Study / S49TNQ31E2020-11-12

Systematic identification of cis-regulatory variants that cause gene expression differences in a yeast cross

Kaushik Renganaath, Rockie Chong, Laura Day, Sriram Kosuri, Leonid Kruglyak et al.

About this study

Sequence variation in regulatory DNA alters gene expression and shapes genetically complex traits. However, the identification of individual, causal regulatory variants is challenging. Here, we used a massively parallel reporter assay to measure the cis-regulatory consequences of 5832 natural DNA variants in the promoters of 2503 genes in the yeast Saccharomyces cerevisiae. We identified 451 causal variants, which underlie genetic loci known to affect gene expression. Several promoters harbored multiple causal variants. In five promoters, pairs of variants showed non-additive, epistatic interactions. Causal variants were enriched at conserved nucleotides, tended to have low derived allele frequency, and were depleted from promoters of essential genes, which is consistent with the action of negative selection. Causal variants were also enriched for alterations in transcription factor binding sites. Models integrating these features provided modest, but statistically significant, ability to predict causal variants. This work revealed a complex molecular basis for cis-acting regulatory variation.

Full author list & citation

Kaushik Renganaath, Rockie Chong, Laura Day, Sriram Kosuri, Leonid Kruglyak, Frank W Albert. Systematic identification of cis-regulatory variants that cause gene expression differences in a yeast cross. 2020-11-12. https://doi.org/10.7554/eLife.62669

Experiments 2

E2ENR7VZ1

Upstream promoter-variant MPRA in Saccharomyces cerevisiae BY4741

The Upstream library tested natural BY/RM variants in 144-bp promoter fragments centered on variants located upstream of yeast genes. Six effective BY4741 replicate groups were assayed by matched plasmid-DNA and reporter-RNA barcode sequencing, with RM and BY allele oligos compared pairwise.

Episomal Plasmid MPRABudding yeastsacCer3
Explore data
E8C98Y3FV

TSS promoter-variant MPRA in Saccharomyces cerevisiae BY4741

The TSS library tested natural BY/RM variants in 144-bp promoter fragments immediately upstream of annotated transcription start sites. Twelve effective BY4741 replicate groups were assayed by matched plasmid-DNA and reporter-RNA barcode sequencing, with single-RM oligos compared against BY reference oligos.

Episomal Plasmid MPRABudding yeastsacCer3
Explore data

Raw source data 20 files

Original supplemental and deposited inputs retained for this study. Download files individually or together as a ZIP; nested folders are preserved. Source reuse terms apply, and sequencing reads may be omitted.

Download all 20 files (ZIP)elife-62669-fig2-data1.xlsxelife-62669-fig2-data2.xlsxelife-62669-fig3-data1.xlsxelife-62669-fig4-data1.xlsxelife-62669-fig5-data1.xlsxelife-62669-fig6-data1.xlsxelife-62669-supp1.xlsxelife-62669-supp2.xlselife-62669-supp3.xlsxelife-62669-supp4.txt.gzelife-62669-supp5.xlsxelife-62669-supp6.vcf.gzelife-62669-supp7.gb.txtelife-62669-table1-data1.xlsxGSE155943_family.soft.gzGSE155943_TSS_countedBarcodesMappedToDesign_200806.txt.gzGSE155943_TSS_countedMappedBarcodes_200806.txt.gzGSE155943_Upstream_countedBarcodesMappedToDesign_200806.txt.gzGSE155943_Upstream_countedMappedBarcodes_200806.txt.gzGSE155944_family.soft.gz

Cite OpenMPRA

Cite the OpenMPRA database. Include your access date because the collection changes over time.

Please also cite the source studies when using their data.