Volume 16 Supplement 12

## Joint 26th Genome Informatics Workshop and 14th International Conference on Bioinformatics: Genomics

# Properly defining the targets of a transcription factor significantly improves the computational identification of cooperative transcription factor pairs in yeast

- Wei-Sheng Wu
^{1}Email author and - Fu-Jou Lai
^{1}

**Published: **9 December 2015

## Abstract

### Background

Transcriptional regulation of gene expression in eukaryotes is usually accomplished by cooperative transcription factors (TFs). Computational identification of cooperative TF pairs has become a hot research topic and many algorithms have been proposed in the literature. A typical algorithm for predicting cooperative TF pairs has two steps. (Step 1) Define the targets of each TF under study. (Step 2) Design a measure for calculating the cooperativity of a TF pair based on the targets of these two TFs. While different algorithms have distinct sophisticated cooperativity measures, the targets of a TF are usually defined using ChIP-chip data. However, there is an inherent weakness in using ChIP-chip data to define the targets of a TF. ChIP-chip analysis can only identify the binding targets of a TF but it cannot distinguish the true regulatory from the binding but non-regulatory targets of a TF.

### Results

This work is the first study which aims to investigate whether the performance of computational identification of cooperative TF pairs could be improved by using a more biologically relevant way to define the targets of a TF. For this purpose, we propose four simple algorithms, all of which consist of two steps. (Step 1) Define the targets of a TF using (i) ChIP-chip data in the first algorithm, (ii) TF binding data in the second algorithm, (iii) TF perturbation data in the third algorithm, and (iv) the intersection of TF binding and TF perturbation data in the fourth algorithm. Compared with the first three algorithms, the fourth algorithm uses a more biologically relevant way to define the targets of a TF. (Step 2) Measure the cooperativity of a TF pair by the statistical significance of the overlap of the targets of these two TFs using the hypergeometric test. By adopting four existing performance indices, we show that the fourth proposed algorithm (PA4) significantly out performs the other three proposed algorithms. This suggests that the computational identification of cooperative TF pairs is indeed improved when using a more biologically relevant way to define the targets of a TF. Strikingly, the prediction results of our simple PA4 are more biologically meaningful than those of the 12 existing sophisticated algorithms in the literature, all of which used ChIP-chip data to define the targets of a TF. This suggests that properly defining the targets of a TF may be more important than designing sophisticated cooperativity measures. In addition, our PA4 has the power to predict several experimentally validated cooperative TF pairs, which have not been successfully predicted by any existing algorithms in the literature.

### Conclusions

This study shows that the performance of computationalidentification of cooperative TF pairs could be improved by using a more biologically relevant way to define the targets of a TF. The main contribution of this study is not to propose another new algorithm but to provide a new thinking for the research of computational identification of cooperative TF pairs. Researchers should put more effort on properly defining the targets of a TF (i.e. Step 1) rather than totally focus on designing sophisticated cooperativity measures (i.e. Step 2). The lists of TF target genes, the Matlab codes and the prediction results of the four proposed algorithms could be downloaded from our companion website http://cosbi3.ee.ncku.edu.tw/TFI/

## Background

In eukaryotes, cooperativity among several transcription factors (TFs) is known to play an important role in transcriptional regulation. A relatively small number of cooperative TFs can set up very complex spatial and temporal patterns of gene expression. Knowing cooperative TFs is helpful for understanding the mechanisms of transcriptional regulation. Therefore, computational identification of cooperative TFs has become a hot research topic in modern biological research.

Many algorithms have been developed to identify cooperative TF pairs in yeast by integrating multiple high-throughput data sources such as gene expression data, ChIP-chip data, protein-protein interaction data, promoter sequence data, etc. [1–15]. The performance of an algorithm varies under different evaluation criteria [16]. A typical algorithm for predicting cooperative TF pairs has two steps. The first step is to define the targets of each TF under study and the second step is to design a measure for calculating the cooperativity of a TF pair based on the targets of these two TFs. While different algorithms propose distinct sophisticated cooperativity measures, the targets of a TF are usually defined using ChIP-chip data. However, there is an inherent weakness in using ChIP-chip data to define the targets of a TF. ChIP-chip analysis can only identify the binding targets of a TF but it cannot distinguish the true regulatory from the binding but non-regulatory targets of a TF [17].

