WormMine

WS294

Intermine data mining platform for C. elegans and related nematodes

Gene :

WormBase Gene ID  ? WBGene00009180 Gene Name  nurf-1
Sequence Name  ? F26H11.2 Brief Description  nurf-1 encodes the C. elegans ortholog of Drosophila NURF301, a component of the NURF chromatin remodeling complex; in C. elegans, nurf-1 acts with isw-1 to regulate vulval development.
Organism  Caenorhabditis elegans Automated Description  Predicted to enable RNA polymerase II cis-regulatory region sequence-specific DNA binding activity and methylated histone binding activity. Involved in positive regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. Predicted to be part of NURF complex. Expressed in several structures, including head; pharyngeal-intestinal valve; pharynx; tail; and vulva. Human ortholog(s) of this gene implicated in Alzheimer's disease; amyotrophic lateral sclerosis; and neurodevelopmental disorder with dysmorphic facies and distal limb anomalies. Is an ortholog of human BPTF (bromodomain PHD finger transcription factor).
Biotype  SO:0001217 Genetic Position  II :22.9649 ±0.001067
Length (nt)  ? 17199
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1 Organism

Name Taxon Id
Caenorhabditis elegans 6239

1 Synonyms

Value
WBGene00009180

Genomics

23 Transcripts

WormMine ID Sequence Name Length (nt) Chromosome Location
Transcript:F26H11.2b.1 F26H11.2b.1 5116   II: 14390713-14401121
Transcript:F26H11.2d.2 F26H11.2d.2 6688   II: 14390713-14407848
Transcript:F26H11.2i.1 F26H11.2i.1 5116   II: 14390713-14401127
Transcript:F26H11.2k.1 F26H11.2k.1 5116   II: 14390714-14401122
Transcript:F26H11.2s.1 F26H11.2s.1 6696   II: 14390714-14407848
Transcript:F26H11.2a.1 F26H11.2a.1 6751   II: 14390714-14407909
Transcript:F26H11.2q.2 F26H11.2q.2 5120   II: 14390716-14401122
Transcript:F26H11.2q.3 F26H11.2q.3 5562   II: 14390718-14401109
Transcript:F26H11.2c.1 F26H11.2c.1 6740   II: 14390718-14407911
Transcript:F26H11.2n.1 F26H11.2n.1 6591   II: 14390720-14407758
Transcript:F26H11.2l.1 F26H11.2l.1 6228   II: 14391754-14407758
Transcript:F26H11.2m.1 F26H11.2m.1 6222   II: 14391754-14407758
Transcript:F26H11.2q.4 F26H11.2q.4 4084   II: 14392581-14401122
Transcript:F26H11.2r.1 F26H11.2r.1 3501   II: 14394772-14401122
Transcript:F26H11.2r.2 F26H11.2r.2 1480   II: 14398991-14401122
Transcript:F26H11.2r.3 F26H11.2r.3 981   II: 14400052-14401127
Transcript:F26H11.2q.1 F26H11.2q.1 975   II: 14400058-14401121
Transcript:F26H11.2d.1 F26H11.2d.1 2540   II: 14400058-14407847
Transcript:F26H11.2o.1 F26H11.2o.1 1707   II: 14401682-14407758
Transcript:F26H11.2p.1 F26H11.2p.1 1359   II: 14403527-14407758
Transcript:F26H11.2e.1 F26H11.2e.1 1218   II: 14404654-14407758
Transcript:F26H11.2f.1 F26H11.2f.1 1745   II: 14405432-14407857
Transcript:F26H11.2j.1 F26H11.2j.1 435   II: 14407276-14407758
 

Other

17 CDSs

WormMine ID Sequence Name Length (nt) Chromosome Location
CDS:F26H11.2a F26H11.2a 6594   II: 14390720-14391012
CDS:F26H11.2b F26H11.2b 4866   II: 14390720-14391012
CDS:F26H11.2i F26H11.2i 4860   II: 14390720-14391012
CDS:F26H11.2s F26H11.2s 6600   II: 14390720-14391012
CDS:F26H11.2n F26H11.2n 6591   II: 14390720-14391012
CDS:F26H11.2l F26H11.2l 6228   II: 14391754-14392340
CDS:F26H11.2m F26H11.2m 6222   II: 14391754-14392340
CDS:F26H11.2r F26H11.2r 702   II: 14400082-14400531
CDS:F26H11.2e F26H11.2e 1218   II: 14404654-14404684
CDS:F26H11.2f F26H11.2f 1533   II: 14405545-14405890
CDS:F26H11.2c F26H11.2c 6585   II: 14390720-14391012
CDS:F26H11.2d F26H11.2d 2427   II: 14400082-14400531
CDS:F26H11.2j F26H11.2j 435   II: 14407276-14407351
CDS:F26H11.2k F26H11.2k 4866   II: 14390720-14391012
CDS:F26H11.2o F26H11.2o 1707   II: 14401682-14401783
CDS:F26H11.2p F26H11.2p 1359   II: 14403527-14403698
CDS:F26H11.2q F26H11.2q 708   II: 14400082-14400531

