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Transcription factor binding site clusters identify target genes with similar tissue-wide expression and buffer against mutations

2018· preprint· en· W4255174926 on OpenAlexafffund
Ruipeng Lu, Peter K. Rogan

Bibliographic record

VenueF1000Research · 2018
Typepreprint
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenomics and Chromatin Dynamics
Canadian institutionsWestern University
FundersNatural Sciences and Engineering Research Council of CanadaCanada Research ChairsCanada Foundation for InnovationWestern UniversityCompute Canada
KeywordsPromoterDNA binding siteBiologyGeneIn silicoGeneticsTranscription factorGene knockdownComputational biologyBinding siteGene expression

Abstract

fetched live from OpenAlex

<ns4:p> <ns4:bold>Background:</ns4:bold> The distribution and composition of <ns4:italic>cis</ns4:italic> -regulatory modules composed of transcription factor (TF) binding site (TFBS) clusters in promoters substantially determine gene expression patterns and TF targets. TF knockdown experiments have revealed that TF binding profiles and gene expression levels are correlated. We use TFBS features within accessible promoter intervals to predict genes with similar tissue-wide expression patterns and TF targets. </ns4:p> <ns4:p> <ns4:bold>Methods:</ns4:bold> Genes with correlated expression patterns across 53 tissues and TF targets were respectively identified from Bray-Curtis Similarity and TF knockdown experiments. Corresponding promoter sequences were reduced to DNase I-accessible intervals; TFBSs were then identified within these intervals using information theory-based position weight matrices for each TF (iPWMs) and clustered. Features from information-dense TFBS clusters predicted these genes with machine learning classifiers, which were evaluated for accuracy, specificity and sensitivity. Mutations in TFBSs were analyzed to <ns4:italic>in silico</ns4:italic> examine their impact on cluster densities and the regulatory states of target genes. </ns4:p> <ns4:p> <ns4:bold>Results:</ns4:bold> We initially chose the glucocorticoid receptor gene ( <ns4:italic>NR3C1</ns4:italic> ), whose regulation has been extensively studied, to test this approach. <ns4:italic>SLC25A32</ns4:italic> and <ns4:italic>TANK</ns4:italic> were found to exhibit the most similar expression patterns to <ns4:italic>NR3C1</ns4:italic> . A Decision Tree classifier exhibited the largest area under the Receiver Operating Characteristic (ROC) curve in detecting such genes. Target gene prediction was confirmed using siRNA knockdown of TFs, which was found to be more accurate than those predicted after CRISPR/CAS9 inactivation. <ns4:italic>In-silico</ns4:italic> mutation analyses of TFBSs also revealed that one or more information-dense TFBS clusters in promoters are required for accurate target gene prediction. </ns4:p> <ns4:p> <ns4:bold>Conclusions</ns4:bold> : Machine learning based on TFBS information density, organization, and chromatin accessibility accurately identifies gene targets with comparable tissue-wide expression patterns. Multiple information-dense TFBS clusters in promoters appear to protect promoters from effects of deleterious binding site mutations in a single TFBS that would otherwise alter regulation of these genes. </ns4:p>

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.057
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.021
GPT teacher head0.300
Teacher spread0.279 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations12
Published2018
Admission routes2
Has abstractyes

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