Central dogma

Fundamentals in Sequence Analysis 1.(part 1)

Hugues Sicotte

NCBI

Review of Basic biology + database searching in Biology.

The Flow of Biotechnology Information

> DNA sequenceAATTCATGAAAATCGTATACTGGTCTGGTACCGGCAACACTGAGAAAATGGCAGAGCTCATCGCTAAAGGTATCATCGAATCTGGTAAAGACGTCAACACCATCAACGTGTCTGACGTTAACATCGATGAACTGCTGAACGAAGATATCCTGATCCTGGGTTGCTCTGCCATGGGCGATGAAGTTCTCGAGGAAAGCGAATTTGAACCGTTCATCGAAGAGATCTCTACCAAAATCTCTGGTAAGAAGGTTGCGCTGTTCGGTTCTTACGGTTGGGGCGACGGTAAGTGGATGCGTGACTTCGAAGAACGTATGAACGGCTACGGTTGCGTTGTTGTTGAGACCCCGCTGATCGTTCAGAACGAGCCGGACGAAGCTGAGCAGGACTGCATCGAATTTGGTAAGAAGATCGCGAACATCTAGTAGA

> Protein sequenceMKIVYWSGTGNTEKMAELIAKGIIESGKDVNTINVSDVNIDELLNEDILILGCSAMGDEVLEESEFEPFIEEISTKISGKKVALFGSYGWGDGKWMRDFEERMNGYGCVVVETPLIVQNEPDEAEQDCIEFGKKIANI

Gene Function

Prequisites to Sequence Analysis

• Basic Biology so you can understand the language of the databases: Central Dogma (transcription; Translation, Prokaryotes, Eukaryotes,CDS, 3´UTR, 5´UTR, introns, exons, promoters, operons, codons, start codons, stop codons,snRNA,hnRNA,tRNA, secondary structure, tertiary structure).

• Before you can analyze sequences.. You have to understand their structure.. And know about Basic Biological Database Searching

Central Dogmas of Molecular Biology

1) The concept of genes is historically defined on the basic of genetic inheritance of a phenotype. (Mendellian Inheritance)

2) The DNA an organism encodes the genetic information. It is made up of a double stranded helix composed of ribose sugars.

Adenine(A), Citosine (C), Guanine (G) and Thymine (T).

[note that only 4 values nees be encode ACGT.. Which can be done using 2 bits.. But to allow redundant letter combinations (like N means any 4 nucleotides), one usually resorts to a 4 bit alphabet.]


3) Each side of the double helix faces it´s complementary base.

A T, and G C.

4) Biochemical process that read off the DNA always read it from the 5´´side towards the 3´ side. (replication and transcription).

5) A gene can be located on either the ´plus strand´ or the minus strand. But rule 4) imposes the orientation of reading .. And rule 3 (complementarity) tells us to complement each base E.g.

If the sequence on the + strand is ACGTGATCGATGCTA, the – strand must be read off by reading the complement of this sequence going ´backwards´

e.g. TAGCATCGATCACGT


6) DNA information is copied over to mRNA that acts as a template to produce proteins.

We often concentrate on protein coding genes, because proteins are the building blocks of cells and the majority of bio-active molecules. (but let´s not forget the various RNA genes)

Prokaryotic genes

Downstream (3’)

Prokaryotes (intronless protein coding genes)

promoter Gene regionUpstream (5’)

Transcription (gene is encoded on minus strand .. And the reverse complement is read into mRNA)

DNA

mRNA5´ UTR 3´ UTRCoDing Sequence (CDS)

ATG

ATG

TAC

Translation: tRNA read off each codons, 3 bases at a time, starting at start codon until it reaches a STOP codon.

protein

Why does Nature bothers with the mRNA?

Why would the cell want to have an intermediate between DNA and the proteins it encodes?

•Gene information can be amplified by having many copies of an RNA made from one copy of DNA. •Regulation of gene expression can be effected by having specific controls at each element of the pathway between DNA and proteins. The more elements there are in the pathway, the more opportunities there are to control it in different circumstances. •In Eukaryotes, the DNA can then stay pristine and protected, away from the caustic chemistry of the cytoplasm.

