4. Genetics Flashcards

1
Q

What is evolution

A

darin’s theory of natural selection of traits associated with higher rates of survival (fitness)
Social dominance to pass on important characteristics (males) and to produce more and healthier offspring (females)
Different types of mate bonding to increase chances of passing on important characteristics

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2
Q

what questions are involved in the dichotomy of thinking?

A

is it biological and psychological?
Is it nature or nurture?
Is it inherited or learned?

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3
Q

what is the complex process of interaction of genes and environment?

A
  1. evolution influences the pool of behaviour-influencing genes available to members of each species
  2. Experience modifies the expression of an individual’s genetic program
  3. Each individual genes initiate a unique program of neural development
  4. Each individual’s genes initiate a unique program of neural development
  5. Each individual’s current behavioural capacities and tendencies are determined by its unique patterns of neural activity, some of which are experienced as thoughts, feelings, memories, etc
  6. Each individual’s current behaviour arises out of interactions among its ongoing patterns of neural activity and its perception of the current situation
  7. the success of each individual’s behaviour influences that likelihood that its genes will be passed on to future generations
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4
Q

Menelian Genetics

A

Mendel studied dichotomous traits in true-breeding lines of pea plants.
Dichotomous traits - occur in one form or another, never in combination
True-breeding lines: interbred members always produce offspring with the same trait

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5
Q

what was step 1 in Mendel’s findings?

A

In the first experimental step, all offspring plants had brown seeds
one parent had two brown seed genes the other had two recessive white seed geners. thus all offspring had one brown and one white gene. Because brown dominant they all had brown seeds
the dominant gene therefore overwrites the recessive gene

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6
Q

What was step 2 of mendel’s findings?

A

A cross between the first generation offspring, 75% of the offspring had brown seeds and 25% with white

each parent had one brown gene and one white gene. therefore 25% of offspring had two brown genes, 50% had one brown and one white and 25% had two white

Since brown genes dominant 75% had brown

the genetic code of the parent plant was mixed - one allele for brown and one allele for white seeds. Hence, 1/4 of the offspring had white seeds (recessive traits show in the homozygous condition of the recessive gene)

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7
Q

Alleles

A

2 genes that control the same trait

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8
Q

homozygous

A

2 identical alleles (BB, ww)

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9
Q

Heterozygous

A

2 different alleles (B,w)

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10
Q

what can genes be?

A

dominant, recessive or intermediate

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11
Q

dominant gene

A

shows a strong effect in either the homozygous or heterozygous condition

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12
Q

recessive gene

A

shoes its effect only in the homozygoys condition

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13
Q

phenotype

A

observable trait

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14
Q

genotype

A

genetic make-up

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15
Q

what are genes a unit of?

A

fundamentally a unit of heredity

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16
Q

what is genetic information carried in?

A

Deoxyribonucleic Acid (DNA) (and RNA)

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17
Q

what does DNA do?

A

DNA is self replicating material that is contained in almost all living organisms.

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18
Q

what is a gene compared to DNA?

A

a gene is a segment of DNA that encodes specific proteins

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19
Q

what does DNA look like?

A

DNA molecules are double strands of nucleotide bases (T, A, G, C) wrapped around each other

A nucleotide (Allele) on strand 1 always pairs with a particular nucleotide on strand 2 (tymine-adenine, guanine-cytosine)

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20
Q

How does DNA fit into the nucleus of a cell?

A

to fit into the nucleus of a cell, DNA is tightly coiled around “spools” (histones). The package of DNA and histones is called Chromatin.. Chromatin gets packed further to form a chromosome. Chromosomes a paired. Chromatid is the exact copy of chromosome during cell devision (sister-chromatid).

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21
Q

chromosomes

A

contain very tightly wound DNA

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22
Q

How many chromosomes to humans have?

A

humans have 23 matched pairs of chromosomes, with an allele on each chromosome (located in same place) 22 autosomes and 1 sex chromosome

23
Q

how do sex chromosomes look?

A

looks different and carry different genes (sex-linked genes)

24
Q

what do sex chromosomes determine?

A

mammalian sex: female (2 X chromosomes) and male (1 X and 1 Y Chromosome)

25
Q

how are sex-linked traits controlled?

A

almost always controlled by X chromosome genes as it is larger and has more genes.

Traits controlled for by X chromosome genes occur more frequently in one sex than the other.

26
Q

dominant traits

A

more likely in females as twice the chance

27
Q

recessive traits

A

less likely in females as they need the recessive gene on both X chromosomes (e.g. colour blindness)

28
Q

what are the two important phases of cell division?

A

meiosis and mitosis

29
Q

meiosis

A

(reproduction and recombination) whereby chromosomes devide and one copy ends up in the produce gamete; genetic recombination happens through cross-obers

30
Q

mitosis

A

(replication) during which the DNA strands unwind, each nucleotide attracts its complementary base (floating in nucleus), making two DNA molecules identical to the original)

31
Q

when can mutation occur?

A

during replication (errors: individual difference)

32
Q

what do genes produce?

A

genes do not directly produce behaviours. Rather they produce proteins that increase the probability that behaviour will develop under certain circumstances

33
Q

What is an example of genes and behaviour?

