Week 8 - Genetics Flashcards

1
Q

What are some relevant nursing actions?

A
  • Standard (social) and aseptic (procedural) hand washing.
  • Personal protective equipment (protection against DNA or RNA viral infections).
  • Genetic counselling
  • Pharmacogenetics
  • Administration of prescribed antibiotics.
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2
Q

What is Sex Chromosomes?

A

Determine maleness /femaleness

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3
Q

What is Genotype?

A

Genetic makeup (DNA sequence)

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4
Q

What is Phenotype?

A

Expression of a genetic trait / characteristic (showing)

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5
Q

What is Alleles?

A

Genes for the same trait that may have different expressions

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6
Q

What is Homozygote?

A

Individual who has identical alleles for a trait

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7
Q

What is Heterozygote?

A

Individual who has different alleles for a trait

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8
Q

What is Dominant?

A

Allele that masks the expression of a less potent allele

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9
Q

What is Recessive?

A

Less potent allele; expressed only in homozygote

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10
Q

What is Centromere?

A

Narrowest region of a chromosome

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11
Q

What is Telomere?

A

Found on both ends of a chromosome

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12
Q

State the number of chromosomes in the nucleus of most human cells

A

46 (23 pairs, one set from each parent)

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13
Q

Identify in which phase of meiosis I and II could a chromosome separation error occur

A
  • Anaphase 1 or 2
  • Chromosomal non-dysfunction, where chromosome pair or chromatid pair not separated
  • Results in wrong number of chromosomes (or chromatids) in sex cells (eggs, sperm)
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13
Q

Once meiosis has been completed, the genetic information in the FOUR new cells is not the same. Describe the three sexual processes that facilitate this genetic diversity

A
  • Genetic recombination (Prophase 1)
  • Independent assortment (Metaphase 1)
  • Random fertilisation
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14
Q

Name the phase of meiosis in which the DNA is replicated so that each chromosome becomes composed of two chromatids

A

Interphase

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15
Q

Explain why men are more likely to have red-green colour blindness and haemophilia

A
  • Women have two X chromosomes, men have one
  • Men have no second chance of inheriting a normal allele if they have one abnormal allele on their X chromosome.
16
Q

Name the phase of meiosis in which the DNA is exchanged between the paternal and maternal chromosomes

17
Q

Identify the major role(s) of meiosis II

A

Split each chromosome (of two chromatids) into two separate chromatids (=chromosomes)

17
Q

Name the phase of meiosis in which the independent assortment of paternal and maternal chromosomes take place

18
Q

State five statements about genetics

A
  • Chromatids, telomeres and centromeres are terms associated with chromosomes
  • Sequence of nitrogenous bases in DNA codes for the sequence of amino acids in proteins
  • Meiosis introduces genetic variability and halves the chromosome number
  • Most traits are determined by the interaction of multiple genes
  • A genotype does not always produce the expected phenotype
19
Q

State five statements about inheritance

A
  • Dominant alleles mask the expression (protein production) of recessive alleles
  • A heterozygote has a different allele for a certain trait (characteristic)
  • Mitochondria possess multiple copies of a circular chromosome
  • Epigenetics markers are chemical tags on DNA that influence gene expression
  • The number of microbiota genes far exceeds the number of human genes
20
Q

DNA in the human body includes that of the nucleus, mitochondria and microbiota. The ratio of microbial to human genes is _____ to one.

21
Q

A disruption to the microbiota is known as _____.