How genes work and such Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

What modifications happen to mRNA after transcription? (post-transcriptional modifications)

A

5’ Capped and 3’ tailed.

5’Cap added to protect 5’ end and allow ribosome binding for translation.

3’ poly(A) tail added to protect tail. (tail circles back onto cap for translation)

Introns spliced out.

mRNA transported to cytoplasm

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is a retrovirus and what are some of its ssRNA components?

A

A ssRNA virus like HIV that carries out reverse transcription, inserting viral DNA into host genome.

Contains Repeat regions at either end for insertion purposes, gag, pol, env

Packaging signal for assembling new viruses from proteins such as:

Gag (group specific antigen): capsid protein

Pol: codes reverse transcriptase

Env: envelope protein.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

How is the RNA in RNA viruses translated?

(and define ambisense genome)

A

Either through reverse transcription to DNA in retroviruses or directly translated from RNA.

Direct translation can only occur if the ssRNA is sense (+) orientation, (runs in correct direction, start codon to stop codon)

If the ssRNA is antisense (-) then the sense + strand is made by viral enzyme RNA-dependent RNA polymerase. RdRp (making dsRNA)

Ambisense genome contains sense and antisense ssRNA.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Describe Genome, Transcriptome, Proteome:

A

Genome is all DNA, coding or not.

Transcriptome is an organism or specific cell’s repertoire of transcribed RNAs (differs between cells/tissues)

Proteome is a cell’s repertoire of translated proteins.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are enhancer regions?

A

Regions that alter (normally enhancing) the expression of a gene by interacting with it.

They can be near to, inside, or far from the enhanced sequence but must interact physically interact with the enhanced sequence.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is the role of small nuclear RNAs (snRNA)

A

They form the spliceosome to splice introns from pre-mRNA.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What is a twintron?

A

An intron within an intron! (intronception)

Small one spliced out first, then surrounding intron.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is the role of small nucleolar RNAs? snoRNA

A

Found in the nucleolus, where Ribosomes are made from rRNA.

snoRNA facilitates modification of rRNA.

By pairing with rRNA it induces methylation of cytosine bases.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Guide RNAs?

A

Guide RNAs are small RNAs found in some species (?humans?) that edit the sequence of other mRNA.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Role of microRNAs? miRNA

A

Post-transcriptional regulation of gene expression.

Bind to mRNA to inhibit translation, and speeds up deadenylation (removal of polyA tail and so destruction)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Production of micro RNAs?

A

miRNAs produced in the form of large stem-loop structures which are transported out of the nucleus and then diced into tiny sequences by dicer.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

siRNA?

A

Small interfering RNA, causes RNAinterference RNAi.

Enters as dsRNA (synthetic or viral) diced by Dicer in cytoplasm.

Binds to mRNA. causing its destruction by RISC (RNA induced silencing complex)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How to use/create synthetic siRNA to artificially silence genes?

A

Create dsRNA identical to the target gene (by incorporating promoters its transcription on both strands of dsDNA)

This dsRNA produced will be diced by Dicer and the segments incorporated into RISC which will then help siRNAs bind and degrade target gene.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What is the C-value paradox?

and how is it resolved?

A

C-value represents the total amount of DNA in the haploid genome.

The C-value paradox is the apparent lack of correlation between phenotypic/morphological complexity of an organism and the size of its c-value.

The paradox is explained because of variable amounts of ‘repetitive/”junk” DNA’

(doesn’t happen in bacteria and viruses because very little repetitive DNA)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Describe some ways some bacteria (and other organisms) can have small genomes (<1Mbp)

A

Simplistic metabolism/life cycle (e.g. endosymbiotic bacteria) Few regulatory genes etc.

Small intergenic regions, and overlapping genes!

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Why do some important bacterial chromosomal genes have increased copy number during DNA replication?

A

Because bacterial chromosomes (circular and typically 1 per bacteria) have only 1 origin of replication (ori) for the whole chromosome, genes closer to the origin are duplicated, relative to more distant genes.

[Genes often oriented in direction of replication (5’–>3’ away from ori (so half on + and half on - strand) so that replication and transcription machinery don’t collide.]

17
Q

What is an operon?

A

A group of genes transcribed as a single mRNA, transcription under the control of one promoter.

(even when not in an operon, genes involved in similar metabolic activities are grouped together in ‘clusters’)

18
Q

How to determine the function of a newly discovered gene?

A

Silence/Knock out the function of the gene and see what happens.

Inactivation of a gene can be acheived by:

Disrupting the sequence of the gene by:

Transposon mutagenesis or Homologous recombination with artificially altered/labelled sequence

Or by silencing gene with RNA interference!

19
Q

How to determine the minimum genome required to sustain cellular life?

A

Compare small bacterial genomes for shared genes.

Knock out all the genes systematically and see which aren’t needed.

Both methods produce a number just under 300 genes

20
Q

Roughly how many genes in the human genome?

A

30,000

about thirty thousand

21
Q

Of the 3200Mb of the human genome how many are associated with genes (what does this include)? and how many are in actual genes?

A

1200Mb (approx1/3) associated with genes (including pseudogenes, introns, untranslated regions)

48Mb of genes (about 1.5% of C-value)

22
Q

Why does DNA contain Thymine (as a pyrimidine pair for Adenine) whereas RNA contains Uracil?

A

Because Cytosine can be spontaneously deaminated to Uracil.

So if Uracil is found in DNA sequence it can be identified as wrong and fixed.

(RNA mutations don’t matter so much as they’re short lived, and Uracil costs less to make than Thymine)

23
Q

Why are CpG dimers so rare in vertebrates genomes?

A

Because the cytosine in CpG dimers is the target for methylation and methylated Cytosine can spontaneously deaminate to form Thymine!

(contrasted with normal cytosine deaminating to uracil)

24
Q

What does Cytosine methylation (of CpG dimers) do?

A

Cytosine methylation silences gene expression by recruiting histone deacetylases, which results in **tight packing of chromatin and so silencing of genes. **(such as in imprinting, X-chromosome inactivation etc)

25
Q

What are CpG islands?

A

Clusters of CpG repeats typically occur at the start of genes near the promoter region.

When unmethylated this indicates the presence of an actively transcribed gene, and their subsequent methylation would silence the gene, such as in imprinting.

26
Q

Why are cytosine methylation modification heritable?

A

Because in DNA replication maintenance methylation occurs, methylating the unmethylated strands opposite existing methylcytosines.

27
Q

Multigene families?

A

A set of related genes, paralogs created by gene duplications.

Similar functions.

28
Q

What are conventional and processed pseudogenes?

A

Conventional pseudogenes are versions of genes inactivated by mutations so they are no longer transcribed. Subsequent mutations can render them almost unrecognisable.

Processed pseudogenes are where mRNA has become reincorporated back into the DNA (by reverse transcription) (they lack introns and promoter sequences)

29
Q

What are interspersed repeated intergenic DNA?

A

All result from ‘transposable’ sequences that copy themselves into different places in the DNA with the help of transposase enzymes.

SINEs, LINEs, LTRs all transposed via RNA intermediates

DNA transposons don’t require an RNA intermediate.

30
Q

What are variable number tandem repeats?

A

Satellites, Minisatellites, Microsatellites.

Variation in copy number caused by replication slippage or by unequal crossing over (problems like NAHR but these aren’t genes)

31
Q

Use of variable number tandem repeats? VNTR

(non-coding, microsatellites, minisatellites etc)

A

Variation between individuals you get a different gel electrophoresis analysis results. (for DNA fingerprinting)

32
Q
A