A3.1 - diversity of organisms Flashcards

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1
Q

centromere

A

a structure on a chromosome that links the two chromatids

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2
Q

diploid

A

a body cell containing pairs of chromosomes

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3
Q

genome

A

all the genetic information of an organism

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4
Q

homologous pair

A

chromosomes that are the same size, having the same genes present at the same location, but with differing alleles

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5
Q

alleles

A

different versions of a gene

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6
Q

nomenclature

A

a system of naming

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7
Q

single-nucleotide polymorphism

A

a position where individual organisms within a species have a different base to each other

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8
Q

speciation

A

the splitting on one species into two or more

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9
Q

Why is variation considered a defining feature of life?

A
  • no 2 individuals are identical in all their traits
  • patterns of variation are complex and are the basis of naming and classifying organisms
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10
Q

What is binomial nomenclature and how are species named using this?

A
  • Every species is given a binomial name.
  • The first part identifies the genus (written with a capital letter) and the second part identifies the species (written with a small letter).
  • It is either written in italics or underlined.
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11
Q

What is the morphological concept of species?

A

Species - a group of organisms with shared traits.
- developed by Linnaeus

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12
Q

What is the biological species concept?

A

Species - a group of organisms that can breed to produce fertile offspring.

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13
Q

What are the 5 limitations of the biological species concept?

A
  1. Not all individuals in a species may be fertile, resulting in a false negative.
  2. May not be possible to see if two individuals can interbreed due to their extinct nature, inability to survive in captivity or inability to accurately track organisms.
  3. Definition doesn’t apply to organisms that reproduce asexually as they do not interbreed.
  4. Hybrids (resulting from parents of closely related species) are infertile.
  5. Arbitrary decision whether 2 populations are regarded as same or different species at a given time during speciation.
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14
Q

How can speciation occur?

A
  • populations becoming more and more different in their traits
  • gradual decline in the success rate of interbreeding
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15
Q

What is the genetic definition of species?

A

Individuals in a species have the same chromosome number and the same types of chromosomes which have the same sequence of genes.

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16
Q

What is the ecological niche definition of species?

A

Group of organisms based on where they live, eat and the molecules they produce.

17
Q

Why do species in the same genus have similar traits to each other?

A
  • similar DNA (sequence) / genome
  • common ancestry
18
Q

What is a genome?

A

all the genetic information of an organism

19
Q

Why are individuals of the same species more similar than those of another species?

A
  • They have the same number of chromosomes and genes in the same location, so share most of their genome.
20
Q

What variation gives diversity in the genome within a species?

A
  • Single-nucleotide polymorphism give some diversity within a species.
21
Q

In what 3 ways does the genome of 2 eukaryotic species differ?

A
  1. Genome size (Gb)
  2. Base sequences / which genes are present
  3. Number of chromosomes
22
Q

What are the chromosomes values for chimpanzees and humans?

A

Humans - 46
Chimpanzees - 48

23
Q

What is whole genome sequencing?

A
  • Determines the sequence of bases present in the whole genome of an organism
24
Q

What are 4 current uses of whole genome sequencing?

A
  1. Research into evolutionary relationships - organisms that share more similar genomes are more closely related.
  2. Searching for genes linked to diseases
  3. Understanding inherited disorders
  4. Tracing human migration patterns
25
Q

Why is whole genome sequencing more accessible than 20 years ago?

A
  • Increasing sequencing speed and decreasing costs allows other uses of genome sequencing.
26
Q

How could whole genome sequencing support personalized medicine in the future?

A
  • Personalised medicine groups people based on their genetic profile and this can be used to predict the effectiveness of particular treatments and to apply ones that are the most effective.
    Advantage - cost-effective and less side effects
    Disadvantage - security of genomic data
27
Q

What is a karyotype?

A

an individuals complete set of chromosomes

28
Q

What is karyotyping?

A

the process of using a karyogram using a karyotype where chromosomes can be collected either with:
1) amniocentesis - taking amniotic fluid that surrounds the fetus
2) chorionic villus sampling - taking tissue from the placenta

29
Q

What is a karyogram?

A

photograph or diagram of homologous pairs of chromosomes that can be analyzed as the chromosomes are arranged in pairs based on size, banding pattern and the position of the centromere.

30
Q

What types of genetic abnormalities could be analyzed using a karyogram?

A
  • missing or extra pieces of chromosomes
  • changes in chromosome number
31
Q

What is the hypothesis on how humans and chimpanzees have evolved to have different chromosome numbers?

A

Chromosome 2 in humans arose from the fusion of chromosomes 12 and 13 with a primate ancestor shared with chimpanzees.

32
Q

What evidence supports the human and chimpanzee hypothesis?

A
  • chromosomes 12 and 13 are the same length as chromosomes 2
  • banding pattern of chromosome 2 matches that of chromosome 12 and 13
  • centromere of chromosome 2 lines up with chromosome 12