Inheritance Flashcards

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1
Q

what is sexual reproduction? (3)

A
  • the fusion of male and female gametes
  • the offspring receives genetic information from both the male and female parents
  • every gamete is different, which means there’s variation in the offspring
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2
Q

what is asexual reproduction? (3)

A
  • only one parent is involved so there’s no fusion of gametes and no mixing of genetic information
  • all offspring are genetically identical because all the gametes are the same
  • only involves mitosis
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3
Q

where does meiosis take place?

A

in the reproductive organs

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4
Q

what is the meiosis process? (3)

A
  1. dna replication
    - the cell duplicates its genetic information, forming ‘two-armed’ chromosomes
    - each ‘arm’ is an exact copy of the other
    -after replication the chromosomes arrange themselves into pairs
  2. first division
    - the chromosomes line up in the centre of the cell
    - they are then pulled apart so each new cell has only one copy of each chromosome
  3. second division
    - chromosomes line up again in the centre of the cell, where the two ‘arms’ are pulled apart
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5
Q

what is the end product of meiosis?

A

four non-identical daughter cells are produced and the chromosomes in these cells are now single - at the beginning, they were in pairs

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6
Q

what happens after fertilisation?

A

the new cell divides by mitosis, producing a clump of identical cells (an embryo)

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7
Q

what is DNA? (3)

A
  • contained within chromosomes
  • determines our inherited features
  • consists of two strands
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8
Q

what is the name of the structure of DNA?

A

double-helix structure

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9
Q

define gene

A

a small section of DNA on a chromosome

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10
Q

what does each gene do?

A

encodes for a specific sequence of amino acids to make a specific protein

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11
Q

define genome

A

the entire genetic material of an organism

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12
Q

define human genome

A

the entire genetic material that makes a human

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13
Q

what are the benefits of scientists studying the entire human genome? (3)

A
  • helps us to search for genes that are linked to certain diseases
  • helps us to understand and treat inherited disorders
  • can use the human genome to trace human migration patterns
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14
Q

define allele

A

versions of a gene

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15
Q

define genotype

A

tells us the allele’s present

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16
Q

define phenotype

A

tells us the characteristics/features of a person based on their alleles

17
Q

define homozygous

A

a person that has two copies of the same allele

18
Q

define heterozygous

A

a person that has two different allele’s

19
Q

in which case would a recessive allele be shown in the phenotype of a person?

A

if there’s two of them (ee, ff, cc)

20
Q

what is cystic fibrosis

A

a disorder of cell membranes

21
Q

which allele’s must a person have in order to have cystic fibrosis?

A

two copies of the defective cell membrane allele (cc)

22
Q

which allele’s must a person have to count as a carrier of cystic fibrosis?

A

one defective allele and one normal allele (Cc)

23
Q

what is polydactyly

A

extra fingers or toes

24
Q

what is polydactyly caused by?

A

a dominant allele

25
Q

define embryo screening

A

in which an embryo is tested to see if they have the allele’s for inherited disorders

26
Q

what is the advantage and disadvantages (2) of embryo screening?

A

ADVANTAGE
scientists may be able to correct faulty allele’s and use this to treat inherited disorders

DISADVANTAGES

expensive - people believe the money should be spent elsewhere in the health service

unethical - some healthy embryos are destroyed; there’s a possibility that in the future we may be able to produce offspring with desire-able features through screening