Prokaryotic genes (operons)

downstream

Prokaryotes (operon structure)

promoterupstream

Gene 1 Gene 2 Gene 3

In prokaryotes, sometimes genes that are part of the same operational pathway are grouped together under a single promoter. They then produce a pre-mRNA which eventually produces 3 separates mRNA´s.

Bacterial genomes have simple gene structure.

- Transcription factor binding site.

- Promoters

-35 sequence (T82T84G78A65C54A45) 15-20 bases

-10 sequence (T80A95T45A60A50T96) 5-9 bases

- Start of transcription : initiation start: Purine90 (sometimes it’s the “A” in CAT)

- translation binding site (shine-dalgarno) 10 bp upstream of AUG (AGGAGG)

- One or more Open Reading Frame

•start-codon (unless sequence is partial)

•until next in-frame stop codon on that strand ..

Separated by intercistronic sequences.

- Termination

Bacterial Gene Structure of signals

Genetic Code

How does an mRNA specify amino acid sequence? The answer lies in the genetic code. It would be impossible for each amino acid to be specified by one nucleotide, because there are only 4 nucleotides and 20 amino acids. Similarly, two nucleotide combinations could only specify 16 amino acids. The final conclusion is that each amino acid is specified by a particular combination of three nucleotides, called a codon:

Each 3 nucleotide code for one amino acid. •The first codon is the start codon, and usually coincides with the Amino Acid Methionine. (M which has codon code ‘ATG’)•The last codon is the stop codon and does NOT code for an amino acid. It is sometimes represented by ‘*’ to indicate the ‘STOP’ codon.

•A coding region (abbreviation CDS) starts at the START codon and ends at the STOP codon.

Codon tableNote the degeneracy of the genetic code. Each amino acid might have up to six codons that specify it. • Different organisms have different frequencies of codon usage. •A handful of species vary from the codon association described above, and use different codons fo different amino acids.

How do tRNAs recognize to which codon to bring an amino acid? The tRNA has an anticodon on its mRNA-binding end that is complementary to the codon on the mRNA. Each tRNA only binds the appropriate amino acid for its anticodon.

RNA

RNA has the same primary structure as DNA. It consists of a sugar-phosphate backbone, with nucleotides attached to the 1' carbon of the sugar. The differences between DNA and RNA are that: 1. RNA has a hydroxyl group on the 2' carbon of the sugar (thus, the difference

between deoxyribonucleic acid and ribonucleic acid.2. Instead of using the nucleotide thymine, RNA uses another nucleotide called

uracil: 3. Because of the extra hydroxyl group on the sugar, RNA is too bulky to form

a stable double helix. RNA exists as a single-stranded molecule. However, regions of double helix can form where there is some base pair complementation (U and A , G and C), resulting in hairpin loops. The RNA molecule with its hairpin loops is said to have a secondary structure.

4. Because the RNA molecule is not restricted to a rigid double helix, it can form many different stable three-dimensional tertiary structures.

tRNA ( transfer RNA)is a small RNA that has a very specific secondary and tertiary structure such that it can bind an amino acid at one end, and mRNA at the other end. It acts as an adaptor to carry the amino acid elements of a protein to the appropriate place as coded for by the mRNA. T

Secondary structure of tRNA

Three-dimensional Tertiary structure

Most of the consensus sequences are known from ecoli studies. So for each bacteria the exact distribution of consensus will change.

Most modern gene prediction programs need to be “trained”. E.g. they find their own consensus and assembly rules given a few examples genes.

A few programs find their own rules from a completely unannotated bacterial genome by trying to find conserved patterns. This is feasible because ORF’s restrict the search space of possible gene candidates.

E.g. selfid program([email protected])

Bacterial Gene Prediction

Open Reading Frames

The simplest bacterial gene prediction techniques simply

1) identify all open reading frames(ORFs),

2) and blastx them against known proteins.

3) The ORFs with the best homology are retained first.

4) This usually densely covers the bacterial genomes with genes. rRNA and tRNA are detected separately using tRNAScan or blastn.

Open Reading Frames (ORF)On a given piece of DNA, there can be 6 possible frames. The ORF can be either on the + or minus strand and on any of 3 possible frames

Frame 1: 1st base of start codon can either start at base 1,4,7,10,...



