AI Article Synopsis

  • A limited number of transcriptional regulatory interactions have been discovered so far, prompting the development of a robust position weight matrix (rPWM) to improve the prediction of transcriptional interactions (TIs) between transcription factors (TFs) and target gene promoters.
  • The AdaFuzzy system, which combines a fuzzy inference system with an interaction type classifier, was used to predict TIs in Saccharomyces cerevisiae and demonstrated superior performance compared to four existing methods, and performed comparably to experimental methods.
  • The results aided in classifying predicted TIs and provided valuable insights into known promoter architectures and transcriptional regulatory mechanisms in yeast.

Article Abstract

Background: To date, only a limited number of transcriptional regulatory interactions have been uncovered. In a pilot study integrating sequence data with microarray data, a position weight matrix (PWM) performed poorly in inferring transcriptional interactions (TIs), which represent physical interactions between transcription factors (TF) and upstream sequences of target genes. Inferring a TI means that the promoter sequence of a target is inferred to match the consensus sequence motifs of a potential TF, and their interaction type such as AT or RT is also predicted. Thus, a robust PWM (rPWM) was developed to search for consensus sequence motifs. In addition to rPWM, one feature extracted from ChIP-chip data was incorporated to identify potential TIs under specific conditions. An interaction type classifier was assembled to predict activation/repression of potential TIs using microarray data. This approach, combining an adaptive (learning) fuzzy inference system and an interaction type classifier to predict transcriptional regulatory networks, was named AdaFuzzy.

Results: AdaFuzzy was applied to predict TIs using real genomics data from Saccharomyces cerevisiae. Following one of the latest advances in predicting TIs, constrained probabilistic sparse matrix factorization (cPSMF), and using 19 transcription factors (TFs), we compared AdaFuzzy to four well-known approaches using over-representation analysis and gene set enrichment analysis. AdaFuzzy outperformed these four algorithms. Furthermore, AdaFuzzy was shown to perform comparably to 'ChIP-experimental method' in inferring TIs identified by two sets of large scale ChIP-chip data, respectively. AdaFuzzy was also able to classify all predicted TIs into one or more of the four promoter architectures. The results coincided with known promoter architectures in yeast and provided insights into transcriptional regulatory mechanisms.

Conclusion: AdaFuzzy successfully integrates multiple types of data (sequence, ChIP, and microarray) to predict transcriptional regulatory networks. The validated success in the prediction results implies that AdaFuzzy can be applied to uncover TIs in yeast.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797023PMC
http://dx.doi.org/10.1186/1471-2105-10-400DOI Listing

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