Genome annotation Flashcards

1
Q

Two diff types of genome annotiaton?

A

Structural and functional

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2
Q

Structural genome annotation?

A

General idea about what each sequence might be–> has a funciton/doesnt

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3
Q

Functional genome annotation?

A

More specific idea of what each sequence it–> mRNA (coding), rRNA (noncoding)

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4
Q

What do a lot of genes start with?

A

ATG–> Methionine

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5
Q

Stop codons?

A

TAA, TAG, TGA

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6
Q

How can algorithm be designed to search for coding genes?

A

Look for start and stop codons in appropriate distances

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7
Q

What must be the same ab a start and stop codon of a possible gene?

A

Must be on the same frame–> within the same multiple of three otherwise they wont be translated together

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8
Q

How many open reading frames are there?

A

6

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9
Q

Why are there 6 ORFs?

A

three possible start places in the DNA bc three nucleotides is a codon, *2 bc of the opposite strand of DNA

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10
Q

Why does ORF scanning work better in pro than in eukaryotes?

A

Smaller genomes, higher gene density, litle gene overlap, introns in eukayotes

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11
Q

What is gene overlap?

A

Opposite strands that face each other in the nucleotide sequence both coding for genes

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12
Q

Why do introns make it difficult to find possible gene sequences?

A

They can put the sequence out of frame

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13
Q

What is codon bias?

A

WHen multiple codons can encode the same AA, diff organisms might have a bias to use some codons to code an AA more than the others that acn code for that AA

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14
Q

Why may codon bias exist?

A

For organisms to be able to differentiate their DNA from foreign DNA
May affect transcription rate

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15
Q

How can codon bias be used to help estimate where a gene is?

A

If a sequence has a lot of codons that aren’t really used by that organism to encode the specific AA, it might not be a coding sequence

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16
Q

What is the intron exon boundary?

A

There is often a GT in between exons and introns

17
Q

How is homology used to find possible gene sequences?

A

If a sequence looks similar to a known sequence that is known to code for a gene then that sequence probably codes for a similar gene

18
Q

Issue with using homology?

A

If the gene you have found is new/unknown, there wont be homology for it

19
Q

What are orthologous genes?

A

present in different species, similar through inheritance from common ancestor

20
Q

What are paralogous genes?

A

similar genes within the same species forming a gene family. Often the result of duplications, followed by neo functionalization

21
Q

What is synteny?

A

When sequence from different species keep genes in the same order across the chromosome

22
Q

Benefits of synteny for gene annotation?

A

Can help confirm predicted genes, and determine function by homology

23
Q

What was observed when looking for coding genes in synteny?

A

Many sequences were in synteny across organisms, but were not actually coding genes

24
Q

Drawbacks of using homology and synteny?

A

Amplification of mistakes in previous genome sequencing

25
How does RNA sequencing help gene identificaiotn?
If the RNA is sequenced it will map to the genome where it came from--> that DNA sequence codes for the RNA and so may be a coding gene
26
Issue with using RNA sequencing for gene identificaiotn?
Genes dont produce RNA all the time, so a genes RNA may not be present in the cell at the time of sequencing
27
Can using RNA to find genes produce false +ves or false -ves?
False -ves
28
What are GO categories?
Assignment of genes to a set of categories
29
What can GO categories be based on?
Molecular function, cellar component, biological processes
30
How can the function of genes be looked at experimentally?
Expression patterns, mutating genes, knockouts
31
What can RNAi be used for?
Silencing a specific sequence
32
Issue with knockouts?
A gene being knocked out and causing a phenotypic effect doesn't necessarily mean that it is the "gene for x"--> other genes could be involved
33
False -ves?
sequences that have a function, but the function has not been identified
34
False -ve e.g.?
small and micro RNAs, genes in hard to sequence regions
35
Possible gene status?
false -ves, predicted genes w/ unknown function, predicted genes w/ predicted function, conformed genes
36
Most important genes to look at across species?
Ones that are v highly conserved
37