(frame –1,-2,-3 are on minus strand)

Some programs have other conventions for naming frames.. (0..5, 1-6, etc)

Gene finding in eukaryotic cDNA uses ORF finding +blastx as well.

http://www.ncbi.nlm.nih.gov/gorf/gorf.html

try with gi=41 ( or your own piece of DNA)

In Eukaryotes ( cells where the DNA is sequestered in a separate nucleus) The DNA does not contain a duplicate of the coding gene, rather exons must be spliced. ( many eukaryotes genes contain no introns! .. Particularly true in ´lower´ organisms)mRNA – (messenger RNA) Contains the assembled copy of the gene. The mRNA acts as a messenger to carry the information stored in the DNA in the nucleus to the cytoplasm where the ribosomes can make it into protein.

Eukaryotic Central Dogma

Eukaryotic Nuclear Gene Structure

Gene prediction for Pol II transcribed genes.

• Upstream Enhancer elements.

• Upstream Promoter elements.

• GC box(-90nt) (20bp), CAAT box(-75 nt)(22bp)

• TATA promoter (-30 nt) (70%, 15 nt consensus (Bucher et al (1990))

• 14-20 nt spacer DNA

• CAP site (8 bp)

• Transcription Initiation.

• Transcript region, interrupted by introns. Translation Initiation (Kozak signal 12 bp consensus) 6 bp prior to initiation codon.

• polyA signal (AATAAA 99%,other)

•Transcript region, interrupted by introns. Each introns

•starts with a donor site consensus (G100T100A62A68G84T63..)

•Has a branch site near 3’ end of intron (one not very conserved consensus UACUAAC)

•ends with an acceptor site consensus. (12Py..NC65A100G100)

AGUACUAAC

introns

•The exons of the transcript region are composed of:

•5’UTR (mean length of 769 bp) with a specific base composition, that depends on local G+C content of genome)

•AUG (or other start codon)

•Remainder of coding region

•Stop Codon

•3’ UTR (mean length of 457, with a specific base composition that depends on local G+C content of genome)

Exons

~6-12% of human DNA encodes proteins(higher fraction in nematode)

~10% of human DNA codes for UTR

~90% of human DNA is non-coding.

Structure of the Eukaryotic Genome

Untranslated regions (UTR’s)

•introns (can be genes within introns of another gene!)

•intergenic regions.

- repetitive elements

- pseudogenes (dead

genes that may(or not) have been retroposed back in the genome as a single-exon “gene”

Non-Coding Eukaryotic DNA

Pseudogenes:

Dna sequence that might code for a gene, but that is unable to result in a protein. This deficiency might be in transcription (lack of promoter, for example) or in translation or both.

Processed pseudogenes:

Gene retroposed back in the genome after being processed by the splicing apperatus. Thus it is fully spliced and has polyA tail.

Insertion process flanks mRNA sequence with short direct repeats.

Thus no promoters.. Unless is accidentally retroposed downstream of the promoter sequence.

Do not confuse with single-exon genes.

Pseudogenes

Each repeat family has many subfamilies.

- ALU: ~ 300nt long; 600,000 elements in human genome. can cause false homology with mRNA. Many have an Alu1 restriction site.

- Retroposons. ( can get copied back into genome)

- Telltale sign: Direct or inverted repeat flank the repeated element. That repeat was the priming site for the RNA that was inserted.

LINEs (Long INtersped Elements)

L1 1-7kb long, 50000 copies

Have two ORFs!!!!! Will cause problems for gene prediction programs.

SINEs (Short Intersped Elements)

Repeats

Low-Complexity Elements

• When analyzing sequences, one often rely on the fact that two stretches are similar to infer that they are homologous (and therefore related).. But sequences with repeated patterns will match without there being any philogenetic relation!

• Sequences like ATATATACTTATATA which are mostly two letters are called low-complexity.

• Triplet repeats (particularly CAG) have a tendency to make the replication machinery stutter.. So they are amplified.

• The low-complexity sequence can also be hidden at the translated protein level.

•To avoid finding spurious matches in alignment programs, you should always mask out the query sequence.

•Before predicting genes it is a good idea to mask out repeats (at least those containing ORFs).

•Before running blastn against a genomic record, you must mask out the repeats.