This work is the first study which aims to investigate whether the performance of computational identification of cooperative TF pairs in yeast could be improved by using a more biologically relevant way to define the targets of a TF.

## Method

### Data sources

Four data sources were used in this study. First, 6017 TF-gene binding pairs for 168 TFs were retrieved from Harbison et al.'s ChIP-chip data with p-value less than 0.001 [2]. Each TF-gene binding pair was supported by the TF binding evidence from the high-throughput genome-wide ChIP-chip experiments in a single publication [2] showing that the TF binds to the promoter of the target gene. Second, 40761 TF-gene binding pairs for 170 TFs were retrieved from the TF binding data deposited in the YEASTRACT database [18]. Each TF-gene binding pair was supported by the TF binding evidence from the detailed gene by gene band-shift, foot-printing experiments or the high throughput genome-wide ChIP-chip experiments in different publications showing that the TF binds to the promoter of the target gene. Third, 165528 TF-gene regulation pairs for 294 TFs were retrieved from the TF perturbation data deposited in the YEASTRACT database [18]. Each TF-gene regulation pair was supported by the TF regulation evidence from the detailed gene by gene analysis or the genome-wide expression analysis in different publications showing that the perturbation (knockout or over-expression) of the TF-encoding gene causes a significant change in the expression of the target gene. Finally, we compiled 8609 TF-gene pairs for 151 TFs from the intersection of the TF binding and TF perturbation data deposited in the YEASTRACT database. Each TF-gene pair was supported by both the TF binding and TF regulation evidence. All the four data sources used in this study could be downloaded from our companion website.

### The four proposed algorithms

where *G* = 6575 is the number of genes in the yeast genome, *N*_{1} is the number of the targets of the first TF, *N*_{2} is the number of the targets of the second TF, *m* is the number of common targets of these two TFs. In summary, the smaller the p-value, the higher the chance that a TF pair has cooperativity.

Note that in Step 1, the targets of 168, 170, 294, and 151 TFs can be defined for the first, second, third, and fourth proposed algorithm, respectively (see Data sources section for details). Therefore, in Step 2, the cooperativity of 14028 (168*167/2), 14365 (170*169/2), 43071 (294*293/2), and 11325 (151*150/2) TF pairs can be computed for the first, second, third, and fourth proposed algorithm, respectively. For each algorithm, these TF pairs were then sorted by their p-values, where the top one TF pair has the smallest p-value and therefore is the most statistically significant cooperative TF pair. For example, the output of the fourth algorithm is a ranked list of 11325 TF pairs. The detailed descriptions of the four proposed algorithms could be found in Additional file 1.

### Four performance comparison indices

We adopt four existing performance comparison indices from the literature to evaluate the performance of an algorithm in identifying cooperative TF pairs. These four indices are introduced in the following subsections.

#### Performance index 1: The statistical significance of the overlap with the benchmark set

Yang et al. [13] compiled a benchmark set of 27 known cooperative TF pairs from the MIPS transcription complex catalogues [21]. Then they computed the statistical significance of the overlap of the set of the predicted cooperative TF pairs (PCTFPs) from an algorithm with the benchmark set to evaluate the performance of an algorithm. The statistical significance (p-value) is calculated using the Fisher exact test. The larger the -log(p-value), the greater the statistical significance. Therefore, the larger the -log(p-value), the better the performance of an algorithm.

