load("../data/candidate_rxlr.RData")

The effectR package is an R package designed to call oomycete RxLR and CRN effectors by searching for the motifs of interest using regular expression searches and hidden markov models (HMM).

Overview

The effectR packages searches for the motifs of interest (RxLR-EER motif for RxLR effectors and LFLAK motif for CRN effectors) using a regular expression search (REGEX). These motifs used by the REGEX effectR search have been reported in the literature (Haas et al., 2009, Stam et al., 2004).

The effectR package aligns the REGEX search results using MAFFT, and builds a HMM profile based on the multiple sequence alignment result using the hmmbuild program from HMMER. The HMM profile is used to search across ORF of the genome of interest using the hmmsearch binary from HMMER. The search step will retain sequences with significant hits to the profile of interest. effectR also combines the redundant sequences found in both REGEX and HMM searches into a single dataset that can be easily exported. In addition, effectR reads and returns the HMM profile to the user and allows for the creation of a MOTIF logo-like plot using ggplot2.

Requirements

External software (REQUIRED)

The effectR package uses MAFFT and HMMER3 to perform the hidden markov model seach across the results from the REGEX step. These two packages should be installed before running any of the effectR functions.

Downloading and installing MAFFT

MAFFT is a multiple sequence alignment program that uses Fourier-transform algorithms to align multiple sequences. We recommend downloading and installing MAFFT by following the instructions and steps in the MAFFT installation web site.

Linux/OS X Users

Make sure that you remember the directory in which MAFFT is installed, of if the installation is sucessful, make sure to obtain the path via bash/tsh/console:

which mafft
/usr/local/bin/mafft

For more information about MAFFT go to the MAFFT website: http://mafft.cbrc.jp/

Windows Users

MAFFT comes in two main distributions for windows:

Please, download and install the all-in-one version. We recommend that you download and save MAFFT in your Desktop, as it will make yyour path easily accesible.

Downloading and installing HMMER

HMMER is used for searching sequence databases for sequence homologs. It uses hidden Markov models (profile HMMs) to search for sequences with hits to similar patterns than the profile. We use three main HMMER tools:

The effectR package requires all of these tools. A correct HMMER installation will install all three programs.

Linux/OS X users

We recommend downloading and installing HMMER by following the instructions and steps in the HMMER installation web site. Make sure that you remember the directory in which HMMER is installed, of if the installation is sucessful, make sure to obtain the path via bash/tsh/console:

which hmmbuild
which hmmpress
which hmmsearch
/usr/local/bin/hmmbuild
/usr/local/bin/hmmpress
/usr/local/bin/hmmsearch

For more information about HMMER go to the HMMER website: http://hmmer.org/

Windows users

To use the effectR package in Windows, the user must download the Windows binaries of HMMER. effectR will not work with any other version of HMMER.

Data input

The effectR package is designed to work with amino acid sequences in FASTA format representing the six-frame translation of every open reading frame (ORF) of an oomycete genome. Using the six-frame translation of all ORF's in a genome is recommended in order to obtain as many effectors as possible from a proteome. To obtain the ORF for a genome, we recommend the use of EMBOSS' getorf.

effectR uses a list of sequences of the class SeqFastadna in order to perform the effector searches. The function read.fasta from the seqinr package reads the FASTA amino acid file into R, creating a list of SeqFastadna objects that represent each of the translated ORF's from the original FASTA file. We will begin our example using a subset of translated ORF's from the P. infestans genome sequenced by Haas et al., (2009):

library(effectR)
pkg <- "effectR"
fasta.file <- system.file("extdata", "test_infestans.fasta", package = pkg)
library(seqinr)
ORF <- read.fasta(fasta.file)
head(ORF, n = 2)

We have created a ORF object that includes the list of translated ORF's from the subset of XX ORF's from the P. infestans genome. For more information on the SeqFastadna objects please read the seqinr manual.

REGEX search

To perform the effector search, effectR searches for the motifs of interest found in RxLR and CRN motifs. We have created the function regex.search to perform the seach of the motif of interest. The function regex.search requires the list of SeqFastadna objects and the gene family of interest. Here we show an example to search for sequences with RxLR-EER motifs from the 27 ORF subset of P. infestans. This ORF example data set contains 17 sequences with RxLR-EER motifs and 27 sequences with the LFLAK motifs found in CRN effectors. We expect to find, then, 17 sequences after using the regex.search function with the motif='RxLR' parameter:

REGEX <- regex.search(sequence = ORF, motif = "RxLR")
length(REGEX)

We observe that the REGEX object has 27 sequences with the RxLR motif. These sequences will be aligned using MAFFT, and used to build a HMM profile to search for similar sequences.