•Most used Programs:

CENSOR:

Repeat Masker:

http://ftp.genome.washington.edu/cgi-bin/RepeatMasker

Masking

More Non-Protein genes

rRNA - ribosomal RNA is one of the structural components of the ribosome. It has sequence complementarity to regions of the mRNA so that the ribosome knows where to bind to an mRNA it needs to make protein from.

snRNA - small nuclear RNA is involved in the machinery that processes RNA's as they travel between the nucleus and the cytoplasm.

hnRNA – hetero-nuclear RNA.small RNA involved in transcription.

The protein as read off from the mRNA may not be in the final form that will be used in the cell. Some proteins contains

• Signal Peptide (located at N-terminus (beginning)), this signal peptide is used to guide the protein out of the nucleus towards it´s final cellular localization. This signal peptide is cleaved-out at the cleavage site once the protein has reach (or is near) it´s final destination.

•Various Post-Translational modifications (phosphorylation)

The final protein is called the “mature peptide”

Protein Processing & localization.

Because the mRNA is actually read off the minus strand of the DNA, the nucleotide sequence are always quoted on the minus strand.

In bioinformatics the sequence format does NOT make a difference between Uracil and Thymine. There is no symbol for Uracil.. It is always represented by a ´T´

Even genomic sequence follows that convention. A gene on the ´plus´ strand is quoted so that it is in the same strand as it´s product mRNA.

Convention for nucleotides in database

Biology Information on the Internet

Biology Information on the Internet

• Introduction to Databases

• Searching the Internet for Biology Information.– General Search methods– Biology Web sites

• Introduction to Genbank file format.

• Introduction to Entrez and Pubmed

• Ref: Chapters 1,2,5,6 of “Bioinformatics”

• Databases:– A collection of Records.

– Each record has many fields.– Each field contain specific information.– Each field has a data type.

» E.g. money, currency,Text Field, Integer, date,address(text field) ,citation (text field)

– Each record has a primary key. A UNIQUE identifier that unambiguously defines this record.

gi Accession version date Genbank Division taxid organims Number of Chromosomes6226959 NM_000014 3 06/01/00 PRI 9606 homo sapiens 22 diploid + X+Y6226762 NM_000014 2 10/12/99 PRI 9606 homo sapiens 22 diploid + X+Y4557224 NM_000014 1 02/04/99 PRI 9606 homo sapiens 22 diploid + X+Y

41 X63129 1 06/06/96 MAM 9913 bos taurus 29+X+Y

Spread-sheet

Flat-file version of a database.



Gi = Genbank Identifier: Unique Key : Primary Key

GI Changes with each update of the sequence record.

Accession Number: Secondary key: Points to same locus and sequence despite sequence updates.

Accession + Version Number equivalent to Gi



gi Accession version date Genbank Division taxid6226959 NM_000014 3 01/06/2000 PRI 96066226762 NM_000014 2 12/10/1999 PRI 96064557224 NM_000014 1 04/02/1999 PRI 9606

41 X63129 1 06/06/1996 MAM 9913

taxid organims Number of Chromosomes9606 homo sapiens 22 diploid + X+Y9913 bos taurus 29+X+Y

Relational Database (Normalizing a database for repeated sub-elements of a database.. Splitting it into smaller databases, relating the sub-databases to the first one using the primary key.)

Types of Relational databases.

• The Internet can be though of as one enormous relational database.– The “links”/URL are the primary keys.

• SQL (Standard Query Language)– Sybase; Oracle ; Access; (Databases systems)

• Sybase used at NCBI.

– SRS(One type of database querying system of use in Biology)

Indexed searches.• To allow easy searching of a database, make

an index.

• An index is a list of primary keys corresponding to a key in a given field (or to a collection of fields)

Genbank divisionPRI 6226959;6226762;4557224;…MAM 41;…

AccessionNM_0000146226959;6226762;4557224;X63129 41;

Indexed searches.• Boolean Query: Merging and Intersecting lists:

– AND (in both lists) (e.g. human AND genome)– +human +genome

– human && genome

– OR (in either lists) (e.g. human OR genome)– human || genome

Search strategies• Search engines use complex strategies that go

beyond Boolean queries.– Phrases matching:

• human genome -> “human genome”

– togetherness: documents with human close to genome are scored higher.