A

Genetic predisposition to a mental disorder does not mean that you will get the mental disorder. There is usually a complex interplay of environment and presence of several predisposing genes required for the mental disorder to surface.

34
Q

How do we get from gene to behaviour?

A

DNA -> RNA -> Protein -> outcomes such as health, looks, behaviours etc

35
Q

how do genes produce protein?

A

Gene segment of DNA strands unwind
Messenger RNA (mRNA) syntehsiized from DNA (transcription): by attracting complementary nucleotides
mRNA leaves nucleus and attaches to ribosomes in the cell’s cytoplasm
Ribosomes synthesizes protein according to 3-base sequences (codons) of mRNA (translation)
Transfer RNA transfers the amino acid to ribosomes

36
Q

what are used for the regulation of gene expression?

A

Enhancers/Promoters
Transcription factors
Epigenetics

37
Q

Enhancers/producers

A

stretches of DNA that determine whether particular structural genes initiate the synthesis of proteins

38
Q

Transcription factors

A

proteins that bind to DNA and influence the extent to which genes are expressed (e.g. by controlling enhancers)

39
Q

Epigenetics

A

the interaction of environment with the actual gene can regulate gene expression

40
Q

The human genome project

A

Driven by the idea that if we are able to identify variations in the human genome and link it to disease we can easily target medical treatment and be good.
•Development of many new techniques to study human genetics
•Discovery that we only have relatively few genes – 20 000 (same as mice and less than corn)
•Difficulty of discovering that many genes link to disease and that interactions amongst genes are often times hard to sort out. Also, sum of all genetic contribution is often times small.

41
Q

Epigents

A

Relatively recent research area (even though idea was around for a long time)

Epigenetics is the study of all mechanisms of inheritance other than the genetic code and its expression (epigenetics does not change the sequence of your genetic code)

42
Q

what have epigenetic studies found?

A

Epigenetic studies have found mechanisms that modify either the histone (histone remodeling) or the DNA (methylation) and other mechanisms acting on RNA.

43
Q

how can epigenetic changes be induced?

A

Epigenetic changes can be induced by particular experiences (e.g. intense stress)

44
Q

how are epigenetic changes passed?

A

Epigenetic changes can be passed on to other generations (transgenerational epigenetics)

45
Q

epigenetics across the human life span

A

What you experience in your lifetime can modify expression of your genetic code, and these changes can be passed down through the generations.

46
Q

what contributes to epigenetic modulation

A
psychological state
social interactions
alternative medication
therapeutic drugs
microbiome
exercise
financial status
drugs of abuse
Toxic chemicals
disease exposure
Diurnal/Seasonal Correlations
Diet
47
Q

what is the importance of environment for genetics?

A

Several study approaches can help exemplify the importance of environment to genetic predisposition:
•Studies of disorder with particular genetic contribution (e.g. Phenylketonuria)
•Animal models (i.e. selective breeding)
•Twin studies

48
Q

Phenylketonuria (PKU)

A

Neurological disorder characterised by intellectual disability, vomiting, seizures, hyperactivity, irritability, brain damage and strange urinal odours
•Pattern of transmission of PKU suggest single recessive gene disorder
•PKU homozygotes lack phenylalanine hydroxylase
•Environmental factor (diet) can significantly reduce health burden of the disorder

49
Q

what was an animal study conducted on genetics and environmental effects?

A

Rats were trained to run a maze with a food reward when they reached the goal

Step 1: Rats that were more successful running the maze (less mistakes) were bred with each other and those that were less successful (more mistakes) Offspring of successful maze runners were more successful than offspring of unsuccessful maze runners Control: Offspring of successful maze runners reared by unsuccessful maze runners and other way around -> same results

Step 2: Test the two different sets of rats on many different tasks:

  • Rats differed in more than one trait
  • Successful maze running rats were less fearful

Step 3: Expose different sets of rats to different environments (impoverished and enriched)  Maze-dull rats did not make significantly more errors than maze-bright rats when both groups were reared in an enriched environment. (Adapted from Cooper & Zubek, 1958.)

50
Q

what did twin studies show?

A

how we share genetic material with out family.
•50% with mother; 50% with father; 50% with full sibling
•Genetic material between non-identical twins: 50%
•Gene material between identical twins: 100%

51
Q

Minnesota study of twins reared apart

A
  • Identical twins more similar than fraternal twins on all psychological dimensions
  • All children were raised by middle-class, tightly scrutinised families in highly industrialised countries yielding little differences in environment
52
Q

Epigenetic effects in monozygotic and dizygotic twins

A
  • Monozygotic twins are indistinguishable early in life but accumulate different sets of epigenetic marks throughout life span
  • Monozygotic and dizygotic twins accumulate different sets of epigenetic marks in a high concordance rate (i.e. no substantial differences in accumulation between dizygotic and monozygotic twin pairs)
53
Q

Environmental effects in monozygotic twins

A

Heritability estimate for IQ dependent on environmental conditions – similar to maze-bright and maze-dull rats. Enriched environments more important for IQ than inheritance.