In addition to the basic functionality of regex.search to obtain both RxLR and CRN candidate genes, we have added the possibility of using a custom regex motif in order to search for non-canonical effectors or other protein motifs from different families of interest. The option motif = "custom" is couple with the reg.pat option, wich allows for the inclusion of any regular expression in the format specified by the regex function in R. For example, if we want to obtain all candidates with a WV motif in the positions 60 to 90 of the aminoacid, we use the following commands:

reg.pat <- "^\\w{50,60}[w,v]"
REGEX <- regex.search(sequence = ORF, motif = "custom", reg.pat = reg.pat)
length(REGEX)

Multiple sequence alignment and HMMER search

To perform the HMM search and obtain all possible effector candidates from a proteome, effectR uses the REGEX results as a template to create a HMM profile and perform a search across the proteome of interest. We have created the hmm.search function in order to perfomr this search. The hmm.search function requires a local installation of MAFFT and HMMER in order to perform the searches. The absolute paths of the binaries must be specified in the mafft.path and hmmer.path options of the hmm.search function.

Note for Windows users: Please use the ABSOLUTE PATH for HMMER and MAFFT or effectR will not work (e.g. mafft.path ="C:/User/Banana/Desktop/mafft/")

In addition, the hmm.function requires the path of the original FASTA file containing the translated ORF's in the original.seq parameter of the function. hmm.search will use this file as a query in the hmmsearch software from HMMER, and search for all sequences with hits against the HMM profile created with the REGEX results.

We will continue or example by performing a hmm.search in our example data set. We will include the original example FASTA file location (stored in the fasta.file object), the location of the MAFFT binary and the location of the HMMER binaries:

candidate.rxlr <- hmm.search(original.seq = fasta.file, regex.seq = REGEX, mafft.path = "/usr/local/bin/", hmm.path = "/usr/local/bin/")

The hmm.search function has resulted in 19 effector candidates. As a reminder, we used the REGEX results of an RxLR motif search, so we can consider this hmm.search results as RxLR candidate effectors. To obtain the CRN candidate effectors we should go back to the regex.search step and modify the motif parameter to motif="CRN and perform the hmm.search again.

The hmm.search object returns a list of 3 elements:

  1. The REGEX sequences used to build the HMM profile in a SeqFastadna class
  2. The sequences from the original translated ORF files with hits to the HMM profile in a SeqFastadna class
  3. The HMM profile table created by HMMER's hmmbuild as a data frame

We can access each one of these elements by using the $ operator in the object obtained from hmm.search:

REGEX results

head(candidate.rxlr$REGEX, n = 2)

HMMER results

head(candidate.rxlr$HMM, n = 2)

HMM profile

head(candidate.rxlr$HMM_Table)

We have included each of these elements to provide the user with the most complete information possible from each of the steps performed until here.

Obtaining non-redundant effectors and motif summaries

The user can extract all of the non-redundant sequences and a summary table with the information about the motifs using the effector.summary function. This function uses the results from either hmm.seach or regex.search functions to generate a table that includes the name of the candidate effector sequence, the number of motifs of interest (RxLR-EER or LFLAK-HVLV) per sequence and its location within the sequence. In addition, when the effector.summary function is used in an object that contains the results of hmm.search, the user will obtain a list of the non-reduntant sequences. If the user provides the results from regex.search, the function will return the motif summary table.

We will use the effector.summary function with our hmm.search results (the candidate.rxlr object):

summary.list <- effector.summary(candidate.rxlr)

Motif table

knitr::kable(summary.list$motif.table)

The motif table has a column called MOTIF. This column summarizes the candidate ORF into one of 4 categories:

Non-redundant sequences

head(summary.list$motif.table, n = 2)
length(summary.list$consensus.sequences)

The summary.list$consensus.sequences has all 27 RxLR candidate genes found in our searches.

Exporting the non-redundant effector candidates

To export the non-redundant effector candidates that resulted from the hmm.search or regex.search functions, we use the write.fasta function of the seqinr package. We recomend the users to read the documentation of the seqinr package Since the objects that result from the hmm.search or regex.search function are of the SeqFastadna class, we can use any of the function of the seqinr package that use this class as well.

To save the results from our example file, we would use the following command:

write.fasta(sequences = getSequence(summary.list$consensus.sequences), names = getName(summary.list$consensus.sequences), file.out = "RxLR_candidates.fasta")

Visualizing the HMM profile using a sequence logo-like plot

To determine if the HMM profile includes the motifs of interest, we have created the function hmm.logo. The function hmm.logo reads the HMM profile (obtained from the hmm.search step) and uses ggplot2 to create a bar-plot. The bar-plot will illustrate the bits (amino acid scores) of each amino acid used to construct the HMM profile according to its consensus position in the HMM profile. To learn more about sequence logo plots visit this wikipedia article.

The hmm.logo is a wrapper that parses the HMM profile table and plots the parsed table results in ggplot2.

To visualize the sequence logo-like plot in our example data set, we use our candidate.rxlr$HMM_Table object in the hmm.search function:

hmm.logo(hmm.table = candidate.rxlr$HMM_Table)


grunwaldlab/effectR documentation built on Sept. 9, 2023, 1:39 a.m.