– Term expansion & synomyms:• human -> homo sapiens

– neigbours:– human genome-> genome projects, chromosomes,genetics

– Frequency of links (www.google.com)• To avoid these term mapping, enclose your queries in quotes:

“human” AND “genome”

Search strategies• Search engines use complex strategies that

go beyond Boolean queries.

• To avoid these term mapping, enclose your queries in quotes: “human” AND “genome”

• To require that ALL the terms in your query be important, precede them with a “+” . This also prevents term mapping.

• To force the order of the words to be important, group sentences within strings. “biology of mammals”.

Indexed searches.Example

• find the advanced query page at http://www.altavista.com

• type human (and hit the Search button)• Type genome: • type human AND genome• type “human genome” (finds the least matches)• type human OR genome (finds the most matches)

• Search Engines:– Web Spiders: Collection of All web pages, but

since Web pages change all the time and new ones appear, they must constantly roam the web and re-index.. Or depend on people submitting their own pages.

• www.google.com (BEST!)

• www.infoseek.com

• www.lycos.com

• www.exite.com

• www.webcrawler.com

• www.lycos.com

• www.looksmart.com (country specific)

http://www.google.com/

• Search Engines:• www.google.com (BEST!)

• Google ranks pages according to how many pages with those terms refer to the pages you are asking for. Not only must one document contain ALL the search terms, but other documents which refer to this one must also contain all the terms.

• Great when you know what you are looking for! You can also use “” to require immediate proximity and order of terms.

• E.g. type» Web server for the blast program.

But google only indexes about 40% of the web.. So you may have to use other web spiders.

(disclaimer.. I don’t own stock in that company.. But I’d like to)

http://www.google.com/

• Search Engines:– Curated Collections: Not comprehensive:

Contains list of best sites for commonly requested topics, but is missing important sites for more specialized topics (like biology)

• www.yahoo.com (Has travel maps too!)

– Answer-based curated collections: Easy to use english-like queries. First looks at list of predefined answers, then refines answers based on user interaction. Also answer new questions.

• www.askjeeves.com• www.magellan.com• www.altavista.com(has translation TOOLS)• www.hotbot.com

• Search Engines:– Meta-Search Engines: Polls several search

engines, and returns the consensus of all results. Is likely to miss sites, but the sites it returns are very relevant to the query.

– Other operating mode is to return the sum of all the results.. Then becomes very sensitive to a very detailled query.

• www.metacrawler.com

• www.savvysearch.com

• www.1blink.com (fast)

• www.metafind.com

• www.dogpile.com

• Virtual Libraries: Curated collections of links for Biologists.(by Biologists)– Pedro’s BioMolecular Research Tools:(1996)

• http://www.public.iastate.edu/~pedro/

– Virtual Library: Bio Sciences• http://vlib.org/Biosciences.html

– Publications and abstract search.• http://www.ncbi.nlm.nih.gov/

– Expasy server• http://www.expasy.ch

– EBI Biocatalog (software & databases list)• http://www.ebi.ac.uk/biocat/

Biological Databases• Nucleotide databases:

– Genbank: International Collaboration• NCBI(USA), EMBL(Europe), DDBJ (Japan and Asia)

• A “bank” No curation.. Submission to these database is required for publication in a journal.

– Organism specific databases (Exercize: Find URLs using search engines)

• FlyBase

• ChickGBASE

• pigbase

• wormpep

• YPD (Yeast Protein Database)

• SGD(Saccharomyces Genome Database)

• Protein Databases:– NCBI:

– Swiss Prot:(Free for academic use, otherwise commercial. Licensing restrictions on discoveries made using the DB. 1998 version free of any licensing)

• http://www.expasy.ch(latest pay version)

• NCBI has the latest free version.

• Translated Proteins from Genbank Submissions

– EMBL• TrEMBL is a computer-annotated supplement of SWISS-PROT

that contains all the translations of EMBL nucleotide sequence entries not yet integrated in SWISS-PROT

– PIR

• Structure databases:– PDB: Protein structure database.

• Http://www.rscb.org/pdb/

– MMDB: NCBI’s version of PDB with entrez links.

