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

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
define dominant allele
* an allele that is expressed * if it is present in the genotype
25
define recessive allele
* an allele that is only expressed * when there's no dominant allele * of the gene present in the genotype
26
what's codominance
* situation in which both alleles in heterozygous organisms * contribute to the phenotype
27
Explain the inheritance of ABO blood groups
* phenotypes are A, B, AB and O blood groups * alleles are IA, IB and Io
28
What's a sex linked characteristic
* 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
give an example of sex-linkage
* red-green colorblindness
30
what's test cross used for
- To identify the genotype of an organism showing the dominant phenotype
31
hows test cross carried out
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
Why are sex-linked diseases usually associated with the X chromosome?
* Y chromosome is much shorter than the X chromosome - Comparatively few genes exist on the shorter Y chromosome
33
Why are X-linked dominant traits more common in females?
- Females have two X chromosomes = two alleles - Either allele may be dominant and cause disease - Can be either homozygous or heterozygous
34
Why are X-linked dominant traits more common in males?
Males have only one X chromosome = one allele - Condition cannot be masked by a second allele
35
For sex-linked diseases:
- Only females can be carriers - Males always inherit X-linked trait from mother - Females cannot inherit X-linked recessive condition from unaffected father