Gene Structure Flashcards
1
Q
Bacterial genomes
A
- organised into operons with similar genes grouped
- distinct boundaries and regulation
- highly evolved
- economical/efficient
2
Q
Eukaryotic genomes
A
- low numbers of protein coding genes
- non coding repeats made up 50% of genome
- small genes hard to locate
- gene density surprisingly low (introns, repeat regions)
- functional RNAs common
- uneven gene distribution with gene rich and gene desert regions
3
Q
Chromosome Structure
A
- two sister chromatids held by a centromere
4
Q
Other DNA
A
- B chromosomes: extra chromosomes to standard complement
- holocentric chromosomes: entire chromosome is a centromere
- extrachromosomal DNA: plasmids/organelle DNA
5
Q
Organelle Genomes
A
- mitochondrial DNA: covalently closed circular DNA
- chloroplast DNA: single closed circular DNA
- photosynthesis genes
6
Q
Genome Sectios
A
- unique and repeat regions
- 62% of genome is an intergenic region between genes (transposons, LINEs, SINEs, LTR elements
7
Q
Repeated Intergenic Regions
A
- differs in GC content
- may have structural role (like telomeres)
- tandemly repeated DNA
- interspersed repeats (genome-wide repeats)
8
Q
Satellite DNA
A
Satellite DNA (satDNA) is the highly repetitive DNA consisting of short sequences repeated a large number of times. It carries a variable AT-rich repeat unit - a and B satellite family
9
Q
Tandemly Repeated DNA
A
- much shorter than satellite DNA
- minisatellites
- associated with structural features
- 10-100 bp
- microsatellites
- simple tandem repeats
- telomeres or dinucleotide repeats
- less than 13 bp
10
Q
Satellite Formation
A
Replication slippage: daughter strand slips back 1 repeating unit
Tandemly repeated DNA: DNA recombination and unequal crossing over
Variable Number Tandem Repeats: used in identificatoin
11
Q
Interspersed Repeats
A
- genome wide repeats (more than 100 bp)
- moderately repetitive
- transposon derived repeats: SINE, LINE, DNA transposons, LTR retrotransposons
12
Q
DNA Transposon
A
- target DNA cut by transposases
- intermediate DNA inserted and ligated into sequence
- flanked by direct repeats
13
Q
Maize Transposon
A
- excision of TE in somatic cells leads to pigment gene
- small spots: late excision
- large spot: excision early in development
- no excision autonomous element not in genome
- revertant: element excised and full expression restored
14
Q
LINEs
A
long interspersed nuclear elements
- RNA transcribed and inserted back into genome at new site
- ORF1: RNA binding protein
- ORF2: reverse transcriptase
15
Q
SINEs
A
short interspersed nuclear elements
- high copy number
- no genes
- transcribed by RNAPIII
- borrows transcriptase synthesized by LINEs
eg. Alu family
16
Q
Retrovirus Related Sequences
A
LTR Retrotransposons
Human endogenous retrovirus
17
Q
Purpose of Repeats
A
- metabolic burden
- rate of propagation must counteract rate of elimination
- maintenance suggests value
- nearly all genome is transcribed
- could cause evolutionary change
- could just be yet to be eliminated
18
Q
How a genome acquires new genes
A
- horizontal gene transfer
- exon shuffling
- duplication
19
Q
Benefits of Duplication
A
- new copy can acquire a new function due to selective pressure advantage
20
Q
Recombination Duplication
A
- unequal crossing over (misalignment)
- unequal sister chromatid exchange
- DNA amplification during replication
- replication slippage (adds extra unit to short repeat)
- retrotransposons
21
Q
Successful Gene Duplication
A
- 1 copy retains original sequence
- 2 copies may increase protein synthesis
- 1 copy may be neutral and become a nonfunctional pseudogene
- 1 copy may acquire new function (neofunctionalism)
22
Q
Neofunctionalism
A
- gene duplicates gaining mutations
- new gene function
- expressed in different time/cell type
eg. chymotrypsin and trypsin are both proteases but recognise slightly different residues : duplication of common ancestor
23
Q
Pseudogenes
A
- copies of functional genes with altered regions
- may contains frameshift mutations and have regulatory roles
- increase genome size
- if transcribed may form RNA homologous to functional RNA and regulate via interaction
24
Q
Processed Pseudogene
A
- tandem duplication of genomic region
- 1 copy lack of selection
- inactivating mutations/incomplete duplication
- missing regulatory regions
25
Q
Non-processed pseudogene
A
- reverse transcriptase activity
- mRNA to cDNA and genome integration
- lacks regulatory regions or introns
- derived from RNA
eg ribosomal pseudogenes: highly conserved large family
26
Q
Multigene families
A
- multigene families can arise from beneficial duplications
eg rRNA genes - tandem gene family on same chromosome
- dispersed gene family on different chromosome
27
Q
Globin Superfamily
A
- example of gene duplication and divergence
- colocation of dispersed clusters of genes
- natural selections coopts existing genes to innovate
- can create new useful properties
- having separate proteins for oxygen storage and transport with different binding affinities is useful
28
Q
Whole Genome Duplication
A
- could be a source of speciation as duplicated genomes can reproduce with parents
29
Q
Polyploidy
A
- multiple sets of chromosomes
- widespread in plant groups as having more DNA creates a larger fruit or flower product
- can induce genomic shock
30
Q
Autoploidy
A
- multiplication of identical species within a single species
- fertilisation by unreduced gametes
- meiosis error accidentally producing diploid gametes so a triploid offspring
- more viable than allopolyploids
- can reproduce with each other permitting speciation
31
Q
Alloploidy
A
