B12 Flashcards

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1
Q

Genome

A

The entire set of genetic material in tan organism

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2
Q

Human genome uses

A

Allows scientists to identify genes in the genome that are linked to different types of disease, knowing these help us develop effective treatments for them
Can trace the migration of certain populations of people around the world. Different populations of people developed tiny differences in their genomes when they migrated away from Africa, which can be investigated using genomes.
Can make many different proteins from the same gene by using it in different ways , or by switching part of a gene on and off

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3
Q

Where do you inherit your mitochondrial DNA from?

A

Your mother, because it comes from the mitochondria in the egg

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4
Q

Disadvantages of human genome

A

Understanding it has taken years of work and billions of pounds

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5
Q

Where does meiosis occur in humans?

A

Only in the reproductive organs(ovaries in females and testes in males)

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6
Q

Process of meiosis

A

1) Before the cell begins to divide, it duplicates its genetic information, forming two armed chromosomes which then arrange themselves into pairs.
2) In the first division in meoisis the chromosome pairs line up in the centre of the cell.
3) The pairs are pulled apart so each new cell only has one copy of each chromosome.
4) In the second division, the chromosomes line up again in the centre of the cell. The arms of the chromosomes are pulled apart.
5) You get four gametes, each with only a single set of chromosomes in it. Each of the gametes is genetically different from the others, since chromosomes are shuffled up in meiosis and each gamete only gets half of them, at random.

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7
Q

What happens to the cell produced by gamete fusion?

A

1) After two gametes have fused during fertilisation, the resulting new cell divides by mitosis to make a copy of itself.
2) Mitosis repeats many times to produce lots of new cells in an embryo.
3) As the embryo develops, these cells start to differentiate into the different types of specialised cell that make up a whole organism.

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8
Q

Which pair of chromosomes decides sex?

A

The 23rd pair - labelled XY(male) or XX(female)

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9
Q

Which chromosome causes male characteristics?

A

The Y Chromosome

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10
Q

Which chromosome causes female characteristics?

A

The X Chromosome

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11
Q

What happens to the X and Y chromosomes when making sperm?

A

When making sperm, the X and Y chromosomes are drawn apart in the first division in meiosis. There’s a 50% chance each sperm cell gets an X-chromosome and a 50% chance it gets a Y-chromosome.

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12
Q

Characteristics controlled by a single gene

A

Mouse fur colour
Red-green colour blindness in humans

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13
Q

How many alleles of every gene in your body do you have?

A

You have two alleles of every gene in your body - one on each chromosome in a pair

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14
Q

Cystic fibrosis

A

A genetic disorder of the cell membranes. It results in the body producing a lot of thick sticky mucus in the air passages and in the pancreas. Caused by a recessive allele

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15
Q

Polydactyly

A

A genetic disorder where a baby’s born with extra fingers or toes - but isn’t life-threatening. Is caused by a dominant allele.

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16
Q

Emrhyonic screening

A

Involves undergoing tests to discover if a person/embryo/foetus has a genetic disorder or is carrying a faulty allele

17
Q

Disadvantages of embryonic screening

A

1)Is expensive.
2) Maybe everyone may want to screen their embryos so they can pick the most ‘desirable’ one e.g. they want a blue-eyed, blond-haired, intelligent boy.
3) An IVF embryo(a potential life) might be destroyed if alleles causing a genetic disorder are found in its genes
4) Tests might not be reliable

18
Q

Advantages of embryonic screening

A

1) Helps stop people suffering.
2) Treating disorders costs the Government(and the taxpayer) a lot of money.
3) There are laws to stop it going too far. At the moment, parents can’t even select the sex of their baby(unless it’s for health reasons).

19
Q

Genetic screening methods

A

Amniocentesis
Chorionic villus sampling
Analysing foetal cells found in the mother’s bloods

20
Q

Pre-natal testing

A

Used to analyse an individual’s DNA or chromosomes before they’re born, can’t detect all inherited disorders

21
Q

Neo-natal testing

A

Used just after a baby has been born, designed to detect genetic disorders that can be treated early

22
Q

How many base pairs/genes are in the human genome?

A

The human genome contains over 3 billion base pairs and almost 21000 genes that code for proteins.

23
Q

Evidence of two organisms being the same species

A

Similar genotype/DNA
Same/similar phenotype
Can breed and produce fertile offspring

24
Q

organisms involved in asexual reproduction

A

Bacteria
Strawberry plant
Daffodils
Smallest plants

25
Q

Organisms reproducing sexually and asexually

A

Malarial parasites produce asexually in the human host, but sexually in the mosquito.
Many fungi reproduce asexually by spores, but also reproduce sexually to give variation.
Many plants produce seeds sexually, but also reproduce asexually by runners such as strawberry plants, or bulb division such as daffodils.
Daffodils reproduce asexually, growing from bulbs. New bulbs can grow from the main one, producing a new identical plant.

26
Q

Advantage of organisms reproducing sexually and asexually

A

It means plants can reproduce even if the flowers have been destroyed by frost or other animals

27
Q

Where does mitosis occur?

A

All body cells except gametes

28
Q

When sperm and egg cells fertilise to produce a new cell, how many chromosomes are in that new cell?

A

46

29
Q

Fusion of gametes in plants(sexual reproduction)

A

Sex cells fertilise to form a seed