Experiment / E1J7OE1DCOther

LRIM1 deletion-mutagenesis enhancer activity

Influence of genetic polymorphism on transcriptional enhancer activity in the malaria vector Anopheles coluzzii

Two natural LRIM1 alleles were shortened symmetrically from both ends to produce 100%, 50%, and 25% derivatives, then tested in the same episomal dual-luciferase reporter system. The panel resolves allele-specific positive and negative regulatory modules within the LRIM1 interval.

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

Basal / Untreated; 24 h after reporter transfection

Deletion derivatives retained 50% or 25% of the initial enhancer length by reducing equally from both ends. The study reports n = 12 per construct and Kruskal–Wallis/post-hoc compact-letter groups; sequence-derived variable-site counts are described in the paper but are not re-calculated here.

Episomal dual-luciferase deletion assay using pGL-Gateway-DSCP firefly reporter plus pRL-ubi-63E Renilla control; the molecular perturbation is symmetric end deletion of a natural enhancer allele and the readout is normalized RLU.

Processed data

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Visible columns (23 of 23)
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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 · 23 definitions
element_id
Enhancer locus tested; all rows are LRIM1.
proximal_gene
Nearest annotated gene used to name the locus.
gene_id
Gene identifier from the paper.
chromosome
Chromosome arm in PEST AgamP4 coordinates.
coordinate_start
1-based inclusive initial LRIM1 interval start.
coordinate_end
1-based inclusive initial LRIM1 interval end.
interval_length_bp
Inclusive initial LRIM1 interval length.
allele_label
Natural LRIM1 allele background used for the derivative.
source_colony
Laboratory colony source of the allele.
colony_origin
Colony initiation population/year reported in Methods.
construct_type
Deletion-mutagenesis construct type.
deletion_fraction
Remaining fraction of the initial enhancer interval (1.0, 0.5, or 0.25).
deletion_description
How the derivative was shortened, following the paper’s symmetric end deletions.
source_fasta_file
Supplementary File S1 FASTA filename retained in raw_data.
source_fasta_record
Exact short-fragment FASTA record used for the sequence column.
sequence_5to3
Ungapped nucleotide sequence reconstructed from the aligned derivative record.
sequence_length_bp
Length of the ungapped derivative sequence.
sequence_md5
MD5 checksum of the ungapped derivative sequence.
relative_luciferase_activity_median_approx
Approximate Figure 6A median of DLX-normalized luciferase activity; digitized from the plotted median bar.
n_measurements
Figure 6A reports n = 12 wells for every construct.
statistical_group
Compact-letter group printed above the Figure 6A distribution.
source_figure
Publication figure supporting the activity value.
qc_pass
All six source-tested deletion constructs retained with n = 12; activity differences are the biological outcome of interest.

Quality control

Retained all six source-tested constructs with n = 12. No technical outlier filter was reported; low or high activity was retained because the experiment is specifically a functional deletion dissection.

Curation notes

Short derivative records come from the separate LRIM1_Alleles-short-fragments.fas file inside Supplementary Dataset 1. The record names encode the derivative, while Figure 6 labels them by allele and percent length; original names are retained for traceability.

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