Mechanisms of Hereditary Flashcards

1
Q

what are monohybrid crosses?

A

parents differ in only one trait (phenotype)

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2
Q

what are the 5 properties of peas that made it very useful for studying genetics?

A
  1. binary traits (2 possible phenotypes)
  2. short generation time
  3. easy to grow
  4. produces lots of offspring
  5. self-fertilise
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3
Q

what are true breeding parents?

A

crosses that results in all offspring having the same phenotype as parents

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4
Q

how did mendel know that parents contribute equally to offspring?

A

reciprocal crosses gave identical results

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5
Q

what is the principle of segregation?

A

two alleles for each trait segregate during gamete formation and then unite randomly at fertilisation

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6
Q

when do we use the product rule of probability?

A

gamete formation

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7
Q

when do we use the sum rule of probability?

A

after gametes fuse

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8
Q

what does it mean if the p value is greater than 0.05?

A

the null hypothesis cannot be rejected, thus there is no significant difference in expected vs observed values

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9
Q

what does it mean if the p value is less than 0.05?

A

the null hypothesis is rejected, and there is a significant difference between the predicted and observed ratios

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10
Q

what are the 5 non mendelian types of inheritance?

A
  • domanince is incomplete
  • lethality
  • phenotype determined by multiple genes and interaction between them
  • sex-linkage
  • linkage
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11
Q

what is complete dominance

A

when you only see the dominant phenotype in 1st generation

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12
Q

what is co dominance?

A

when the offspring show two traits (e.g. blood types)

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13
Q

what is incomplete dominance?

A

when a new phenotype occurs that doesnt look like either of the parents

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14
Q

what is lethality (non mendelian inheritance)

A

an allele or specific genotype leads to death or non-viablity of organism

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15
Q

what are complementation tests?

A

way to determine whether 2 mutants (with the same phenotype) are defective in the same gene or in different genes

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16
Q

what does it mean if you cross two mutants together and see a mutant phenotype in the F1 generation?

A

mutants are defective in the same gene

17
Q

what does it mean if you cross two mutants together and see a wild type phenotype in the F1 generation?

A

mutants are defective in different genes

18
Q

what is a complementation group?

A

a group of mutations that are all defective in the same gene, the groups dont complement one another

19
Q

what do complementation groups tell you about the number of genes the mutants are defective in

A

nr of comp groups = nr of different genes mutants are defective in

20
Q

what is recessive epistasis?

A

homozygosity for a recessive allele at one locus masks genotype at a second locus (e.g. recessive allele determines whether pigment is deposited or not)

21
Q

what is dominant epistasis?

A

having a dominant allele mask the phenotype coded by the second allele

22
Q

what is the expected phenotypic ratio of recessive epistasis?

A

9:3:4

A-B- : aaB- : A-bb + aabb

23
Q

what is the expected phenotypic ratio of dominant epistasis?

A

12:3:1

A-B- + aaB- : A-bb : aabb

24
Q

what is penetrance?

A

% of individuals with phenotype

25
what is the difference between mitosis and meiosis
in mitosis there is one round of nuclear division but in meiosis there are two rounds of nuclear division
26
what is a barr body?
an inactivated X chromosome that ensures dosage compensation between males & females
27
what makes humans bad for experiments?
* long lifespan * small nr of offspring (chance plays larger role) * ethics * can't self fertilise * most of our traits are multi genic
28
what clues should we look for on a pedigree to determine if the disease is x-linked recessive?
* M >> F * skips a generation
29
what clues should we look for on a pedigree to determine if the disease is x-linked dominant?
* F >> M * is found in all generations
30
what clues should we look for on a pedigree to determine if the disease is autosomal dominant ?
* equally in males and females * in every generation
31
what clues should we look for on a pedigree to determine if the disease is autosomal recessive?
* equally in males & femaes * skips a generation
32
what is sry
sex determining region of y - drives male development and kicks off signalling cascades to lead to production of male sex hormones