630 likes | 810 Views
Clustered Repeats and Regulatory Sites. Abdulrahman Alazemi , Shahroze Abbas, Liam Lewis, Donald Ta, Ann Vo. Overview. Clustered repeats Wide variety of functions History largely unknown Regulatory Sites A segment capable of altering expression of specific genes
E N D
Clustered Repeats and Regulatory Sites AbdulrahmanAlazemi, Shahroze Abbas, Liam Lewis, Donald Ta, Ann Vo
Overview • Clustered repeats • Wide variety of functions • History largely unknown • Regulatory Sites • A segment capable of altering expression of specific genes • Various classifications of regulatory sequences • Found in non-coding regions • Functions at the transcriptional level
Identification • Consensus sequences • Utilize PSSM • How? • Determine consensus
Clustered repeats and potential regulatory sequences AbdulrahmanAlazemi
Background; • Transcription factors? • Activators Vs Repressors.
Thoughts; - My questions; Can I apply a known method/tool with a known results to other phage and get the same/similar result?
The known case; • Examine the proven Repressor and Cro binding sites (operators) of Phage Lambda. • Bioinformatics method in the notes. • First “Name of Lambda in BioBike”. • Go to BioBike/Phantome.
The known case; • Second; Motifs in for the upstream sequence of phage Lambda. • Labeled, DNA, Multiple-Hits-ok.
The known case; • Results of motifs in. • More than one interesting case. • Motifs 1, 2 , 3.
The known case; • BioBike function; • Description-analysis submenu, Genes-proteins menu. • Now, we have an idea about where to look.
The known case; • Used the function sequence-of from Genome menu. • Go to the specific region in the genome
The known case; • Finding the operators. • Directly Vs inversion of.
Thoughts; - My concern/focus; Would I find some sort of generality between operators of different phages?
My experiment; • Twenty one random phages of different phage families. • Eight of them don't have repressors. (eliminated) • Three of the 13 phages left didn't display a map because of linear amplicon. • Ten phages out of 21 went through all the steps of the method/tool successfully and gave me back out come that I can work with. • Three out of 10 have similar results to phage Lambda.
Outcome analysis; - Similar to phage lambda: -Bacillus-phage-1
Outcome analysis; -Similar to phage Lambda: -Listeria-phage-A006
Outcome analysis; -Similar to phage lambda: -Lactobacillus-johnsonii-prophage-Lj928
First conclusion; - Out of 21 or 10 phages, only 3 phages are similar to phage Lambda. - Less than 50%. - No Generality. - Appropriate conclusion; - Phage Lambda, Bacillus-phage-1, Listeria-phage-A006 , and Lactobacillus-johnsonii-prophage-Lj928 have a similarity/generality between their operators that the repressors bind to.
Inspiration; - Dead end. - The articles !!!! - Extend my research. - look for something interesting.
First interesting case; - In Burkholderia-phage-Bcep1. - Six similar sequence in one intergenic region - another 6 similar sequences in another intergenic region. - Palindromic sequences. - 6 or 3 sequences ? - Bacillus-phage-1 is similar to Burkholderia-phage-Bcep1 somehow.
Second interesting case; • - In phage Clostridium-phage-39-O. • - Eight nucleotides sequence (TTACTACA) repeated 10 times in one intergenic sequence. • - Again the same sequence repeated 8 times in another intergenic sequence in another place on the phage.
Conclusion; - Goals; - Pick one interesting case. - Research it. - Make sense of it.
A. Comparison of Pseudomonas putidaand Azotobacter REP sequences Donald Ta
REPs • Repetitive Extragenic Palindromic Sequences • Found mainly in abundance in Enterobacteriaecae • Can be anywhere around 20 to 40 nt long • Clustered into structures called BIMEs (bacterial interspersed mosaic element) as two inverted tandem repeats separated by a short linker of variable length
What do REPs do? • Regulate Gene Expression • Structuring DNA • Specific target sites for bacterial insertion sequences • Possibly more that are undiscovered
Previous Study • I. Aranda-Olmedo 2002 used BLAST (Basic local alignment search tool) to find regions of local similarity between sequences downloaded from the National Center for Biotechnology Information (NCBI) • Used database with all contigs of Pseudomonas putidaalready available in The Institute for Genome Research • Developed their own program to screen all of the strains against the 35 nt sequence 5’-CCGGCCTCTTCGCGGGTAAGCCCGCTCCTACAGGG-3’
Implications from that study They suggest that the 35 bp element they found is species specific in P. putida First time that REP sequences have been described and characterized in a group of non-enterobacteriaceae
What am I doing? • Comparing REP sequence element of Pseudomonas putidaKT2440 with Azotobactervanlandii • Why? • Order Pseudomonadales • Used the REP element that is most common among Pseudomonas species “GCGGGnnnnCCCGC”
Methods • Used built-in functions of BioBike to scan a sequence for possibly loose matches of a pattern • “****GCGGG****CCCGC****” sequence iterated over the sequence of the organism of interest and then whenever there was a match it was displayed on the output • “*” means an unspecified amino acid
Findings • 52 sequence hits in Azotobactervanlandiithat appear to have the same conserved region found in Pseudomonas putida • The species share similar REP elements with the same conserved central palindromic region • “GCGGG****CCCGC”
Significance • REP sequences mainly found abundantly in Enterobacteriacaea • Study by Bao Ton-Hoang 2012 suggested that transposases could’ve been responsible for the proliferation of REP sequences in the genomes of bacteria in Enterobacteriacaea • Possibly suggest a similar origin of REP sequences/elements for Pseudomonas and Enterobacteriacaea?
Problems? • Found 2 hits in E. Coli K-12 that had the REP element • Maybe suggests similar origin? • Could be just a fluke/just by chance that these two organisms share the same REP element in abundance • Past Study found 804 REP sequences with that REP element in Pseudomonas putida • I found 52 in Azotobactervanlandii
Possible plans of the future/near future? • Compare with other bacteria in the order of Pseudomondas to see if I get similar results • Possibly try to find a link to how REP sequences started proliferating in bacteria outside of Enterobacteriacae
Positional Preference of Rho-Independent Transcriptional Terminators in E. Coli Ann Vo
Transcriptional Terminators • Rho-independent • Specific activities poorly understood • Occurs in ssDNA and RNA • Unique characteristics: • T-Tract: 12-15 nt • GC-rich stem: 4-18 nt
Transcriptional Terminators • Available algorithms: • RNAMotif • TransTermHP • ARNold • About 317 natural terminators found in E. Coli • Lai et al. (2013) found a positional preference between other regulatory sequences Do transcriptional terminators have a positional preference relative to the end of the gene?
ARNold • Erpin • Scores input sequences • Compares against 1,200 known terminators from Bacillus subtilitisand Escherichia coli • RNAMotif • Used descriptors to find possible terminators • Scores free energy of hairpin formation
Matching Sequences • BioBIKE/PhAnToMe • Extracted the 50 nucleotides following every gene • Python • Compared sequences to terminators • Calculated distance to terminator downstream sequence terminator CAGGACGGTTTACCGGGGAGCCATAAACGGCTCCCTTTTCATTGTTATCA ACGGTTTACCGGGGAGCCATAAACGGCTCCCTTTTCATTGTTA