- hybridisation between 2 reproductively compatible species
- via unreduced gametes from 2 diploid species (one step model)
- via hybridisation between haploid gametes and somatic doubling (two step model)
32
Q
Triploid Wheat-Rye Hybrid
A
- yield of wheat with disease tolerance of rye
- tetraploid wheat crossed with diploid rye to give triploid triticale seed
- can artificially double chromosomes in sterile plant for fertilization with doubled gametes to give fertile offspring
33
Q
Hox Gene Family
A
- WGD in metazoa led to evolution of organisational body plan complexity
- homeobox gene clusters in animal development are TF regulating developing with DBD
- different organisms have different repeats and clusters
34
Q
Hox Gene Expression
A
- expression in different embryo regions
- gene order reflects expression order
- spatial and temporal colinearity
- each specifies body segment structures
35
Q
2R/3R Theory
A
- Based on this model, two rounds of genome duplication occurred early in the vertebrate evolution [2, 3], but see also [4, 5]. An ancestral genome was duplicated to two copies after the first genome duplication (1R), and then to four copies after the second (2R) duplication [6, 7]. Recent data suggest that an additional whole genome duplication occurred in the fish lineage (3R or fish-specific genome duplication)
- Humans have 4 duplications
36
Q
Benefits of WGD
A
- evolutionary diversification
- defence against mutation
- colonisation of new environments
- improved fitness
- duplication of regulatory regions generates biological complexity like body plans
37
Q
Exon Shuffling Theory
A
- eukaryotic proteins are mosaics of motifs
- each domain has a specific function
- primordial exons correspond to domains
- duplication/insertion/rearrangements generate novel genes and proteins
38
Q
Illegitimate Nonhomologous Recombination
A
- process by which two unrelated double stranded segments of DNA are joined.
Duplication - unequal crossing over
- replication slippage
- increases gene length
Shuffling - domains from different genes joined together
- retrotransposition or INHR
eg. aA-crystallin gene transfected into mouse - heat shock protein
- domain duplication by illegitimate recombination and unequal crossing over
- TOPOI nicks DNA and ligates non-homologous ends
39
Q
LINEs and Gene Shuffling
A
- jump around using RNA intermediate and retrotransposition into genome
- transposition can take piece of DNA (3’ transduction)
- transcription reads through weak terminating signal
- domain retrotransposed
40
Q
Transposons and Gene Shuffling
A
- mutator like transposable elements
- inverted terminal repeats flanking exons/introns
- encode transposase moving themselves and other MULEs
41
Q
Intron Phases
A
- insertions and duplications affect reading frame
- need exact multiples of 3 in an exon to prevent this
- need intron phases the same
- either 2,1/1,2/3,0 insertions on either side
- Phase 0: introns lie between 2 codons (3,0)
- Phase 1: introns located after first nucleotide (1,2)
- Phase 2: introns located after second nucleotide (2,1)
42
Q
Splice Frame Rule
A
following a successful shuffling event a newly acquired exon will be flanked by 2 introns of the same phase otherwise it will produce a frameshift in resulting coding sequence
- preserving reading frame makes less of a target for purifying selection (no loss of function with frameshift)
43
Q
Evidence of Shuffling
A
multicellular structure
- adhesion/receptor molecules benefit from swapping domains to tune interactions
Franca et al.
- Phase 0 most common
- excess of symmetric exons compared to asymmetric
44
Q
Exon 1-1 Shuffling
A
- phase 0 introns more ancient and prevalent in non-Metazoan lineages
- 1/1 shuffling associated with emergence of necessary features of multi-cellularity
- 1:1 shuffle compatible with glycine codons (interupted)
- easily split
- increases efficiency of creating mosaic proteins
- acquisition of domain must overcome structural limitations
- small and flexible domains fold independently
- linker sequences have glycine more frequently
45
Q
Collagen Gene Shuffling
A
- a2 type 1 collagen gene
- highly repetitive sequence of glycine:x:y
- exons very glycine rich and can be split with 1:1 exon phase meaning they are compatible with large and repetitive protein collagen
46
Q
Tissue Plasminogen Activator Shuffling
A
- found in blood clotting in vertebrates
- 4 exons
- growth factor domain and plasminogen gene
- upstream exon encodes finger module
- ancestors from 3 domains formed the TPA structure
- common ancestor formed by duplication and adding exons to genes
47
Q
Exon Phases
A
These include the symmetric exons 0-0, 1-1, and 2-2 and the asymmetric exons 0-1, 0-2, 1-0, 1-2, 2-0, and 2-1, which can be joined into symmetric combinations. The symmetric exons (or exon sets) are the only ones that can be inserted into introns (of the same phase), undergo tandem duplication, or be deleted without disturbing the reading frame.
48
Q
Protein Protein Interaction
A
- mosaic proteins can interact with several proteins to become hubs of PPI networks
- shuffling promotes self interaction capacity
- formation of homodimeric proteins with self interacting domains
- new connection networks
49
Q
Amyloid Precursor Protein
A
- alternative splicing generates isoforms
- APP undergoes protease processing by a-secretase to give soluble APP
- processing by B scretase and gamma secretase to also give B-amyloid protein (amyloid plaques in Alzheimers)
- processing determined by KPI domain presence inhibiting a-secretase
- KPI domain gained by shuffling
- domain is flanked by introns
- similarity to metazoan protein