36 RNAi Result

WormBase ID
WBRNAi00045698
WBRNAi00045699
WBRNAi00045700
WBRNAi00045701
WBRNAi00086214
WBRNAi00013983
WBRNAi00025262
WBRNAi00025263
WBRNAi00086209
WBRNAi00086213
WBRNAi00086228
WBRNAi00086227
WBRNAi00086230
WBRNAi00086234
WBRNAi00086233
WBRNAi00086235
WBRNAi00086252
WBRNAi00086254
WBRNAi00086253
WBRNAi00086256
WBRNAi00086255
WBRNAi00086212
WBRNAi00086215
WBRNAi00086226
WBRNAi00086229
WBRNAi00086232
WBRNAi00086231
WBRNAi00031472
WBRNAi00082609
WBRNAi00086246

462 Allele

Public Name
gk963801
gk963053
WBVar01320047
WBVar01320051
WBVar01320052
WBVar01320055
WBVar01320056
WBVar01320057
WBVar01320058
WBVar01320067
WBVar01320068
WBVar01320069
WBVar01320073
WBVar01320076
WBVar01320078
WBVar01320080
WBVar01320091
WBVar01320092
WBVar01320096
gk962684
gk487481
WBVar02040996
gk847682
WBVar00556821
cxTi8305
WBVar02068480
WBVar02068484
WBVar02068483
WBVar02068482
WBVar02068481

1 Chromosome

WormBase ID Organism Length (nt)
II Caenorhabditis elegans 15279421  

1 Chromosome Location


Feature . Primary Identifier
Start End Strand
WBGene00009180 14390713 14407911 1

4 Data Sets

Name URL
WormBaseAcedbConverter  
GO Annotation data set  
C. elegans genomic annotations (GFF3 Gene)  
Panther orthologue and paralogue predictions  

1 Downstream Intergenic Region

WormBase ID Name Sequence Name Length (nt) Chromosome Location Organism
intergenic_region_chrII_14407912..14408611   700 II: 14407912-14408611 Caenorhabditis elegans

