lecture 22 - human genome Flashcards

1
Q

What were the aims of the 1990 human genome project?

A

Identify all human genes and their roles, and analyse genetic variation between humans and other species.

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2
Q

How many base pairs are found in nuclear DNA?

A

6 billion

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3
Q

How many genes are found in the human genome?

A

Approximately 20,000

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4
Q

What is the structure of mitochondrial DNA?

A

Single stranded, circular

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5
Q

How many base pairs are found in mitochondrial DNA?

A

approx. 16500

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6
Q

Where is mitochondrial DNA inherited from?

A

The mother exclusively

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7
Q

How many genes are found on mitochondrial DNA?

A

37

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8
Q

What percentage of genes code for proteins?

A

<2%

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9
Q

What percentage of genes are coding (exons)?

A

<2%

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10
Q

What percentage of the DNA sequence is introns (non-coding segments)?

A

20%

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11
Q

What percentage of the human genome has unknown function?

A

20%

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12
Q

What does SNPs stand for?

A

Single Nucleotide Polymorphisms.

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13
Q

What are SNPs?

A

Nucleotide sites that commonly vary within populations.

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14
Q

What distinguishes an SNP from a mutation?

A

If a particular combination has more than 1% prevalence in the population, it is considered at SNP.

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15
Q

What is the prevalence of SNPs in the human genome?

A

1 in 300 base pairs.

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16
Q

Where do SNPs mainly originate from?

A

Inheritance from parents, as opposed to just mutation.

17
Q

What is a linked SNP?

A

An SNP that is outside a gene, and has no effect on protein production or function.

18
Q

What are causative SNPs?

A

SNPs found in a gene.

19
Q

What are non-coding SNPs?

A

causative SNPs of a gene that change the amount of proteins produced.

20
Q

What are coding SNPs?

A

Causative SNPs that change amino acid sequence, and therefore the protein coded for by the gene.

21
Q

Why is there greatest genetic variation in the African Continent, compared to the rest of the world?

A

The rest of the world’s populations evolved from a bottle-neck population that migrated from Africa - the ‘founder effect.’

22
Q

What does STRs stand for?

A

Short Tandem Repeats

23
Q

What are STR?

A

repeats of 2-5 nucleotides, found in specific regions of the genome. In each allele, there are many different possible numbers of repeats possible. You may inherit an allele with a different number from each parent.

24
Q

What are InDels?

A

Small insertions or deletions in DNA that can cause ‘frame shift’ which changes the way DNA is read in protein coding regions.

25
Q

What does CNVs stand for?

A

copy number variations

26
Q

What are CNVs?

A

Chunks of DNA greater than 500 base pairs long that are present at different amounts or ‘copy numbers’ relative to a reference
genome. (More or fewer of a certain type of segment).

27
Q

How many CNVs do humans have?

A

10,000 within and between genes.

28
Q

Are CNVs exclusive to single genes?

A

No - they can span multiple genes.

29
Q

The human genome project showed that what percentage of genes code for proteins?

A

Less than 2%