• Http://www.ncbi.nlm.nih.gov

• Genome Mapping Information:– http://www.il-st-acad-sci.org/health/genebase.html

– NCBI(Human)– Genome Centers:

• Stanford, Washington University, Stanford

– Research Centers and Universities

• Litterature databases:– NCBI: Pubmed: All biomedical litterature.

• Www.ncbi.nlm.nih.gov• Abstracts and links to publisher sites for

– full text retrieval/ordering– journal browsing.

– Publisher web sites.– Biomednet: Commercial site for litterature

search.

• Pathways Database:– KEGG: Kyoto Encyclopedia of Genes and

Genomes: www.genome.ad.jp/kegg/kegg/html

• Database Identifiers: Primary keys– GI (changes with each sequence update for

NCBI only)• Annotation may change without the gi changing!

– Accession(stable)– version(changes with each sequence update)– “Version” also refers to Accession.version– Secondary accession: Records may have been

merged in the past.. So the records which were not chosen as the primary were made secondary.

Primary Databases

• A primary Database is a repository of data derived from experiments or from research knowledge.– Genbank (Nucleotide repository)– Protein DB, Swissprot– PDB (MMDB) are primary databases.– Pubmed (litterature)– Genome Mapping databases.– Kegg Database.(pathways)

Secondary Databases

• A secondary database contains information derived from other sources.– Refseq (Currated collection of Genbank at

NCBI)– Unigene (Clustering of ESTs at NCBI)

• Organism-specific databases are often a mix between primary and secondary.

Genbank Records• A Bank: No attempt at reconciliation.• Submit a sequence Get an Accession Number!

– Cannot modify sequences without submitter’s consent. – No attempt at reconciliation.(not a unique collection

per LOCUS/gene)– Entries of various sequence quality and different

sources==> Separate in various divisions based on• High Quality sequences in taxon specific divisions.• Low Quality sequences in Usage specific databases.

• A Collaboration between NCBI, EMBL and DDBJ. They contain (nearly) the same information, only the data format differs.

EMBL does not differentiate between the different types of RNA records, while NCBI (and DDBJ) do. In Entrez EMBL records are patched up to add that information.

Refseq and LocusLink• Attempt to produce 1 mRNA, 1 protein, and

1 genomic gene for each frequently occuring allele of a protein expressing gene.

• www.ncbi.nlm.nih.gov/LocusLink• Special non-genbank Accession numbers

– NM_nnnnnn mRNA refseq– NP_nnnnnn protein refseq– NC_nnnnnn refseq genomic contig– NT_nnnnnn temporary genomic contig– NX_nnnnnn predicted gene

http://www.ncbi.nlm.nih.gov/LocusLink

Genbank divisions

Sequences in genbank are split into various categories based on

1) The quality and type of sequences

2) The high quality nucleotide sequences are divided into organism-dependant divisions.

• Genbank Entry type: (and query to restrict to that field)– mRNA (1/10000 errors)

• biomol_mRNA [PROP]– cDNA (EST, 95-99% accuracy, single pass )

• gbdiv_EST [PROP]– genomic ( biomol_genomic [PROP])

• in HTGS division: >99% accuracy;– gbdiv_HTG [PROP]

• GSS(low-quality genome survey sequences)– gbdiv_GSS [PROP]

• rest of Genbank; 1/10000 accuracy.– Human gbdiv_PRI [PROP]– mouse gbdiv_ROD [PROP]– bovine gbdiv_MAM [PROP]

– STS(EST or cDNA used in mapping)• gbdiv_STS [PROP]

FASTA Format

>identifier descriptive text

nucleotide of amino-acid

sequence on multiple lines if needed.

Example:>gi|41|emb|X63129.1|BTA1AT B.taurus mRNA for alpha-1-anti-trypsin

GACCAGCCCTGACCTAGGACAGTGAATCGATAATGGCACTCTC

CATCACGCGGGGCCTTCTGCTGCTGGC ….

MOST important data format!!!

Modified FASTA Format

1) A few tools follow the convention that lower case sequences are masked. (repeat masker, some versions of blast, megablast, blastz)

2) A few analysis tools (like CLUSTAL) want a simplified identifier on the defline.. So they can have a short string for the alignment.

>X63129.1GACCAGCCCTGACCTAGGACAGTGAATCGATAATGGCACTCTCCATCACGCGGGGCCTTCTGCTGCTGGC ….