199 Expression Clusters

Regulated By Treatment Description Algorithm Primary Identifier
  Coexpression clique No. 256, pek-1_22220-pek-1_33, on the genome-wide coexpression clique map for the nematode GPL200 platform. All available microarray datasets for the GPL200 platform (Affymetrix C. elegans Genome Array) were obtained from the GEO repository. This included 2243 individual microarray experiments. These were normalized against each other with the software RMAexpress (Bolstad, 2014). Based on these normalized values, Pearsons correlation coefficients were obtained for each probe-probe pair of the 22,620 probes represented on this array type. The resulting list of correlation coefficients was then ranked to generate the ranked coexpression database with information on each probe represented on the GPL200 platform. WBPaper00061527:pek-1_22220-pek-1_33
  Transcripts that showed significantly increased expression in L1 neural cells comparing to in adult neural cells. DESeq2 (v1.18.1) fold change > 2, P-adj<0.05, using BenjaminiHochberg correction. WBPaper00060811:L1_vs_adult_upregulated_neural
  Transcripts expressed in neuronal cells, by analyzingfluorescence-activated cell sorted (FACS) neurons. DESeq. False discovry rate (FDR) < 0.1. WBPaper00048988:neuron_expressed
adult vs dauer larva Transcripts that showed differential expression in adult vs dauer lava in N2 animals at 20C. N.A. WBPaper00050488:adult_vs_dauer_regulated_N2_20C
  mRNAs that showed decreased expression in 1 cell mebryo comparing to in oocyte, according to RNAseq analysis. Gaussian error propagation. As cutoff for the up-regulated genes authors used log2 fold change > 1 and P < 0.05 and as cutoff for the down-regulated genes authors used log2 fold change < -1 and P < 0.05. WBPaper00045420:fertilization_downregulated_transcript
  Genes that were downregulated in lin-15B(n744). For each gene in each microarray hybridization experiment, the ratio of RNA levels from the two samples was transformed into a log2 value and the mean log2 ratio was calculated. The log2 ratios were normalized by print-tip Loess normalization (Dudoit and Yang, 2002). All genes with a false discovery rate of <= 5% (q <= 0.05) (Storey and Tibshirani, 2003) and a mean fold-change ratio of >= 1.5 were selected for further analysis. WBPaper00038168:lin-15B(n744)_downregulated
  Transcripts that showed significantly increased expression after animals were treated with 50uM Rifampicin and 250uM Allantoin from day 1 to day 3 adult hermaphradite. DESeq2(v1.14.1), fold change > 2, p-value < 0.05 WBPaper00055354:Rifampicin-Allantoin_upregulated
  Transcripts that showed significantly increased expression after animals were treated with 50uM Rifampicin from day 1 to day 3 adult hermaphradite. DESeq2(v1.14.1), fold change > 2, p-value < 0.05 WBPaper00055354:Rifampicin_upregulated
  Transcripts that showed significantly increased expression after animals were treated with 100uM Psora and 250uM Allantoin from day 1 to day 3 adult hermaphradite. DESeq2(v1.14.1), fold change > 2, p-value < 0.05 WBPaper00055354:Psora-Allantoin_upregulated
  Transcripts that showed significantly increased expression after animals were treated with 100uM Rapamycin and 50mM Metformin from day 1 to day 3 adult hermaphradite. DESeq2(v1.14.1), fold change > 2, p-value < 0.05 WBPaper00055354:Rapamycin-Metformin_upregulated
Heat shock: 35C for 1 hour. Transcripts that showed significantly increased expression immediately after 1-day post L4 adult hermaphrodite endu-2(tm4977) animals were exposed to 35C for 1 hour. The DESeq2 (GalaxyVersion 2.11.40.6 + galaxy1) was used to determine differentiallyexpressed features from count tables of differential transcript abundances. log2FC > 1, FDR < 0.01. WBPaper00065749:Heat-Shock_upregulated_endu-2(tm4977)
Heat shock: 35C for 1 hour. Transcripts that showed significantly increased expression immediately after 1-day post L4 adult hermaphrodite N2 animals were exposed to 35C for 1 hour. The DESeq2 (GalaxyVersion 2.11.40.6 + galaxy1) was used to determine differentiallyexpressed features from count tables of differential transcript abundances. log2FC > 1, FDR < 0.01. WBPaper00065749:Heat-Shock_upregulated_N2
  Transcripts expressed in the epithelial tissues surrounding the pharynx that includes the arcade and intestinal valve (AIV) cells, according to PAT-Seq analysis using Pbath-15-GFP-3XFLAG mRNA tagging. Cufflinks FPKM value >=1. WBPaper00050990:arcade_intestinal-valve_expressed
  Genes significantly enriched in NSM neurons (isolated by FACS) versus the reference, according to RNAseq analysis towards total RNA. Gene expression quantification and differential expression was analyzed using cufflinks v2.2.1. Enriched contains only genes significantly enriched (differentially expressed >= 2.4 fold in total RNA or >= 3.2 fold in DSN treated total RNA) in the NSM neurons versus the reference. WBPaper00045974:NSM_enriched_totalRNA_RNAseq
  Transcripts expressed in body muscle, according to PAT-Seq analysis using Pmyo-3-GFP-3XFLAG mRNA tagging. Cufflinks FPKM value >=1. WBPaper00050990:body-muscle_expressed
  Transcripts expressed in GABAergic neuron, according to PAT-Seq analysis using Punc-47-GFP-3XFLAG mRNA tagging. Cufflinks FPKM value >=1. WBPaper00050990:GABAergic-neuron_expressed
