inheritance Flashcards

1
Q

Define chromosomes

A

Chromosomes are made of DNA; which contains genetic information * in the form of genes.

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2
Q

Define gene

A

length of DNA
* that codes for a protein

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3
Q

Define allele

A

alternative form of gene!

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4
Q

what does sex determination depend on?

A
  • All eggs have one X chromosome.
  • However a sperm can have either X or Y chromosome.
  • Therefore sex determination depends on whether the sperm that fertilizes the egg carries a Y or X chromosome.
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5
Q

what determines the sequence of amino acids used to make a specific protein?

A
  • sequences of bases in a gene
  • different sequences of amino acids give different shapes to protein molecules
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6
Q

How does DNA control cell function?

A
  • controlling the production of proteins
    including enzymes, membrane carriers & receptors for neurotransmitters
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7
Q

Explain how a protein is made

A
  • the gene coding for the protein remains in the nucleus
  • messenger RNA (mRNA) is a copy of a gene
  • mRNA molecules are made in the nucleus and move to the cytoplasm
  • the mRNA passes through ribosomes
  • the ribosome assembles amino acids into protein molecules
  • the specific sequence of amino acids is determined by the sequence of bases in the mRNA
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8
Q

Are all proteins made in all cells?

A

no.
most body cells in an organism contain the same genes, but many genes in a particular cell are not expressed
* because the cell only makes the specific proteins it needs

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9
Q

What’s a haploid nucleus?

A

nucleus containing a single set of chromosomes

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10
Q

What’s a diploid nucleus?

A

nucleus containing two sets of chromosomes

i.e. all body cells except gametes
- One pair of each type of chromosome
- 23 pairs in a human

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11
Q

define mitosis

A

nuclear division giving rise to
genetically identical cells

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12
Q

role of mitosis

A

growth, repair of damaged tissues, replacement of cells and
asexual reproduction

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13
Q

How does mitosis occur?

A

Chromosomes replicate before mitosis occurs
- Copies of chromosomes separate
- Chromosome number is maintained in each daughter cell

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14
Q

define stem cells

A
  • unspecialised cells that divide by mitosis
  • to produce daughter cells
  • that can become specialised for specific functions
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15
Q

define meiosis

A
  • reduction division in which the chromosome number is halved from diploid to haploid
  • resulting in genetically different cells
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16
Q
A
16
Q

Role of meiosis

A
  • involved in production of gametes
  • takes place in testes/ovaries
17
Q

why is meiosis known as reductive division?

A
  • Chromosome number is halved (from diploid to haploid)
  • Results in genetically varied daughter cells
  • New combinations of maternal and paternal genes made
18
Q

define inheritance

A
  • the transmission of genetic information
  • from generation to generation
19
Q

define genotype

A
  • Genetic make-up of an organism
  • i.e. which alleles are present in the organism’s genome
20
Q

define phenotype

A

observable features of an organism

21
Q

homozygous

A
  • having 2 identical alleles of a particular gene
22
Q

what happens when 2 homozygous individuals?

A

it’ll be pure-breeding

23
Q

define heterozygous

A

having 2 different alleles of a particular gene

24
Q

define dominant allele

A
  • an allele that is expressed
  • if it is present in the genotype
25
Q

define recessive allele

A
  • an allele that is only expressed
  • when there’s no dominant allele
  • of the gene present in the genotype
26
Q

what’s codominance

A
  • situation in which both alleles in heterozygous organisms
  • contribute to the phenotype
27
Q

Explain the inheritance of ABO blood groups

A
  • phenotypes are A, B, AB and O blood groups
  • alleles are IA, IB and Io
28
Q

What’s a sex linked characteristic

A
  • a feature in which the gene responsible is located on a sex chromosome
  • and that this makes the characteristic more common in one sex than in the other
29
Q

give an example of sex-linkage

A
  • red-green colorblindness
30
Q

what’s test cross used for

A
  • To identify the genotype of an organism showing the dominant phenotype
31
Q

hows test cross carried out

A

Cross the unknown individual with individual showing recessive phenotype
- Offspring either 50% dominant and 50% recessive OR all dominant
- If any offspring have recessive phenotype → unknown individual was heterozygous
- If no offspring have recessive phenotype → unknown individual was homozygous

32
Q

Why are sex-linked diseases usually associated with the X chromosome?

A
  • Y chromosome is much shorter than the X chromosome
  • Comparatively few genes exist on the shorter Y chromosome
33
Q

Why are X-linked dominant traits more common in females?

A
  • Females have two X chromosomes = two alleles
  • Either allele may be dominant and cause disease
  • Can be either homozygous or heterozygous
34
Q

Why are X-linked dominant traits more common in males?

A

Males have only one X chromosome = one allele
- Condition cannot be masked by a second allele

35
Q

For sex-linked diseases:

A
  • Only females can be carriers
  • Males always inherit X-linked trait from mother
  • Females cannot inherit X-linked recessive condition from unaffected father