geWorkbench

Overview

The Promoter component scans one or more sequence profiles against nucleotide sequences that the user has loaded into geWorbench. Motifs from the JASPAR database of transcription factor binding sites are included with the component. Additional motifs can be added by the user.

The Promoter component will also display the results of hits found in the Pattern Discovery component.

JASPAR CORE database

The promoter component of geWorkbench includes version 3.0 of the JASPAR CORE database (http://jaspar.genereg.net/). It contains 138 curated, non-redundant profiles. These "profiles are derived from published collections of experimentally defined transcription factor binding sites for multi-cellular eukaryotes. The database represents a curated collection of target sequences" (JASPAR Documentation).

The datafile used "MATRIX_DATA.txt" can be found at http://jaspar.genereg.net/html/DOWNLOAD/mySQL/JASPAR_CORE_2008/.

The profiles represent counts of how many times each of the four nucleotide bases occurs at a particular position in the aligned promoter sequences.

Working with the Promoter graphical interface

Prerequisites

• To use the Promoter component, first check that it has been loaded in the Component Configuration Manager.
• The Promoter component appears when a data node of type "sequence" has been loaded in the Project Folders component.
• The Promoter component appears in the upper-right quadrant of geWorkbench, in the "Visual Area".

Layout

The figure shows the display of profile "TBP:TATA-box:MA0108" from the list of those included in JASPAR. The main features of the component include

• The TF Mapping tab at left. This area allows profiles to be searched for and selected for use in a sequence scan.
• The Logo, Parameters and Sequence tabs at right. These provide respectively visual display of the profile, the parameters, and the scan results.
• Control buttons at bottom left to manage scans and results.

Further details of each part of the component are provided below.

TF Mapping tab

List of available transcription factors

TF list - The TF list contains the names of available transcription factor binding site sequence profiles from JASPAR and those that have been loaded from files using Add TF. Double-click on TF signatures in the TF list box (upper box) to add TF's to the Selected TF (lower box). This lower list displays transcription factors which can be searched against the available genomic sequences by clicking on Scan. Double-clicking on a TF name clears it from the Selected TF list and returns it to the TF List.

Multiple profiles can be moved to the selected list for scanning.

• Search - Enter a portion of a TF name in the Search text box. The list scrolls to and highlights the TF containing the text string. Click Find Next to highlight the TF containing the text string. If nothing matches the text string, the entered text is changed to red.

• Find Next - continue scanning the list for the next occurrence of the search string.

Selected TF

This list contains the profiles that will be used in the next scan. Entries on the Selected TF list can be moved back up to the "available TFs" list by again double-clicking on their entry.

Here the TATA-box entry has been moved to the selected list.

Controls

Scan

Scans the sequences in the Selected TF list against the available genomic sequences. If the Selected TF list is empty, the system displays an error message.

Add TF

Not currently available. This button is disabled.

The profile should consist of a tab delimited series of counts, one for each position in the profile. It should could four lines, in the order A, C, G, T. There are no header lines or row labels, just the numeric matrix. For example, here is a profile showing the first six columns:

0 12 0 0 1 0

49 0 20 23 3 45

0 37 29 2 45 4

0 0 0 25 0 0

Because the normalization step uses the count total (sequences aligned to generate the profile), loading a frequency matrix is not currently supported.

Save

Saves to file a list of hits by a profile to a nucleotide sequence, including the sequence identifier, the transcription factor name and the start and stop points of the match along the sequence, as shown here:

gi|65508003

ATHB5:HOMEO-ZIP:MA0110 2104 2113

ATHB5:HOMEO-ZIP:MA0110 2115 2106

ATHB5:HOMEO-ZIP:MA0110 2882 2891

ATHB5:HOMEO-ZIP:MA0110 2893 2884

Retrieve

Not currently available. This button is disabled.

Stop

Stop the current scan.

The LOGO tab

LOGO display

The LOGO display implements the method of Schneider and Stephens (1990) to display the information at each position in a motif. Briefly, the total height of the column of letters at a position shows the information available, on a scale of 0 to 2 bits (the information needed to represent the 4 possible nucleotide bases at each position). The relative heights of each letter in a column show their individual contribution to the information at that position.

