Introduction to genetic traits Flashcards

(45 cards)

1
Q

Where is DNA found?

A

In the nucleus

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2
Q

What acid is present in DNA?

A

Nucleic acid?

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3
Q

What is DNA?

A

molecule containing the genetic code of an organism, it determines inheritance (heredity)

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4
Q

Describe DNA in different cells around the body

A

Almost every cell in the human body has the same DNA

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5
Q

The DNA nucleotide is made up of what 3 parts?

A

5-carbon deoxyribose unit (a sugar)
phosphate group
nitrogenous base

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6
Q

What 4 types of nucleotide subunit make up DNA?

A

Adenine (purine)
Thymine (pyrimidine)
Guanine (purine)
Cytosine (pyrimidine)

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7
Q

DNA is composed of two what?

A

Complementary DNA strands made up of nucleotides

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8
Q

The DNA strands are held together by what?

A

Hydrogen bonds between the nitrogenous bases of the nucleotides.

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9
Q

What forms the DNA backbone?

A

Alternating deoxyribose and phosphate units

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10
Q

How many H bonds bind A and T?

A

2

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11
Q

How many H bonds bind G and C?

A

3

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12
Q

The two DNA strands form what?

A

A double helix

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13
Q

Describe down syndrome

A

aka trisomy 21
additional copy of chromosome 21
individuals have 47 chromosomes
Example of aneuploidy - anything other than diploid number of chromosomes
caused by errors in or failure of chromosomes to separate during meiosis = non-disjunction
characteristics: learning difficulties, distinctive physical features, congenital heart disease

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14
Q

Klinefelter syndrome

A

XXY genotype
Characteristics: Long limbs, reduced testosterone, reduced fertility, learning difficulties

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15
Q

Where are chromosomes found?

A

In the nucleus

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16
Q

What are nucleosomes?

A

DNA wrapped around histones

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17
Q

What forms fibres of chromatin?

A

Nucleosomes coiled together

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18
Q

What forms chromosomes?

A

CHROMATIN FOLDED WITH THE HELP OF PROTEINS

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19
Q

Why is DNA packaged?

A

Allows it to fit inside the nucleus and prevents damage during cell division

20
Q

What are the chromosomes 1-22

21
Q

What are chromosomes 23

A

Sex chromosomes

22
Q

What is a trait?

A

Specific characteristic of an organism

23
Q

What is the karyotype?

A

The particular collection of chromosomes an individual has

24
Q

What is each pair of autosomes referred to as?

A

Homologous chromosomes
They are the same size and contain comparable genes for the same characteristics
However, the genes may not be identical

25
What is an allele?
Term used to describe different forms of the same gene
26
What is genetics?
The study of genes and variation in the inheritance of traits
27
What is inheritance?
Passing of traits from parents to offspring. Also known as heredity
28
What are traits?
Specific characteristics of an organism Determined by interaction between genes and the environment
29
What is a gene?
Section of DNA which when copied to mRNA codes for the production of a protein. DNA copied to mRNA via transcription mRNA gives rise to protein via process of translation.
30
What is the central dogma of molecular biology?
States that genetic information flows in a specific direcion: DNA -> mRNA -> Proteins
31
What are structural genes?
Code for proteins via transcription and translation
32
What are regulatory genes?
Control for structural genes
33
What is a mutation?
Any alteration to the structure of a gene some good, some bad produces genetic variation can cause ageing, disease mutations in germ cells can result in transmission of mutation to offspring
34
Genotype
Genetic aspect contributing to a trait
35
Phenotype
How traits appear as a result of interaction between genes and environment observable traits e.g. hair colour
36
Alleles
Different forms of the same gene
37
Locus
The particular (fixed) location of a gene on a chromosome
38
Dominant
Demonstrated or takes precedence in the body and the phenotype
39
Recessive
Alleles masked by dominant allele and are not displayed in phenotype
40
Co-dominance
Both alleles of equal dominance e.g. AB blood group
41
Autosomal dominant inheritance
Only one copy of mutated dominant allele needed to cause disease. Therefore not possible to be a carrier
42
Autosomal recessive inheritance
Two copies of mutated recessive allele are required to cause disease X-linked recessive - linked to female X chromosmes
43
Single gene inheritance
Gene altered by one nucleotide and this single nucleotide change alters one amino acid. aka single point genetic condition e.g. huntingtons disease
44
Polygenic inheritance
Phenotype is a result of several genes Results in a wide range of phenotypic variation e.g. height, eye colour, hair colour, weight
45
Multifactorial inheritance
Combined effect of more than one gene and environmental variables determine phenotype wide range of phenotypic variation e.g. skin, personality, inteligence e.g. alzheimers = genetic element + head injury e.g. asthma = genetic element + environmental triggers