How To Identify Targets Of A Transcription Factor ?
9
16
Entering edit mode
14.3 years ago

I have a list of transcription factors from a high-throughput experiment. I would like to know about the probable target genes of these transcription factors. For example using OregAnno, I found that target gene of KLF6 is LTC4S. OregAnno seems to be not up-to-date. Is there any other bioinformatics resource where I can find the human TF->Target information ?

transcription • 29k views
ADD COMMENT
1
Entering edit mode

i think by reverse engineering tools such as ARACNe you can define Targets Of A Transcription Factor

ADD REPLY
6
Entering edit mode
14.3 years ago

Tough question. Most people want to go from gene to TF regulating that gene instead of TF to all genes under its (partial) control. What also makes this tough are: 1) tissue-specificity, 2) predictions of one or few binding sites when in vitro/in vivo data would suggest that the particular TF needs to bind multiple times, typically in cooperative fashion, in order to promote transcription. Other complications are different mRNA isoforms under control of different, perhaps overlapping TFs and genome variation altering regulation by a particular TF.

I know that none of this points you to a database of TF-gene interactions. I know of none that would address the above points - and those are relevant to the way I look at this question.

ADD COMMENT
1
Entering edit mode

I don't know but I doubt they consider these items. The real deep detailed stuff I have seen puts focus on just one TF. But one of ~2000 certainly won't cut it for your work.

ADD REPLY
0
Entering edit mode

Larry: Thanks for your suggestions on why this is difficult. I am wondering whether or OregAnno or other database that reports target information consider these important aspects.

ADD REPLY
0
Entering edit mode

Thanks for your suggestions.

ADD REPLY
6
Entering edit mode
13.6 years ago

I recently used "Investigate Gene Sets" options in MSigDB to find the transcription factor target information of my dataset. Adding this here as an answer for future googlers.

The data is curated from TRANSFAC, you can do a 'Compute Overlap' of your genes with the list of genes in the dataset. Output includes a p-value to indicate statistical significance and a Gene/geneset overlap matrix to visualize the gene categorized into different transcription factor targets.

Data set is available here.

ADD COMMENT
1
Entering edit mode

Looks like a good resource! Thanks!

ADD REPLY
5
Entering edit mode
14.3 years ago

You could try http://pazar.info/ and http://itfp.biosino.org/itfp/ for starters.

ADD COMMENT
1
Entering edit mode

This new paper describes another database server which might fit the bill (haven't checked it yet): http://www.ncbi.nlm.nih.gov/pubmed/20709693?dopt=Abstract

ADD REPLY
0
Entering edit mode

I will check these resources and get back to you.

ADD REPLY
4
Entering edit mode
11.0 years ago
Travis ★ 2.8k

Old question but still relevant and think this resource answers it:

http://rulai.cshl.edu/cgi-bin/TRED/tred.cgi?process=searchTFGeneForm

ADD COMMENT
0
Entering edit mode

@Travis, I think so too, except I have not gotten it to work yet.

ADD REPLY
2
Entering edit mode
9.7 years ago
Kamil ★ 2.3k

You might be interested in this R package: https://github.com/slowkow/tftargets

It summarizes 6 datasets:

See make_rdata.R for the script that converts the raw data into lists of gene sets.

Usage Example

  • Show the names of the lists.
  • Show the names of the first 5 transcription factors in TRRUST.
  • Show the gene targets for the AIP transcription factor.

screenshot

ADD COMMENT
1
Entering edit mode
13.9 years ago
Dejian ★ 1.3k

I agree with Larray on that people usually try to search for TFs acting on the interested genes. I have two suggesions to solve this problem. First, we can do it as usual, or find the TFs for all the genes in the genome (if available) of your research species and then select those genes posessing your TFs.This poissibly will take much time for computation. Furthermore, this probably has been done for model organisms and relavant databases may be available.Replicate the procedure and apply it to your own species.MAPPER can help do this. Second, try to find some ChIP data about your TF.If you are lucky and such kind of data is available,it will be a great help.The two suggestions may turn out to be useless since they are based on some preconditions that may be unavailable.

ADD COMMENT
0
Entering edit mode

Thanks Balance.

ADD REPLY
1
Entering edit mode
13.9 years ago
Michael 55k

There is also the Transfac database which is a commercial database of TF and interactions with subscription (now, I thought they had had a free portion before?).

As a wet-lab approach the exact solution to your question would be ChIP-sequencing (or ChIP-chips).

ADD COMMENT
0
Entering edit mode

Michael, Thanks,

ADD REPLY
1
Entering edit mode
13.6 years ago
Gurado ▴ 280

If you are happy to go with predictions have a look at the MEME suite http://meme.sdsc.edu/ Just be aware that you are getting plenty of false positives. To get a more accurate picture for a particular scenario have a go with ChipSeq.

ADD COMMENT
0
Entering edit mode
9.1 years ago
nivi1972 • 0

I am working in the same.I have a list of Transcription factors, their target genes and miRNAs all involved in skin cancer. Actually I want to make a directed regulatory network. But the problem is how to make it direct because all the databases mentioned above not provide information about what kind of regulation exist? weather it is activation or inhibition or coactivation like that. Manual annotation seems very difficult for me as I have huge data. Please suggest any database, plugins or method so that I can get such type of regulatory information.

Thanks

ADD COMMENT
0
Entering edit mode

SIREN package by can identify activation or inhibition type of regulation

http://baderlab.org/PegahKhosravi/SIREN

ADD REPLY

Login before adding your answer.

Traffic: 1766 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6