Genome Projects Flashcards

1
Q

What is heterosis

A
Hybrid vigour (only in F1 offspring)
utilised by farmers to increase yields of hybrids by 15 - 60% relatice to inbred parents.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

size of maize genome

how much is TE?

A

2.9Gb size

85%

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

which approaches were used to sequence maize genome

A
  • Cultivar B73 selected because of widespread use in breeding
  • hierarchial approach to get sequence - BAC to BAC (30x coverage). 3 different BAC lbraries produced with 3 restriction enzymes.
  • 350253 BAC clones fingerprinted and assembled to 1500 contigs.
  • minimum tiling path of 16848 BACS picked for sequencing.
  • predicted protein encoding genes and miRNA genes from assembled BAC contigs using mix of evidence based and ab inito approaches.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are Helitrons?

How are they important for variation btw maize cultivars?

A
Very active class of DNA transposons in plants animals and fungi. 
Maize has 8 families of helitrons, forming 20000 copies. 
located in gene rich regions and often move gene fragments when transposed, moving genes and creating variation.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

mechanism of helitrons translocating

A

transposase molecules cleave donor and target sites.
ss TE inserts into target and may also move a flanking sequence from donor into target DNA.
replication of inserted sequence.

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

What did anchoring reference sequence of B73 maize to a genetic map show?

A

Unequal rate of meiotic recombination per megabase.

Highest recombination rate observed at the end of the chromosomes
low recombination rates were found surrounding the centromere.

Correlates with gene density

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

What caused a lot of chromosomal rearrangements in maize genome?

A

Whole genome duplication event, 5-12mya.
returned to diploid state.
Associated with numerous chr breakages and fusions - seen by alignment with genomes of sorghum and rice.
-most duplicated genes lost sue to extensive chr rearrangement, has retained just 8110 genes as duplicates.

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

what other methods was used to genetate maize genome, in 2017

A

whole genome shotgun approach.
using PacBio SMRT, assembled almost 3000 contigs. N50contig = 1.18Mb.

high quality optical map used on this assembly to create 625 scaffolds N50 scaffold length = 9.56Mb.

Error correction using Illumina short read seq.

new B73 assembly total size 2,105Mb.

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

difference in no genes in 2 versions of maize genome

A

version 2 had 39,324 genes, 6,784 more than version 1. 20%

Result of differences in assembly and annotation. no biological significance.

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

what is the Pan genome idea

A

pan-genome describes all genes and genetic variation within a species. - core genome portion common to all individuals, - dispensable genome is only in a subset or unique to individuals.

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

What is the HapMap project?

A

Haplotype map

  • 2012 published for maize
  • focussed on sequence diversity across 103 different maize lines +19 wild relatives.
  • sequenced with illumina and aligned to 2009 B73 reference genome. 4.2x coverage of each maize line.
  • 55million SNPs identified. 21% associated with genic region (a lot since only 1-2% of genome codes genes).
  • thousands of structural rearrangements.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

When was th ehuman genome project completed

What methods.

A

june 2000. 10 year effort.
Competition between public hierarchal approach, sector and private, Shotgun approach.
agreed a tie in june 2000.

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

what is the 1000 genomes project?

A

description of common human genetic variation.
whole genome sequencing to diverse set of individuals from multiple pops.
Completed 2015.
Discovered 60,000 structural variants.

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

How many structural variants in a typical human genome?

A

2100 - 2500

affect approx 20 million bases

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

How did the 1000 genomes project support ‘out of africa’ model of human origin?

A

showed individuals from African acestry had greatest number of variant sites.

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

why is sequencing ancient DNA difficult?

A

usually it is degraded into small molecules, <200bp, chemically modified and extracts contain large amounts of exogeneous DNA from microbes.

17
Q

How was neanderthal draft genome sequenced?

A

2010
21 bones from different sites
extracted and enriched DNA
seq on Illumina, 454 n solexa platformns

18
Q

what did analysis of neanderthal genome suggest?

A

gene flow from neanderthals into ancestors of non Africans occured before divergence of Eurasian groups.
1-4% of genome fo modern humans in Eurasia share genetic variants with neanderthals.