(Submitter supplied) chip-seq for MoIug4 in rice, putative transcription factor MoIug4 was secrected from M. oryzae to the nucleus of rice. Here, we performed of MoAtf1 chip-seq assays to uncovered the regulation network
Organism:
Oryza sativa
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL9147
1 Sample
Download data: BW
Series
Accession:
GSE188802
ID:
200188802
10.

The function of CEBiP in the chitin elicitor signaling in rice cells

(Submitter supplied) To see the function of CEBiP in the chitin elicitor signaling in rice cells, a plasmid for the gene-specific knock-down by RNA interference (RNAi) was constructed by using a sequence for the 3’-terminal region of CEBiP and transformed into the rice cells by using Rhizobium radiobacter (Agrobacterium tumefaciens). chitinoligomer was added (or not added) to the medium. For the control of them, rice cells that non transformed wild type was used. more...
Organism:
Oryza sativa
Type:
Expression profiling by array
Platform:
GPL3642
4 Samples
Download data: TXT
Series
Accession:
GSE4645
ID:
200004645
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