  Transcripts expressed in hypodermis, according to PAT-Seq analysis using Pdpy-7-GFP-3XFLAG mRNA tagging. Cufflinks FPKM value >=1. WBPaper00050990:hypodermis_expressed
  Transcripts expressed in intestine, according to PAT-Seq analysis using Pges-1-GFP-3XFLAG mRNA tagging. Cufflinks FPKM value >=1. WBPaper00050990:intestine_expressed
  Maternal class (M): genes that are called present in at least one of the three PC6 replicates. A modified Welch F statistic was used for ANOVA. For each gene, regressed error estimates were substituted for observed error estimates. The substitution is justified by the lack of consistency among the most and least variable genes at each time point. Regressed error estimates were abundance-dependent pooled error estimates that represented a median error estimate from a window of genes of similar abundance to the gene of interest. A randomization test was used to compute the probability Pg of the observed F statistic for gene g under the null hypothesis that developmental time had no effect on expression. P-values were not corrected for multiple testing. [cgc5767]:expression_class_M
  Transcripts expressed in NMDA neuron, according to PAT-Seq analysis using Pnmr-1-GFP-3XFLAG mRNA tagging. Cufflinks FPKM value >=1. WBPaper00050990:NMDA-neuron_expressed
  Transcripts expressed in pharynx, according to PAT-Seq analysis using Pmyo-2-GFP-3XFLAG mRNA tagging. Cufflinks FPKM value >=1. WBPaper00050990:pharynx_expressed
  Genes with expression level regulated by genotype (N2 vs CB4856) and age at old adults stage (214 hours at 24 centigrade). For model 2, authors used 100 permutations to estimate the FDR threshold. Per permutation, genotypes and ages were independently randomly distributed, keeping the among-gene structure intact. Then for each spot (23,232) on the array, model 2 was tested. The obtained P-values were used to estimate a threshold for each of the explanatory factors. Authors also used a genome-wide threshold of -log10 P-value = 2, which resembles an FDR of 0.072 and 0.060 for marker and the interaction age-marker for the developing worms and FDR of 0.050 and 0.065 for marker and age-marker for the aging worms. For the physiological age effect, authors used a log10 P-value = 8 in developing worms (0.012 FDR) and -log10 P-value = 6 (0.032 FDR). WBPaper00040858:eQTL_age_regulated_aging
  Genes with expression level regulated by genotype (N2 vs CB4856) and age at L3 larva and Late reproduction stage (96 hours at 24 centigrade). For model 2, authors used 100 permutations to estimate the FDR threshold. Per permutation, genotypes and ages were independently randomly distributed, keeping the among-gene structure intact. Then for each spot (23,232) on the array, model 2 was tested. The obtained P-values were used to estimate a threshold for each of the explanatory factors. Authors also used a genome-wide threshold of -log10 P-value = 2, which resembles an FDR of 0.072 and 0.060 for marker and the interaction age-marker for the developing worms and FDR of 0.050 and 0.065 for marker and age-marker for the aging worms. For the physiological age effect, authors used a log10 P-value = 8 in developing worms (0.012 FDR) and -log10 P-value = 6 (0.032 FDR). WBPaper00040858:eQTL_age_regulated_developing
  Transcripts expressed in seam cells, according to PAT-Seq analysis using Pgrd-10-GFP-3XFLAG mRNA tagging. Cufflinks FPKM value >=1. WBPaper00050990:seam_expressed
  Genes with expression level regulated by genotype (N2 vs CB4856) at L3 larva and Late reproduction stage (96 hours at 24 centigrade). For model 2, authors used 100 permutations to estimate the FDR threshold. Per permutation, genotypes and ages were independently randomly distributed, keeping the among-gene structure intact. Then for each spot (23,232) on the array, model 2 was tested. The obtained P-values were used to estimate a threshold for each of the explanatory factors. Authors also used a genome-wide threshold of -log10 P-value = 2, which resembles an FDR of 0.072 and 0.060 for marker and the interaction age-marker for the developing worms and FDR of 0.050 and 0.065 for marker and age-marker for the aging worms. For the physiological age effect, authors used a log10 P-value = 8 in developing worms (0.012 FDR) and -log10 P-value = 6 (0.032 FDR). WBPaper00040858:eQTL_regulated_developing
  Transcripts expressed in vulva. FPKM >= 1. WBPaper00064122:vulva_transcriptome
Bacteria diet: Sphingomonas aquatilis Yellow. Fed for 30 generations. Transcripts that showed significantly decreased expression after fed by bacteria Sphingomonas aquatilis (Yellow) for 30 generations comparing to animals fed by E. coli OP50. DESeq2 fold change > 2, p-value < 0.01. WBPaper00061007:S.aquatilis_downregulated
  Transcripts that showed significantly increased expression in aak-1(tm1944);aak-2(ok524) animals comparing to in N2. DEseq 1.18.0, adjusted p-value < 0.05. WBPaper00056471:aak-1(tm1944);aak-2(ok524)_upregulated
Bacteria infection: Staphylococcus aureus MW2. 4 hours of exposure. Transcripts that showed significantly increased expression after N2 animals had 4 hours of infection by Staphylococcus aureus (MW2). DEseq 1.18.0, adjusted p-value < 0.05. WBPaper00056471:S.aureus-4h_upregulated_N2
  Transcripts that showed significantly changed expression in 6-day post-L4 adult hermaphrodite comparing to in 1-day post L4 adult hermaphrodite animals. Sleuth WBPaper00051558:aging_regulated

