1.3 Exam Prep Flashcards

To prepare (45 cards)

1
Q

The different alleles in a population

A

Variation

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2
Q

The physical expression of a trait

A

Phenotype

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3
Q

The combinations of alleles that an organism possesses. Represented with capital letters for dominant, and lowercase for recessive.

A

Genotype

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4
Q

A double-stranded molecule which is made up of nucleotides. This stores the genetic information made to produce the organism.

A

DNA

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5
Q

DNA is made up of these bonded together. These are made up of a phosphate, sugar, and a base

A

Nucleotides

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6
Q

This is a long, thread-like structure made of DNA and proteins that contains genetic information. It helps to organize and protect the DNA, ensuring that genes are passed on during cell division. Humans typically have 46 chromosomes, arranged in 23 pairs.

A

Chromosome

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7
Q

GeneA small strand of DNA which codes for a certain trait.

A

Gene

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8
Q

Where a gene is located on a chromosome

A

Loci

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9
Q

An alternate form of a geneAllele

A

Allele

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10
Q

Two chromosomes with the same genes (one from the sperm, one from the egg) but with potentially different alleles.

A

Homologous Pair

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11
Q

The order of the bases (A,T,C,G) in an allele

A

Base sequence

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12
Q

Permanent change in the DNA base sequence

A

Mutation

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13
Q

Something which causes a mutation

A

Mutagen

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14
Q

A change in the base sequence that doesn’t change the amino acid sequence, so it doesn’t change the protein.

A

Silent Mutation

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15
Q

A permanent change in the DNA base sequence gives the organism a mutation, making survival easier.

A

Beneficial Mutation

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16
Q

A permanent change in the DNA base sequence gives the organism a mutation making survival more difficult.

A

Harmful Mutation

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17
Q

A mutation that is not in a gamete so it cannot be passed down to offspring (meaning it’s somatic)

A

Non-inherited mutation

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18
Q

A cell which isn’t a gamete (sex cell)

A

A cell which isn’t a gamete (sex cell)

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19
Q

A genetically unique sperm fertilizes a genetically unique egg and produces offspring which has a combination of alleles, different from both parents.

A

Sexual Reproduction

20
Q

Where a haploid sperm and haploid egg fuse together to create a zygote.

A

Fertilisation

21
Q

An organism or cell having only one complete set of chromosomes

22
Q

A cell having two sets of chromosomes (one from each parent)

23
Q

A sex cell such as an egg or sperm which unite during sexual reproduction to produce a zygote.

24
Q

A fertilised egg

25
A type of cell division that results in four haploid daughter gametes, each genetically different from each other
Meiosis
26
Exchange of alleles between homologous chromosomes during meiosis. This results in recombined chromosomes with some alleles from the mother and some from the father.
Crossing over
27
When homologous chromosomes line up independently, they create a random order of maternal/paternal chromosomes in the gametes.
Independent Assortment
28
Allele pairs are separated during meiosis so each gamete has only 1 instead of 2 alleles for a trait
Segregation
29
Two of the same alleles for a trait
Homozygous
29
Two different alleles for a trait
Heterozygous
30
An allele that is always shown in the phenotype, which masks the recessive allele.
Dominant allele
31
Alleles will only appear in the phenotype when dominant alleles are absent.
Recessive Allele
32
A tool used to predict inheritance
Punnet Squares
33
Compares something to another
Ratios
34
A tool to show the inheritance of a trait across generations
Pedigree charts
35
When humans decide which individuals breed together
Selective Breeding
36
Individuals with the best alleles in the given environment will survive to reproduce and pass the alleles on. These alleles will then become more common, and those with less-suited alleles are less likely to survive, making the alleles rarer.
Natural Selection
37
Being able to find food and resources to live as long as they can
Survival
38
Something new in the environment (e.g. predator, disease) that influences if certain individuals live or die.
Environmental Change
39
Closely related individuals having offspring
Inbreeding
40
A reduction in the ability to survive and reproduce due to inbreeding, as well as reduced variation.
Inbreeding depression
41
Figuring out what the sequence of bases is for a gene.
DNA Sequencing
42
Testing an individual to see if they have a specific sequence of bases (or genes)
DNA screening
43
Matching an individual’s genetic markers to another individual to see how they are related to each other.
DNA profiling
44
Using a genetic marker/base sequence/gene that only occurs in one species to see whether an unknown individual is that species or not.
DNA barcoding