Introduction to Genetics and Genomics - key concepts Flashcards Preview

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Flashcards in Introduction to Genetics and Genomics - key concepts Deck (39)
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1

Define: gene

Specific stretch of DNA where the sequence contains genetic instructions

2

What are a few different ways in which variation in the genome arises?

1) alterations in the sequence of bases in a specific section of DNA - single nucleotide polymorphism (SNPs) or small deletions or duplications (few bases)

2) Larger deletions/duplications (copy number variation) of DNA segment - include one to many genes

3) Changes in the number or structure of chromosomes

SNPs are the most common mutations

3

What is the difference between chromosomal rearrangements and single base changes?

Chromosomal rearrangements are large
Single base changes are small

4

What is the difference between single nucleotide polymorphisms in population and mutations in a gene in one family?

SNPs in population = common
Mutation in a gene in one family = rare

5

What is the difference between non-harmful polymorphisms and variations that disrupt gene function

Non-harmful polymorphisms are non-pathogenic, whereas when gene function is disrupted they are pathogenic

6

When are polymorphisms not harmful?

occur in non-functional DNA
occur within gene but does not change amino acid
changes the amino acid but not the protein function

7

What is a defining factor in being a SNP?

a base changes has to have a frequency of >1%

8

What is PCR?

PCR takes advantage of the ability of nucleic acids to hybridise
Its a medical research and diagnostic tool
- take template DNA and add nucleotides and this reaction links nucleotides together to amplify the amount of DNA to enable you to carry out experiments

9

What is microarray analysis?

tells you which genes are turned on in different cells
- base level
-large blocks of DNA

10

What is karotyping?

using light microscopy you can look for differences between chromosomes to check for crossover for example

11

When do mutations occur and what causes them?

Cell division
Intrinsic and extrinsic attacks on DNA

12

What can be seen in interphase?

nuclear envelope intact
No chromosomes visible

13

What can be seen in prophase?

Chromosomes condense and become visible
Bipolar spindle develops

14

What can be seen in prometaphase?

Nuclear envelope dissolves
Chromosomes begin to migrate to equatorial plane and are seen to contain 2 chromatids

15

What can be seen in metaphase?

Chromosomes fully condensed and located at metaphase plate
Tension on kinetochores at centromeres facing opposite directions

16

What can be seen in anaphase?

Each centromere splits
The two chromatids of each chromosome are pulled to opposite poles

17

What can be seen in telophase?

Chromosomes reach poles and start to decondense
Nuclear membrane reforms
Cytoplasm starts to divide

18

What can be seen in cytokinesis?

Cytoplasm division completed to give two daughter cells

19

What questions need be considered at the different checkpoints of the cell division process?

Checkpoint in mitosis:
- Are all chromosomes properly attached to the mitotic spindle
G1 Checkpoint:
- Is the environment favourable
G2 checkpoint:
- Is all the DNA replicated?
- Is all DNA damage repaired?

20

How could errors in DNA replication and mitotic cell division cause human disease?

DNA replication: new mutations =copying errors
Chromosome segregation at mitotic cell division: anomalies of chromosome number = non-dysjunction

21

What is mosaicism?

some cells are affected by chromosomal anomalies while other cells are normal

22

What are the functions of meiosis?

Reduction division (23 chromosomes per gamete)
Reassortment of genes
Independent segregation of chromosomes crossing over

23

What is the mechanism of meiosis?

Each homologue replicates to give two chromatids -homologues pair
Exchange of material between non-sister chromatids - crossing over/recombination
Chiasmata (visible cytologically) are physical manifestations of crossing over - 2 chromosomes are linked to one another

24

How many potential different combinations are there after independent assortment of maternal and paternal homologues after meiosis 1?

8.4 million different combinations

25

What are the differences between gametogenesis in females and males?

In females you end up with one egg and in males you end up with 4 mature spermatozoa

26

How many cells divisions and how many oocytes have been produced by 5 months gestation in a female?

22 cell divisions producing a stock of 2,600,000 oocytes

27

What does deletion/insertion and substitution mutations cause?

cause gain of function or loss of function

28

What are silent mutations/sequence variant mutations?

A base pair change that does not change the amino acid sequence

29

What are missense mutations?

Missense: changes to a codon for another amino acid (can be harmful mutation or neutral polymorphism)

30

What is a non-sense mutation?

Non-sense:change from an amino acid codon to a stop codon