11 Expression Patterns

Remark Reporter Gene Primary Identifier Pattern Subcellular Localization
    Expr9824 Very broad GFP expression was seen from early embryogenesis to the mature adult. Many cells expressed GFP in the head, including nerve cells, cells in the pharynx and the hypodermis. Many neurons in the tail also showed GFP expression. Body wall expression of GFP was observed throughout the length of the body, in the hypodermis and possibly muscle cells. GFP could also be seen in the intestine and reproductive system. The level of GFP and the number of cells with detectable levels of GFP was reduced in the adult.  
    Expr9826 Very broad GFP expression was seen from early embryogenesis to the mature adult. Many cells expressed GFP in the head, including nerve cells, cells in the pharynx and the hypodermis. Many neurons in the tail also showed GFP expression. Body wall expression of GFP was observed throughout the length of the body, in the hypodermis and possibly muscle cells. GFP could also be seen in the intestine and reproductive system. The level of GFP and the number of cells with detectable levels of GFP was reduced in the adult.  
    Expr9827 Very broad GFP expression was seen from early embryogenesis to the mature adult. Many cells expressed GFP in the head, including nerve cells, cells in the pharynx and the hypodermis. Many neurons in the tail also showed GFP expression. Body wall expression of GFP was observed throughout the length of the body, in the hypodermis and possibly muscle cells. GFP could also be seen in the intestine and reproductive system. The level of GFP and the number of cells with detectable levels of GFP was reduced in the adult.  
    Expr1034005 Tiling arrays expression graphs  
Clone: pUL#JRH/AG10   Expr7522 Expression is seen in 3 cells in the terminal bulb of the pharynx and in the junction between the pharynx and intestine, late embryo onwards, weakening through the larval stages. There is also expression in the developing gonad, possibly the spermathecae. However, all the expression is quite weak.  
    Expr9842 Non-nuclear-localized GFP was observed from early embryogenesis GFP was seen in the body wall in the head and tail. Particularly high levels of GFP were seen in the rectal cells, in some unidentified cells in the head and in the adult vulva. Two other independently generated strains, transgenic for the same reporter gene fusion construction, gave similar GFP expression patterns but the transmission of the transgenic array was very low and these strains were not retained.  
    Expr9828 No GFP expression was seen in two independent transgenic strains.  
    Expr2014533 Single cell embryonic expression. Only cell types with an expression fraction of greater 0.2 of the maximum expressed fraction are labeled (Full data can be downloaded from http://caltech.wormbase.org/pub/wormbase/datasets-published/packer2019/). The colors represent the broad cell class to which the cell type has been assigned. The size of the point is proportional to the log2 of the numbers of cells in the dataset of that cell type. Interactive visualizations are available as a web app (https://cello.shinyapps.io/celegans/) and can also be installed as an R package (https://github.com/qinzhu/VisCello.celegans).  
    Expr2032772 Single cell embryonic expression. Only cell types with an expression fraction of greater 0.2 of the maximum expressed fraction are labeled (Full data can be downloaded from http://caltech.wormbase.org/pub/wormbase/datasets-published/packer2019/). The colors represent the broad cell class to which the cell type has been assigned. The size of the point is proportional to the log2 of the numbers of cells in the dataset of that cell type. Interactive visualizations are available as a web app (https://cello.shinyapps.io/celegans/) and can also be installed as an R package (https://github.com/qinzhu/VisCello.celegans).  
    Expr1149612 Developmental gene expression time-course. Raw data can be downloaded from ftp://caltech.wormbase.org/pub/wormbase/datasets-published/hashimshony2015  
    Expr1017951 Developmental gene expression time-course. Raw data can be downloaded from ftp://caltech.wormbase.org/pub/wormbase/datasets-published/levin2012  

11 GO Annotation

Annotation Extension Qualifier
  located_in
has_input(WB:WBGene00002015),happens_during(GO:0001666) involved_in
  involved_in
  involved_in
  involved_in
  enables
  enables
  enables
  part_of
  part_of
  located_in

4 Homologues

Type
least diverged orthologue
least diverged orthologue
least diverged orthologue
least diverged orthologue

1 Locations


Feature . Primary Identifier
Start End Strand
WBGene00009180 14390713 14407911 1

11 Ontology Annotations

Annotation Extension Qualifier
  located_in
has_input(WB:WBGene00002015),happens_during(GO:0001666) involved_in
  involved_in
  involved_in
  involved_in
  enables
  enables
  enables
  part_of
  part_of
  located_in

0 Regulates Expr Cluster

1 Sequence

Length
17199

1 Sequence Ontology Term