Experiment / E6RPALXJMTargeted Genomic Integration MPRA

Inter-specific S. cerevisiae × S. uvarum CRE-seq time course

Cis-regulatory variants affect gene expression dynamics in yeast

An integrated CRE-seq library tested 130-bp promoter windows from S. cerevisiae and S. uvarum, including both parental alleles and reciprocal distal/proximal chimeras, in an Oak × S. uvarum diploid. Four random 10-bp barcodes were designed per construct, and barcode RNA/DNA activity was measured over 27 timepoints.

Processed tables are specific to each experiment. Column names, units, measurements, and table structure are not standardized across the database. Check this experiment’s column definitions and quality-control notes before comparing or combining data.

Perturbation & assay details

Diauxic-shift time course in YPD at 30°C; no exogenous treatment

CRE-seq reporter assay: pooled 200-bp synthetic oligos were cloned into pIM202, YFP was placed between the cis-regulatory element and barcode, and the reporter library was integrated at the URA3 locus in yeast. RNA barcode counts measure reporter expression and combined DNA1/DNA27 barcode counts measure library abundance; the processed activity is the per-barcode log2 RNA/DNA ratio after library-size normalization. Allele tokens 3 and 4 are reciprocal distal/proximal chimeras.

Processed data

50 rows per page. Click a cell to inspect its full value.

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Filters apply to this table only. The CSV download contains the complete processed table; filtered rows are available through the API.

Column dictionary · 55 definitions
element_id
Unique CRE construct identifier without the barcode sequence.
gene_id
Systematic S. cerevisiae gene identifier targeted by the promoter region.
region_id
Gene and promoter-window identifier in the form gene:region.
region
Promoter window index; 0 is proximal to the TSS and 4 is most distal.
allele
Library allele token: 1 S. cerevisiae, 2 S. uvarum, 3 CU chimera, or 4 UC chimera.
allele_label
Human-readable parental or chimera label; the first chimera letter is distal and the second is proximal.
construct_type
Functional class of the tested construct.
promoter_sequence
Synthetic cis-regulatory sequence used in the reporter construct.
promoter_sequence_length
Length in bases of promoter_sequence.
oligo_length
Designed synthetic oligo length in bases.
num_snp_differences
Number of SNP differences annotated for the parental region.
num_indel_differences
Number of insertion/deletion differences annotated for the parental region.
allele_length_1
Length of the S. cerevisiae allele in the type annotation.
allele_length_2
Length of the S. uvarum allele in the type annotation.
aligned_length
Alignment length reported in the CRE type annotation.
n_barcodes_total
Number of barcodes designed for the construct.
n_barcodes_qc
Number of barcode rows retained after the author and region-support QC filters.
qc_pass_rate
n_barcodes_qc divided by n_barcodes_total.
qc_barcodes
Semicolon-separated barcode sequences retained after QC.
region_qc_retained
Indicates that the region passed the final parental-replicate support filter; 1 means yes.
region_correlated_with_rnaseq
Author annotation indicating whether the promoter region correlated with endogenous RNA-seq expression (1=yes, 0=no).
region_parent_dynamics_significant
Author significance flag for parental expression dynamics (1=significant, 0=not significant).
region_parent_levels_significant
Author significance flag for parental expression levels (1=significant, 0=not significant).
region_parent_fdr_levels
Author FDR for the parental CRE expression-level comparison for this region.
region_parent_fdr_dynamics
Author FDR for the parental CRE expression-dynamics comparison for this region.
region_distal_fdr_levels
Author FDR for the distal chimera genotype expression-level test.
region_proximal_fdr_levels
Author FDR for the proximal chimera genotype expression-level test.
region_distal_fdr_dynamics
Author FDR for the distal chimera genotype expression-dynamics test.
region_proximal_fdr_dynamics
Author FDR for the proximal chimera genotype expression-dynamics test.
region_cu_vs_cc_fdr_dynamics
Author FDR for CU versus S. cerevisiae parental dynamics.
region_cu_vs_uu_fdr_dynamics
Author FDR for CU versus S. uvarum parental dynamics.
region_uc_vs_cc_fdr_dynamics
Author FDR for UC versus S. cerevisiae parental dynamics.
region_uc_vs_uu_fdr_dynamics
Author FDR for UC versus S. uvarum parental dynamics.
region_cu_vs_cc_fdr_levels
Author FDR for CU versus S. cerevisiae parental levels.
region_cu_vs_uu_fdr_levels
Author FDR for CU versus S. uvarum parental levels.
region_uc_vs_cc_fdr_levels
Author FDR for UC versus S. cerevisiae parental levels.
region_uc_vs_uu_fdr_levels
Author FDR for UC versus S. uvarum parental levels.
distance_cc_uu
Author Euclidean expression distance between the two parental genotypes.
distance_cc_cu
Author Euclidean expression distance between S. cerevisiae parent and CU chimera.
distance_uu_cu
Author Euclidean expression distance between S. uvarum parent and CU chimera.
distance_cc_uc
Author Euclidean expression distance between S. cerevisiae parent and UC chimera.
distance_uu_uc
Author Euclidean expression distance between S. uvarum parent and UC chimera.
distance_cu_uc
Author Euclidean expression distance between the two chimeras.
timepoint
CRE-seq RNA sampling label from T1 through T27.
time_hours
Sampling time in hours during the diauxic shift, from the authors' CRE_analysis.R time vector.
n_barcodes_with_activity
Number of retained barcodes with nonzero RNA and positive DNA used for the activity summary at this timepoint.
mean_rna_count
Mean raw RNA barcode count across retained barcodes for this construct and timepoint.
mean_dna_count
Mean combined DNA1+DNA27 barcode count across retained barcodes for this construct.
mean_rna_cpm
Mean RNA count after per-timepoint library-size normalization to counts per million.
mean_dna_cpm
Mean combined DNA count after library-size normalization to counts per million.
mean_log2_activity
Mean barcode-level log2[(RNA CPM)/(combined DNA CPM)] at this timepoint; zero-RNA barcodes are omitted.
sem_log2_activity
Standard error of the barcode-level log2 activity mean at this timepoint.
mean_activity_over_time
Mean of mean_log2_activity across timepoints with nonmissing activity for this construct.
sd_activity_over_time
Standard deviation of mean_log2_activity across informative timepoints for this construct.
n_timepoints_with_activity
Number of timepoints with a nonmissing construct activity summary.

Quality control

Author-described QC was applied to the raw barcode counts: perfect matches to library barcodes were retained, technical replicate libraries were combined, and a barcode was removed if it had zero RNA reads in more than one-third of the 27 RNA timepoints, fewer than 100 total DNA1+DNA27 reads, or fewer than 2,700 total RNA reads (100 average reads per timepoint). This retained 5,013 of 7,232 barcode rows. For the final processed table, the author analysis' region-level support filter was also applied: at least two QC-passing barcodes were required for each parental allele, retaining 4,223 barcode rows, 1,383 constructs, and 348 promoter regions. Zero RNA timepoints are omitted from activity means and standard errors. The processed activity uses transparent library-size-normalized CPM RNA divided by combined-DNA CPM; the original count files and author statistics are included in raw_data.

Curation notes

The paper labels this library YJF1484 and reports the 5,013-row barcode QC result. The source paper has a typo calling that retained inter-specific count intra-specific in one sentence; this package uses inter.counts.csv and the inter-specific metadata. The final region support filter matches the analysis script's removal of regions with fewer than two parental barcode replicates.

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