The LOGO display in geWorkbench implements the "small sample correction" described by Schneider, the magnitude of which depends on the number of sequences aligned to generate the profile. The correction is subtracted from the calculated information content at each position, with a minimum value (floor) of zero being displayed.

Table display

A table is used to show the numeric data from which the LOGO diagram is generated. The table depicts each position in the profile as a column, and has a row for each of the four nucleotide bases A, C, G and T. The user can choose to display the data either as the original counts or as frequencies.

• Display: Counts or Frequencies

The Parameters tab

Background sequence and scoring threshold determination

A background sequence is used to estimate an appropriate scoring threshold. This background can be generated in two ways.

1. determine base composition of input sequence and from this generate random sequence.
2. (13K) - use a set of 13,000 promoter sequences as background.

• The length of background sequence scanned is given by 1000*Iterations/PValue.

• The threshold value is calculated by scanning the background sequence with the profile and finding the top 100 scores. The 100th score is used as the threshold.

• Calculated p-values are Bonferroni corrected and also corrected for duplicates in the list of 100 top scores.

• Positive and negative strands are scanned and values above threshold are reported.

Parameters

• PValue / 1K -
• Use Thr. - Use threshold - if checked, use a user-input threshold rather than a calculated threshold for scoring a match.
• 13K Set - If not checked (default), use the random background sequence described above. If checked, use the 13K sequences as background.
• Iterations -
• Pseudocount - a small-sample correction factor (default 1.0). See above description.

Results

Total hits and Sequences with hits

Total hits counts all hits regardless of how many times one sequence is hit.

• Expected - number of hits expected by chance.
• Actual - observed number of hits.
• Enrich. p-value - p-value for chance of getting this outcome by chance.
•  % with hits

5' hits and 3'hits

• Expected - Expected number of hits
• Actual - Actual number of hits.

The Sequence tab

The Sequence tab can display either a line or a full character representation of the sequence which was searched against. Clicking on a position along the line or character representation will cause that portion of the sequence to be displayed in the detail box at the bottom of the component. This box also displays numbers representing position along the sequence, relative to the start of that particular sequence (not its genomic location). Both the character and detail views will show the location and extent of any profile match to the sequence.

If matches are found, the sequence will include blocks in various colors with solid arrows indicating the match orientation (forward or reverse complement). Individual hits can be identified by positioning the mouse pointer over them, which will display a tool tip. Clicking on an area with a match will show it in the Sequence Detail at the bottom with the hits shown as boxes around the characters.

The tooltip format is as follows: numeric position, Transcription Factor name <numeric position of the first character of the pattern, numeric position of last matching pattern character>.

• View - Line or Full Sequence. Line represents the sequence as a simple line, with any hits positioned along it. Full shows the entire sequence as characters.
• Show Patterns - display hits from Pattern Discovery (this is a separate component, not part of the Promoter component). Implementation note - these hits are represented in the "Active Patterns" data-structure.
• Show TFs - show hits from a search in this component. Implementation note - these hits are represented in the "Active TFs" data-structure.
• Clear All - clear all hits from the sequence window (and from the associated data structures). Note this will also clear the two adjacent check boxes. The relevant box must be re-checked to see further results.

The full character display shows any hits in white with a red background, and a small red arrow marks the start of the match and its direction.

Implementation details

1. Each time that a transcription factor (TF) matching operation is run, the "Active TFs" data structure is *AUGMENTED* with the results of the discovery operation (i.e., contents due to previous runs are maintained). The "Active TFs" data structure is not affected by pattern discovery.
2. Each time that a Pattern Discovery analysis is run, the contents of the "active patterns" structure are *REPLACED* with the results of the discovery operation (i.e., contents due to previous runs are cleared).

Scan Implementation

Normalization and the Pseudocount

The count matrices are normalized to frequencies using an algorithm which includes a "pseudocount" (see Nishida 2009). The pseudocount is a way to compensate for the effects of small sample sizes in the original observations used to generate the profiles. Nishida et al. studied how to determine an appropriate value for the pseudocount. They found that the optimal values were independent of the sample size and were correlated with the entropy of the original matrices. They say that this implies that the less-conserved the binding site, the larger a value should be used for the pseudocount. They find that 0.8 is a good value "for practical uses". They do not recommend use of the square root of the total count.

geWorkbench allows a pseudocount factor to be directly entered, or it can be selected to be the square root of the total count of sequences used to generate the profile. Prior to geWorkbench 1.8.0, setting the pseudocount to the square root of the total counts was directly coded and not changeable. The current default is to set the pseudocount equal to 1.0.

