Cell division, inheritance and genetics Flashcards

1
Q

Define the term inheritance

A

Inheritance is the passage of hereditary traits from one generation to another

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2
Q

Define the term Genetics

A

Genetics is the branch of biology that deals with inheritance

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3
Q

Define the term Genotype

A

Genotype if the genetic makeup of an individual E.g. Pp

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4
Q

Define phenotype

A

Phenotype if the physical characteristics determined by the genotype and the environment E.g. brown hair, blue eyes

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5
Q

Define the term mutation

A

A mutation is a permanent, heritable change in a gene that causes it to have a different effect than it has previously

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6
Q

Define the term “Autosome”

A

A normal chromosome that is not a sex chromosome: in humans, one of the 22 oher pairs

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7
Q

Define X-linked (sex) chromosomes

A

a chromosomes concerned in determining the sex of a person

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8
Q

Explain what is meant by dominant and recessive alleles

A
  • dominant alleles is an allele that is always expressed, or evident, in a person. it does this by overriding the influence of the corresponding allele on the other homologous chromosomes E.g. Pp a dominant allele can show up and a homozygous (PP) or heterozygous (Pp)
  • recessive alleles is an allele that is completely hidden or masked by the presence of a dominant allele. A recessive allele is only expressed when no dominant allele is present E.g. pp (homozygous recessive)
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9
Q

Explain Autosomal dominant dominant genetic conditions and give an example of a condition

A
  • Pp
  • caused by mutation of a single gene on a chromosome
  • one heterozygous parent will have a 50% chance o having a child with the disease
  • E.g. huntington’s disease
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10
Q

Explain Autosomal recessive genetic conditions and give an example of a condition

A
  • pp
  • caused by mutation of two gene pairs on a chromosome
  • E.g. cystic fibrosis
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11
Q

Explain X-linked recessive genetic conditions and give an example of a condition

A
  • caused by a mutation on the X chromosome
  • more common in men as have only one X chromosome
  • E.g. colorblindness and hemophilia
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12
Q

Define multiple allele inheritance and give on example of a genetic trait carried by this type of inheritance

A
  • Three or more alternative forms of a gene (allele) that can occupy the same ocous.
  • However, only two of the alleles can be present in a single organism. For example, the ABO system of blood groups is controlled by three alleles, only two of which are present in an individual
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13
Q

Define complex inheritance and give one example of a genetic trait carried by this type of inheritance

A
  • Most inherited traits are not controlled by one gene but by:
  • the combined effects of two or more genes or
  • combined effects of many genes and environmental factors E.g. skin colour, hair colour, height, body weight, build and metabolism rate.
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14
Q

Explain why many X-linked conditions primarily affect males

A
  • genes for X-linked traits appear on X chromosomes, bu many of them are absent from Y chromosomes.
  • primarily affect males because there are no counterbalancing dominant genes on the Y chromosomes
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15
Q

Explain the term Trisomy and give an example

A
  • a Trisomy is a type of polysomy in which there are three instances of the particular chromosome, instead of the normal two.
    (2n+1) has an extra chromosome (trisomy)
  • E.g. downs syndrome
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16
Q

Explain the term Monosomy and give an example

A
  • Monosomy is when a diploid organism has only one copy of one of its chromosomes instead of two
  • (2n-1) is missing a chromosome (monosomy)
  • E.g. turners syndrome
17
Q

What are the functions of the Nucleus?

A
  • stores DNA, contains the information needed to make proteins
  • controls cellular structure
  • directs cellular activities
  • produced ribosomes
18
Q

What are the contents of a nucleus?

A
  • Nucleoli

- genes- genes are arranged along Chromosomes

19
Q

What is an allele?

A
  • alleles are alternative forms of genes
20
Q

What are homozygous alleles?

A

-homozygous alleles have identical information for a trait

21
Q

What are heterozygous alleles?

A
  • heterozygous alleles have different information for a trait
22
Q

name two different types of cell division

A
  • somatic cell division and reproductive cell devision
23
Q

Describe somatic cell division

A
  • The aim is to replicate cells to replace dead or injured cells or add new cells during growth
  • occurs through mitosis and cytokinesis
  • the end product is 2 identical diploid cells with 46 chromosomes
  • occurs in somatic (regular) body cells
  • mutation that occurs in somatic division are not passed onto offspring
24
Q

Describe reproductive cell division

A
  • aim to produce the gamete cells (sperm and oocyte) required for the next generation.
  • occurs through meiosis
  • occurs only in sex cells
  • end product is 4 different haploid cells (gametes) with 23 chromosomes each.
25
Q

Explain how genetic variation occurs

A

crossing over increases genetic variation
- occurs in meiosis

  • the exchange of genes between homologous ( paired chromosome
26
Q

Define cancer

A

cancer is a group of diseases that results from uncontrolled or abnormal cell proliferation
- uncontrolled cell division results in excess tissue called a tumor ( or neoplasm)

27
Q

What is a malignant tumor?

A

malignant tumors undergo metastasis (the spread of cancerous cells to other parts of the body)

28
Q

What is a benign tumor?

A
  • benign tumors do not metastasis ( they do not spread)
29
Q

Name the type of cancer that arises from epithelial tissue

A

carcinoma

30
Q

Name the type of cancer that arises from melanocytes

A

melanoma

31
Q

Name the type of cancer that arises from lymphatic tissue

A

lymphoma

32
Q

Name the type of cancer that arises from leukocytes

A

leukaemia

33
Q

State 3 causes of cancer

A
  • Environmental agents ( e.g. chemical and radiation, these chemicals and radiation are called carcinogens and include: cigarette tar, radon gas and UV light)
  • Viruses (e.g. human papillomavirus (HPV) cause cervical cancer by stimulating abnormal proliferation of cells)
  • Genes (abnormalities of the genes that control and regulate cell division