#### Performance index 2: The similarity of protein-protein interaction (PPI) partners between the two TFs of each PCTFP

The similarity of PPI partners between two TFs may suggest that they participate in the same regulatory mechanism. This rationale has been used in previous studies [15, 16] to evaluate the biological plausibility of a PCTFP. The physical PPI data were downloaded from the BioGRID database [22]. The PPI partners similarity score of a TF pair, denoted as -log(p-value), is calculated using Equation (1). Note that *G* = 6575 is the number of genes in the yeast genome, *N*_{1} is the number of proteins which have physical PPI with the first TF, *N*_{2} is the number of proteins which have physical PPI with the second TF, and *m* is the number of common PPI partners of these two TFs. Here we use the average of the PPI partners similarity scores of all PCTFPs from an algorithm to evaluate the performance of an algorithm. The larger the average, the better the performance of an algorithm.

#### Performance index 3: The shortest path length of two TFs in the physical PPI network

Aguilar and Oliva [23] observed that a cooperative TF pair has a shorter path length in the physical PPI network than random expectation. The physical PPI network is constructed using the physical PPI data retrieved from the BioGRID database [22]. Here we use the average of the reciprocals of the shortest path lengths of all PCTFPs from an algorithm to evaluate the performance of an algorithm. The larger the average, the better the performance of an algorithm.

#### Performance index 4: The functional similarity of two TFs

Since a cooperative TF pair co-regulates the expression of a set of genes, they should have similar functions. Functional similarity has been used in several previous studies [10, 15, 16] to evaluate the biological plausibility of a PCTFP. The functional similarity score of a TF pair, which is calculated based on their GO semantic similarity, was retrieved from Yang et al.'s study [24]. Here we use the average of the functional similarity scores of all PCTFPs from an algorithm to evaluate the performance of an algorithm. The larger the average, the better the performance of an algorithm.

## Results and discussion

By adopting four existing performance comparison indices from the literature, we have the following discoveries.

### The performance of computational identification of cooperative TF pairs could be improved by using a more biologically relevant way to define the targets of a TF

In this study, the four proposed algorithms (denoted as PA1, PA2, PA3, and PA4) use different ways to define the targets of a TF. The targets of a TF defined by PA1 and PA2 (using ChIP-chip data and TF binding data, respectively) are bound but not necessarily are regulated by this TF. The targets of a TF defined by PA3 (using TF perturbation data) are regulated but not necessarily are bound by this TF. The targets of a TF defined by PA4 (using the intersection of the TF binding and TF perturbation data) are bound and regulated by this TF. Therefore, the targets of a TF defined by PA4 are more biologically relevant than those defined by the other three algorithms.

### Performance comparison of the fourth proposed algorithm (PA4) with 12 existing sophisticated algorithms in the literature

^{-15}as the PCTFPs of our PA4. Reporting the top 50 TF pairs seems reasonable because the number of the PCTFPs of most existing algorithms [1, 3, 5, 6, 8, 9, 15] falls between 20 and 60. For completeness of the comparison, we also consider the top 50 PCTFPs from PA1, PA2 and PA3 as their predictions. Figure 3 shows that PA4 is the best performing algorithm, which has the smallest average rank, among the 16 compared algorithms. Moreover, the performance of PA2, PA1 and PA3 ranks 2, 10, and 16, respectively, among the 16 compared algorithms. Note that the comparison is on the PCTFPs but not on the algorithms themselves since different algorithms cannot be compared fairly due to using different kinds of data sources. In summary, our finding suggests that properly defining the targets of a TF may be more important than designing sophisticated cooperativity measures.

### The fourth proposed algorithm (PA4) is robust against different p-value thresholds for determining the PCTFPs

^{-15}as the p-value threshold of the hypergeometric test and reported 50 PCTFPs whose p-values are less than the threshold. We then showed that the PCTFPs from our PA4 are more biologically meaningful than those from the 12 existing algorithms in the literature. To check the robustness of our PA4 against different p-value thresholds, here we evaluate the performance of our PA4 using three other different p-value thresholds (10

^{-25}, 10

^{-20}and 10

^{-10}), which reports 22, 33, 88 PCTFPs, respectively. Figure 4 shows that no matter which p-value threshold is used, our PA4 always has a smaller average rank than do the 12 existing algorithms in the literature. This suggests that our PA4 is indeed robust against different p-value thresholds.