• WIM now will talk about GCG …

Feature table(NCBI;EMBL/DDBJ)

• http://www.ncbi.nlm.nih.gov/collab/FT/index.html

http://www.ncbi.nlm.nih.gov/collab/FT/index.html

http://www.ncbi.nlm.nih.gov/collab/FT/index.html

Genbank Data format

• LOCUS BTA1AT 1380 bp mRNA MAM 30-APR-1992

• DEFINITION B.taurus mRNA for alpha-1-antitrypsin.

• ACCESSION X63129

• NID g41

• VERSION X63129.1 GI:41

• KEYWORDS alpha-1 antitrypsin; serine protease inhibitor; serpin.

• SOURCE Bos taurus.

• ORGANISM Bos taurus

• Eukaryota; Metazoa; Chordata; Vertebrata; Mammalia; Eutheria;

• Artiodactyla; Ruminantia; Pecora; Bovoidea; Bovidae; Bovinae; Bos.

41

http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=41&form=6&db=n&Dopt=g

Genbank References• LOCUS BTA1AT 1380 bp mRNA MAM 30-APR-1992

• ...

• REFERENCE 1 (bases 1 to 1380)

• AUTHORS Sinha,D.

• TITLE Direct Submission

• JOURNAL Submitted (22-OCT-1991) D. Sinha, Dept of Biochemistry, Temple University, 3400 North Broad Street, Philadelphia, PA

19140, USA

• REFERENCE 2 (bases 1 to 1380)

• AUTHORS Sinha,D., Bakhshi,M.R. and Kirby,E.P.

• TITLE Complete cDNA sequence of bovine alpha 1-antitrypsin

• JOURNAL Biochim. Biophys. Acta 1130 (2), 209-212 (1992)

• MEDLINE 92223096

• FEATURES Location/Qualifiers

•

Genbank Source Qualifier• LOCUS BTA1AT 1380 bp mRNA MAM 30-APR-1992

• ...

• FEATURES Location/Qualifiers

• source 1..1380

• /organism="Bos taurus"

• /db_xref="taxon:9913"

• /tissue_type="liver"

• /cell_type="hepatocyte"

• /clone_lib="lambda gt11"

• /clone="2f-Ic"

• mRNA <1..>1380

• sig_peptide 33..104

• ...

Genbank mRNA+CDS features• mRNA <1..>1380

• sig_peptide 33..104

• CDS 33..1283

• /codon_start=1

• /product="alpha-1-antitrypsin"

• /protein_id="CAA44840.1"

• /db_xref="PID:g42"

• /db_xref="GI:42"

• /db_xref="SWISS-PROT:P34955"

• /translation="MALSITRGLLLLAALCCLAPISLAGVLQGHAVQETDDTSHQEAACHKIAPNLANFAFSIYHHLAHQSNTSNIFFSPVSIASAFAMLSLGAKGNTHTEILKGLGFNLTELAEAEIHKGFQHLLHTLNQPNHQLQLTTGNGLFINESAKLVDTFLEDVKNLYHSEAFSINFRDAEEAKKKINDYVEKGSHGKIVELVKVLDPNTVFALVNYISFKGKWEKPFEMKHTTERDFHVDEQTTVKVPMMNRLGMFDLHYCDKLASWVLLLDYVGNVTACFILPDLGKLQQLEDKLNNELLAKFLEKKYASSANLHLPKLSISETYDLKSVLGDVGITEVFSDRADLSGITKEQPLKVSKALHKAALTIDEKGTEAVGSTFLEAIPMSLPPDVEFNRPFLCILYDRNTKSPLFVGKVVNPTQA"

• mat_peptide 105..1280

• /product="alpha-1-antitrypsin"