The normalization forumula used in calculating frequencies is then, where b is the pseudocount, and counts(i, j) is the observed count in a particular entry in the matrix,

freq(i, j) = (counts(i, j) + b/4) / (totalCounts + b).

The resulting frequency matrix is used in the subsequent scan.

Because the pseudocount is a settable parameter, the frequency matrix is recalculated for each scan from the original counts.

Scoring

• Calculated p-values are Bonferroni corrected and also corrected for duplicates in the list of 100 top scores found during the background scan.

• Positive and negative strands are scanned and values above threshold are reported.

Example: Running and viewing a scan

Prerequisites

The Promoter component is only available when a sequence has been loaded, either from disk or for example using the Sequence Retriever component to obtain genomic sequence.

For this example, we will obtain upstream genomic sequence for CDH2, the N-Cadherin gene. However, using the Sequence Retriever component requires that a microarray dataset and its annotations be loaded. Here, we will use the JB-ccmp_0120.txt file, which is an Affymetrix HG-U95Av2 MAS5 format text file and is part of the geWorkbench tutorial dataset.

The Affymetrix HG-U95Av2 annotation file can be obtain from the Affymetrix website. Please see instructions on the geWorkbench FAQ.

1. In the Project Folders component, load the file JB-ccmp_0120.txt as type MAS5/GCOS.

2. When prompted, associate the HG-U95Av2 annotation file.

3. In the Markers component, search for the gene name "CDH2" using the Find Next button. On this chip type, marker 2053_at represents the CDH2 gene.

4. You can double-click on the marker to add it to the default "Selection" set. Or you can right-click on it and add it to a named set, such as "Cadherins". This is depicted below.

5. "Activate" (check the box next to) the set to which you added the marker.

6. Any activated markers will appear in the Sequence Retriever component, as shown below.

7. Set the retrieval limits to 2000 base pairs up- and downstream from the transcription start site.

8. Make sure the retrieval type is set to DNA, UCSC (the Santa Cruz genome sequence database).

9. Click "Get Sequence".

10. Once the sequence has been retrieved, check the box next to the sequence and then hit the button "Add to Project". We now have the genomic sequence available for other components to use.

Running the scan

1. In the Promoter component, search for "ap2", which corresponds to transcription factor activator protein 2 alpha.

2. Double-click on the TFAP2A entry to move it down to the search list.

3. Hit the "Scan" button. The result is displayed in the Sequence tab of the Promoter component as shown here.

4. Setting the View to Full Sequence shows the hits in white on the sequence. Red arrows indicate whether the hit is to the forward (right arrow) or reverse (complementary) (left-arrow) strand.

5. The parameters tab displays the actual threshold values calculated during the run, and displays the enrichment results.

References

• Lawrence and Reilly (1990) Searching putative regulatory sequences against a collection of known transcription factor DNA-binding signatures represented as a position weight matrices (PWMs) (citation unknown). See perhaps: Lawrence, C. and Reilly, A. (1990). An expectation maximization (EM) algorithm for the identification and characterization of common sites in unaligned biopolymer sequences. Proteins, 7 (1), 41-51. Link to Abstract
• Nishida K, Frith MC, Nakai K. (2009) Pseudocounts for transcription factor binding sites. Nucleic Acids Res. Feb;37(3):939-44. link to paper
• Sandelin A, Alkema W, Engstrom P, Wasserman WW, Lenhard B. (2004) JASPAR: an open-access database for eukaryotic transcription factor binding profiles. Nucleic Acids Res. Jan 1;32(Database issue):D91-4 (link to paper).
• Schneider TD, Stephens RM. (1990) Sequence logos: a new way to display consensus sequences. Nucleic Acids Res. Oct 25;18(20):6097-100. (link to paper)
• Vlieghe D, Sandelin A, De Bleser PJ, Vleminckx K, Wasserman WW, van Roy F, Lenhard B. (2006) A new generation of JASPAR, the open-access repository for transcription factor binding site profiles. Nucleic Acids Res. Jan 1;34(Database issue):D95-7.