### The fourth proposed algorithm (PA4) predicts nine unique cooperative TF pairs

Nine unique PCTFPs (among the 50 PCTFPs) which are predicted by the fourth proposed algorithm but not by any existing algorithms

Rank | PCTFP | Experimental evidence | The biological process in which both TFs are involved |
---|---|---|---|

1 |
| Jorgensen et al. [25] | Regulation of ribosomal protein gene transcription |

2 |
| Wade et al. [26] | Regulation of ribosomal protein gene transcription |

16 | Msn2-Ste12 | Stress response | |

17 | Msn2-Tec1 | Stress response | |

20 |
| Schawalder et al. [27] | Regulation of ribosomal protein gene transcription |

30 | Msn2-Pdr1 | Stress response | |

42 | Sok2-Ste12 | Pseudohyphal growth | |

44 |
| Roth [28] | Chromatin-mediated transcription regulation |

46 | Msn2-Rap1 | Stress response |

Two PCTFPs Ifh1-Sfp1 and Ifh1-Rap1 are noteworthy. These two pairs are the top two most statistically significant (ranked first and second) cooperative TF pairs predicted by our PA4 and they have not been predicted by any existing algorithm. Remarkably, these two PCTFPs have been experimentally validated in the literature. It is known that Sfp1 influences the nuclear localization of Ifh1, which binds to ribosomal protein (RP) gene promoters. The absence of Sfp1 causes Ifh1 to localize to nucleolar regions, thus reducing RP gene transcription [25]. In addition, the RP gene promoter is characterized by upstream binding of the general TF Rap1 followed by the RP gene specific TF Ifh1 via the forkhead-associated domain of Fhl1 [26].

The fact that only our PA4 but no existing algorithms can predict the four experimentally validated cooperative TF pairs (Ifh1-Sfp1, Ifh1-Rap1, Ifh1-Fhl1, and Rap1-Tup1) convincingly demonstrates the usefulness of our PA4.

## Conclusions

In this study, we investigated whether the performance of computational identification of cooperative TF pairs could be improved by using a more biologically relevant way to define the targets of a TF. We developed a simple algorithm (i.e. the fourth proposed algorithm PA4) which integrates TF binding data and TF perturbation data to define the biologically plausible targets of a TF. Our PA4 predicts nine unique PCTFPs, which have not been predicted by any existing algorithms. Remarkably, four of the nine unique pairs are experimentally validated cooperative TF pairs, convincingly demonstrating the usefulness of our PA4. Moreover, by adopting four existing performance comparison indices from the literature, we have two discoveries. First, the performance of computational identification of cooperative TF pairs is improved when integrating TF binding and TF perturbation data instead of using ChIP-chip data alone, TF binding data alone or TF perturbation data alone to define the targets of a TF. This suggests that using a more biologically relevant way to define the targets of a TF indeed helps identify cooperative TF pairs. Second, the cooperative TF pairs predicted by our simple PA4 are more biologically relevant than those predicted by the 12 existing sophisticated algorithms. This suggests that properly defining the targets of a TF may be more important than designing sophisticated cooperativity measures. In conclusion, our study shows that how to define the targets of a TF in a more biologically relevant way is critical for successful identification of cooperative TF pairs. Researchers should put more effort on properly defining the targets of a TF rather than totally focus on designing sophisticated cooperativity measures.

## Declarations

### Acknowledgements

This study was supported by National Cheng Kung University and Ministry of Science and Technology of Taiwan MOST-103-2221-E-006-174-MY2.

**Declarations**

The publication of this paper was funded by National Cheng Kung University and Ministry of Science and Technology of Taiwan MOST-103-2221-E-006-174-MY2.

This article has been published as part of *BMC Genomics* Volume 16 Supplement 12, 2015: Joint 26th Genome Informatics Workshop and 14th International Conference on Bioinformatics: Genomics. The full contents of the supplement are available online at http://www.biomedcentral.com/bmcgenomics/supplements/16/S12.

## Authors’ Affiliations

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