• polyA_signal 1343..1348

• polyA_site 1368

Genbank Sequence format• ...• BASE COUNT 357 a 413 c 322 g 288 t• ORIGIN • 1 gaccagccct gacctaggac agtgaatcga taatggcact ctccatcacg cggggccttc• 61 tgctgctggc agccctgtgc tgcctggccc ccatctccct ggctggagtt ctccaaggac• 121 acgctgtcca agagacagat gatacatccc accaggaagc agcgtgccac aagattgccc• 181 ccaacctggc caactttgcc ttcagcatat accaccattt ggctcatcag tccaacacca• 241 gcaacatctt cttctccccc gtgagcatcg cttcagcctt tgcgatgctc tccctgggag• 301 ccaagggcaa cactcacact gagatcctga agggcctggg tttcaacctc actgagctcg• 361 cagaggctga gatccacaaa ggctttcagc atcttctcca caccctgaac cagccaaacc• ...• 1321 gtccccccac tccctccatg gcattaaagg atgactgacc tagccccgaa aaaaaaaaaa• //

EMBL DATA FORMAT

• Embl: http://www.ebi.ac.uk/Databases/

• http://www.ebi.ac.uk/cgi-bin/emblfetch

• Use Accession X63129

http://www.ebi.ac.uk/Databases/

http://www.ebi.ac.uk/cgi-bin/emblfetch

DDBJ DATA FORMAT

• DDBJ: http://www.ddbj.nig.ac.jp/

• http://ftp2.ddbj.nig.ac.jp:8000/getstart-e.html

• Use Accession X63129

• Flat file format same as NCBI/Genbank format.

http://www.ddbj.nig.ac.jp/

Entrez• Index Based search system. Each field in

the database is searchable individually or as agregate. – (e.g. CDS [FKEY]) – default is agregate [ALL FIELDS] *

• All primary databases are interlinked as one big relational database.– (e.g. Pubmed links in Genbank records)

• Phrase matching.– Human genome -> “human genome”

Entrez

• Available neighbours (related documents or related sequences)

• In Pubmed searches: Term mapping to neighbouring documents and neighbouring terms.

• Term mapping to chemical names.– In pubmed: term [All Fields] is term mapped to

chemical names + MeSH terms + Text Fields.

– .. Unless “term” is whithin double quotes.

Entrez

• http://www.ncbi.nlm.nih.gov/Entrez/

• Tutorials:• http://www.ncbi.nlm.nih.gov/Class/

MLACourse/Genetics/index.html • http://www.ncbi.nlm.nih.gov/Literature/pubmed_s

earch.html• http://www.ncbi.nlm.nih.gov/Database.tut1.html

http://www.ncbi.nlm.nih.gov/Entrez/

http://www.ncbi.nlm.nih.gov/Literature/pubmed_search.html

http://www.ncbi.nlm.nih.gov/Literature/pubmed_search.html

http://www.ncbi.nlm.nih.gov/Database.tut1.html









SWISSPROT

1. Core data: protein sequence data; the citation information and the

taxonomic data2. Annotation

• Function(s) of the protein • Domains and sites. For example calcium binding regions, ATP-

binding sites, zinc fingers, homeobox, kringle, etc. • Post-translational modification(s). For example carbohydrates,

phosphorylation, acetylation, GPI-anchor, etc. • Secondary structure • Quaternary structure. For example homodimer, heterotrimer, etc. • Similarities to other proteins • Disease(s) associated with deficiencie(s) in the protein • Sequence conflicts, variants, etc.

http://www.expasy.ch/sprot/sprot_details.html

SWISSPROT

http://www.expasy.ch/cgi-bin/get-random-entry.pl?S

REBASE (Restriction enzymes dataBASE)

Restriction enzymes have a pattern recognition sequence, and then within or a few bases away from that pattern is the actual cutting site

http://rebase.neb.com/rebase/rebase.htmlI prefer the bairoch format (SWISSPROT format)http://rebase.neb.com/rebase/rebase.f19.htmlID enzyme name ET enzyme type OS microorganism name PT prototype RS recognition sequence, cut site MS methylation site (type) CR commercial sources for the restriction enzyme CM commercial sources for the methylase RN [count] RA authors RL jour, vol, pages, year, etc.

http://rebase.neb.com/rebase/rebase.html

http://rebase.neb.com/rebase/rebase.f19.html

Exercises

•You can work in teams for this.

•1a) Use the first 6000 bases of your genomic piece [ or find a bacterial genomic or mRNA sequence in Entrez with length between 2000:10000 ]

•b) Use the ORF finder to find the gene(s). Compare the answer you get to the annotation you can infer from using blastn against genbank and to using blastx against a protein database.

•Do the Entrez exercizes. ( separate word document)

Education

Central dogma